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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
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)
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
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
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
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)
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
Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection., Guo, Dong-Chuan, Regalado Ellen S., Minn Charles, Tran-Fadulu Van, Coney Joshua, Cao Jiumei, Wang Min, Yu Robert K., Estrera Anthony L., Safi Hazim J., et al. , Circulation. Cardiovascular genetics, 2011 Feb, Volume 4, Issue 1, p.36-42, (2011) Abstract
ABCF1 extrinsically regulates retinal pigment epithelial cell phagocytosis., Guo, Feiye, Ding Ying, Caberoy Nora, Alvarado Gabriela, Wang Feng, Chen Rui, and Li Wei , Molecular biology of the cell, 2015 Apr 22, (2015) Abstract
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) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease., Guo, Dong-Chuan, Papke Christina L., Tran-Fadulu Van, Regalado Ellen S., Avidan Nili, Johnson Ralph Jay, Kim Dong H., Pannu Hariyadarshi, Willing Marcia C., Sparks Elizabeth, et al. , American journal of human genetics, 2009 May, Volume 84, Issue 5, p.617-27, (2009) Abstract
Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene., Guo, W., Worley K., Adams V., Mason J., Sylvester-Jackson D., Zhang Y. H., Towbin J. A., Fogt D. D., Madu S., and Wheeler D. A. , Nature genetics, 1993 Aug, Volume 4, Issue 4, p.367-72, (1993) Abstract

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