1. Bioinformatics and Statistical Genomics
001 : Abdurashitov et al : A physical map of human Alu repeats cleavage by restriction endonucleases 002 : Acharya et al : Prediction of deleterious Human Membrane Transporter Polymorphisms 003 : Ansari et al : ISSPred: Identification of Intein proteins and their Splice Sites 004 : Anurag et al : Unleashing the unstructured proteins as potential drug target: A case study on Mycobacterium Tuberculosis 005 : Anwar : Beyond Next Gen Sequencing: Applying Bioinformatics to Obtain Biological Answers 006 : Basu et al : Using Clusters Of Short Invariant Peptides in PepCluster To Explore Protein Function 007 : Bourque et al : Evolution of the mammalian transcription factor binding repertoire via transposable elements 008 : Brookes et al : GEN2PHEN: An International Effort To Harmonise And Optimise The Databasing Of Gene-Disease Relationships 009 : Bruford et al : The HGNC Database: an essential resource for the human genome 010 : Chandra et al : Flow of information in the M.tuberculosis interactome network: Pathways to drug resistance 011 : Chatterjee et al : Use of Molecular Modelling and QSAR for the design of beta-lactamase inhibitors 012 : De et al : Understanding Wnt cascades through modularization 013 : Dhar et al : Identification of phosphorylation sites and molecular modeling of DICER 014 : Dubey et al : In silico designing of inhibitor against Tin2 for aging 015 : Fulton et al : Unraveling the Regulatory Code of Myelin Genes 016 : Ghosh : A Novel Transmission Disequilibrium Test For Quantitative Traits 017 : Hegde et al : Dynamic Changes in Protein Functional Linkage Networks Revealed by Integration with Gene Expression Data 018 : Ibn Ayub et al : 'Sexual dysfunction' in the brain: An uncharacterized gene's apparent role in male erectile dysfunction 019 : Ikeda et al : Genetic variants of constitutive androstane receptor (CAR) gene and the diseases in the Japanese elderly population 020 : Jana et al : Target Identification by In-silico Studies on NS1 Proteins of Bird Flu Virus 021 : Kapushesky et al : Meta-analysis of condition-specificity of gene expression: an integrated statistical framework for analysing 20,000+ transcriptomics assays across multiple studies and platforms in ArrayExpress 022 : Kondo et al : Assembly-based analysis protocol of metagenomic short-read sequence data 023 : Koressaar et al : Enhancements in widely used primer design program Primer3 024 : Kundu et al : GeneScan: A context independent gene finding program 025 : Lata et al : Softwares and Databases developed for innate immunity 026 : Lehman et al : Obesity, Diet and Type II Diabetes Risk in Indians 027 : Madan Babu et al : Expression divergence during human evolution is shaped by change in genomic neighbourhood of genes 028 : Madhyastha et al : Predicting signaling networks upon inflammation caused by PAR-1 activation: application of the ExPlainTM Analysis Platform 029 : Mitra et al : Omega parameters - a novel integrated approach for feature detection in nucleic acid structures 030 : Mitra et al : GC-rich special short sequences dominate eukaryotic promoter regions 031 : Mitra et al : Analysis of Regulatory motif binding site - an effective approach for identifying upregulated genes in the human oncogenome 032 : Mukhopadhyay et al : Association tests using kernel-based measures of multilocus genotype similarity between individuals 033 : Nandi et al : Classifiers for genome annotation built on Gene Ontology 034 : Narayanaswamy et al : Prediction of protein-protein interactions between a malarial parasite and human 035 : Okada et al : Genomic Control for Fisher's Exact Test 036 : Orlov et al : Statistics of transcription factor binding sites data sets obtained by high-throughout sequencing and chromatin IP in human genome 037 : Palta et al : The nature and heritability of the retention of heterozygosity (ROH) areas in human genome 038 : Pandey et al : Genome annotation of Anopheles gambiae mosquito using tandem mass spectrometry-derived data 039 : Poddar et al : In Silico Studies On Structure And Function Of Phylogenetically Related Dengue Virus Nonstructual And Human (Host) Proteins 040 : Pundhir et al : SSPred: a prediction server based on SVM for the identification and classification of proteins involved in bacterial secretion systems 041 : Putta et al : Structural Domain Prediction for Transcription Factor Binding Sequences 042 : Raju et al : NetPath: A Public Resource of Curated Signal Transduction Pathways - Development of an initial set of immune signaling pathways 043 : Ramachandran et al : MalVac: Database of Malarial Vaccine Candidates 044 : Ramamoorthy et al : Evolution of diversity in Polycomb homologues 045 : Rangannan et al : Genome wide application of DNA stability for the annotation of promoter regions 046 : Rao et al : Motifs as Markers in Diseased proteins: In Silico Investigations of Potential Drug Targets 047 : Rawal et al : ELAN: A server based tool for genome wide analysis of mobile genetic elements 048 : Roy et al : Identification of translational regulatory elements in 5' UTRS of hiv genomes - Possible targets for designed Aptamers 049 : Sachidanandam et al : Computational identification of functional SNPs at 5' splice sites 050 : Saharinen et al : From genome wide association towards underlying genetic association networks: GWANA 051 : Samarakoon et al : The Sri Lankan Genome Variation Database 052 : Sarmah et al : dbSNP-lite: A derivative from each build of dbSNP that tracks and consolidates core rsID marker and allele changes from each previous build 053 : Sengupta et al : Multiple pseudoknot motifs in Wilms' Tumor associated genes - an in silico perspective 054 : Singh et al : Fully disordered proteins in human proteome 055 : Singh et al : DLact: An antimicrobial resistance gene database 056 : Singhal et al : Understanding Human Genome organization based on physico-chemical properties of DNA 057 : Sriram et al : A Novel Glocal Alignment of Protein Sequences with Evolutionarily Conserved Subsequences 058 : Srivastava et al : Co-Transcription of Genes Into Single Transcripts: Another Regulatory Mechanism For Gene Expression In Vertebrates 059 : Surendranath et al : Identifying components of Alzheimer's Disease using a genome-wide Endoribonuclease-prepared siRNAs library 060 : Swati : Identification of telomeric and sub-telomeric signature sequences of small eukaryotic chromosomes using Information Theory 061 : Tandon et al : Disease Gene Mapping in Populations with Mixed Ancestry 062 : Taneja et al : PepCluster: A web-tool to annotate bacterial proteins by consensus and core invariant peptide signatures 063 : Telikicherla et al : A Resource of Molecular Alterations in Breast Cancer 064 : Thakur et al : Dissecting the Transcriptional Regulation of Metastasis 065 : Thakur et al : Markov segmentation of human X chromosome 066 : Thalamuthu et al : Joint Association Analysis of Multiple Genes in a Biological Pathway 067 : Thomas et al : Global Gene Profiling to Predict Radiation Response in Indian Women with Cervical Cancer 068 : Thorisson et al : HGVbaseG2P: A Central Genetic Association Study Database 069 : Thummala : Comprehensive Analysis of the Splice Site Regions by Comparative Genomics 070 : Tomilov et al : Human chromosomal DNA digestion with restriction endonucleases in vitro and in silico 071 : Verma et al : Identification of Proteins Secreted by Malaria Parasite into Erythrocyte using SVM and PSSM profiles 072 : Wadhwa et al : Gene Expression Analysis Studies for Acute Myeloid Leukemia to find out putative drug targets using in-silico approach 073 : Yadav et al : In silico analysis of cloned seed storage protein promoters of wheat, oat and rice for genetic manipulation of triticin gene, a possible target for wheat nutritional quality improvement 074 : Yajnik et al : GenePython: A Framework for ab initio Genome Annotation2. Single Gene Disorders
