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Dawn of ocular gene therapy: implications for molecular diagnosis in retinal disease., Zaneveld, Jacques, Wang Feng, Wang Xia, and Chen Rui , Science China. Life sciences, 2013 Feb, Volume 56, Issue 2, p.125-33, (2013) Abstract
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy., Yang, Zhao, Bowles Neil E., Scherer Steven E., Taylor Michael D., Kearney Debra L., Ge Shuping, Nadvoretskiy Vyacheslav V., DeFreitas Gilberto, Carabello Blasé, Brandon Lois I., et al. , Circulation research, 2006 Sep 15, Volume 99, Issue 6, p.646-55, (2006) Abstract
A Drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases., Yamamoto, Shinya, Jaiswal Manish, Charng Wu-Lin, Gambin Tomasz, Karaca Ender, Mirzaa Ghayda, Wiszniewski Wojciech, Sandoval Hector, Haelterman Nele A., Xiong Bo, et al. , Cell, 2014 Sep 25, Volume 159, Issue 1, p.200-14, (2014) Abstract
Deletion screening at the hypoxanthine-guanine phosphoribosyltransferase locus in Chinese hamster cells using the polymerase chain reaction., Xu, Z. D., Yu Y. J., Hsie A. W., Caskey C. T., Rossiter B., and Gibbs R. A. , Teratogenesis, carcinogenesis, and mutagenesis, 1989, Volume 9, Issue 3, p.177-87, (1989) Abstract
De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea., Xia, Fan, Bainbridge Matthew N., Tan Tiong Yang, Wangler Michael F., Scheuerle Angela E., Zackai Elaine H., Harr Margaret H., Sutton Reid V., Nalam Roopa L., Zhu Wenmiao, et al. , American journal of human genetics, 2014 May 1, Volume 94, Issue 5, p.784-9, (2014) Abstract
DVL1 Frameshift Mutations Clustering in the Penultimate Exon Cause Autosomal-Dominant Robinow Syndrome., White, Janson, Mazzeu Juliana F., Hoischen Alexander, Jhangiani Shalini N., Gambin Tomasz, Alcino Michele Calijorne, Penney Samantha, Saraiva Jorge M., Hove Hanne, Skovby Flemming, et al. , American journal of human genetics, 2015 Mar 25, (2015) Abstract
Differentiation of embryonic stem cells into corneal epithelium., Wang, Zhichong, Ge Jian, Huang Bing, Gao Qianying, Liu Bingqian, Wang Linghua, Yu Ling, Fan Zhigang, Lu Xiaoming, and Liu Jingbo , Science in China. Series C, Life sciences / Chinese Academy of Sciences, 2005 Oct, Volume 48, Issue 5, p.471-80, (2005) Abstract
Developing a tissue resource to characterize the genome of pancreatic cancer., Voidonikolas, Georgios, Gingras Marie-Claude, Hodges Sally, McGuire Amy L., Chen Changyi, Gibbs Richard A., Brunicardi Charles F., and Fisher William E. , World journal of surgery, 2009 Apr, Volume 33, Issue 4, p.723-31, (2009) Abstract
DNA deletion confined to the iduronate-2-sulfatase promoter abolishes IDS gene expression., Timms, K. M., Huckett L. E., Belmont J. W., Shapira S. K., and Gibbs R. A. , Human mutation, 1998, Volume 11, Issue 2, p.121-6, (1998) Abstract
Dicer-mediated upregulation of BCRP confers tamoxifen resistance in human breast cancer cells., Selever, Jennifer, Gu Guowei, Lewis Michael T., Beyer Amanda, Herynk Matthew H., Covington Kyle R., Tsimelzon Anna, Dontu Gabriela, Provost Patrick, Di Pietro Attilio, et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2011 Oct 15, Volume 17, Issue 20, p.6510-21, (2011) Abstract
Dissection of K+ currents in Caenorhabditis elegans muscle cells by genetics and RNA interference., Santi, C. M., Yuan A., Fawcett G., Wang Z. - W., Butler A., Nonet M. L., Wei A., Rojas P., and Salkoff L. , Proceedings of the National Academy of Sciences of the United States of America, 2003 Nov 25, Volume 100, Issue 24, p.14391-6, (2003) Abstract
Disruptive TP53 mutation is associated with aggressive disease characteristics in an orthotopic murine model of oral tongue cancer., Sano, Daisuke, Xie Tong-Xin, Ow Thomas J., Zhao Mei, Pickering Curtis R., Zhou Ge, Sandulache Vlad C., Wheeler David A., Gibbs Richard A., Caulin Carlos, et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2011 Nov 1, Volume 17, Issue 21, p.6658-70, (2011) Abstract
