NDLI: Advances in basic and clinical researchin laminopathies

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Advances in basic and clinical researchin laminopathies

Content Provider	PubMed Central
Author	Politano, Luisa Carboni, Nicola Madej-pilarczyk, Agnieszka Marchel, Michael Nigro, Gerardo Anna, Fidziaóska Opolski, Grzegorz Hausmanowa-petrusewicz, Irena
Abstract	Lamins (LMNA) are the main proteins of the nuclear lamina considered to be the ancestors of all intermediate filament proteins. They form complex protein assemblies with integral proteins of the inner nuclear membrane, transcriptional regulators, histones and chromatin modifiers. During recent years, interest in lamins has greatly increased due to the identification of many distinct heritable human disorders associated with lamin mutations. These disorders, collectively termed laminopathies, range from muscular dystrophies to premature aging. They may affect muscle, fat, bone, nerve and skin tissues. The workshop was addressed to understand lamin organization and its roles in nuclear processes, mutations in lamins affecting cell and tissues functions, the biology of the nucleus and laminopathic disease mechanisms, all aspects important for designing future therapies.
Starting Page	18
File Format	PDF
ISSN	11282460
e-ISSN	11282460
Journal	Acta Myologica
Issue Number	1
Volume Number	32
Language	English
Publisher	Pacini Editore SpA
Publisher Date	2013-05-01
Access Restriction	Open
Rights Holder	Pacini Editore SpA
Subject Keyword	Research in Higher Education
Content Type	Text
Resource Type	Article
Subject	Cardiology and Cardiovascular Medicine

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