075 : Angalena et al : Prenatal and Postnatal diagnosis for beta thalassemia and sickle cell anemia 076 : Ansar et al : CC2D1A is involved in autosomal recessive non-syndromic mental retardation in a Pakistani Family 077 : Balakrishnan et al : Molecular analysis in Pediatric Wilson's disease: 13 novel mutations 078 : Bhattacharya et al : Modifier gene mutations in beta thalassemia 079 : Chavali et al : Not so simple! Hemophilia B as a quasi-quantitative condition with mutations showing variable penetrance 080 : Gilyazova et al : Mutational analysis of PMP22, MPZ, GJB1 and EGR2 genes in Charcot-Marie-Tooth Neuropathy (type1) patients from Bashkortostan Republic of Russia 081 : Gudzenko et al : Novel mutations in FRMD7 in Russian families with X-linked congenital motor nystagmus 082 : Hooper et al : Molecular screening approach for identification of mutations causing familial hypercholesterolaemia in Western Australia 083 : Kabra et al : Prenatal Diagnosis of Single Gene Disorders - 10 Years Experience from a Referral Center 084 : Karunas et al : Mutational analysis of ATP7B gene and genotype-phenotype correlation in Wilson's disease patients from the Volga-Ural region of Russia 085 : Keerthikumar et al : Primary Immunodeficiency disease database: A discovery tool for the genomics research 086 : Khlebnikova et al : DNA-diagnostics of choroideremia in Russian family 087 : Kumar et al : Molecular genetics of primary microcephaly in Indian families 088 : Kumar et al : X-linked Adrenoleukodystrophy Gene Polymorphisms and Mutation in Indian Population 089 : Kumaramanickavel et al : Application of Human Genome Knowledge in a Tertiary Ophthalmic Institution in India 090 : Lai et al : Simple and cost-effective approach for quantitative detection of heterozygous deletion genotypes in diagnosis of DMD/BMD carriers 091 : Maksimova et al : Novel CUL7 mutation in 49 Yakut patients with short stature syndrome 092 : Mohammed et al : SCA-LSVD - A new locus specific disease database (LSDB) for cataloging variations associated with Spinocerebellar ataxias 093 : Mondal et al : Heterozygous deletion of the 3' region of TYR is one of the potential mutations which remains uncharacterized in 15% of the OCA1 patients worldwide 094 : Padma et al : Mitochondrial Gene Mutations as a cause of Non-Syndromic Hearing Impairment among Probands from Andhra Pradesh 095 : Poltavets et al : Seven new mutations have been found in STX11, PRF1 and UNC13D genes in a group of Russian FHL patients 096 : Praveen et al : Genetic polymorphism and expression analysis of Glutathione S-Transferases in breast cancer patients 097 : Purushotham et al : Identification of disease causing mutations in Familial Hypertrophic Cardiomyopathy patients from Andhra Pradesh 098 : Sarkar et al : Molecular Heterogeneity of Beta-Thalassaemia and associated Disorders in Multiethnic setting of Southern Bengal, India 099 : Sengupta et al : Molecular Characterization Of Oculocutaneous Albinism Type 1 (OCA1) Mutations Found In Indian Population 100 : Sharma et al : NPHS2 and WT1 Mutations In Indian Children With Steroid-Resistant Nephrotic Syndrome 101 : Sheynin et al : Study of the Gene Causing Congenital Insensitivity to Pain among Israeli-Beduins 102 : Shukla et al : Mutation Analysis in Indian Patients with X-linked Adrenoleukodystrophy 103 : Singh et al : Genetic analysis of families with autosomal recessive retinal degenerations 104 : Srivastava et al : Origin of Friedreich's ataxia (FRDA) mutation predates divergence of Indian and Caucasian populations 105 : Vedam et al : SNP based genome wide homozygosity mapping in consanguineous families with autosomal recessive retinitis pigmentosa: Identification of a novel loci/mutations 106 : Wee et al : Genotype analysis in a multi-racial population: Co-inheritance of α-thalassaemia with heterozygous β-thalassaemia in Malaysia 107 : Yeasmin et al : Mutations in HBB gene in thalassemia patients from Bangladesh and correlating them with phenotypic severity of thalassemia3. Genome Variation Diversity and Evolution
108 : Adimoolam et al : Updating Phylogeny of Mitochondrial DNA Macrohaplogroup M in India 109 : Bachtrog : Evolutionary dynamics of the human Y chromosome 110 : Balakrishnan et al : Polymorphisms in ACTN3 and KCNJ11 genes and athletic performance in South Indian athletes 111 : Basu et al : Allele frequency and haplotype diversity in three hyaluronan metabolic genes in 24 Indian populations 112 : Becerra-Contreras et al : Frequency of C3435T single nucleotide ABCB1 genetic polymorphism in Native and Mestizo Mexican Populations 113 : Bhardwaj : The Growth Hormone Receptor Gene and its association with mandibular height - a PCR based research study 114 : Biswas et al : Structure of human genomic regions by functionality: An assessment of selective effects 115 : Chaubey : The genetic origin of Austro-Asiatic speakers 116 : Chaudhary et al : Red Cell Enzyme Polymorphism in Gond, Korku and Keer Tribes inhabiting Pachmari Biosphere of Madhya Pradesh 117 : Deng et al : HapMap based whole genome scan for positive selection signals and the construction of database SNP@Evolution 118 : Dey et al : Involvement of functional polymorphisms in the promoter regions of matrix metalloproteinase-2, -3 and -9 in the susceptibility of gastric cancer 119 : Dissanayake et al : The prevalence of variant alleles of functionally significant polymorphisms in the methylenetetrahydrofolate reductase, factor V, and prothrombin genes in the Sri Lankan population 120 : Eaaswarkhanth et al : The Genetic Legacy of Indian Muslims 121 : Farheen et al : Yin-Yang Haplotype Structure at the ACE Locus in Indian Populations 122 : Giddaluru et al : Haplotype diversity in disease candidate genes analyzed in the Indian Genome Variation project 123 : Hardy et al : Genomic medicine and developing countries: creating a room of their own 124 : Hidalgo-Miranda et al : The Mexican Genome Diversity Project: Analysis of genetic structure in Mestizo and Amerindian populations of Mexico 125 : Hong et al : Genomic analysis of mitochondrial DNA in the Indigenous groups of Malaysia 126 : Jha et al : Analysis of Genome-Wide Copy Number Variations in diverse Indian Populations 127 : Kato et al : Patterns of high-resolution recombination rates in human genes 128 : Khusnutdinova et al : Y-chromosome diversity in Southern-Ural Bashkirs 129 : Kumar et al : Simple Sequence Repeats as beneficial mutators in the evolution of Yersinia pestis 130 : Kushniarevich et al : Genetic portrait of modern Belarusians: mitochondrial DNA and Y-chromosome perspective 131 : Laval et al : A genome-wide scan of balancing selection in the human genome 132 : Manna et al : Evolutionary Constraints on Hub and Non-hub Proteins in Human Protein Interaction Network: Insight from Protein Connectivity and Intrinsic Disorder 133 : Metspalu et al : High resolution phylogeographic study of mtDNA macrohaplogroup M in South Asia 134 : Modak et al : Darwin's Dream: Multi-parametric Consesus Phylogenetic Tree in 3-D 135 : Mukherjee et al : Genetic Variation and Haplotype Structures of Innate Immunity Genes in Eastern India 136 : Mukhopadhyay et al : Application of Indian Genome Variation data as guidelines for future disease association studies from population sub-structure perspective 137 : Nandan et al : Phylogeography of selected tribal populations of Orissa, India 138 : Nayak et al : Single nucleotide polymorphisms of ADH and ALDH2 gene among the Bondo-Highlanders of Orissa 139 : Nothnagel et al : Population structure inference and genetic matching in European samples using genome-wide marker sets 140 : Padmanabham et al : Establishment of a National Repository for Human Genetic Research: An Initiative 141 : Park : Relative nucleotide substitution rates from allele frequency spectrum of human gene loci 142 : Pimenoff et al : Fine-scale recombination and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene subfamily regions in European populations and implications for association studies of complex pharmacogenetic traits 143 : Podder et al : Impact of Multifunctionality in shaping molecular evolution of human housekeeping and tissue-specific interactome over connectivity 144 : Prabhakar et al : Adaptive human-specific gain of function in a developmental enhancer 145 : Premi et al : Unique Signatures of the Natural Background Radiation on the Human Y chromosomes from Kerala (India) 146 : Purushottam et al : Allele frequencies at neutral loci suggest a recent bottleneck in southern India: Impact on susceptibility and co-morbidity in schizophrenia 147 : Ramesar et al : Genomic Studies on Indigenous African Populations 148 : Ruan : Individual cancer genome sequencing using SOLiD-PET revealed extensive large SVs and provided architectural framework for completion 149 : Sarbajna et al : Meiotic recombination in the human Xp/Yp pseudoautosomal region 1 150 : Sarkar et al : G6PD, Natural Selection and the Evolution of India-specific Deficiency Variants 151 : Sarkar Roy et al : An evaluation of tSNP portability across isolated population groups 152 : Sengupta et al : Genetic Differentiation and Ancestral Histories of Indian Population Groups: Inferences from Y-chromosomal Markers 153 : Shah et al : Genetic affinities and admixture among Siddis, a recent migrant population from Africa 154 : Sharma et al : Diversity of mitochondrial and y-haplogroups in TB patients of Sahariya tribe of Central India 155 : Sharma et al : Phylogenomic study of a concealed Ladakh tribe of the Great Himalayas 156 : Singh et al : Genetic heritage of Indian Jews population 157 : Singh et al : Identification and analysis of genetic signatures of selection in Indian populations 158 : Singh : RISC - Repeat Induced Sequence Changes 159 : Stepanov et al : Population history of North Eurasia revealed by X-chromosome ZFX haplotypes 160 : Stobdan et al : High altitude population stratification based on SNPs in genes of cardiopulmonary function: IGVdb application 161 : Tamang et al : High frequency of rare Y chromosome and mtDNA haplogroup suggests unique origin of Darjeeling populations 162 : Tateno : Tree of life constructed by genome-wide information 163 : Varma et al : Detection of mitochondrial DNA heteroplasmy in low quantity samples: Whole genome amplification (WGA) vs nested PCR 164 : Yadav et al : Going India to Australia: New Genetic Evidence on Modern Human Colonization 165 : Yamaguchi-Kabata et al : Structure of Japanese population based on SNP genotypes from 7,003 individuals in comparison to other ethnic groups: Effects on population-based association studies4. Genomics of Microbial Pathogens and Host-Pathogen Interactions
