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Manfred Wehnert

Showing results (11-20 of 41) with videos related to

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Acta Bio-Medica : Atenei Parmensis|May 1, 2007
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndromeNadir M Maraldi, Cristina Capanni, Elisabetta Mattioli, et al.
Brain Pathology (Zurich, Switzerland)|November 17, 2006
Myofiber degeneration in autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) (LGMD1B)Michel Mittelbronn, Frank Hanisch, Marc Gleichmann, et al.
European Journal of Cell Biology|May 5, 2012
LINC complex alterations in DMD and EDMD/CMT fibroblastsSurayya Taranum, Eva Vaylann, Peter Meinke, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|January 29, 2010
Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle developmentK Natalie Randles, Le Thanh Lam, Caroline A Sewry, et al.
European Journal of Pediatrics|November 21, 2008
Restrictive dermopathy--a lethal congenital laminopathy. Case report and review of the literaturePaulo Morais, Sofia Magina, Maria do Céu Ribeiro, et al.
Neurogenetics|December 1, 2006
Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophySabine Rudnik-Schöneborn, Elke Botzenhart, Thomas Eggermann, et al.
Experimental Cell Research|December 20, 2002
Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophyCatherine Favreau, Emmanuelle Dubosclard, Cecilia Ostlund, et al.
Neuromuscular Disorders : NMD|February 19, 2017
Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathologyPhu Le Thanh, Peter Meinke, Nadia Korfali, et al.
Cell Cycle (Georgetown, Tex.)|September 1, 2012
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistributionCristina Capanni, Stefano Squarzoni, Vittoria Cenni, et al.
Nucleus (Austin, Tex.)|March 5, 2015
Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cellsKatrin Bercht Pfleghaar, Pekka Taimen, Veronika Butin-Israeli, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Acta Bio-Medica : Atenei Parmensis|May 1, 2007
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndromeNadir M Maraldi, Cristina Capanni, Elisabetta Mattioli, et al.
Brain Pathology (Zurich, Switzerland)|November 17, 2006
Myofiber degeneration in autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) (LGMD1B)Michel Mittelbronn, Frank Hanisch, Marc Gleichmann, et al.
European Journal of Cell Biology|May 5, 2012
LINC complex alterations in DMD and EDMD/CMT fibroblastsSurayya Taranum, Eva Vaylann, Peter Meinke, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|January 29, 2010
Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle developmentK Natalie Randles, Le Thanh Lam, Caroline A Sewry, et al.
European Journal of Pediatrics|November 21, 2008
Restrictive dermopathy--a lethal congenital laminopathy. Case report and review of the literaturePaulo Morais, Sofia Magina, Maria do Céu Ribeiro, et al.
Neurogenetics|December 1, 2006
Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophySabine Rudnik-Schöneborn, Elke Botzenhart, Thomas Eggermann, et al.
Experimental Cell Research|December 20, 2002
Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophyCatherine Favreau, Emmanuelle Dubosclard, Cecilia Ostlund, et al.
Neuromuscular Disorders : NMD|February 19, 2017
Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathologyPhu Le Thanh, Peter Meinke, Nadia Korfali, et al.
Cell Cycle (Georgetown, Tex.)|September 1, 2012
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistributionCristina Capanni, Stefano Squarzoni, Vittoria Cenni, et al.
Nucleus (Austin, Tex.)|March 5, 2015
Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cellsKatrin Bercht Pfleghaar, Pekka Taimen, Veronika Butin-Israeli, et al.
Pageof 5