Zobrazeno 1 - 10
of 1 044
pro vyhledávání: '"Finnell Richard H"'
Autor:
Lu, Lei, Bai, Meizhu, Zheng, Yufang, Wang, Xiukun, Chen, Zhongzhong, Peng, Rui, Finnell, Richard H., Zhao, Tongjin, Li, Chengtao, Wu, Bo, Lei, Yunping, Li, Jinsong, Wang, Hongyan
Publikováno v:
In Science Bulletin 30 July 2024 69(14):2260-2272
Autor:
Chen, Shuxia, Lei, Yunping, Yang, Yajun, Liu, Chennan, Kuang, Lele, Jin, Li, Finnell, Richard H., Yang, Xueyan, Wang, Hongyan
Publikováno v:
In Journal of Genetics and Genomics April 2024 51(4):433-442
Autor:
Wolujewicz, Paul, Aguiar-Pulido, Vanessa, Thareja, Gaurav, Suhre, Karsten, Elemento, Olivier, Finnell, Richard H., Ross, M. Elizabeth
Publikováno v:
In Genetics in Medicine Open 2024 2
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Pisano M Michele, Greene Robert M, Shaw Gary M, Chapa Claudia J, Yang Wei, Guzman Adrian R, Lu Wei, Lammer Edward J, Finnell Richard H, Zhu Huiping
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 141 (2010)
Abstract Background Spina bifida is a malformation of the neural tube and is the most common of neural tube defects (NTDs). The etiology of spina bifida is largely unknown, although it is thought to be multi-factorial, involving multiple interacting
Externí odkaz:
https://doaj.org/article/9f8c61e8939145f29914c53a57478d6b
Autor:
Hogan Michael E, Wong David, Finnell Richard H, Hardin Jill, Horovitz Joy, Shu Jenny, Shaw Gary M
Publikováno v:
BMC Genetics, Vol 10, Iss 1, p 38 (2009)
Abstract Background Neonatal blood, obtained from a heel stick and stored dry on paper cards, has been the standard for birth defects screening for 50 years. Such dried blood samples are used, primarily, for analysis of small-molecule analytes. More
Externí odkaz:
https://doaj.org/article/eaea0392a9d24c7fa95dc9c421242ad1
Autor:
Shaw Gary M, Lu Wei, Zhu Huiping, Yang Wei, Briggs Farren BS, Carmichael Suzan L, Barcellos Lisa F, Lammer Edward J, Finnell Richard H
Publikováno v:
BMC Medical Genetics, Vol 10, Iss 1, p 49 (2009)
Abstract Background Folic acid taken in early pregnancy reduces risks for delivering offspring with several congenital anomalies. The mechanism by which folic acid reduces risk is unknown. Investigations into genetic variation that influences transpo
Externí odkaz:
https://doaj.org/article/19665f40d6204be49881338efb7768b8
Publikováno v:
In Trends in Endocrinology & Metabolism September 2023 34(9):539-553
Autor:
Bauer Linda K, Eudy James D, van Waes Michael, Wilberding Justin, Smith Lynette M, Maddox Joyce R, Gelineau-van Waes Janee, Finnell Richard H
Publikováno v:
BMC Genomics, Vol 9, Iss 1, p 156 (2008)
Abstract Background The reduced folate carrier (RFC1) is an integral membrane protein and facilitative anion exchanger that mediates delivery of 5-methyltetrahydrofolate into mammalian cells. Adequate maternal-fetal transport of folate is necessary f
Externí odkaz:
https://doaj.org/article/c05f50e28c944c3287a1e524dc44b862
Publikováno v:
BMC Medical Genetics, Vol 8, Iss 1, p 12 (2007)
Abstract Background CFL1 encodes human non-muscle cofilin (n-cofilin), which is an actin-depolymerizing factor and is essential in cytokinesis, endocytosis, and in the development of all embryonic tissues. Cfl1 knockout mice exhibit failure of neural
Externí odkaz:
https://doaj.org/article/1c3c5404f965404faafeb8becb90c2d6