166 : Ahmed : Genomic plasticity of Helicobacter pylori and impact on evolution of novel virulence mechanisms 167 : Bandyopadhyay et al : Molecular characterization of Mycobacterium tuberculosis PII protein 168 : Basak et al : Unusual codon usage bias in lowly expressed genes of Vibrio cholerae 169 : Bharadwaj et al : Genetic variations in TNF-LTA locus and susceptibility to HPV mediated cervical cancer in North Indian women 170 : Bhattacharjee et al : Use of D-Limonene as an antimicrobial agent against Hemolytic streptococci - An in silico and in vitro approach 171 : Das et al : Global gene expression analysis of P. vivax parasites causing severe malaria and interaction with the host genome 172 : Dey et al : Host cell contact induces expression of virulence factors in Vibrio cholerae 173 : Gautam et al : An integrated proteomic and transcriptomic approach to study the effect of amphotericin B on Aspergillus fumigatus 174 : Gupta et al : Cloning, overexpression and purification of Leishmania donovani enolase 175 : Ho Sui et al : A bioinformatics pipeline to identify bacterial protein drug targets: Integration of novel gene discovery and existing annotations 176 : Joon et al : A gain-of-function mutation in a multidrug resistant clinical isolate of M. tuberculosis 177 : Kalia : Genomic Aid in Search of Pathogens of Tomorrow and Novel Drug Targets 178 : Kumar et al : Studies on genetic variation among Leishmania major, L. tropica and L.donovani by AFLP analysis 179 : Kumar et al : DnaA Protein Mediated Helix Opening of Mycobacterium tuberculosis OriC occurs at a precise location and is inhibited by a Putative IciA like Protein 180 : Kurupati et al : Bacterial toxin induced stress response in murine macrophages 181 : Kyaw et al : Predicting Protein-Protein Interactions from metagenomics datasets 182 : Mattoo et al : Spo0B - A snapshot in kinase evolution 183 : Mishra et al : TLR2 arg753gln and Vitamin D Receptor (VDR) gene polymorphisms in tuberculosis patients of Ahirwars and Muslim population from Uttar Pradesh, India 184 : Nilsson et al : De novo genome assembly of a highly virulent Burkholderia pseudomallei isolate assisted by genome paired-end ditag sequencing 185 : Pandit et al : Analysis of codon usage pattern in HIV-1genome and genes 186 : Ponnuraj et al : HIV-1: Identification of a novel kinase as a potential drug target 187 : Prasad et al : Use of mass spectrometry derived data to annotate genome of Candida albicans 188 : Ram et al : 'Codon-shuffling' method, a potential strategy to combat human pathogens 189 : Roychoudhury et al : Effect of IL1B Promoter Polymorphism on Down Regulation of Gastrin through Signalling Intermediates NFKB and SMAD7 190 : Sachdeva et al : Protein Phosphorylation and Stress-Dependent Sigma Factor Regulation in Mycobacterium tuberculosis 191 : Saxena et al : The Apicoplast Genome Of Plasmodium vivax 192 : Sengupta et al : Sequence variations within HPV16 isolates among Indian women: prediction of causal role of rare non-synonymous variations within intact isolates in cervical cancer pathogenesis 193 : Sinha et al : Variants of host adhesion and immune regulatory molecules and Plasmodium falciparum disease severity in a malaria endemic and non-endemic region of India 194 : Srivastava et al : Higher chlamydial heat shock protein specific levels of Interferon-gamma, Interleukin-10 and Tumor Necrosis Factor-alpha at the site of infection is associated with infertility in women 195 : Verma et al : Development of molecular markers for the authentic detection of Staphylococcus aureus by polymerase chain reaction 196 : Wong et al : Genetic polymorphisms in TLR1 are associated with susceptibility to leprosy 197 : Misra et al : Genome-wide transcription analysis of interaction between the human macrophage and Mycobacterium tuberculosis during concurrent drug administration by conventional and novel methods5. Disease Proteomics
198 : Ahmad et al : Serum Profiling For Candidate Biomarkers: Decrypting the Chrono Encryption 199 : Bagchi et al : Homology Modelling of Fumerate Hydratase (FH) mutation protein and Docking of Fumerate Hydratase (FH) mutation protein with 17- ketosteroid 200 : Biswas et al : Aberrant glycosylation of plasma and synovial fluid proteins in rheumatoid arthritis 201 : Chaerkady et al : Quantitative proteomic approaches to identify biomarkers for hepatocellular carcinoma 202 : Dube et al : A proteomic-based approach for the identification of potential Th-1 stimulatory novel proteins in a subunit vaccine (68-97.4kDa) of soluble antigens of Leishmania donovani promastigotes that protects against fatal visceral leishmaniasis 203 : Dutta et al : Identification of Cancer Markers and their Correlation to Cancer Diagnosis and Prognosis 204 : Gedela et al : Quantification of Inflammatory Mediators in Diabetic Nephropathy: An Experimental Design Approach 205 : George et al : Proteomic Analysis of Differentially Expressed Proteins in Swiss Mice Following Glyphosate Exposure 206 : Ghosh Chakraborty et al : Changes in expression of CD80, CD86, TLR2 and TLR4 in CD14-mononuclear cells after vaccination with an oral cholera vaccine 207 : Gupta et al : Two Natural Missense Mutations at Intersubunit Contact Domain in Human Pyruvate Kinase M2 (PK-M2) Isozyme with Differential Behavior 208 : Harsha et al : A multi-pronged proteomic approach to study pancreatic cancers 209 : Kalle M et al : Cyclooxygenase 2-dependent multidrug resistance 1 overexpression confers resistance to Imatinib in chronic myeloid leukemia cell line-K562 210 : Kaur et al : To study the effect of benzimidazole analogues (DNA minor groove binding ligands) on the protein expression of U87, a Glioblastoma cell line under Ionizing radiation 211 : Kothandaraman et al : Use of In-silico approaches to identify promoter elements and transcription factors associated with malignancy in ovarian cancer followed by validation of potential targets in tissues and serum samples of patients with ovarian cancer using proteomic approaches 212 : Maniraja et al : BIOBASE Knowledge LibraryTM (BKL) Disease View and HGMD®: A comprehensive literature-derived disease information management system 213 : Mitra et al : Methylation status of EpCAM in y79 retinoblastoma cell line: Proteomic analysis shows modification of various other proteins 214 : Polisetty et al : Analysis of proteins and their fragments released by human glioma cell lines as potential tumor markers 215 : Rajeswari et al : Proteomics Of The Outer Membrane Of Native And β-lactam Resistant Strains Of Acinetobacter baumannii 216 : Rakesh et al : Embryonic stem cells, their biomedical potential and proteomics approach for quality control 217 : Sen et al : Mechanistic studies of antiproliferative activity of Phyllanthus emblica extract on HeLa cells 218 : Shanmugam et al : Identification of differences in protein pattern and differentially expressed protein in wildtype Schizosaccharomyces pombe and Pol-gamma null strain depleted of mitochondrial genome using two dimensional gel electrophoresis and mass spectrometry 219 : Sharma et al : Functional characterization of putative disease proteins in Type 2 Diabetes Mellitus 220 : Shukla et al : Development of Novel Biomarkers for Breast Cancer in North Indian Population 221 : Sidana : Pigment Epithelium-Derived Factor Treatment for Cervical Cancer 222 : Tran The et al : Glycosylated and Thermostable Proteins in Serum of Type 2 Diabetes Mellitus Patients 223 : Tripathi et al : Glutathione-S-transferase with reduced allergenicity has therapeutic potential in mice model of asthma 224 : Vinay et al : Identification of Rheumatoid Arthritis causing protein and interpretting the treatment for the disease 225 : Yadav et al : Rapid identification of Human Plasma Proteins by mass fingerprinting using PLASMASS search engine6. Computational Biology and Structural Proteomics
