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The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Gerhard, Daniela S., Wagner Lukas, Feingold Elise A., Shenmen Carolyn M., Grouse Lynette H., Schuler Greg, Klein Steven L., Old Susan, Rasooly Rebekah, Good Peter, et al. , Genome research, 2004 Oct, Volume 14, Issue 10B, p.2121-7, (2004) Abstract
Stargazin and other transmembrane AMPA receptor regulating proteins interact with synaptic scaffolding protein MAGI-2 in brain., Deng, Fang, Price Maureen G., Davis Caleb F., Mori Mayra, and Burgess Daniel L. , The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006 Jul 26, Volume 26, Issue 30, p.7875-84, (2006) Abstract
SSTR5 P335L monoclonal antibody differentiates pancreatic neuroendocrine neuroplasms with different SSTR5 genotypes., Zhou, Guisheng, Gingras Marie-Claude, Liu Shi-He, Sanchez Robbi, Edwards Dean, Dawson David, Christensen Kurt, Paganelli Giovanni, Gibbs Richard, Fisher William, et al. , Surgery, 2011 Dec, Volume 150, Issue 6, p.1136-42, (2011) Abstract
Squamous Cell Carcinoma of the Oral Tongue in Young Non-Smokers Is Genomically Similar to Tumors in Older Smokers, Pickering, C. R., Zhang J., Neskey D. M., Zhao M., Jasser S. A., Wang J., Ward A., Tsai C. J., Ortega Alves M. V., Zhou J. H., et al. , Clinical Cancer Research, 07/2014, Volume 20, Issue 14, p.3842 - 3848, (2014)
Spontaneous mutagenesis is elevated in protease-defective cells., Al Mamun, Abu Amar M., and Humayun Zafri M. , Molecular microbiology, 2009 Feb, Volume 71, Issue 3, p.629-39, (2009) Abstract
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation., Lalani, Seema R., Safiullah Arsalan M., Fernbach Susan D., Harutyunyan Karine G., Thaller Christina, Peterson Leif E., McPherson John D., Gibbs Richard A., White Lisa D., Hefner Margaret, et al. , American journal of human genetics, 2006 Feb, Volume 78, Issue 2, p.303-14, (2006) Abstract
Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study., Volcik, Kelly A., Ballantyne Christie M., Coresh Josef, Folsom Aaron R., and Boerwinkle Eric , Atherosclerosis, 2007 Nov, Volume 195, Issue 1, p.e76-82, (2007) Abstract
Sources of variation in hair cortisol in wild and captive non-human primates., Fourie, Nicolaas H., Brown Janine L., Jolly Clifford J., Phillips-Conroy Jane E., Rogers Jeffrey, and Bernstein Robin M. , Zoology (Jena, Germany), 2016 Feb 2, (2016) Abstract
Source identification in two criminal cases using phylogenetic analysis of HIV-1 DNA sequences., Scaduto, Diane I., Brown Jeremy M., Haaland Wade C., Zwickl Derrick J., Hillis David M., and Metzker Michael L. , Proceedings of the National Academy of Sciences of the United States of America, 2010 Dec 14, Volume 107, Issue 50, p.21242-7, (2010) Abstract
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence., Bidichandani, S. I., Purandare S. M., Taylor E. E., Gumin G., Machkhas H., Harati Y., Gibbs R. A., Ashizawa T., and Patel P. I. , Human molecular genetics, 1999 Dec, Volume 8, Issue 13, p.2425-36, (1999) Abstract
Somatic mutations affect key pathways in lung adenocarcinoma., Ding, Li, Getz Gad, Wheeler David A., Mardis Elaine R., McLellan Michael D., Cibulskis Kristian, Sougnez Carrie, Greulich Heidi, Muzny Donna M., Morgan Margaret B., et al. , Nature, 2008 Oct 23, Volume 455, Issue 7216, p.1069-75, (2008) Abstract
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma., Davis, Caleb F., Ricketts Christopher J., Wang Min, Yang Lixing, Cherniack Andrew D., Shen Hui, Buhay Christian, Kang Hyojin, Kim Sang Cheol, Fahey Catherine C., et al. , Cancer cell, 2014 Sep 8, Volume 26, Issue 3, p.319-330, (2014) Abstract
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10., Matsuura, Tohru, Fang Ping, Lin Xi, Khajavi Mehrdad, Tsuji Kuniko, Rasmussen Astrid, Grewal Raji P., Achari Madhureeta, Alonso Maria E., Pulst Stefan M., et al. , American journal of human genetics, 2004 Jun, Volume 74, Issue 6, p.1216-24, (2004) Abstract
