Literature DB >> 7501167

Laminin beta 2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy).

U M Wewer1, M E Durkin, X Zhang, H Laursen, N H Nielsen, J Towfighi, E Engvall, R Albrechtsen.   

Abstract

Muscular dystrophy may be caused by disturbances in a number of muscle proteins that appear to be part of a chain of interacting molecules that includes cytoskeletal, cell membrane, and basement membrane components. We found that the skeletal muscle cells in two cases of Walker-Warburg syndrome were severely deficient in the laminin beta 2 chain and in adhalin. The findings indicate that these two proteins are key molecules in the interactive protein complex conferring muscle stability and cell survival.

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Year:  1995        PMID: 7501167     DOI: 10.1212/wnl.45.11.2099

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  9 in total

1.  Laminin expression in adult and developing retinae: evidence of two novel CNS laminins.

Authors:  R T Libby; M F Champliaud; T Claudepierre; Y Xu; E P Gibbons; M Koch; R E Burgeson; D D Hunter; W J Brunken
Journal:  J Neurosci       Date:  2000-09-01       Impact factor: 6.167

2.  Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle.

Authors:  U M Wewer; L E Thornell; F Loechel; X Zhang; M E Durkin; S Amano; R E Burgeson; E Engvall; R Albrechtsen; I Virtanen
Journal:  Am J Pathol       Date:  1997-08       Impact factor: 4.307

3.  Collagen XVII and BPAG1 expression in the retina: evidence for an anchoring complex in the central nervous system.

Authors:  Thomas Claudepierre; Mary K Manglapus; Nathan Marengi; Stephanie Radner; Marie-France Champliaud; Kaisa Tasanen; Leena Bruckner-Tuderman; Dale D Hunter; William J Brunken
Journal:  J Comp Neurol       Date:  2005-06-27       Impact factor: 3.215

4.  Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy.

Authors:  P H Vachon; H Xu; L Liu; F Loechel; Y Hayashi; K Arahata; J C Reed; U M Wewer; E Engvall
Journal:  J Clin Invest       Date:  1997-10-01       Impact factor: 14.808

5.  Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.

Authors:  Daniel Beltrán-Valero de Bernabé; Sophie Currier; Alice Steinbrecher; Jacopo Celli; Ellen van Beusekom; Bert van der Zwaag; Hülya Kayserili; Luciano Merlini; David Chitayat; William B Dobyns; Bru Cormand; Ana-Elina Lehesjoki; Jesús Cruces; Thomas Voit; Christopher A Walsh; Hans van Bokhoven; Han G Brunner
Journal:  Am J Hum Genet       Date:  2002-10-04       Impact factor: 11.025

6.  Laminins in normal, keratoconus, bullous keratopathy and scarred human corneas.

Authors:  Berit Byström; Ismo Virtanen; Patricia Rousselle; Kaoru Miyazaki; Christina Lindén; Fatima Pedrosa Domellöf
Journal:  Histochem Cell Biol       Date:  2007-05-11       Impact factor: 2.531

7.  Laminin γ3 plays an important role in retinal lamination, photoreceptor organisation and ganglion cell differentiation.

Authors:  Birthe Dorgau; Majed Felemban; Alexander Sharpe; Roman Bauer; Dean Hallam; David H Steel; Susan Lindsay; Carla Mellough; Majlinda Lako
Journal:  Cell Death Dis       Date:  2018-05-23       Impact factor: 8.469

Review 8.  The role of defective glycosylation in congenital muscular dystrophy.

Authors:  Harry Schachter; Jiri Vajsar; Wenli Zhang
Journal:  Glycoconj J       Date:  2004       Impact factor: 3.009

9.  Merosin and laminin in myogenesis; specific requirement for merosin in myotube stability and survival.

Authors:  P H Vachon; F Loechel; H Xu; U M Wewer; E Engvall
Journal:  J Cell Biol       Date:  1996-09       Impact factor: 10.539

  9 in total

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