226 : Amineni et al : In silico Putative Drug targets in Leptospira interrogans and Homology Modeling of UDP-N-acetylglucosamine 1-carboxyvinyltransferase MurA 227 : Aparoy et al : Comparative analysis of R and S isoforms of 12-Lipoxygenases: Homology modeling and docking studies 228 : Bansal et al : Intrinsic versus induced effects in DNA structure 229 : Bhasin et al : Using support vector machine for the identification of disease-associated missense SNPs 230 : Bhattacharyya et al : Structure-Function correlations in LuxS from bacteria: Analysis of protein-protein interface clusters by graph theoritical approach 231 : Chetnani et al : A novel mechanism of action of Mycobacterium tuberculosis pantothenate kinase involving mobility of ligands 232 : Dutta et al : Three-dimensional structure of Vibrio cholerae Hemolysin oligomer by Cryoelectron Microscopy 233 : Guruprasad et al : Identification and Analysis of Novel Repeats and Domains in Human proteome 234 : Kalidas et al : Targetability of Mycobacterium tuberculosis: Comparison of host and pathogen pocketomes 235 : Karuturi et al : DNA Replication Firing Efficiency Profiling of Human Chromosomes 21 and 22 by Mathematical Modeling 236 : Loveland et al : High Quality Manual Genome Annotation at WTSI 237 : Morozova et al : Defining expression signatures of known cancer genes using seriation analysis of SAGE libraries from Cancer Genome Anatomy Project (CGAP) 238 : Nagal et al : Design of Human non-pancreatic secretory phospholipase A2 (hnps-PLA2) inhibitors: A Qsar Based approach and its confirmation with structure-based studies 239 : Nargotra et al : Structural Characterization and Refinement of NorA, a multidrug resistant efflux pump 240 : Paila et al : Recompilation of amino acid substitution matrices for sequence searches of a biased genome 241 : Pattanayak et al : Structure determination of cysteine conjugate-beta lyase 1 (CCBL1) a key enzyme for nephro/neurotoxicity through computational approaches 242 : Prakash et al : Binding of Gastrin-Releasing Peptide Hormone to the Membrane Bilayers: Investigation of Preferred Orientation Using Molecular Dynamics Studies 243 : Reddy et al : Functional correlation of cyclooxygenases-1, -2 and -3 from amino acid sequences 244 : Saha et al : Structural Analysis Of Factor IX Variants For Genotype Phenotype Correlation In Hemophilia B Patients 245 : Selvaraj et al : Mobility in Mycobacterium tuberculosis ribosome recycling factor 246 : Shamim et al : Development of a new SVM-based method for protein fold recognition 247 : Singh et al : Computational methods of protein network identification in Acinetobacter baylyi 248 : Smita et al : Substrate, Positional and Stereospecificity of 12R-LOX : Positional and Functional correlation studies7. Genomics of Complex Disorders I
249 : Ahluwalia et al : Higher order gene-gene interactions: Association of CCL2, CCR5, IL8, AGT, ACE and AGTR1 gene variants with type 2 diabetic nephropathy in Asian Indians 250 : Ali et al : Common polymorphisms of Angiotensinogen (AGT) and susceptibility to hypertension: Prospective implementation of IGVdb 251 : Balam-Ortiz et al : Association of Angiotensinogen G-6A and C4072T polymorphisms with hypertension in Mexican population 252 : Banerjee et al : Chronic arsenic exposure impairs macrophage functions and alters inflammatory cytokine profile 253 : Bashyam et al : The Cancer Genome: A-ray of hope 254 : Bhanushali et al : Impact of Genetic Polymorphisms in Apolipoprotein A5 on Lipid Variables and its Association with Coronary Artery Disease in Indians 255 : Bhaskar et al : TCF7L2 Gene Polymorphisms do not Predict Susceptibility to Diabetes in Tropical Calcific Pancreatitis but May Interact with SPINK1 and CTSB Mutations 256 : Bhoopathy et al : Contribution of A116C polymorphisms in conferring risk for essential hypertension - a case control study 257 : Chakraborty et al : Genetic alterations of the TP53 gene and their influence on the risk of cervical cancer development among HPV16/18 positive Indian women 258 : Cutiongco-de la Paz et al : CYP1A1, CYP2E1 and GSTP1 polymorphisms and lung cancer risk among Filipinos 259 : Das et al : HLA B serological types relevant for HPV16 positive cervical cancer development among Indian women: significant impact on some viral factors 260 : Das et al : Functional role of Acidic Mammalian Chitinase polymorphisms in atopic asthma 261 : Das et al : Genotype and tissue specific effects on alternative splicing of the transcription factor 7-like 2 (TCF7L2) gene in tissues important to type 2 diabetes (T2DM) pathogenesis 262 : Das Roy et al : Risk of oral leukoplakia and cancer in relation to HPV infection, polymprphisms at XRCC1 and TP53 and mutation in TP53 gene 263 : Dash et al : A Common Genomic Variant in 9p21 Associated with Premature Coronary Artery Disease in Asian Indians 264 : Datta et al : Gilbert's syndrome: Genetic factors and their interactions 265 : Dube et al : Possible protective role of ARNT gene in low risk for Type 2 Diabetes Mellitus in Raica community of Rajasthan 266 : Dutta et al : A case of Balanced Reciprocal Translocation t(3;14)(p12;q12~13) associated with Bad Obstetric History 267 : Fortier et al : The Generic-DataSHaPER, a step towards the global harmonization of biobanks 268 : Ghasemi et al : Evaluation of the Frequency of PCOS in patients with breast cancer 269 : Gupta et al : Evaluation of Single Nucleotide Polymorphisms in Peroxisome Proliferator Activator Receptor-γ (PPARG) and Tumor Necrosis Factor-α (TNF) Genes in Obese Asian Indians: A Population Based Study 270 : Gupta et al : Expression-based Gene Interaction Networks for breast cancer 271 : Hofmann et al : A genome-wide association study identifies a novel sarcoidosis disease gene with potential relevance for related granulomatous inflammatory phenotypes 272 : Indira Somarajan et al : Association of ACE I/D, ADD1 G460W polymorphisms in Ischemic and Hemorrhagic Stroke in North Indian Patients 273 : Janipalli et al : FTO Gene Variants are Strongly Associated with Type 2 Diabetes but only weakly with Obesity in South Asian Indians 274 : Jiménez-Morales et al : Interleukin 13 gene is a risk genetic factor to asthma in Mestizo-Mexican childhood 275 : Kapoor et al : Leptin (LEP) gene: The missing link between the Depression, Obesity and Metabolic disorders 276 : Kapur et al : APOE and CAPN gene and risk for the metabolic complications in diabetes 277 : Kepp et al : Hypervariable polymprphism in SLC8A1 intronic region is associated with cardiovascular traits and serum lipids 278 : Kim et al : Negative association of all ten non-HLA single-nucleotide polymorphisms identified in a British genome-wide scan with rheumatoid arthritis in Koreans 279 : Kumar et al : Polymorphisms in non-coding region of IFNG gene and their association with atopic asthma 280 : Kumar : Physiological Effect of Human Angiotensinogen Haplotypes on Blood Pressure in Transgenic Mice 281 : Kumar et al : Single nucleotide polymorphisms in homocysteine metabolism pathway genes: Association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia 282 : Kumar et al : Interactive effect of Angiotensinogen gene polymorphisms in essential hypertension 283 : Kundu et al : Epidemiological, Cytogenetic and Molecular Approaches to Decipher Arsenic Susceptibility 284 : Kuppuswamy et al : Association of Apolipoprotein A4 polymorphisms Asn147Ser and Thr347Ser with type 2 diabetes in an Asian Indian population 285 : Laan et al : Genome-wide association study with blood pressure traits 286 : Ladha et al : Identification of unique primary and secondary Glioblastoma Multiforme (GBM) specific networks and molecular connections using protein-protein interaction tools 287 : LaFramboise et al : Somatic DNA Amplification as a Phenotype in Cancer 288 : Mahurkar et al : A Comprehensive Approach Towards analysis of Complex Disorders: Tropical Calcific Pancreatitis as a Model 289 : Maitra et al : Association of the Pituitary Growth Hormone and Its Receptor Gene Polymorphisms with Premature Coronary Artery Disease in Asian Indians 290 : Malik et al : Association of Xenobiotic metabolizing enzymes genetic polymorphisms with esophageal and gastric cancers in Kashmir valley: Influence of smoking and consumption of salted tea 291 : Mallik et al : Association of polymorphic markers in candidate genes with quantitative precursors of Coronary Artery Disease: A study in an isolated population group of India 292 : Mani et al : CYP17A1 (T-34C), CYP19A1 (Trp39Arg), and FGFR2 (C-906T) polymorphisms and the risk of Breast Cancer in South Indian Women Population 293 : Mani et al : Clinical, biochemical and genetic analysis of Leigh syndrome patients with atypical presentation 294 : Mehra et al : Multiple HLA-DR3 haplotypes associated with autoimmunity in North Indians 295 : Mohamed et al : Mutations in the APC gene in families with Familial Adenomatouos Polyposis (FAP) 296 : Munjal et al : Gene expression profiling of the hepatic transcriptome in the presence of TNF α 297 : Muthuswamy et al : Differntially expressed transcripts in the adipose tissue of 'sumo rats' (WNIN/Ob) 298 : Pandey et al : Attenuation of hepatic insulin sensitivity by TNFα 299 : Pasha et al : Balancing the role of gene and environment: High-altitude adaptation and mal-adaptation 300 : Patkar et al : Association of Insertion Deletion Polymorphism in intron 16 of ACE gene with Essential Hypertension 301 : Ramachandran et al : Genetic Predisposition To DNA Repair And Its Effects On Tumor Response To Radiation Therapy In Oral Cancer 302 : Raman et al : Molecular genetic analyses of tumours from colorectal cancer patients suggest existence of alternate tumourigenesis pathway(s) in young patients from India 303 : Ramírez-Bello et al : Association of FCRL3 polymorphisms with juvenile rheumatoid arthritis in Mexican population 304 : Ranade et al : Development of a web-enabled system for patient data management and genetic analysis of diabetes mellitus (DM) 305 : Rani et al : Interaction and integration of genes involved in immune responses with special reference to HLA-DRB1, HLA-B, Cytokine genes, Vitamin D Receptor and Protein Tyrosine phosphatase non-receptor 22 genes in type 1 diabetes 306 : Rautanen et al : Association between CLEC7A gene and pneumocystis pneumonia (PCP) susceptibility