The soluble epoxide hydrolase gene harbors sequence variation associated with susceptibility to and protection from incident ischemic stroke., Fornage, Myriam, Lee Craig R., Doris Peter A., Bray Molly S., Heiss Gerardo, Zeldin Darryl C., and Boerwinkle Eric , Human molecular genetics, 2005 Oct 1, Volume 14, Issue 19, p.2829-37, (2005) Abstract
Software for automated analysis of DNA fingerprinting gels., Fuhrmann, Daniel R., Krzywinski Martin I., Chiu Readman, Saeedi Parvaneh, Schein Jacqueline E., Bosdet Ian E., Chinwalla Asif, Hillier Ladeana W., Waterston Robert H., McPherson John D., et al. , Genome research, 2003 May, Volume 13, Issue 5, p.940-53, (2003) Abstract
SNPdetector: a software tool for sensitive and accurate SNP detection., Zhang, Jinghui, Wheeler David A., Yakub Imtiaz, Wei Sharon, Sood Raman, Rowe William, Liu Paul P., Gibbs Richard A., and Buetow Kenneth H. , PLoS computational biology, 2005 Oct, Volume 1, Issue 5, p.e53, (2005) Abstract
A SNP discovery method to assess variant allele probability from next-generation resequencing data., Shen, Yufeng, Wan Zhengzheng, Coarfa Cristian, Drabek Rafal, Chen Lei, Ostrowski Elizabeth A., Liu Yue, Weinstock George M., Wheeler David A., Gibbs Richard A., et al. , Genome research, 2010 Feb, Volume 20, Issue 2, p.273-80, (2010) Abstract
Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci., Oeltjen, J. C., Liu X., Lu J., Allen R. C., Muzny D., Belmont J. W., and Gibbs R. A. , Mammalian genome : official journal of the International Mammalian Genome Society, 1995 May, Volume 6, Issue 5, p.334-8, (1995) Abstract
Single-Molecule Sequencing Reveals Estrogen-Regulated Clinically Relevant lncRNAs in Breast Cancer., Jonsson, Philip, Coarfa Cristian, Mesmar Fahmi, Raz Tal, Rajapakshe Kimal, Thompson John F., Gunaratne Preethi H., and Williams Cecilia , Molecular endocrinology (Baltimore, Md.), 2015 Nov, Volume 29, Issue 11, p.1634-45, (2015) Abstract
Single stimulus fMRI produces a neural individual difference measure for Autism Spectrum Disorder., Lu, James, Kishida Ken, De Asis Cruz Josepheen, Lohrenz Terry, Deering Diane Treadwell, Beauchamp Michael, and Montague Read P. , Clinical psychological science : a journal of the Association for Psychological Science, 2015 May 1, Volume 3, Issue 3, p.422-432, (2015) Abstract
Single nucleotide polymorphisms in genes for 2'-5'-oligoadenylate synthetase and RNase L inpatients hospitalized with West Nile virus infection., Yakub, Imtiaz, Lillibridge Kristy M., Moran Ana, Gonzalez Omar Y., Belmont John, Gibbs Richard A., and Tweardy David J. , The Journal of infectious diseases, 2005 Nov 15, Volume 192, Issue 10, p.1741-8, (2005) Abstract
Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study., Morrison, Alanna C., Bare Lance A., Luke May M., Pankow James S., Mosley Thomas H., Devlin James J., Willerson James T., and Boerwinkle Eric , Cerebrovascular diseases (Basel, Switzerland), 2008, Volume 26, Issue 4, p.420-4, (2008) Abstract
Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma., Cotton, Ronald T., Li Donghui, Scherer Steven E., Muzny Donna M., Hodges Sally E., Catania Robbi L., Witkiewicz Agnieszka K., Brody Jonathan R., Kennedy Eugene P., Yeo Charles J., et al. , HPB : the official journal of the International Hepato Pancreato Biliary Association, 2009 Aug, Volume 11, Issue 5, p.435-44, (2009) Abstract
Single nucleotide polymorphism (SNP) analysis of mouse quantitative trait loci for identification of candidate genes., Yan, Y., Wang M., Lemon W. J., and You M. , Journal of medical genetics, 2004 Sep, Volume 41, Issue 9, p.e111, (2004)

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