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T Sejersen

Showing results (31-40 of 41) with videos related to

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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 originsA 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 cellsS 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 cellsS 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 myositisD 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 formationG 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 cardiomyopathiesA 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 StabilizationE 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 mannerK 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 childhoodA Muravyev, T Vershinina, P Tesner, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 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 originsA 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 cellsS 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 cellsS 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 myositisD 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 formationG 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 cardiomyopathiesA 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 StabilizationE 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 mannerK 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 childhoodA Muravyev, T Vershinina, P Tesner, et al.
Pageof 5