Biomechanical characterization of a desminopathy in primary human myoblasts-Reference-Cited by-同舟云学术

Biomechanical characterization of a desminopathy in primary human myoblasts

Published:2012-03 Issue:4 Volume:419 Page:703-707
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Bonakdar Navid,Luczak Justyna,Lautscham Lena,Czonstke Maja,Koch Thorsten M.,Mainka Astrid,Jungbauer Tajana,Goldmann Wolfgang H.,Schröder Rolf,Fabry Ben

Funder

Deutsche Gesellschaft für Muskelkranke (DGM)

Johannes und Frieda Marohn-Stiftung

Deutsche Forschungsgesellschaft (DFG)

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference16 articles.

1. Primary desminopathies;Schröder;J. Cell Mol. Med.,2007

2. Myofibrillar myopathies: a clinical and myopathological guide;Schröder;Brain Pathol.,2009

3. Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro;Bar;Hum. Mol. Genet.,2005

4. Molecular pathology of myofibrillar myopathies;Ferrer;Expert Rev. Mol. Med.,2008

5. Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset dominant myopathies are associated with the desmin mutation R350P;Walter;Brain,2007

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