Skip to Content

Publications

Filters: First Letter Of Last Name is P  [Clear All Filters]
A B C D E F G H I J K L M N O [P] Q R S T U V W X Y Z   [Show ALL]
[
[Theory of microcirculation. 1: Misinterpretations in Starling's hypothesis of microcirculation]., Petrow, J. M. , Zeitschrift für die gesamte innere Medizin und ihre Grenzgebiete, 1990 Sep 15, Volume 45, Issue 18, p.531-5, (1990)
[Results of treatment of flexion spasms in children]., Popielarska, A., Gregorczuk J., Suffczyńska-Kotowska M., and Mazurowa M. , Neurologia i neurochirurgia polska, 1971, Volume 5, Issue 3, p.387-91, (1971)
Z
Zebrafish dax1 is required for development of the interrenal organ, the adrenal cortex equivalent., Zhao, Y., Yang Z., Phelan J. K., Wheeler D. A., Lin S., and McCabe E. R. B. , Molecular endocrinology (Baltimore, Md.), 2006 Nov, Volume 20, Issue 11, p.2630-40, (2006) Abstract
W
WormBase: a multi-species resource for nematode biology and genomics., Harris, Todd W., Chen Nansheng, Cunningham Fiona, Tello-Ruiz Marcela, Antoshechkin Igor, Bastiani Carol, Bieri Tamberlyn, Blasiar Darin, Bradnam Keith, Chan Juancarlos, et al. , Nucleic acids research, 2004 Jan 1, Volume 32, Issue Database issue, p.D411-7, (2004) Abstract
Why primate models matter., Phillips, Kimberley A., Bales Karen L., Capitanio John P., Conley Alan, Czoty Paul W., 't Hart Bert A., Hopkins William D., Hu Shiu-Lok, Miller Lisa A., Nader Michael A., et al. , American journal of primatology, 2014 Apr 10, (2014) Abstract
Whole-genome sequence–based analysis of high-density lipoprotein cholesterol, Morrison, Alanna C., Voorman Arend, Johnson Andrew D., Liu Xiaoming, Yu Jin, Li Alexander, Muzny Donna, Yu Fuli, Rice Kenneth, Zhu Chengsong, et al. , Nature Genetics, 6/2013, Volume 45, Issue 8, p.899 - 901, (2013)
Whole-genome sequence-based analysis of high-density lipoprotein cholesterol., Morrison, Alanna C., Voorman Arend, Johnson Andrew D., Liu Xiaoming, Yu Jin, Li Alexander, Muzny Donna, Yu Fuli, Rice Kenneth, Zhu Chengsong, et al. , Nature genetics, 2013 Aug, Volume 45, Issue 8, p.899-901, (2013) Abstract
Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytes., Wang, L., Swierczek S. I., Drummond J., Hickman K., Kim Sj, Walker K., Doddapaneni H., Muzny D. M., Gibbs R. A., Wheeler D. A., et al. , Leukemia, 2014 Apr, Volume 28, Issue 4, p.935-8, (2014)
Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia., Pehlivan, Davut, Karaca Ender, Aydin Hatip, Beck Christine R., Gambin Tomasz, Muzny Donna M., Bilge Geckinli B., Karaman Ali, Jhangiani Shalini N., Gibbs Richard A., et al. , European journal of human genetics : EJHG, 2014 Jan 15, (2014) Abstract
Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis., Wang, Xia, Wang Hui, Cao Ming, Li Zhe, Chen Xianfeng, Patenia Claire, Gore Athurva, Abboud Emad B., Al-Rajhi Ali A., Lewis Richard A., et al. , Human mutation, 2011 Dec, Volume 32, Issue 12, p.1450-9, (2011) Abstract
Whole genome sequences of three Treponema pallidum ssp. pertenue strains: yaws and syphilis treponemes differ in less than 0.2% of the genome sequence., Cejková, Darina, Zobaníková Marie, Chen Lei, Pospíšilová Petra, Strouhal Michal, Qin Xiang, Mikalová Lenka, Norris Steven J., Muzny Donna M., Gibbs Richard A., et al. , PLoS neglected tropical diseases, 2012 Jan, Volume 6, Issue 1, p.e1471, (2012) Abstract
Whole genome sequence of Treponema pallidum ssp. pallidum, strain Mexico A, suggests recombination between yaws and syphilis strains., Pětrošová, Helena, Zobaníková Marie, Čejková Darina, Mikalová Lenka, Pospíšilová Petra, Strouhal Michal, Chen Lei, Qin Xiang, Muzny Donna M., Weinstock George M., et al. , PLoS neglected tropical diseases, 2012, Volume 6, Issue 9, p.e1832, (2012) Abstract
