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 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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Nuclear sequestration of -sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytes

By Heydemann Ahlke   Demonbreun Alexis   Hadhazy Michele   Earley Judy U.   McNally Elizabeth M.  

Human Molecular Genetics, Vol. 16, Iss. 4, 2007-02 ,pp. : 355-363

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

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Partial recessive IFN-R1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds

By Sologuren Ithaisa   Boisson-Dupuis Stéphanie   Pestano Jose   Vincent Quentin Benoit   Fernández-Pérez Leandro   Chapgier Ariane   Cárdenes María   Feinberg Jacqueline   García-Laorden M. Isabel   Picard Capucine   Santiago Esther   Kong Xiaofei   Jannière Lucile   Colino Elena   Herrera-Ramos Estefanía   Francés Adela   Navarrete Carmen   Blanche Stéphane   Faria Emilia   Remiszewski Paweł   Cordeiro Ana   Freeman Alexandra   Holland Steven   Abarca Katia   Valerón-Lemaur Mónica   Gonçalo-Marques José   Silveira Luisa   García-Castellano José Manuel   Caminero José   Pérez-Arellano José Luis   Bustamante Jacinta   Abel Laurent   Casanova Jean-Laurent   Rodríguez-Gallego Carlos  

Human Molecular Genetics, Vol. 20, Iss. 8, 2011-04 ,pp. : 1509-1523

Oxford University Press

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