Literature DB >> 11360268

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy.

P Sabatelli1, G Lattanzi, A Ognibene, M Columbaro, C Capanni, L Merlini, N M Maraldi, S Squarzoni.   

Abstract

Electron microscopy study of muscle biopsies from patients with autosomal-dominant Emery-Dreifuss muscular dystrophy revealed nuclear alterations in about 10% of the preserved muscle fibers. The major findings consisted of peripheral heterochromatin loss or detachment from the nuclear envelope, and of interchromatin texture alterations. These abnormalities are similar to those reported in an animal model of the disease and to those found in the X-linked form of Emery-Dreifuss muscular dystrophy. These results suggest that an abnormal ultrastructural arrangement of the nuclear periphery is a common feature in the known forms of Emery-Dreifuss muscular dystrophy, and that several proteins of the nuclear scaffold are necessary in muscle cells to maintain the nuclear structural/functional integrity and a normal muscle cell metabolism. Copyright 2001 John Wiley & Sons, Inc.

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Year:  2001        PMID: 11360268     DOI: 10.1002/mus.1076

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  21 in total

Review 1.  Lamin-binding Proteins.

Authors:  Katherine L Wilson; Roland Foisner
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-02-17       Impact factor: 10.005

Review 2.  Nuclear lamins: major factors in the structural organization and function of the nucleus and chromatin.

Authors:  Thomas Dechat; Katrin Pfleghaar; Kaushik Sengupta; Takeshi Shimi; Dale K Shumaker; Liliana Solimando; Robert D Goldman
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Review 3.  The Nucleoskeleton.

Authors:  Stephen A Adam
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-02-01       Impact factor: 10.005

4.  Barrier-to-Autointegration Factor influences specific histone modifications.

Authors:  Rocío Montes de Oca; Paul R Andreassen; Katherine L Wilson
Journal:  Nucleus       Date:  2011-11-01       Impact factor: 4.197

5.  Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.

Authors:  V Cenni; P Sabatelli; E Mattioli; S Marmiroli; C Capanni; A Ognibene; S Squarzoni; N M Maraldi; G Bonne; M Columbaro; L Merlini; G Lattanzi
Journal:  J Med Genet       Date:  2005-03       Impact factor: 6.318

6.  Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment.

Authors:  M Columbaro; C Capanni; E Mattioli; G Novelli; V K Parnaik; S Squarzoni; N M Maraldi; G Lattanzi
Journal:  Cell Mol Life Sci       Date:  2005-11       Impact factor: 9.261

7.  Protein Tpr is required for establishing nuclear pore-associated zones of heterochromatin exclusion.

Authors:  Sandra Krull; Julia Dörries; Björn Boysen; Sonja Reidenbach; Lars Magnius; Helene Norder; Johan Thyberg; Volker C Cordes
Journal:  EMBO J       Date:  2010-04-20       Impact factor: 11.598

Review 8.  Emerin in health and disease.

Authors:  Adam J Koch; James M Holaska
Journal:  Semin Cell Dev Biol       Date:  2013-12-21       Impact factor: 7.727

Review 9.  Nuclear lamins and chromatin: when structure meets function.

Authors:  Thomas Dechat; Stephen A Adam; Robert D Goldman
Journal:  Adv Enzyme Regul       Date:  2008-12-31

10.  Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

Authors:  Jason Cowan; Duanxiang Li; Jorge Gonzalez-Quintana; Ana Morales; Ray E Hershberger
Journal:  Circ Cardiovasc Genet       Date:  2009-11-17
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