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Frontiers in Cell and Developmental Biology
|
March 30, 2022
Desmin Modulates Muscle Cell Adhesion and Migration
Coralie Hakibilen, Florence Delort, Marie-Thérèse Daher, et al.
Experimental Cell Research
|
October 14, 2011
Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins
Isabelle Duband-Goulet, Stephanie Woerner, Sylvaine Gasparini, et al.
Human Mutation
|
July 26, 2006
Variable pathogenic potentials of mutations located in the desmin alpha-helical domain
Bertrand Goudeau, Fernando Rodrigues-Lima, Dirk Fischer, et al.
FEBS Letters
|
June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies
Christoph S Clemen, Dirk Fischer, Udo Roth, et al.
Human Molecular Genetics
|
March 7, 2003
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria
Rolf Schröder, Bertrand Goudeau, Monique Casteras Simon, et al.
Acta Neuropathologica
|
January 20, 2009
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study
Kristl G Claeys, Peter F M van der Ven, Anthony Behin, et al.
Neuromuscular Disorders : NMD
|
May 11, 2006
Different early pathogenesis in myotilinopathy compared to primary desminopathy
Dirk Fischer, Christoph S Clemen, Montse Olivé, et al.
Circulation
|
October 7, 2020
Dual Functional States of R406W-Desmin Assembly Complexes Cause Cardiomyopathy With Severe Intercalated Disc Derangement in Humans and in Knock-In Mice
Harald Herrmann, Eva Cabet, Nicolas R Chevalier, et al.
European Journal of Human Genetics : EJHG
|
December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy
Alexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Frontiers in Cell and Developmental Biology
|
March 30, 2022
Desmin Modulates Muscle Cell Adhesion and Migration
Coralie Hakibilen, Florence Delort, Marie-Thérèse Daher, et al.
Experimental Cell Research
|
October 14, 2011
Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins
Isabelle Duband-Goulet, Stephanie Woerner, Sylvaine Gasparini, et al.
Human Mutation
|
July 26, 2006
Variable pathogenic potentials of mutations located in the desmin alpha-helical domain
Bertrand Goudeau, Fernando Rodrigues-Lima, Dirk Fischer, et al.
FEBS Letters
|
June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies
Christoph S Clemen, Dirk Fischer, Udo Roth, et al.
Human Molecular Genetics
|
March 7, 2003
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria
Rolf Schröder, Bertrand Goudeau, Monique Casteras Simon, et al.
Acta Neuropathologica
|
January 20, 2009
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study
Kristl G Claeys, Peter F M van der Ven, Anthony Behin, et al.
Neuromuscular Disorders : NMD
|
May 11, 2006
Different early pathogenesis in myotilinopathy compared to primary desminopathy
Dirk Fischer, Christoph S Clemen, Montse Olivé, et al.
Circulation
|
October 7, 2020
Dual Functional States of R406W-Desmin Assembly Complexes Cause Cardiomyopathy With Severe Intercalated Disc Derangement in Humans and in Knock-In Mice
Harald Herrmann, Eva Cabet, Nicolas R Chevalier, et al.
European Journal of Human Genetics : EJHG
|
December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy
Alexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Page
of 5