among HIV-infected individuals 307 : Rocamora et al : Glutathione-S-Transferase P1 (GSTP1) Polymorphism and Breast, Colorectal and Oral Cavity Cancer Risk Among Filipinos 308 : Roy et al : Enhancement of risk of oral leukoplakia and cancer by combinations of polymorphisms at NAT1, NAT2 and XRCC1 309 : Sannappa et al : Polymorphisms in the IL6 gene in Asian Indian families with premature coronary artery disease - The Indian Atherosclerosis Research Study 310 : Santos-Cortez et al : Metabolic Enzyme Gene Variants and Oral Cavity Cancer among Filipinos 311 : Selvi Rani et al : Novel genetic variations in TNNT2 gene are associated with hypertrophic and dilated cardiomyopathies of Indian origin 312 : Shanker et al : Genetic studies on the APOA1-APOC3-APOA5 gene cluster in Asian Indians with premature Coronary Artery Disease 313 : Sharad et al : Role of OPRM1 gene in T2DM susceptibility and its prevalence in North-West Part of Rajasthan 314 : Sinha et al : MTHFR gene polymorphisms among Aggarwals: A community specific case control study for CAD 315 : Srivastava et al : Role of DNA Repair Gene Polymorphisms in Gallbladder Cancer 316 : Subhashini et al : Dilated Cardiomyopathy caused by a mutation in Phospholamban 317 : Subodh et al : APOBEC3 Insertion/Deletion polymorphism among patients infected with hepatitis B virus 318 : Tabassum et al : Genetic variants of FOXA2: Risk of type 2 diabetes and effect on metabolic traits in North Indians 319 : Tirunilai et al : Risk conferred by Leptin (LEP) and Leptin receptor (LEPR) gene polymorphisms to essential hypertension irrespective of obesity 320 : Tripathi et al : Genetic Predisposition of MTHFR Polymorphism in Coronary Artery Disease (CAD): SGPGI Experience 321 : Vadapalli et al : Molecular Markers in Idiopathic Pulmonary Arterial Hypertension 322 : Vannberg et al : Genome wide study of tuberculosis susceptibility in West Africans reveal novel associations 323 : Velazquez et al : SNPs in FTO and GNB3 are associated to obesity in Mexican Mestizos 324 : Venkatesan et al : Genetic studies in type 2 diabetes in south Indian population8. Epigenomics
325 : Aburatani : Epigenomic regulation of p53 pathway 326 : Barbhuiya et al : Methylation Pattern of a few Tumor Suppressor Genes in Gall Bladder Cancer Patients amongst North Central Indian Population 327 : Bhatia et al : A possible dual role of a chromatin remodeling protein INO80 328 : Bhavani et al : Role of BRCA1 and 17BHSD 2 methylation in the aetiology of sporadic Breast Cancer 329 : Chanda et al : Epigenetic Alteration of Human DNA When Chronically Exposed to Arsenic by Drinking Water 330 : Damineni et al : CYP17A1 and CYP19A1 Gene Polymorphisms and Breast Cancer Risk 331 : Deobagkar et al : The DNA methylation profile of genes from the inactive X chromosome from human fibroblasts 332 : Handoko : Dynamic of genome organization in mouse embryonic stem cells and neural-committed stem cells 333 : He et al : IGF2/H19 Domain Epigenetic Alteration in Sib Pairs with Schizophrenia 334 : Hussain et al : Analysis of Promoter Methylation of E-Cadherin (CDH1) Gene in Esophageal Squamous Cell Carcinoma 335 : Joseph et al : High throughput sequencing technologies revealed correlation of histone methylation pattern on estrogen response element utilization of binding sites in MCF-7 human breast cancer cell line 336 : Kabekkodu et al : CpG Island Microarray Based Identification of Differentially Methylated Genes During Cervical Cancer Progression 337 : Khosla et al : DNMT3L: epigenetic correlation with cancer 338 : Kundu et al : Alteration of genome function by modulating epigenetic marks: Implication in diseases 339 : Mishra et al : Nuclear matrix, genome organization and regulation of genes 340 : Rico et al : Whole Genome Bisulphite Sequencing by high-throughput oligonucleotide ligation sequencing 341 : Satti et al : TP53 Gene Polymorphisms and Breast Cancer Risk 342 : Sharma et al : Homocysteine mediated DNA methylation and its potential role in Coronary Artery Disease 343 : Shehi et al : MS-FLAG, a Novel Real-Time Signal Generation Method for Methylation-Specific PCR 344 : Singh et al : Epigenetic mapping of Human Y-chromosome reveals the role of non-coding elements in genome organization 345 : Srivastava et al : Role of H2AX, a DNA damage response protein and a histone H2A variant, in sporadic breast cancer 346 : Tögl et al : A reproducible high-throughput Methylome analysis of a single cell 347 : Vasanthi et al : Epigenetic regulation of genes during development: a conserved theme from flies to mammals 348 : Wei : Dynamics of genome organizations and epigenetic networks during pluripotent cell differentiation9. Pharmacogenomics and Toxicogenomics
349 : Abdul Vahab et al : Evaluating the effect of genotype and haplotype frequencies of ABCB1 (MDR1) polymorphisms in medically refractory epilepsy patients of an Indian population 350 : Bhattacharya et al : Mechanism of Black Tea Polyphenols Theaflavins and Thearubigins Induced Apoptosis in Human Skin Cancer Cells: Involvement of Oxidative Stress Induced MAP kinase pathways 351 : Chakravarty et al : Genotype-Phenotype correlation in β-Thalassemia patients (both major and intermedia) responding to Hydroxyurea Treatment and Common β-Thalassemia Mutations in the Eastern Indian population 352 : Chauhan et al : Genotypic Variability of CYP2C9 and CYP2C19 in Indian Population: Correlation with Pharmacokinetic Based Phenotype 353 : Chowdhury et al : Arsenic-induced Gene Expression Changes in Human Peripheral Lymphocytes and its Association with Carcinogenesis 354 : De Chaudhuri et al : Arsenic induced premature senescence: A biomarker study in exposed population from West Bengal, India 355 : Dhawan et al : Genetic Variations in TCF7L2 Influence Therapeutic Response to Sulfonylureas in Indian Diabetics 356 : Ghosh et al : Gene Expression Profiling in Lymphocytes of Arsenic Exposed Individuals 357 : Glubb et al : An Acute Antidepressant Pharmacogenomic Study and Association of ADM, a Paroxetine-Regulated Gene, with Antidepressant Response 358 : Goel et al : Cytotoxic and apoptogenic effects of coumarin derivatives on human lung adenocarcinoma cell line 359 : Grover et al : Pharmacogenomics of first line anti-epileptic drugs (AEDs) in Indian population 360 : Gupta et al : Interindividual variability in drug response to risperidone treatment in schizophrenia: Role of dopaminergic pathway gene polymorphisms 361 : Kanive Parashiva et al : Role of NBN gene polymorphisms in DNA repair 362 : Kim et al : Pharmacogenetics on drugs for rheumatic diseases 363 : Korivi Jyothiraj et al : Role of GSTM1, GSTP1 and GSTT1 polymorphisms in the succeptibility to Acute Lymphoblastic Leukemia and the influence of SNPs in the TPMT gene to the tolerance of Thiopurines in the ALL patients 364 : Kukreti et al : Pharmacogenomics and Predictive Therapy for Complex Diseases 365 : Kumari et al : Pharmacogenomic Study of Drug Transporter ABCB1 and Drug Target SCN1A in Epilepsy Patients from North India 366 : Mathew et al : Investigating the Role of Polymorphisms in ABCB1 and MTHFR with Teratogenicity of Antiepileptic Drugs 367 : Mittal et al : Pharmacogenomic Study of Drug Transporter ABCB1 and CYP3A4*1B, CYP3A5*3 Polymorphisms associated with Daily Dose Requirement of Cyclosporine A to Prevent Renal Allograft Rejection in North India 368 : Mohamed Ali et al : Association between Cholinesterase Activity and Human Paraoxonase (PON1) Polymorphisms in Workers Exposed to Organophosphate 369 : Muramatsu et al : HLA genotypes in carbamazepine-induced severe cutaneous adverse drug response: difference between Japanese and Han-Chinese 370 : Poduri et al : Polymorphisms in Statin Metabolism Pathway Genes Predict Statin Mediated LDL Cholesterol Lowering in Coronary Artery Disease Patients 371 : Rai et al : Polymorphism of serine hydroxymethyltransferase gene (SHMT1 C1420T) and risk of colon cancer: An Indian case-control study 372 : Rao et al : Genetic Variations and Haplotypes of the 5' regulatory region of CYP2C19 in South Indian population 373 : Setia et al : Apolipoprotein E polymorphisms influence the response of lipids to Atorvastatin in hypercholesterolemic patients with Coronary artery disease 374 : Tripathi et al : ACE gene polymorphism: a potent risk factor for End Stage Renal Disease among North Indians 375 : Vibhuti et al : Genetic variants of ACE, NOS3, GSTP1 and EPHX1 and oxidative stress markers associates with COPD10. Genes Chromosomes and Disease
