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pro vyhledávání: '"Chodirker, Bernard N"'
Akademický článek
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Autor:
Roychaudhury, Arkaprava, Lee, Yu‐Ri, Choi, Tae‐Ik, Thomas, Mervyn G., Khan, Tahir N., Yousaf, Hammad, Skinner, Cindy, Maconachie, Gail, Crosier, Moira, Horak, Holli, Constantinescu, Cris S., Kim, Tae‐Yoon, Lee, Kang‐Han, Kyung, Jae‐Jun, Wang, Tao, Ku, Bonsu, Chodirker, Bernard N., Hammer, Michael F., Gottlob, Irene, Norton, William H. J.
Publikováno v:
Annals of Neurology; Nov2024, Vol. 96 Issue 5, p914-931, 18p
Publikováno v:
Application of Clinical Genetics; Jul2022, Vol. 15, p87-95, 9p
Publikováno v:
Canadian Journal of Pathology; feb2022, Vol. 14 Issue 1, p28-37, 10p
Autor:
Salman, Michael S.1,2 (AUTHOR) msalman@hsc.mb.ca, Chodirker, Bernard N.2,3 (AUTHOR)
Publikováno v:
Neuro-Ophthalmology. Jun2015, Vol. 39 Issue 3, p125-131. 7p.
Publikováno v:
In Obstetrics & Gynecology 2002 99(4):531-536
Publikováno v:
BMC Pregnancy and Childbirth, Vol 6, Iss 1, p 23 (2006)
Abstract Background Although maternal serum alpha-fetoprotein (MSAFP) is a highly sensitive marker for certain congenital malformations such as open neural tube and ventral wall defects, its usefulness as a screening test for fetal hydrocephalus is u
Externí odkaz:
https://doaj.org/article/4cddfb29fbd74a9e80d8e51edd925d38
Autor:
Greenberg Cheryl R, Evans Jane A, Björklund Natalie K, Seargeant Lorne E, Schneider Carol E, Chodirker Bernard N
Publikováno v:
Reproductive Biology and Endocrinology, Vol 2, Iss 1, p 65 (2004)
Abstract Introduction The C677T MTHFR variant has been associated with the same third trimester pregnancy complications as seen in women who have elevations of maternal serum α-fetoprotein (MSAFP). We hypothesized that these women with third trimest
Externí odkaz:
https://doaj.org/article/42fb82734b6b4de5800355fdb48b74a5
Autor:
Szajkowski, Terrence P.1 terry_szaj@hotmail.com, Chodirker, Bernard N.1,2 BChodirker@exchange.hsc.mb.ca, MacDonald, Karen M.1 KMacDonald@exchange.hsc.mb.ca, Evans, Jane A.1,2 jevans@ms.umanitoba.ca
Publikováno v:
BMC Pregnancy & Childbirth. 2006, Vol. 6, p23-5. 5p. 2 Charts.
Autor:
Wheway, Gabrielle, Schmidts, Miriam, Mans, Dorus A, Szymanska, Katarzyna, Nguyen, Thanh-Minh T, Racher, Hilary, Phelps, Ian G, Toedt, Grischa, Kennedy, Julie, Wunderlich, Kirsten A, Sorusch, Nasrin, Abdelhamed, Zakia A, Natarajan, Subaashini, Herridge, Warren, van Reeuwijk, Jeroen, Horn, Nicola, Boldt, Karsten, Parry, David A, Letteboer, Stef J F, Roosing, Susanne, Adams, Matthew, Bell, Sandra M, Bond, Jacquelyn, Higgins, Julie, Morrison, Ewan E, Tomlinson, Darren C, Slaats, Gisela G, van Dam, Teunis J P, Huang, Lijia, Kessler, Kristin, Giessl, Andreas, Logan, Clare V, Boyle, Evan A, Shendure, Jay, Anazi, Shamsa, Aldahmesh, Mohammed, Al Hazzaa, Selwa, Hegele, Robert A, Ober, Carole, Frosk, Patrick, Mhanni, Aizeddin A, Chodirker, Bernard N, Chudley, Albert E, Lamont, Ryan, Bernier, Francois P, Beaulieu, Chandree L, Gordon, Paul, Pon, Richard T, Donahue, Clem, Giles, Rachel H, UK10K Consortium
Defects in primary cilium biogenesis underlie the ciliopathies, a growing group of genetic disorders. We describe a whole-genome siRNA-based reverse genetics screen for defects in biogenesis and/or maintenance of the primary cilium, obtaining a globa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10691::f3fd7dafc78123d6256feba30d6330af
https://dspace.library.uu.nl/handle/1874/332913
https://dspace.library.uu.nl/handle/1874/332913