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Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida., Agopian, A. J., Bhalla Angela D., Boerwinkle Eric, Finnell Richard H., Grove Megan L., Hixson James E., Shimmin Lawrence C., Sewda Anshuman, Stuart Colin, Zhong Yu, et al. , Birth defects research. Part A, Clinical and molecular teratology, 2013 Sep, Volume 97, Issue 9, p.597-601, (2013) Abstract
Exome sequencing of head and neck squamous cell carcinoma reveals inactivating mutations in NOTCH1., Agrawal, Nishant, Frederick Mitchell J., Pickering Curtis R., Bettegowda Chetan, Chang Kyle, Li Ryan J., Fakhry Carole, Xie Tong-Xin, Zhang Jiexin, Wang Jing, et al. , Science (New York, N.Y.), 2011 Aug 26, Volume 333, Issue 6046, p.1154-7, (2011) Abstract
Escherichia coli cells bearing mutA, a mutant glyV tRNA gene, express a recA-dependent error-prone DNA replication activity., Al Mamun, A. A., Rahman M. S., and Humayun M. Z. , Molecular microbiology, 1999 Aug, Volume 33, Issue 4, p.732-40, (1999) Abstract
Elevated expression of DNA polymerase II increases spontaneous mutagenesis in Escherichia coli., Al Mamun, Abu Amar M. , Mutation research, 2007 Dec 1, Volume 625, Issue 1-2, p.29-39, (2007) Abstract
Escherichia coli DNA polymerase II can efficiently bypass 3,N(4)-ethenocytosine lesions in vitro and in vivo., Al Mamun, Abu Amar M., and Humayun Zafri M. , Mutation research, 2006 Jan 29, Volume 593, Issue 1-2, p.164-76, (2006) Abstract
The Escherichia coli UVM response is accompanied by an SOS-independent error-prone DNA replication activity demonstrable in vitro., Al Mamun, A. A., Yadava R. S., Ren L., and Humayun M. Z. , Molecular microbiology, 2000 Oct, Volume 38, Issue 2, p.368-80, (2000) Abstract
The extent of genetic variation in the CCR5 gene., Ansari-Lari, M. A., Liu X. M., Metzker M. L., Rut A. R., and Gibbs R. A. , Nature genetics, 1997 Jul, Volume 16, Issue 3, p.221-2, (1997)
Expression of human immunodeficiency virus type 1 reverse transcriptase in trans during virion release and after infection., Ansari-Lari, M. A., and Gibbs R. A. , Journal of virology, 1996 Jun, Volume 70, Issue 6, p.3870-5, (1996) Abstract
Estrogen Receptor-Positive Breast Cancer Cells Drive CAFs to Secrete Leptin and Support Tumor Invasiveness, Barone, Ines, Catalano Stefania, Gelsomino Luca, Panza Salvatore, Marsico Stefania, Giordano Cinzia, Bonofiglio Daniela, Casaburi Ivan, Covington Kyle R., Fuqua Suzanne, et al. , The FASEB Journal, Volume 26, p.142–7, (2012)
Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI., Bayram, Yavuz, Aydin Hatip, Gambin Tomasz, Akdemir Zeynep Coban, Atik Mehmed M., Karaca Ender, Karaman Ali, Pehlivan Davut, Jhangiani Shalini N., Gibbs Richard A., et al. , American journal of medical genetics. Part A, 2015 Apr 6, (2015) Abstract
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information., Bonnen, Penelope E., Lowe Jennifer K., Altshuler David M., Breslow Jan L., Stoffel Markus, Friedman Jeffrey M., and Pe'er Itsik , European journal of human genetics : EJHG, 2010 Mar, Volume 18, Issue 3, p.309-16, (2010) Abstract
Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia., Bonnen, Penelope E., Pe'er Itsik, Plenge Robert M., Salit Jackie, Lowe Jennifer K., Shapero Michael H., Lifton Richard P., Breslow Jan L., Daly Mark J., Reich David E., et al. , Nature genetics, 2006 Feb, Volume 38, Issue 2, p.214-7, (2006) Abstract
