The truncated prelamin A in Hutchinson–Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers

By Delbarre Erwan   Tramier Marc   Coppey-Moisan Maïté   Gaillard Claire   Courvalin Jean-Claude   Buendia Brigitte  

Human Molecular Genetics, Vol. 15, Iss. 7, 2006-04 ,pp. : 1113-1122

Oxford University Press

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Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy

By Boguslavsky Revekka L.   Stewart Colin L.   Worman Howard J.  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 653-663

Oxford University Press

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A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

By Lloyd D.J.   Trembath R.C.   Shackleton S.  

Human Molecular Genetics, Vol. 11, Iss. 7, 2002-04 ,pp. : 769-777

Oxford University Press

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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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A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features

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Molecular Syndromology, Vol. 1, Iss. 3, 2010-09 ,pp. : 127-132

Karger

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