Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling

By Zwerger Monika   Jaalouk Diana E.   Lombardi Maria L.   Isermann Philipp   Mauermann Monika   Dialynas George   Herrmann Harald   Wallrath Lori L.   Lammerding Jan  

Human Molecular Genetics, Vol. 22, Iss. 12, 2013-06 ,pp. : 2335-2349

Oxford University Press

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Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

By Arimura Takuro  

Human Molecular Genetics, Vol. 14, Iss. 1, 2005-01 ,pp. : 155-169

Oxford University Press

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Distinct PAR/IQGAP expression patterns during murine development: implications for thrombin-associated cytoskeletal reorganization

By Cupit Lisa  

Mammalian Genome, Vol. 15, Iss. 8, 2004-08 ,pp. : 618-629

Springer Publishing Company

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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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Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells

By Kandert Sebastian   Lke Yvonne   Kleinhenz Tobias   Neumann Sascha   Lu Wenshu   Jaeger Verena M.   Munck Martina   Wehnert Manfred   Mller Clemens R.   Zhou Zhongjun   Noegel Angelika A.   Dabauvalle Marie-Christine   Karakesisoglou Iakowos  

Human Molecular Genetics, Vol. 16, Iss. 23, 2007-12 ,pp. : 2944-2959

Oxford University Press

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