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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
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
Demographic histories and patterns of linkage disequilibrium in Chinese and Indian rhesus macaques., Hernandez, Ryan D., Hubisz Melissa J., Wheeler David A., Smith David G., Ferguson Betsy, Rogers Jeffrey, Nazareth Lynne, Indap Amit, Bourquin Traci, McPherson John, et al. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.240-3, (2007) Abstract
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles., Boone, Philip M., Campbell Ian M., Baggett Brett C., Soens Zachry T., Rao Mitchell M., Hixson Patricia M., Patel Ankita, Bi Weimin, Cheung Sau Wai, Lalani Seema R., et al. , Genome research, 2013 Sep, Volume 23, Issue 9, p.1383-94, (2013) Abstract
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification., Chamberlain, J. S., Gibbs R. A., Ranier J. E., Nguyen P. N., and Caskey C. T. , Nucleic acids research, 1988 Dec 9, Volume 16, Issue 23, p.11141-56, (1988) 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
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome., Koekkoek, S. K. E., Yamaguchi K., Milojkovic B. A., Dortland B. R., Ruigrok T. J. H., Maex R., De Graaf W., Smit A. E., VanderWerf F., Bakker C. E., et al. , Neuron, 2005 Aug 4, Volume 47, Issue 3, p.339-52, (2005) Abstract
Deeper into the genome., Gibbs, Richard , Nature, 2005 Oct 27, Volume 437, Issue 7063, p.1233-4, (2005)
Deep sequencing of systematic combinatorial libraries reveals β-lactamase sequence constraints at high resolution., Deng, Zhifeng, Huang Wanzhi, Bakkalbasi Erol, Brown Nicholas G., Adamski Carolyn J., Rice Kacie, Muzny Donna, Gibbs Richard A., and Palzkill Timothy , Journal of molecular biology, 2012 Dec 7, Volume 424, Issue 3-4, p.150-67, (2012) Abstract
Deep resequencing reveals excess rare recent variants consistent with explosive population growth., Coventry, Alex, Bull-Otterson Lara M., Liu Xiaoming, Clark Andrew G., Maxwell Taylor J., Crosby Jacy, Hixson James E., Rea Thomas J., Muzny Donna M., Lewis Lora R., et al. , Nature communications, 2010, Volume 1, p.131, (2010) Abstract
Deep resequencing and association analysis of schizophrenia candidate genes., Crowley, J. J., Hilliard C. E., Kim Y., Morgan M. B., Lewis L. R., Muzny D. M., Hawes A. C., Sabo A., Wheeler D. A., Lieberman J. A., et al. , Molecular psychiatry, 2013 Feb, Volume 18, Issue 2, p.138-40, (2013)
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy., Fu, Y. H., Friedman D. L., Richards S., Pearlman J. A., Gibbs R. A., Pizzuti A., Ashizawa T., Perryman M. B., Scarlato G., and Fenwick R. G. , Science (New York, N.Y.), 1993 Apr 9, Volume 260, Issue 5105, p.235-8, (1993) Abstract
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome., Bainbridge, Matthew N., Hu Hao, Muzny Donna M., Musante Luciana, Lupski James R., Graham Brett H., Chen Wei, Gripp Karen W., Jenny Kim, Wienker Thomas F., et al. , Genome medicine, 2013 Feb 5, Volume 5, Issue 2, p.11, (2013) 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
dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions., Liu, Xiaoming, Jian Xueqiu, and Boerwinkle Eric , Human mutation, 2011 Aug, Volume 32, Issue 8, p.894-9, (2011) 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
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
DANPOS: dynamic analysis of nucleosome position and occupancy by sequencing., Chen, Kaifu, Xi Yuanxin, Pan Xuewen, Li Zhaoyu, Kaestner Klaus, Tyler Jessica, Dent Sharon, He Xiangwei, and Li Wei , Genome research, 2013 Feb, Volume 23, Issue 2, p.341-51, (2013) Abstract

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