Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

By Cao Henian   Hegele Robert A.  

Human Molecular Genetics, Vol. 9, Iss. 1, 2000-01 ,pp. : 109-112

Oxford University Press

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Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration

By Melcon Gisela   Kozlov Serguei   Hernandez Lidia   Zhao Po   Mitchell Stephanie   Nader Gustavo   Bakay Marina   Rottman Jeff N.   Hoffman Eric P.   Stewart Colin L.  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 637-651

Oxford University Press

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The Emery-Dreifuss Muscular Dystrophy Protein, Emerin, is a Nuclear Membrane Protein

By Manilal S.   Man Nguyen thi   Sewry C. A.   Morris G. E.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 801-808

Oxford University Press

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Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells

By Arocena Dolores Garcia   Iwahashi Christine K.   Won Nelly   Beilina Alexandra   Ludwig Anna L.   Tassone Flora   Schwartz Philip H.   Hagerman Paul J.  

Human Molecular Genetics, Vol. 14, Iss. 23, 2005-12 ,pp. : 3661-3671

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Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?

By Masny Peter S.  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1857-1871

Oxford University Press

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