Zobrazeno 1 - 10
of 871
pro vyhledávání: '"Sarah A. Curtis"'
Autor:
Caroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, Hemma Murali, Casey Tsimbal, Eileen Dalessandro, Shannon H. Carroll, Simren Kochhar, Sarah W. Curtis, Ching Hsun Eric Cheng, Feng Wang, Eric Kutschera, Russ P. Carstens, Yi Xing, Kai Wang, Elizabeth J. Leslie, Eric C. Liao
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-14 (2024)
Abstract Orofacial cleft (OFC) is a common human congenital anomaly. Epithelial-specific RNA splicing regulators ESRP1 and ESRP2 regulate craniofacial morphogenesis and their disruption result in OFC in zebrafish, mouse and humans. Using esrp1/2 muta
Externí odkaz:
https://doaj.org/article/d34d269b32354c1e9fa1ec00b6085b6b
Autor:
Karen L. Oliver, Ingrid E. Scheffer, Colin A. Ellis, Bronwyn E. Grinton, Samuel F. Berkovic, Melanie Bahlo, Zaid Afawi, Dina Amrom, Eva Andermann, Jocelyn F. Bautista, Susannah T. Bellows, Judith Bluvstein, Gregory D. Cascino, Seo-Kyung Chung, Patrick Cossette, Sarah W. Curtis, Norman Delanty, Orrin Devinsky, Dennis Dlugos, Michael P. Epstein, Catharine Freyer, Micheline Gravel, Rebekah V. Harris, Erin L. Heinzen, Olivia J. Henry, Heidi E. Kirsch, Robert C. Knowlton, Eric H. Kossoff, Rebecca Loeb, Daniel H. Lowenstein, Anthony G. Marson, Heather C. Mefford, Paul V. Motika, Terence J. O'Brien, Ruth Ottman, Juliann M. Paolicchi, Slave Petrovski, William O. Pickrell, Mark I. Rees, Lynette G. Sadleir, Jerry J. Shih, Rani K. Singh, Michael C. Smith, Philip E.M. Smith, Rhys H. Thomas, Judith Weisenberg, Peter Widdess-Walsh, Melodie R. Winawer
Publikováno v:
EBioMedicine, Vol 109, Iss , Pp 105404- (2024)
Summary: Background: Phenotypic variability within families with epilepsy is often observed, even when relatives share the same monogenic cause. We aimed to investigate whether common polygenic risk for epilepsy could explain the penetrance and pheno
Externí odkaz:
https://doaj.org/article/0d0f5424442d4240b5c116f34ead7cf1
Autor:
Clark, Linda L.
Publikováno v:
Journal of Social History, 2001 Dec 01. 35(2), 461-463.
Externí odkaz:
https://www.jstor.org/stable/3790204
Autor:
Alaimo, Kathleen
Publikováno v:
History of Education Quarterly, 2001 Oct 01. 41(3), 456-458.
Externí odkaz:
https://www.jstor.org/stable/369220
Autor:
Harrison, Carol E.
Publikováno v:
The Journal of Modern History, 2014 Jun 01. 86(2), 451-453.
Externí odkaz:
https://www.jstor.org/stable/10.1086/675887
Autor:
Toshiyuki Itai, Fangfang Yan, Andi Liu, Yulin Dai, Chihiro Iwaya, Sarah W. Curtis, Elizabeth J. Leslie, Lukas M. Simon, Peilin Jia, Xiangning Chen, Junichi Iwata, Zhongming Zhao
Publikováno v:
HGG Advances, Vol 5, Iss 3, Pp 100313- (2024)
Summary: Orofacial clefts (OFCs) are common congenital birth defects with various etiologies, including genetic variants. Online Mendelian Inheritance in Man (OMIM) annotated several hundred genes involving OFCs. Furthermore, several hundreds of de n
Externí odkaz:
https://doaj.org/article/d1da2bc8f18746018552c2282332f15a
Autor:
Horvath-Peterson, Sandra
Publikováno v:
The American Historical Review, 2012 Jun 01. 117(3), 942-943.
Externí odkaz:
https://www.jstor.org/stable/23310693
Autor:
Toner, Fred L.
Publikováno v:
The French Review, 2010 Feb 01. 83(3), 707-708.
Externí odkaz:
https://www.jstor.org/stable/25614123
Autor:
Moulinet, Daniel
Publikováno v:
Revue de l'histoire des religions, 2005 Jul 01. 222(3), 372-374.
Externí odkaz:
https://www.jstor.org/stable/23617790
Autor:
THIVEND, Marianne
Publikováno v:
Histoire de l'education, 2004 Jan 01(101), 105-108.
Externí odkaz:
https://www.jstor.org/stable/41160124