The DNA sequence of the human X chromosome., Ross, Mark T., Grafham Darren V., Coffey Alison J., Scherer Steven, McLay Kirsten, Muzny Donna, Platzer Matthias, Howell Gareth R., Burrows Christine, Bird Christine P., et al. , Nature, 2005 Mar 17, Volume 434, Issue 7031, p.325-37, (2005) Abstract
Designing new microsatellite markers for linkage and population genetic analyses in rhesus macaques and other nonhuman primates., Raveendran, Muthuswamy, Harris Alan R., Milosavljevic Aleksandar, Johnson Zach, Shelledy Wendy, Cameron Judy, and Rogers Jeffrey , Genomics, 2006 Dec, Volume 88, Issue 6, p.706-10, (2006) Abstract
Dual regulation and redundant function of two eye-specific enhancers of the Drosophila retinal determination gene dachshund., Pappu, Kartik S., Ostrin Edwin J., Middlebrooks Brooke W., Sili Beril Tavsanli, Chen Rui, Atkins Mardelle R., Gibbs Richard, and Mardon Graeme , Development (Cambridge, England), 2005 Jun, Volume 132, Issue 12, p.2895-905, (2005) Abstract
Differentially expressed nucleolar TGF-beta1 target (DENTT) in mouse development., Ozbun, Laurent L., Martínez Alfredo, Angdisen Jerry, Umphress Sarah, Kang Yang, Wang Min, You Ming, and Jakowlew Sonia B. , Developmental dynamics : an official publication of the American Association of Anatomists, 2003 Mar, Volume 226, Issue 3, p.491-511, (2003) Abstract
The DNA sequence, annotation and analysis of human chromosome 3., Muzny, Donna M., Scherer Steven E., Kaul Rajinder, Wang Jing, Yu Jun, Sudbrak Ralf, Buhay Christian J., Chen Rui, Cree Andrew, Ding Yan, et al. , Nature, 2006 Apr 27, Volume 440, Issue 7088, p.1194-8, (2006) Abstract
Determining Factors Important to Guiding Under Represented Minorities toward Research Careers., Murray, D., and Rivera H. , 50th Annual Meeting of the American Society for Cell Biology., Volume 20, (2010)
Developing Pathways for Underrepresented Minorities into Genomic Science., Murray, D., and Rivera H. , 176th Meeting of the American Association for the Advancement of Science., San Diego, CA., p.p128., (2010)
Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasia, Murali, Chaya, Lu James T., Jain Mahim, Liu David S., Lachman Ralph, Gibbs Richard A., Lee Brendan H., Cohn Daniel, and Campeau Philippe M. , Molecular Genetics and Metabolism Reports, 2014, Volume 1, p.213 - 219, (2014)
Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study., Meyer, Tamra E., Boerwinkle Eric, Morrison Alanna C., Volcik Kelly A., Sanderson Maureen, Coker Ann L., Pankow James S., and Folsom Aaron R. , Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010 Feb, Volume 19, Issue 2, p.558-65, (2010) Abstract
Dnmt3a loss predisposes murine hematopoietic stem cells to malignant transformation., Mayle, Allison, Yang Liubin, Rodriguez Benjamin, Zhou Ting, Chang Edmund, Curry Choladda V., Challen Grant A., Li Wei, Wheeler David, Rebel Vivienne I., et al. , Blood, 2015 Jan 22, Volume 125, Issue 4, p.629-38, (2015) Abstract
Demographic, environmental, and genetic predictors of metabolic side effects of hydrochlorothiazide treatment in hypertensive subjects., Maitland-van der Zee, Anke-Hilse, Turner Stephen T., Schwartz Gary L., Chapman Arlene B., Klungel Olaf H., and Boerwinkle Eric , American journal of hypertension, 2005 Aug, Volume 18, Issue 8, p.1077-83, (2005) Abstract
The Drosophila melanogaster Genetic Reference Panel., Mackay, Trudy F. C., Richards Stephen, Stone Eric A., Barbadilla Antonio, Ayroles Julien F., Zhu Dianhui, Casillas Sònia, Han Yi, Magwire Michael M., Cridland Julie M., et al. , Nature, 2012 Feb 9, Volume 482, Issue 7384, p.173-8, (2012) Abstract
dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations., Liu, Xiaoming, Jian Xueqiu, and Boerwinkle Eric , Human mutation, 2013 Sep, Volume 34, Issue 9, p.E2393-402, (2013) Abstract

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