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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
August 17, 2011
Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins
A Kostareva, G Sjoberg, A Gudkova, et al.
Experimental Lung Research
|
September 18, 2001
Lung clearance in children with Duchenne muscular dystrophy or spinal muscular atrophy with and without CPAP (continuous positive airway pressure)
B Klefbeck, K Svartengren, P Camner, et al.
Pediatric Research
|
March 1, 1991
Serum factors induce C-fos expression and rapid cell proliferation in adolescent but not in infant rat proximal tubule cells
S H Larsson, A Hultgårdh-Nilsson, S Kölare, et al.
Oncogene
|
December 1, 1988
Chromosome localization and expression pattern of Lmyc and Bmyc in murine embryonal carcinoma cells
S Ingvarsson, S Sundaresan, P Jin, et al.
Neuromuscular Disorders : NMD
|
January 1, 1997
Tenascin-C expression correlates with macrophage invasion in Duchenne muscular dystrophy and in myositis
D Gullberg, T Velling, G Sjöberg, et al.
Human Molecular Genetics
|
November 5, 1999
A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation
G Sjöberg, C A Saavedra-Matiz, D R Rosen, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 14, 2007
Desmin mutations in a St. Petersburg cohort of cardiomyopathies
A Kostareva, A Gudkova, G Sjoberg, et al.
Cytoskeleton (Hoboken, N.J.)
|
February 22, 2026
Filamin C Modulates Cellular Mechanoresponse Through Focal Adhesion Turnover and Actin Stabilization
E S Klimenko, M Yu Sorokina, K S Sukhareva, et al.
Cell and Tissue Research
|
June 5, 2023
Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner
K S Sukhareva, N A Smolina, A I Churkina, et al.
Orphanet Journal of Rare Diseases
|
September 14, 2022
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
A Muravyev, T Vershinina, P Tesner, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
August 17, 2011
Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins
A Kostareva, G Sjoberg, A Gudkova, et al.
Experimental Lung Research
|
September 18, 2001
Lung clearance in children with Duchenne muscular dystrophy or spinal muscular atrophy with and without CPAP (continuous positive airway pressure)
B Klefbeck, K Svartengren, P Camner, et al.
Pediatric Research
|
March 1, 1991
Serum factors induce C-fos expression and rapid cell proliferation in adolescent but not in infant rat proximal tubule cells
S H Larsson, A Hultgårdh-Nilsson, S Kölare, et al.
Oncogene
|
December 1, 1988
Chromosome localization and expression pattern of Lmyc and Bmyc in murine embryonal carcinoma cells
S Ingvarsson, S Sundaresan, P Jin, et al.
Neuromuscular Disorders : NMD
|
January 1, 1997
Tenascin-C expression correlates with macrophage invasion in Duchenne muscular dystrophy and in myositis
D Gullberg, T Velling, G Sjöberg, et al.
Human Molecular Genetics
|
November 5, 1999
A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation
G Sjöberg, C A Saavedra-Matiz, D R Rosen, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 14, 2007
Desmin mutations in a St. Petersburg cohort of cardiomyopathies
A Kostareva, A Gudkova, G Sjoberg, et al.
Cytoskeleton (Hoboken, N.J.)
|
February 22, 2026
Filamin C Modulates Cellular Mechanoresponse Through Focal Adhesion Turnover and Actin Stabilization
E S Klimenko, M Yu Sorokina, K S Sukhareva, et al.
Cell and Tissue Research
|
June 5, 2023
Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner
K S Sukhareva, N A Smolina, A I Churkina, et al.
Orphanet Journal of Rare Diseases
|
September 14, 2022
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
A Muravyev, T Vershinina, P Tesner, et al.
Page
of 5