Reduced Levels of Dystrophin Associated Proteins in the Brains of Mice Deficient for Dp71

By Greenberg David S.   Schatz Yechezkel   Levy Zehava   Pizzo Paola   Yaffe David   Nudel Uri  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1299-1303

Oxford University Press

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OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation

By Ban Tadato   Heymann Jrgen A.W.   Song Zhiyin   Hinshaw Jenny E.   Chan David C.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2113-2122

Oxford University Press

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Cystatin B-deficient mice have increased expression of apoptosis and glial activation genes

By Lieuallen K.  

Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1867-1871

Oxford University Press

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Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller–Dieker syndrome

By Carter Mark G.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 413-419

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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