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Manfred Wehnert

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

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Human Molecular Genetics|September 21, 2007
Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cellsSebastian Kandert, Yvonne Lüke, Tobias Kleinhenz, et al.
Molecular Biology of the Cell|April 22, 2005
Lamin A/C-dependent localization of Nesprin-2, a giant scaffolder at the nuclear envelopeThorsten Libotte, Hafida Zaim, Sabu Abraham, et al.
Journal of Proteome Research|September 24, 2008
Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cellsVittoria Cenni, Jessika Bertacchini, Francesca Beretti, et al.
Aging|October 18, 2014
Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamicsVittoria Cenni, Cristina Capanni, Elisabetta Mattioli, et al.
Ebiomedicine|December 22, 2019
A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanismPeter Meinke, Alastair R W Kerr, Rafal Czapiewski, et al.
The Journal of Biological Chemistry|April 3, 2024
Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomereChen Li, Derek T Warren, Can Zhou, et al.
American Journal of Medical Genetics. Part A|May 15, 2008
Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644CJulia Rankin, Michaela Auer-Grumbach, Warwick Bagg, et al.
American Journal of Human Genetics|September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophyLucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
Neuromuscular Disorders : NMD|August 6, 2003
108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The NetherlandsGisèle Bonne, Rabah Ben Yaou, Christophe Béroud, et al.
Human Molecular Genetics|September 1, 2007
Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrityQiuping Zhang, Cornelia Bethmann, Nathalie F Worth, et al.
Pageof 5

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

Sort By:
Pageof 5
Human Molecular Genetics|September 21, 2007
Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cellsSebastian Kandert, Yvonne Lüke, Tobias Kleinhenz, et al.
Molecular Biology of the Cell|April 22, 2005
Lamin A/C-dependent localization of Nesprin-2, a giant scaffolder at the nuclear envelopeThorsten Libotte, Hafida Zaim, Sabu Abraham, et al.
Journal of Proteome Research|September 24, 2008
Lamin A Ser404 is a nuclear target of Akt phosphorylation in C2C12 cellsVittoria Cenni, Jessika Bertacchini, Francesca Beretti, et al.
Aging|October 18, 2014
Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamicsVittoria Cenni, Cristina Capanni, Elisabetta Mattioli, et al.
Ebiomedicine|December 22, 2019
A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanismPeter Meinke, Alastair R W Kerr, Rafal Czapiewski, et al.
The Journal of Biological Chemistry|April 3, 2024
Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomereChen Li, Derek T Warren, Can Zhou, et al.
American Journal of Medical Genetics. Part A|May 15, 2008
Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644CJulia Rankin, Michaela Auer-Grumbach, Warwick Bagg, et al.
American Journal of Human Genetics|September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophyLucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
Neuromuscular Disorders : NMD|August 6, 2003
108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The NetherlandsGisèle Bonne, Rabah Ben Yaou, Christophe Béroud, et al.
Human Molecular Genetics|September 1, 2007
Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrityQiuping Zhang, Cornelia Bethmann, Nathalie F Worth, et al.
Pageof 5