Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith–Magenis syndrome

By Bi Weimin   Ohyama Tomoko   Nakamura Hisashi   Yan Jiong   Visvanathan Jaya   Justice Monica J.   Lupski James R.  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 983-995

Oxford University Press

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Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome

By Burns Brooke   Schmidt Kristie   Williams Stephen R.   Kim Sun   Girirajan Santhosh   Elsea Sarah H.  

Human Molecular Genetics, Vol. 19, Iss. 20, 2010-10 ,pp. : 4026-4042

Oxford University Press

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WIF1 causes dysfunction of heart in transgenic mice

By Lu Dan   Dong Wei   Zhang Xu   Quan Xiongzhi   Bao Dan   Lu Yingdong   Zhang Lianfeng  

Transgenic Research, Vol. 22, Iss. 6, 2013-12 ,pp. : 1179-1189

Springer Publishing Company

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Paraquat induces dopaminergic dysfunction and proteasome impairment in DJ-1-deficient mice

By Yang Wonsuk   Chen Linan   Ding Yunmin   Zhuang Xiaoxi   Kang Un Jung  

Human Molecular Genetics, Vol. 16, Iss. 23, 2007-12 ,pp. : 2900-2910

Oxford University Press

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Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice

By Beck Tyler F.   Veenma Danielle   Shchelochkov Oleg A.   Yu Zhiyin   Kim Bum Jun   Zaveri Hitisha P.   van Bever Yolande   Choi Sunju   Douben Hannie   Bertin Terry K.   Patel Pragna I.   Lee Brendan   Tibboel Dick   de Klein Annelies   Stockton David W.   Justice Monica J.   Scott Daryl A.  

Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 1026-1038

Oxford University Press

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