Whole Exome Sequencing of Polycythemia Vera Reveals Novel Recurrent Somatic and Germline Variation, Wang, Linghua, Swierczek Sabina, Piterkova Lucie, Hickman Kimberly, Wheeler David A., and Prchal Josef T. , Blood, Volume 120, Number 21, (2012)
Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome., Bayram, Yavuz, Pehlivan Davut, Karaca Ender, Gambin Tomasz, Jhangiani Shalini N., Erdin Serkan, Gonzaga-Jauregui Claudia, Wiszniewski Wojciech, Muzny Donna, Elcioglu Nursel H., et al. , American journal of medical genetics. Part A, 2014 Sep, Volume 164A, Issue 9, p.2328-34, (2014) Abstract
What everybody should know about the rat genome and its online resources., Twigger, Simon N., Pruitt Kim D., Fernández-Suárez Xosé M., Karolchik Donna, Worley Kim C., Maglott Donna R., Brown Garth, Weinstock George, Gibbs Richard A., Kent Jim, et al. , Nature genetics, 2008 May, Volume 40, Issue 5, p.523-7, (2008) Abstract
WebWise: guide to the Baylor College of Medicine Human Genome Sequencing Center's web site., Pruitt, K. D. , Genome research, 1998 Mar, Volume 8, Issue 3, p.170-4, (1998)
U
Using a pericentromeric interspersed repeat to recapitulate the phylogeny and expansion of human centromeric segmental duplications., Horvath, J. E., Gulden C. L., Bailey J. A., Yohn C., McPherson J. D., Prescott A., Roe B. A., de Jong P. J., Ventura M., Misceo D., et al. , Molecular biology and evolution, 2003 Sep, Volume 20, Issue 9, p.1463-79, (2003) Abstract
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype., Perrault, Isabelle, Estrada-Cuzcano Alejandro, Lopez Irma, Kohl Susanne, Li Shiqiang, Testa Francesco, Zekveld-Vroon Renate, Wang Xia, Pomares Esther, Andorf Jean, et al. , PloS one, 2013, Volume 8, Issue 1, p.e51622, (2013) Abstract
Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy., Majewski, Tadeusz, Lee Sangkyou, Jeong Joon, Yoon Dong-Sup, Kram Andrzej, Kim Mi-Sook, Tuziak Tomasz, Bondaruk Jolanta, Lee Sooyong, Park Weon-Seo, et al. , Laboratory investigation; a journal of technical methods and pathology, 2008 Jul, Volume 88, Issue 7, p.694-721, (2008) Abstract
T
Two Novel Simian Arteriviruses in Captive and Wild Baboons (Papio spp.)., Bailey, Adam L., Lauck Michael, Sibley Samuel D., Pecotte Jerilyn, Rice Karen, Weny Geoffrey, Tumukunde Alex, Hyeroba David, Greene Justin, Correll Michael, et al. , Journal of virology, 2014 Sep 3, (2014) Abstract
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum., Davis, Erica E., Zhang Qi, Liu Qin, Diplas Bill H., Davey Lisa M., Hartley Jane, Stoetzel Corinne, Szymanska Katarzyna, Ramaswami Gokul, Logan Clare V., et al. , Nature genetics, 2011 Mar, Volume 43, Issue 3, p.189-96, (2011) Abstract
A transposon-like element in the deletion-prone region of the dystrophin gene., Pizzuti, A., Pieretti M., Fenwick R. G., Gibbs R. A., and Caskey C. T. , Genomics, 1992 Jul, Volume 13, Issue 3, p.594-600, (1992) Abstract
Transcriptomic analysis supports similar functional roles for the two thymuses of the tammar wallaby., Wong, Emily S. W., Papenfuss Anthony T., Heger Andreas, Hsu Arthur L., Ponting Chris P., Miller Robert D., Fenelon Jane C., Renfree Marilyn B., Gibbs Richard A., and Belov Katherine , BMC genomics, 2011, Volume 12, p.420, (2011) Abstract
Transcriptome of Treponema pallidum: gene expression profile during experimental rabbit infection., Smajs, David, McKevitt Matthew, Howell Jerrilyn K., Norris Steven J., Cai Wei-Wen, Palzkill Timothy, and Weinstock George M. , Journal of bacteriology, 2005 Mar, Volume 187, Issue 5, p.1866-74, (2005) Abstract
TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities., Wiszniewski, Wojciech, Hunter Jill V., Hanchard Neil A., Willer Jason R., Shaw Chad, Tian Qi, Illner Anna, Wang Xueqing, Cheung Sau W., Patel Ankita, et al. , American journal of human genetics, 2013 Aug 8, Volume 93, Issue 2, p.197-210, (2013) Abstract


about seo