PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease
暂无分享,去创建一个
Jing Chen | Bruce J. Aronow | Anil G. Jegga | Sivakumar Gowrisankar | B. Aronow | A. Jegga | Jing Chen | S. Gowrisankar | Sivakumar Gowrisankar
[1] S. Henikoff,et al. Automated assembly of protein blocks for database searching. , 1991, Nucleic acids research.
[2] S Ichii,et al. The APC gene, responsible for familial adenomatous polyposis, is mutated in human gastric cancer. , 1992, Cancer research.
[3] Francis S. Collins,et al. Variations on a Theme: Cataloging Human DNA Sequence Variation , 1997, Science.
[4] A. Chakravarti. It's raining SNPs, hallelujah? , 1998, Nature Genetics.
[5] Anders Isaksson,et al. First International SNP Meeting at Skokloster, Sweden, August 1998. Enthusiasm mixed with scepticism about single-nucleotide polymorphism markers for dissecting complex disorders , 1999, European Journal of Human Genetics.
[6] T. N. Bhat,et al. The Protein Data Bank , 2000, Nucleic Acids Res..
[7] D. Valle,et al. Online Mendelian Inheritance In Man (OMIM) , 2000, Human mutation.
[8] P. Bork,et al. Towards a structural basis of human non-synonymous single nucleotide polymorphisms. , 2000, Trends in genetics : TIG.
[9] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[10] J. Moult,et al. SNPs, protein structure, and disease , 2001, Human mutation.
[11] P. Bork,et al. Human non-synonymous SNPs: server and survey. , 2002, Nucleic acids research.
[12] Minoru Kanehisa,et al. The KEGG database. , 2002, Novartis Foundation symposium.
[13] S. Amladi,et al. Online Mendelian Inheritance in Man 'OMIM'. , 2003, Indian journal of dermatology, venereology and leprology.
[14] Steven Henikoff,et al. SIFT: predicting amino acid changes that affect protein function , 2003, Nucleic Acids Res..
[15] Russ B. Altman,et al. MutDB: annotating human variation with functionally relevant data , 2003, Bioinform..
[16] A. Valencia,et al. A gene network for navigating the literature , 2004, Nature Genetics.
[17] Sivakumar Gowrisankar,et al. Pattern of sequence variation across 213 environmental response genes. , 2004, Genome research.
[18] N. Campbell. Genetic association database , 2004, Nature Reviews Genetics.
[19] Cynthia L. Smith,et al. The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information , 2004, Genome Biology.
[20] Aleksey A. Porollo,et al. Accurate prediction of solvent accessibility using neural networks–based regression , 2004, Proteins.
[21] Timothy R. Rebbeck,et al. Assessing the function of genetic variants in candidate gene association studies , 2004, Nature Reviews Genetics.
[22] Matthew B Schabath,et al. An Evolutionary Perspective on Single-Nucleotide Polymorphism Screening in Molecular Cancer Epidemiology , 2004, Cancer Research.
[23] H. Ozçelik,et al. Identifying functional genetic variants in DNA repair pathway using protein conservation analysis. , 2004, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[24] Simon Kasif,et al. topoSNP: a topographic database of non-synonymous single nucleotide polymorphisms with and without known disease association , 2004, Nucleic Acids Res..
[25] I. M. Jones,et al. Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function. , 2004, Genomics.
[26] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[27] Chu Chen,et al. Screening for Deleterious Nonsynonymous Single-Nucleotide Polymorphisms in Genes Involved in Steroid Hormone Metabolism and Response , 2005, Cancer Epidemiology Biomarkers & Prevention.
[28] Alan F. Scott,et al. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders , 2004, Nucleic Acids Res..
[29] Lincoln Stein,et al. Reactome: a knowledgebase of biological pathways , 2004, Nucleic Acids Res..
[30] David Haussler,et al. LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources , 2005, Bioinform..
[31] Tatiana A. Tatusova,et al. NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins , 2004, Nucleic Acids Res..
[32] A. Sidow,et al. Physicochemical constraint violation by missense substitutions mediates impairment of protein function and disease severity. , 2005, Genome research.
[33] Peng Yue,et al. SNPs3D: Candidate gene and SNP selection for association studies , 2006, BMC Bioinformatics.
[34] Modesto Orozco,et al. PMUT: a web-based tool for the annotation of pathological mutations on proteins , 2005, Bioinform..
[35] Sean D. Mooney,et al. Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis , 2005, Briefings Bioinform..
[36] John B. Anderson,et al. CDD: a Conserved Domain Database for protein classification , 2004, Nucleic Acids Res..
[37] David Haussler,et al. The UCSC Proteome Browser , 2004, Nucleic Acids Res..
[38] C. Ouzounis,et al. Expansion of the BioCyc collection of pathway/genome databases to 160 genomes , 2005, Nucleic acids research.
[39] Joost Schymkowitz,et al. Bioinformatics Applications Note Snpeffect V2.0: a New Step in Investigating the Molecular Phenotypic Effects of Human Non-synonymous Snps , 2022 .
[40] Tatiana Tatusova,et al. NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins , 2004, Nucleic Acids Res..