Literature DB >> 10469836

Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy.

G E Morris1, S Manilal.   

Abstract

Emery-Dreifuss muscular dystrophy has some remarkably specific features, with only cardiac and skeletal tissues being affected. Equally remarkably, the disease is caused by mutations in widely expressed genes for the nuclear membrane/lamina proteins, emerin and lamin A/C. How do mutations in proteins at the heart of the cell lead to stiff joints and sudden heart failure? This and related questions are the subject of this review.

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Year:  1999        PMID: 10469836     DOI: 10.1093/hmg/8.10.1847

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  21 in total

Review 1.  Lipoatrophic diabetes and other related syndromes.

Authors:  Elif Arioglu Oral
Journal:  Rev Endocr Metab Disord       Date:  2003-03       Impact factor: 6.514

Review 2.  Molecular genetics and pathogenesis of cardiomyopathy.

Authors:  Akinori Kimura
Journal:  J Hum Genet       Date:  2015-07-16       Impact factor: 3.172

Review 3.  Diseases of the Nucleoskeleton.

Authors:  James M Holaska
Journal:  Compr Physiol       Date:  2016-09-15       Impact factor: 9.090

4.  Skeletal myopathy in a family with lamin A/C cardiac disease.

Authors:  Subha Ghosh; Rahul Renapurkar; Subha V Raman
Journal:  Cardiovasc Diagn Ther       Date:  2016-10

5.  MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans.

Authors:  Jun Liu; Kenneth K Lee; Miriam Segura-Totten; Ester Neufeld; Katherine L Wilson; Yosef Gruenbaum
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-08       Impact factor: 11.205

6.  Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein.

Authors:  Ewa Markiewicz; Thomas Dechat; Roland Foisner; Roy A Quinlan; Christopher J Hutchison
Journal:  Mol Biol Cell       Date:  2002-12       Impact factor: 4.138

7.  Head and/or CaaX domain deletions of lamin proteins disrupt preformed lamin A and C but not lamin B structure in mammalian cells.

Authors:  M Izumi; O A Vaughan; C J Hutchison; D M Gilbert
Journal:  Mol Biol Cell       Date:  2000-12       Impact factor: 4.138

8.  Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

Authors:  M Raffaele Di Barletta; E Ricci; G Galluzzi; P Tonali; M Mora; L Morandi; A Romorini; T Voit; K H Orstavik; L Merlini; C Trevisan; V Biancalana; I Housmanowa-Petrusewicz; S Bione; R Ricotti; K Schwartz; G Bonne; D Toniolo
Journal:  Am J Hum Genet       Date:  2000-03-16       Impact factor: 11.025

Review 9.  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

10.  Tyrosine phosphorylation of nuclear-membrane protein emerin by Src, Abl and other kinases.

Authors:  Kathryn E Tifft; Katherine A Bradbury; Katherine L Wilson
Journal:  J Cell Sci       Date:  2009-09-29       Impact factor: 5.285

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