376 : Aggarwal et al : Genetic variations in Endothelin-1 but not in endothelial Nitric Oxide Synthase and Angiotensin Converting Enzyme are associated with preeclampsia 377 : Aggarwal et al : Extensive alternative splicing of Dmrt1 during gonadogenesis in Indian mugger, a species exhibiting temperature-dependent sex-determination 378 : Al Ali : Centre for Arab Genomics Studies: Current focus and future direction 379 : Banerjee et al : Evolution of human trifunctional GART gene and identification of elements important for gene transcription in neurodevelopment 380 : Banerjee et al : Gene-gene interaction between SLC6A4 and HTR1B contributing to the risk of ADHD in Indian population 381 : Bhardwaj et al : CompreSNPdb: Comprehensive Data-mining Workflow for SNPs, Genes,Diseases and Pathways 382 : Bhat et al : Mutation in ATPase gene regulating oxidative phosphorylation in sperm mitochondria and low seminal antioxidant levels in idiopathic asthenozoospermic men 383 : Bhattacharjya et al : Interleukin 1 Beta (IL1B) As Potential Host Susceptibility Factor In Helicobacter Pylori Mediated Duodenal Ulcer In Eastern Indian Population 384 : Bhushan et al : NF-kB signaling pathway in acute leukemia: A study on expression of cell survival and proliferative genes by Real Time RT-PCR 385 : Biswas et al : Evaluation of PINK1 variants in Indian Parkinson's disease patients 386 : Chakraborty et al : Chromosomal aberrations and micronuclei as biomarkers of arsenicosis; a study in an arsenic exposed population in West Bengal, India 387 : Chatterjee et al : GST polymorphism, micronuclei frequencies-risk markers for oral cancerous lesions and their prevalence in other oral mucosal lesions 388 : Chattopadhyay et al : Differential expression of MAPK and GPCR pathway in esophageal cancer of North-east region of India 389 : Chauhan et al : Immunophenotypic and clinical findings in adult Acute Myeloid Leukemia with FLT3 Internal Tandem duplication 390 : Cheah et al : Genome Wide Search for Novel Cancer Gene in Familial Adenomatous Polyposis (FAP) Variant Patients without Detectable APC Mutation 391 : Cooke et al : Modelling potential CNV effects on human fertility by manipulating meiosis in mice 392 : Dada et al : Analysis of sperm and blood mtDNA mutations in infertile oligoasthenozoospermic (OA) men 393 : Dangi et al : Mutational Analysis in Beta-Thalassaemics in Bhopal 394 : Das et al : Gene expression profiling to understand the mechanism of action of Enhancing Factor (EF) in the Tg-K14EF transgenic mice 395 : Datta et al : Regulation of transcription by HIPPI and its molecular partner, Huntingtin Interacting Protein HIP1 396 : Deeba et al : Investigation on Angiotensin Converting Enzyme gene I/D polymorphism of Vitiligo in South Indian population 397 : Dunna et al : NPM1/FLT3 ITD Gene Mutation Profiling in Acute leukemia: A Pilot study 398 : Dwivedi et al : Genetic association of promoter and structural gene variants of Mannan-Binding Lectin (MBL2) gene with susceptibility to vitiligo 399 : Gecz et al : Systematic resequencing of the coding exons of the X chromosome in X-linked mental retardation 400 : Gijselinck et al : Identification of a novel chromosomal locus in a Belgian FTLD-MND family 401 : Gireesha et al : Identification of tuberous sclerosis causing gene and finding the treatment for the disease 402 : Guastadisegni et al : The Secondary Use of Samples. Lessons from the Italian Paediatric Diabetes Studies (ISPED) 403 : Gupta et al : Association of mannose binding lectin gene variant with leprosy in an Indian cohort 404 : Hansmann et al : Repetitive elements flank both breakpoints of a chromosome 3 inversion in a 3-generation family with short stature 405 : Hussain et al : Genotype - Molecular Phenotype Correlation using Lymphoblastoid Cell Lines from Patients with Multiple Primary Neoplasia 406 : Ihsan et al : Significance of TP53 codon 72 polymorphism in breast and lung cancer showing different xenobiotic potential spectrum 407 : Ilencikova et al : Comprehensive characterization of genetic aberrations in T-lymphomas in children 408 : Indra et al : Evidence of CHEK1 and EI24 as candidate tumor suppressor genes associated with the development of uterine cervical carcinoma 409 : Iourov et al : Intercellular genomic variations manifesting as aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain 410 : Jha et al : Genome wide structural variations in malignant glioma samples of Indian population 411 : Kavsan et al : Molecular markers of human brain tumors and their participation in cellular signaling pathways 412 : Khattri et al : Role of CaMKIV and PRM genes in idiopathic male infertility 413 : Kishore et al : Profiling of esophageal squamous cell carcinoma using whole genome mRNA and aCGH arrays 414 : Krishna Murthy et al : Apparently balanced, de novo Complex Chromosome Rearrangement (CCR) - 46, XY, t(8;10;12) associated with Autism - Cytogenetic and molecular studies 415 : Kumar : Genomic disorders: A new class in the taxonomy of human disease 416 : Kumar et al : Centric Fission of Chromosome 5 in a couple with Recurrent Spontaneous Abortions 417 : Kumar et al : Cytogenetic Analysis in Myelodysplastic Syndrome (MDS) 418 : Laddha et al : Association of TNF -308 and -238 promoter polymorphisms with vitiligo susceptibility in Gujarat population 419 : Lee et al : Mutation Analysis of PAH Gene and Characterization of a Recurrent Deletion Mutation in Korean Patients with Phenylketonuria 420 : Minocherhomji et al : Identification of chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype 421 : Misra et al : Studies on Interplay among TP53, TP73 and MDM2 Loci at the Risk of Tobacco Associated Leukoplakia and Oral Cancer and Analysis of Apoptotic Property of Wild Type and Mutant TP53 Gene under Different Polymorphic Background 422 : Mittal et al : Genetic Susceptibility to Gallbladder Cancer: Role of Polymorphisms in Candidate Genes 423 : Mondal et al : MLH1 -93G>A promoter polymorphism and risk of head and neck squamous cell cancer 424 : Murthy et al : Clinical implications of array-CGH: Detection and characterization of submicroscopic chromosomal alterations in complex diseases and its significance in genetic diagnosis and counseling 425 : Naiya et al : Molecular pathogenesis of dystonia: Role of GCH1 gene in Indian patients 426 : Nath et al : Expression profile of SAC genes in HNSCC samples and study of transcriptional regulation of a key SAC gene, CDC20 upon DNA damage 427 : Nava-Salazar et al : Polymorphisms of HIF1A gene in Mexican patients with preeclampsia 428 : Pal et al : Analysis of DNA damage - death receptor apoptotic pathway gene SNPs in sporadic breast cancer - An interactive study 429 : Paliwal et al : Molecular genetic, histopathological and clinical examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophies 430 : Paliwal et al : Chymotrypsin C (CTRC) gene polymorphisms predict susceptibility to tropical calcific pancreatits 431 : Panda et al : Candidate tumor suppressor genes in the short arms of chromosomes 3 and 9 differentially associate with the development of head and neck squamous cell carcinoma 432 : Paul et al : Role of arsenic in blood cancer 433 : Phipps et al : SLE in Asia - Genetic Insights towards better management 434 : Ponnala et al : Spectrum Of chromosomal imbalances associated with Mental retardation 435 : Qiang et al : Nectin-like molecule 1 is a glycoprotein with a single N-glycosylation site at N290KS which influences its adhesion activity 436 : Ramachandra et al : Maternal grandmothers with advance-age reproduction are more likely to have Down syndrome grandchildren 437 : Rudra et al : Prevalance of iron deficiency and haemoglobinopathies in the population 438 : Sadhukhan et al : Molecular pathogenesis of Parkinson's disease: Role of DJ1 and LRRK2 genes in Indian patients 439 : Sailaja et al : GST M1 and GST T1 gene deletion polymorphisms in Chronic Myeloid Leukemia 440 : Saluja et al : Different domains of SIN3B interact with various co-repressors 441 : Sandhya et al : Association of Vitamin D Receptor Polymorphisms with Myopia Development 442 : Sawabe et al : Phenome scan (genotype/dense phenotype association studies) of a comprehensive clinicopathological database derived from large numbers of autopsy cases 443 : Silao et al : PCR-Based Detection of Southeast Asian (--Sea) and Filipino (--Fil) Alpha-Thalassemia Deletions in Filipino Patients 444 : Singh et al : Analysis of methylation of 5'-flanking region of Fmr-1 gene and its modulation by sex steroids hormones in aging mouse brain 445 : Soni et al : Androgen signaling and androgen-related gene polymorphisms and the risk prostate carcinoma 446 : Sowjanya et al : Persistent infection with human papilloma virus, 3q chromosomal gain and presence of circulating RNA component of the telomerase (TERC) in cervical neoplasia 447 : Tadmouri : Genetic Disorders in Arab Populations Reflect a Remarkable Diversity 448 : Thavanati et al : Genetic Factors related to ethnic variation in plasma levels of the evolutionary conserved IGF1 gene: A study evaluated towards the susceptibility of breast cancer in Mexico 449 : Thoudam et al : Differential gene expression profile of stomach and oral cancer in high risk region of India 450 : Togarrati et al : Role of genetic alterations in E-cadherin gene in Gallbladder cancer and in early Gallbladder epithelial lesions 451 : Venkatesh et al : 2, 17 novel translocation in a severely oligozoospermic infertile man 452 : Vorsanova et al : Mitotic (non-meiotic) instability of the genome is associated with early spontaneous fetal death 453 : Wang et al : HSD11 regulates the sensitivity of HeLa cells to multiple apoptotic stimuli through Bcl-xL 454 : Wu et al : Induction of tumorigenesis by APLP2 through regulation of cell survival and cell apoptosis 455 : Yadav et al : Codon 72 of TP53 gene Polymorphism in oral cancer and stomach cancer in high-risk region of India 456 : Yuan et al : Cooperation between EZH2, NSPc1-mediated histone H2A ubiquitination and Dnmt1 in HOX gene silencing 457 : Yurov et al : Somatic genome instability closely associates with cerebellar neurodegeneration in the ataxia telangiectasia 458 : Zack et al : Mutations in Acute myeloid leukemia -1 gene result in down regulation of RUNX2 and LAT gene expression 459 : Zahir et al : Genotype-phenotype correlations for CNVs identified in patients with mental retardation; increased array resolution refines detected CNVs, selects candidate genes and diagnoses known syndromes 460 : Zeng et al : Co-transcription and intergenic splicing in vertebrates11. Technology Developments and Applications
