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Bayesian estimation of genomic copy number with single nucleotide polymorphism genotyping arrays., Guo, Beibei, Villagran Alejandro, Vannucci Marina, Wang Jian, Davis Caleb F., Man Tsz-Kwong, Lau Ching, and Guerra Rudy , BMC research notes, 2010, Volume 3, p.350, (2010) Abstract
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections., Guo, Dong-Chuan, Pannu Hariyadarshi, Tran-Fadulu Van, Papke Christina L., Yu Robert K., Avidan Nili, Bourgeois Scott, Estrera Anthony L., Safi Hazim J., Sparks Elizabeth, et al. , Nature genetics, 2007 Dec, Volume 39, Issue 12, p.1488-93, (2007) Abstract
Concatenation cDNA sequencing for transcriptome analysis., Gunaratne, Preethi H., Wu Jiaqian, Garcia Angela M., Hulyk Steven, Worley Kim C., Margolin Judith F., and Gibbs Richard A. , Comptes rendus biologies, 2003 Oct-Nov, Volume 326, Issue 10-11, p.971-7, (2003) Abstract
Advances in genome biology and technology., Gunaratne, Preethi H. , Expert review of molecular diagnostics, 2004 Nov, Volume 4, Issue 6, p.757-60, (2004)
Enhancer and promoter elements directing activation and glucocorticoid repression of the alpha 1-fetoprotein gene in hepatocytes., Guertin, M., LaRue H., Bernier D., Wrange O., Chevrette M., Gingras M. C., and Bélanger L. , Molecular and cellular biology, 1988 Apr, Volume 8, Issue 4, p.1398-407, (1988) Abstract
Orphan nuclear receptor GCNF is required for the repression of pluripotency genes during retinoic acid-induced embryonic stem cell differentiation., Gu, Peili, LeMenuet Damien, Chung Arthur C. - K., Mancini Michael, Wheeler David A., and Cooney Austin J. , Molecular and cellular biology, 2005 Oct, Volume 25, Issue 19, p.8507-19, (2005) Abstract
FMR2 function: insight from a mouse knockout model., Gu, Y., and Nelson D. L. , Cytogenetic and genome research, 2003, Volume 100, Issue 1-4, p.129-39, (2003) Abstract
Orphan nuclear receptor LRH-1 is required to maintain Oct4 expression at the epiblast stage of embryonic development., Gu, Peili, Goodwin Bryan, Chung Arthur C. - K., Xu Xueping, Wheeler David A., Price Roger R., Galardi Cristin, Peng Li, Latour Anne M., Koller Beverly H., et al. , Molecular and cellular biology, 2005 May, Volume 25, Issue 9, p.3492-505, (2005) Abstract
Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island., Gu, Y., Shen Y., Gibbs R. A., and Nelson D. L. , Nature genetics, 1996 May, Volume 13, Issue 1, p.109-13, (1996) Abstract
Novel microRNA candidates and miRNA-mRNA pairs in embryonic stem (ES) cells., Gu, Peili, Reid Jeffrey G., Gao Xiaolian, Shaw Chad A., Creighton Chad, Tran Peter L., Zhou Xiaochuan, Drabek Rafal B., Steffen David L., Hoang David M., et al. , PloS one, 2008, Volume 3, Issue 7, p.e2548, (2008) Abstract
Targeting Thyroid Receptor b in Estrogen Receptor Negative Breast Cancer, Gu, G., Covington K., Rechoum Y., O'Malley B., Mangelsdorf D., Minna J., Webb P., and Fuqua S. , Cancer Research, Volume 72, Number 24 Supplement 3, (2012)
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium., Grove, Megan L., Yu Bing, Cochran Barbara J., Haritunians Talin, Bis Joshua C., Taylor Kent D., Hansen Mark, Borecki Ingrid B., Cupples Adrienne L., Fornage Myriam, et al. , PloS one, 2013, Volume 8, Issue 7, p.e68095, (2013) Abstract
Relationship of HIV testing and high-risk behaviors among clients in methadone maintenance treatment., Grella, C. E., Campos M., and Anglin M. D. , AIDS education and prevention : official publication of the International Society for AIDS Education, 1998 Oct, Volume 10, Issue 5, p.403-16, (1998) Abstract