Evolution of human immunodeficiency virus type 1 nucleotide sequence diversity among close contacts., Burger, H., Weiser B., Flaherty K., Gulla J., Nguyen P. N., and Gibbs R. A. , Proceedings of the National Academy of Sciences of the United States of America, 1991 Dec 15, Volume 88, Issue 24, p.11236-40, (1991) Abstract
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling., Chaki, Moumita, Airik Rannar, Ghosh Amiya K., Giles Rachel H., Chen Rui, Slaats Gisela G., Wang Hui, Hurd Toby W., Zhou Weibin, Cluckey Andrew, et al. , Cell, 2012 Aug 3, Volume 150, Issue 3, p.533-48, (2012) Abstract
Expression of the murine Duchenne muscular dystrophy gene in muscle and brain., Chamberlain, J. S., Pearlman J. A., Muzny D. M., Gibbs R. A., Ranier J. E., Caskey C. T., and Reeves A. A. , Science (New York, N.Y.), 1988 Mar 18, Volume 239, Issue 4846, p.1416-8, (1988) Abstract
Evidence that multiple genetic variants of MC4R play a functional role in the regulation of energy expenditure and appetite in Hispanic children., Cole, Shelley A., Butte Nancy F., Voruganti Saroja V., Cai Guowen, Haack Karin, Kent Jack W., Blangero John, Comuzzie Anthony G., McPherson John D., and Gibbs Richard A. , The American journal of clinical nutrition, 2010 Jan, Volume 91, Issue 1, p.191-9, (2010) Abstract
Exome sequencing of a patient with suspected mitochondrial disease reveals a likely multigenic etiology., Craigen, William J., Graham Brett H., Wong Lee-Jun, Scaglia Fernando, Lewis Richard Alan, and Bonnen Penelope E. , BMC medical genetics, 2013, Volume 14, p.83, (2013) Abstract
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci., Demerath, Ellen W., Guan Weihua, Grove Megan L., Aslibekyan Stella, Mendelson Michael, Zhou Yi-Hui, Hedman Åsa K., Sandling Johanna K., Li Li-An, Irvin Marguerite R., et al. , Human molecular genetics, 2015 Aug 1, Volume 24, Issue 15, p.4464-79, (2015) Abstract
EAnnot: a genome annotation tool using experimental evidence., Ding, Li, Sabo Aniko, Berkowicz Nicolas, Meyer Rekha R., Shotland Yoram, Johnson Mark R., Pepin Kymberlie H., Wilson Richard K., and Spieth John , Genome research, 2004 Dec, Volume 14, Issue 12, p.2503-9, (2004) Abstract
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction., Do, Ron, Stitziel Nathan O., Won Hong-Hee, Jørgensen Anders Berg, Duga Stefano, Angelica Merlini Pier, Kiezun Adam, Farrall Martin, Goel Anuj, Zuk Or, et al. , Nature, 2015 Feb 5, Volume 518, Issue 7537, p.102-6, (2015) Abstract
Evidence for Stabilizing Selection on Codon Usage in Chromosomal Rearrangements of Drosophila pseudoobscura., Fuller, Zachary L., Haynes Gwilym D., Zhu Dianhui, Batterton Matthew, Chao Hsu, Dugan Shannon, Javaid Mehwish, Jayaseelan Joy C., Lee Sandra, Li Mingmei, et al. , G3 (Bethesda, Md.), 2014 Oct 17, (2014) Abstract
Evolutionary and biomedical insights from the rhesus macaque genome., Gibbs, Richard A., Rogers Jeffrey, Katze Michael G., Bumgarner Roger, Weinstock George M., Mardis Elaine R., Remington Karin A., Strausberg Robert L., Venter Craig J., Wilson Richard K., et al. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.222-34, (2007) Abstract
Evolving methods for the assembly of large genomes., Gibbs, R. A., and Weinstock G. M. , Cold Spring Harbor symposia on quantitative biology, 2003, Volume 68, p.189-94, (2003)
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
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

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