461 : Brahmachari et al : Open Source Drug Discovery for Infectious Diseases - a case application on Tuberculosis (Phase I) 462 : Chen et al : Testing SNP Markers for Human Identification Application 463 : Davidson et al : Enhanced Workflow for Sequencing PCR Products by Capillary Electrophoresis 464 : Fullwood et al : ERα-bound chromatin interactions are prevalent and functional in the human breast cancer genome 465 : Glavac et al : Novel biomarkers in early stages of lung adenocarcinoma identified with oligonucleotide based DNA microarrays 466 : Goel et al : Development of a high-throughput Pyrosequencer with integrated sample preparation 467 : Hogan : The Evolution of a High-Capacity, Multi-user Sample Management Network 468 : Hyland et al : Human whole genome sequencing by high-throughput, short read oligonucleotide ligation 469 : Kaplinski et al : Evaluation of factors affecting the success of multiplex PCR 470 : Khanna : The Potential Of Rna Interference - An Overview 471 : Maercker et al : A new assay in functional genomics: Monitoring cell differentiation in live cell chips by electric cell-substrate impedance sensing 472 : Majumdar et al : Keeping pace with the innovation: An easily adaptable technique for rapidly generating humanized animal models in the era of human genome 473 : Makrigiorgos et al : Replacing PCR with COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing 474 : McInnes et al : A new alternative for two dimensional gel electrophoresis: OFFGEL electrophoresis combined with high sensitivity protein sizing on microchips 475 : Mishra et al : Anti-Leishmanial Efficacy study of a new Liposomal Amphotericin B preparation in mouse model using Quantitative Real Time PCR 476 : Parihar et al : Polymorphism of xenobiotics metabolic genes and risk prediction: A potential tool for cancer prevention 477 : Patnaik et al : Novel PEI based nanoparticles for delivery of nucleic acids 478 : Raghavachari et al : Characterization of whole blood gene expression profiles in sickle cell disease with enhanced transcript detection using globin mRNA reduction 479 : Sethi et al : A novel photoreactive heterobifunctional reagent, 1-N-(maleimidohexanoyl)-6-N-(anthraquinon-2-oyl) hexanediamine (MHAHD) for the preparation of oligonucleotide microarrays on modified glass surfaces 480 : Sharma et al : MetaBioME: Comprehensive Metagenomic BioMining Engine to Search Novel Biocatalysts in Metagenomic Datasets 481 : Xiao et al : 'Universal' control assay selection and evaluation using comparative genomics approach for copy number variation detection12. Genomics of Complex Disorders II
482 : Banerjee et al : A nonsynonymous SNP in CYP1B1 is associated with Primary Open Angle Glaucoma 483 : Chakraborty et al : Involvement of IL1 gene cluster in glaucoma pathogenesis 484 : Das et al : Association of MAPT haplotype-tagging SNPs with Parkinson's disease among Indians 485 : Das Bhowmik et al : Analysis of Association between Genetic Polymorphisms and Aggressive Traits in Intellectually Disabled Individuals from Eastern India 486 : Ganguli et al : In Silico analysis reveals Pyrroloquinoline quinine is an effective ligand for α - synuclein - a key player in Parkinson's disease 487 : Ghosh et al : A study of GRIK1 gene polymorphism in mental retardation related to Down syndrome 488 : Godbole et al : Neural tube defects in India occur despite normal maternal folate status and low frequency of T allele at C677T polymorphism in the MTHFR gene 489 : Guhathakurta et al : Preliminary analysis of SLC6A4 gene polymorphisms indicates the possibility of a positive association of the gene with autism in Indian population 490 : Kaur et al : Contributions of the ARMS2 (LOC387715) and HTRA1 Variants in the Risk of Age-Related Macular Degeneration Among Indian Patients 491 : Kazantseva et al : The influence of SLC6A3 and DRD2 genes variation on personality traits modified by gender - ethnicity confounding 492 : Kranthi Kumar et al : High Prevalence of Infantile Encephalitic Beriberi with Overlapping Features of Leigh's Disease 493 : Mohd-Yusuf et al : PDCD1 and SLE in Malaysian cohort 494 : Mookherjee et al : Functional Implication of CYP1B1 in Primary Open Angle Glaucoma 495 : Murthy A et al : A putative genetic locus for bipolar affective disorder at chromosome 6pter-p24.3 496 : Neetha et al : Association Studies of Neurotransmitter Receptor and Transporter Genes in the Theranostics of Schizophrenia in a South Indian Population 497 : Negi et al : Molecular correlates of extreme human constitution types defined in Ayurveda: The Indian traditional system of medicine 498 : Pal et al : Role of alcohol metabolizing genes in alcohol induced Pancreatitis 499 : Periyasamy et al : Mitochondrial dysfunction: a major cause for neuromuscular diseases 500 : Phan Van et al : A study of A3243G mutation in mitochondrial tRNALeu among Vietnamese MELAS patients 501 : Ray et al : Molecular pathogenesis of Parkin gene related Parkinson's disease in Indian population 502 : Saha et al : Integrin Beta 3 gene (ITGB3) polymorphisms and Autism Spectrum Disorder: An association study in the Indian population from West Bengal 503 : Saldaña-Alvarez et al : Polymorphisms analysis in the leptin gene promoter and the leptin receptor gene in a sample of Mexican obesity patients 504 : Sarkar et al : Role of SNAP25 genetic polymorphisms in the etiology of Attention Deficit Hyperactivity Disorder in eastern Indian subjects 505 : Shipra et al : T-47C variation in CRYGB gene: protection against steroid induced pediatric cataract? 506 : Singh et al : Lack of association of three SNP markers (A-1438G, T102C and C1354T) of serotonin receptor 2A gene (HTR2A) with Autism Spectrum Disorder (ASD): A Genetic Study on Indian population 507 : Subhashree et al : Epistatic interactions in psychiatric disorders 508 : Sukka Ganesh et al : Is C-A substitution in exon-2 of CRYAA gene (F71L) causally related to age-related cataracts? 509 : Taneja et al : Exploring the molecular association of Transthyretin Amyloidosis with Spinocerebellar Ataxia and Glaucoma 510 : Tripathi et al : PAX6 interacts with SPARC, Ras and P53 that links Akt and TGFbeta pathways and influences on neural functions in brain 511 : Weerasekera et al : A descriptive study of the prevalence of factor V (F5) 1691 G>A, prothrombin (F2) 20210G>A and methylenetetrahydrofolate reductase (MTHFR) 677C>T polymorphisms among patients with thromboembolism in the Sri Lankan population 512 : Çaglayan et al : A susceptibility locus for juvenile absence epilepsy13. Micro RNA and Non-Coding DNA and Repeats
513 : Agrawal et al : In silico approach towards discovering novel small molecules as potential inhibitors of oncogenic microRNA processing 514 : Agrawal et al : piRNABank: A tool to annotate and analyze functional relevance of piwi interacting RNAs at genome wide scale 515 : Ahluwalia et al : Human encoded microRNA interferes with HIV-1 replication and nef expression 516 : Anand et al : A novel non-coding RNA in developing gonads of Crocodilus palustris: a candidate gene having a role in sex determination 517 : Bargaje et al : Integrated analysis of gene expression by correlating the transcriptome and miRNome 518 : Brahmachari et al : Incomplete penetrance and variable expressivity: the microRNA connection 519 : Chaurasia et al : Involvement of repeats in non-random genomic divergence in 5' upstream regions of Human and Chimpanzee genes of different biological processes 520 : Das et al : Determination of relative telomere length in normal, obese and hypertensive individuals: A quantitative real time PCR approach 521 : De Sarkar et al : Signatures of recent positive selection in human miRNA genes based on a genome-wide analysis 522 : Dutta : MicroRNAs and non-micro-short RNAs (nmsRNAs) in cell quiescence and cancer 523 : Fang et al : Mir-29 is Up-Regulated During Skeletal Muscle Differentiation 524 : Ganesan et al : Involvement of a nuclear restricted, Drosha processed Non-coding RNA in gene regulation 525 : Ganesh et al : The human satellite III non-coding RNA is involved in general stress response and modulates the cellular toxicity of misfolded proteins associated with neurodegenerative disorders 526 : George et al : Genome wide analysis and discovery of MicroRNA - associated regulatory motifs in two mammalian genomes 527 : Girijadevi et al : MicroRNAs in Cervical Carcinogenesis 528 : Hariharan et al : More to Intronic miRNAs: 'Double Locks' and