Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nicholas Warr"'
Autor:
Jehangir N. Ahmed, Radiya G. Ali, Nicholas Warr, Heather M. Wilson, Helen M. Bellchambers, Kristen S. Barratt, Amelia J. Thompson, Ruth M. Arkell
Publikováno v:
Disease Models & Mechanisms, Vol 6, Iss 3, Pp 755-767 (2013)
SUMMARY The ZIC transcription factors are key mediators of embryonic development and ZIC3 is the gene most commonly associated with situs defects (heterotaxy) in humans. Half of patient ZIC3 mutations introduce a premature termination codon (PTC). In
Externí odkaz:
https://doaj.org/article/6d3b4c00b6344c7a9e083b9e338dc3e4
Autor:
Nicholas Warr, Helen M. Bellchambers, Ruth M. Arkell, Jehangir N. Ahmed, Kristen S. Barratt, Radiya G. Ali, Koula E. M. Diamand, Kieran Neill
Publikováno v:
Journal of Cell Science. 134
Zinc finger of the cerebellum (Zic) proteins act as classic transcription factors to promote transcription of the Foxd3 gene during neural crest cell specification. Additionally, they can act as co-factors that bind proteins from the T-cell factor/ly
Autor:
Nicholas Warr, Dominic P. Norris, Nicola Powles-Glover, Ruth M. Arkell, Joan E. Robson, Anna Chappell
Publikováno v:
Human Molecular Genetics. 17:2986-2996
The putative transcription factor ZIC2 is associated with a defect of forebrain development, known as Holoprosencephaly (HPE), in humans and mouse, yet the mechanism by which aberrant ZIC2 function causes classical HPE is unexplained. The zinc finger
Autor:
Nicholas Warr
The bloody, month-long battle for the Citadel in Hue during 1968 pitted U.S. Marines against an entrenched, numerically superior North Vietnamese Army force. By official U.S. accounts it was a tactical and moral victory for the Marines and the United
Autor:
Helen M. Bellchambers, Kristen S. Barratt, Nicholas Warr, Heather L. Wilson, Amelia J. Thompson, Radiya G. Ali, Jehangir N. Ahmed, Ruth M. Arkell
Publikováno v:
Disease Models & Mechanisms, Vol 6, Iss 3, Pp 755-767 (2013)
Disease Models & Mechanisms
Disease Models & Mechanisms
SummaryThe ZIC transcription factors are key mediators of embryonic development and ZIC3 is the gene most commonly associated with situs defects (heterotaxy) in humans. Half of patient ZIC3 mutations introduce a premature termination codon (PTC). In
Autor:
Manik Ahuja, Robert Aseltine, Nicholas Warren, Susan Reisine, Pam Holtzclaw Williams, Andy Cislo
Publikováno v:
Pilot and Feasibility Studies, Vol 4, Iss 1, Pp 1-7 (2018)
Abstract Background State health agencies (SHA) and local health agencies (LHA) face several challenges with the dissemination of local health data using Web-Based Data Query Systems (WDQS). To help guide future research, this study aimed to utilize
Externí odkaz:
https://doaj.org/article/f7a5b99a4dde40deb1bf6926a9f0da83
Publikováno v:
The Journal of Military History. 62:228
Autor:
Carole Oddoux, Andrew Friedman, Charles Farmer, Andrew H. Crosby, Johnny Loke, Nicholas Warr, Alexander Pearlman, Eric D. Brooks, Andy Greenfield, Lisa Chin, Shahin Shajahan, David Brauer, Jenny J. Couper, Tessa Homfray, Bridget Riley, Cédric Le Caignec, Albert David, John Willan, Harry Ostrer, Andrew H. Sinclair, Giovanna Camerino, Stefan J. White
Publikováno v:
The American Journal of Human Genetics. (6):898-904
Investigations of humans with disorders of sex development (DSDs) resulted in the discovery of many of the now-known mammalian sex-determining genes, including SRY, RSPO1, SOX9, NR5A1, WT1, NR0B1, and WNT4. Here, the locus for an autosomal sex-determ