Natural killer cell regulation of implantation and early lung growth of H-ras-transformed 10T1/2 fibroblasts in mice., Greenberg, A. H., Egan S. E., Jarolim L., Gingras M. C., and Wright J. A. , Cancer research, 1987 Sep 15, Volume 47, Issue 18, p.4801-5, (1987) Abstract
Genetic diversity among type emm28 group A Streptococcus strains causing invasive infections and pharyngitis., Green, Nicole M., Beres Stephen B., Graviss Edward A., Allison James E., McGeer Allison J., Vuopio-Varkila Jaana, LeFebvre Rance B., and Musser James M. , Journal of clinical microbiology, 2005 Aug, Volume 43, Issue 8, p.4083-91, (2005) Abstract
Reporting genomic sequencing results to ordering clinicians: incidental, but not exceptional., Green, Robert C., Lupski James R., and Biesecker Leslie G. , JAMA : the journal of the American Medical Association, 2013 Jul 24, Volume 310, Issue 4, p.365-6, (2013)
Demographic history and rare allele sharing among human populations., Gravel, Simon, Henn Brenna M., Gutenkunst Ryan N., Indap Amit R., Marth Gabor T., Clark Andrew G., Yu Fuli, Gibbs Richard A., and Bustamante Carlos D. , Proceedings of the National Academy of Sciences of the United States of America, 2011 Jul 19, Volume 108, Issue 29, p.11983-8, (2011) Abstract
Genetic linkage and imprinting effects on body mass index in children and young adults., Gorlova, Olga Y., Amos Christopher I., Wang Nancy W., Shete Sanjay, Turner Stephen T., and Boerwinkle Eric , European journal of human genetics : EJHG, 2003 Jun, Volume 11, Issue 6, p.425-32, (2003) Abstract
The molecular characterisation of HPRT CHERMSIDE and HPRT COORPAROO: two Lesch-Nyhan patients with reduced amounts of mRNA., Gordon, R. B., Dawson P. A., Sculley D. G., Emmerson B. T., Caskey C. T., and Gibbs R. A. , Gene, 1991 Dec 15, Volume 108, Issue 2, p.299-304, (1991) Abstract
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy., Gonzaga-Jauregui, Claudia, Harel Tamar, Gambin Tomasz, Kousi Maria, Griffin Laurie B., Francescatto Ludmila, Ozes Burcak, Karaca Ender, Jhangiani Shalini N., Bainbridge Matthew N., et al. , Cell reports, 2015 Aug 18, Volume 12, Issue 7, p.1169-83, (2015) Abstract
Human genome sequencing in health and disease., Gonzaga-Jauregui, Claudia, Lupski James R., and Gibbs Richard A. , Annual review of medicine, 2012, Volume 63, p.35-61, (2012) Abstract
Mutations in COL27A1 cause Steel syndrome and suggest a founder mutation effect in the Puerto Rican population, Gonzaga-Jauregui, Claudia, Gamble Candace N., Yuan Bo, Penney Samantha, Jhangiani Shalini, Muzny Donna M., Gibbs Richard A., Lupski James R., and Hecht Jacqueline T. , European Journal of Human Genetics, 07/2014, (2014)
Mutations in VRK1 Associated With Complex Motor and Sensory Axonal Neuropathy Plus Microcephaly., Gonzaga-Jauregui, Claudia, Lotze Timothy, Jamal Leila, Penney Samantha, Campbell Ian M., Pehlivan Davut, Hunter Jill V., Woodbury Suzanne L., Raymond Gerald, Adesina Adekunle M., et al. , JAMA neurology, 2013 Oct 14, (2013) Abstract
The genome sequence of Mannheimia haemolytica A1: insights into virulence, natural competence, and Pasteurellaceae phylogeny., Gioia, Jason, Qin Xiang, Jiang Huaiyang, Clinkenbeard Kenneth, Lo Reggie, Liu Yamei, Fox George E., Yerrapragada Shailaja, McLeod Michael P., McNeill Thomas Z., et al. , Journal of bacteriology, 2006 Oct, Volume 188, Issue 20, p.7257-66, (2006) Abstract
Paradoxical DNA repair and peroxide resistance gene conservation in Bacillus pumilus SAFR-032., Gioia, Jason, Yerrapragada Shailaja, Qin Xiang, Jiang Huaiyang, Igboeli Okezie C., Muzny Donna, Dugan-Rocha Shannon, Ding Yan, Hawes Alicia, Liu Wen, et al. , PloS one, 2007, Volume 2, Issue 9, p.e928, (2007) Abstract

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