Feedback Loops 529 : Jadhav et al : Application of artificial microRNA in antiviral therapeutics 530 : Jesudasan et al : Novel non-coding RNA from human Yq12 heterochromatic block provides a testis-specific 5'UTR to CDC2L2 mRNA by trans-splicing 531 : Kanduri et al : Mechanistic insights into Kcnq1ot1 non-coding antisense RNA-mediated transcriptional silencing of the chromosomal domains 532 : Kota et al : Endogenous XIST complementary small RNA and RNAi machinery in human X dosage compensation 533 : Krishnan et al : The predicted microRNA regulation and target identification on candidate genes involved in congestive heart failure 534 : Kumar et al : GATA repeat associated regions of human Y chromosome mark chromatin domain boundaries and facilitate long-range interactions 535 : Kurochkin et al : Identification of long non-coding RNAs regulated by retinoic acid during neuronal differentiation of the human neuroblastoma cells 536 : Mandal et al : Alu repeat mediated transcriptome diversity through antisense, editing and exonization 537 : Pandey et al : Probing the involvement of HSF elements within Alu repeats in global heat shock response 538 : Pillai et al : Role of transcriptional dysregulation in polyglutamine mediated neuronal cell death 539 : Rossbach et al : Dissecting RNA Mediated Gene Silencing Pathways in Murine Embryonic Stem Cells 540 : Salowsky et al : Quality control of miRNA in biological extractions 541 : Scaria et al : In silico models of microRNA regulatory networks in host-pathogen crosstalk 542 : Shekar et al : Argonaute 2 is dispensable in self-renewal and differentiation of murine ES cells 543 : Singh : Sequence based method of Riboswitch detection 544 : Soni et al : Maternal inheritance of a microRNA with pleiotropic tissue specific effects 545 : Sripathi et al : Screening for human miRNA targets on the genetic pathway in Type II Diabetes Mellitus 546 : Tanzi et al : A SOLiDTM Approach to Small RNA Discovery and Profiling using Ligase Enhanced Genome Detection 547 : Trivedi et al : Micro RNA, Simple Sequence Repeats and Neuron Specific Genes 548 : Vaz et al : Prediction and Validation of precursor miRNAs in Human Genomic sequences 549 : Wahlestedt : Noncoding RNAs in Nervous System Function14. Genomics of Model Organisms
550 : Agrawal et al : Genomic Dissection of the Cellular Exocytic Machinery Regulating Airway Mucus Secretion 551 : Bandyopadhyay et al : Gene expression profile in glucocorticoid-induced hypertrophied heart in rat 552 : Brahmachari et al : Mining the human genome for components of cellular memory modules 553 : Farhan et al : A Drosophila systems model of locomotor plasticity relevant in epileptogenesis 554 : Withdrawn : 555 : Goode et al : Investigating the influence of cis-regulatory elements in differential roles of the PAX258 gene family 556 : Joe et al : Positional cloning identifies variants of A disintegrin-like metalloproteinase with thrombospondin motifs 16 linked to hypertension in a rat model and in humans 557 : Joshi : Lessons from the Fruitfly: Interaction between members of a Conserved Wnt gene cluster 558 : Joshi et al : Identification of potential drug targets in Acinetobacter baylyi using Genomics Approach 559 : Karar et al : Differential Gene Expression in Mice Exposed to Acute Hypobaric Hypoxia 560 : Kasturia et al : Genetic analysis of γ-Glutamylcysteine synthetase enzyme involved in Glutathione biosynthesis in model organism Saccharomyces cerevisiae 561 : Kumar et al : Study of the gamma glutamyl cycle in yeast 562 : Kumar et al : Homocysteine induces mitochondrial stress mediated cell death in Saccharomyces cerevisiae 563 : Kumar et al : Role of intracellular Calcium in Drosophila larval growth and viability: A Microarray analysis 564 : Kushwaha et al : In silico identification of novel DOF (DNA binding with one finger) genes from Sorghum bicolor using comparative genomics approach 565 : Lufkin et al : Cell-type specific transcriptional profiling in developing mouse embryos 566 : Lyons et al : Genetic Variation and Population Structuring of the Domestic Cat 567 : Maity et al : Gene expression profile in hyperthyroid induced hypertrophied heart in rat 568 : Manoj et al : G-protein coupled signaling in Ciona intestinalis : a comparative genomics perspective 569 : Mathavan et al : Comparative transcriptomic analysis identifies functional conservation of estrogen responsiveness between zebrafish and human cancer cell lines 570 : Mathur et al : Analysis of the mechanisms of differential facultative chromatin organization in a model system 571 : Meli et al : Community annotation of the zebrafish genome: a wiki solution 572 : Mishra et al : Transcriptional profile of immune response genes in mammals at high altitude 573 : Mukherjee et al : Study of the role of genetic heterogeneity in response to Low dose ionizing radiation using mice as model system 574 : Palmes-Saloma et al : Evaluation of Potential Risk on Mammalian Embryos of Nanoparticles Introduced Systemically on the Mother during Pregnancy 575 : Sharma et al : Genomic mechanism of levetiracetam action in a Drosophila systems model 576 : Singh et al : Insertional Mutagenesis Screen In Zebrafish Using Gene Breaking Trap Approach 577 : Singh et al : Paradoxical signature of antiepileptic drugs in a Drosophila genomic model 578 : Singh et al : Application of Comparative Genomics for identification of genes involved in plant stress from Octodecanoid and Jasmonic acid pathway of Rice and Arabidopsis thaliana 579 : Singh et al : Creation and characterization of Wdr13 gene deficient mouse 580 : Sivasubbu et al : Genome-wide gene trapping identifies novel transcripts in zebrafish 581 : Sultana et al : Boundary element separates the differentially expressing genes myoglianin and eyeless on the fourth chromosome of Drosophila melanogaster 582 : Thakur et al : Pgt1, a glutathione transporter from the fission yeast Schizosaccharomyces pombe 583 : Visa et al : Preliminary characterization of the IGF-II binding domain of the fugu fish mannose 6-phosphate/IGF-II receptor protein 584 : Yadav et al : A Comparative analysis of the sulphur assimilatory pathways in Candida glabrata with other yeasts 585 : Zhang et al : Gene identification signature (GIS) analysis for Zebrafish transcriptome characterization and genome annotation15. Chemical Genomics and Molecular Medicine
586 : Anantha Ramanan et al : Use of natural analogs as AchE inhibitor for treatment of early stage Alzheimer's Disease 587 : Arya : Challenges and Opportunities in the Post-Genomic Chemical Biology Age: The Hunt for Small Molecule, Chemical Dissectors of Signaling Networks 588 : Balhara et al : S29 ribosomal protein regulates balance between cell death and survival in Hep2 cells through MAPK/mitochondrial pathway 589 : Bodzioch et al : The effects of humanin peptides on mitochondrial functions and global gene expression 590 : Chopra et al : Novel paradigm in lipid metabolic network of Mycobacterium tuberculosis 591 : Gonsalves et al : Novel RNAi-based Chemical Genetic Screen to Identify Small Molecule Modulators of the Wnt/wg Signaling Pathway 592 : Han et al : TRIM69/HSD34 protein, a RING finger protein, functions as an E3 ligase in regulating cell cycle and apoptosis by interacting with HUS1 protein 593 : Maity et al : Potentiation of macrophage function by cigarette smoke against Leishmania donovani infection 594 : Nallari et al : Novel Mutations in Sarcomeric and Desmosomal genes in Cardiomyopathies - An Indian Study 595 : Nandy et al : A High-throughput Generation of Flavonoid Natural Product-Inspired Chemical Probes: The Discovery of a Novel Class of Cell Motility Inhibitor 596 : Withdrawn : 597 : Nowak et al : Heterozygous I171V mutation of the nibrin (NBN) gene as a risk factor for solid malignant tumors 598 : Poondra et al : Exploring the Indoline Alkaloid Natural Product-Inspired Space in a Search of Chemical Probes of FAK Signaling Networks 599 : Prakesch et al : A High-throughput Generation of Natural Product-Inspired Compounds: The Discovery of Chemical Modulators of Cell Death Pathways Involving Bcl-XL/Mcl-1 600 : Saarma : Novel neurotrophic factors for the treatment of neurodegenerative diseases 601 : Sahu et al : In-silico Designing of Novel Triazole Derivatives as substitute for Novel Fungicides 602 : Saxena et al : Predicting the activity and druggability of compounds from Medicinal plants through in silico approach 603 : Song et al : RSA-14-44 interacts with PSMB5, a proteasome subunit, in spermatogenic cells 604 : Swami et al : A novel PEG cross-linked PEI nanoparticle: An efficient transfection agent in vitro and in vivo 605 : Vedadi et al : Application of Small Molecule Screening to Investigate Binding Specificity of Protein Families 606 : Wu et al : SPAG8, a testis specific protein, decreased the cell proliferation and prolongated G2/M phase in cell cycle 607 : Xu et al : GADD153, a critical nodal point protein in selenite-induced apoptosis of NB4 cells
Page maintained by
webperson.hgm2008@hgu.mrc.ac.uk
webperson.hgm2008@hgu.mrc.ac.uk
AbProcess V4.30 - Written by Alastair F. Brown
Copyright (C) 1999-2008 Alastair F. Brown
Copyright (C) 1999-2008 Alastair F. Brown