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Manfred Wehnert

Showing results (1-10 of 41) with videos related to

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Neurology|May 31, 2007
What message does the nuclear envelope hold?Hanns Lochmüller, Manfred Wehnert
Neuromuscular Disorders : NMD|June 11, 2013
Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutationMatthias Türk, Manfred Wehnert, Rolf Schröder, et al.
Neuromuscular Disorders : NMD|May 16, 2006
Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium compositionIan Holt, Thi Man Nguyen, Manfred Wehnert, et al.
Experimental Cell Research|May 16, 2009
Nuclear protein import is reduced in cells expressing nuclear envelopathy-causing lamin A mutantsAlbert Busch, Tilman Kiel, Wolfgang-M Heupel, et al.
European Journal of Cell Biology|July 11, 2009
Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA geneSebastian Kandert, Manfred Wehnert, Clemens R Müller, et al.
Nucleus (Austin, Tex.)|October 11, 2011
Distinct association of the nuclear pore protein Nup153 with A- and B-type laminsTeiba Al-Haboubi, Dale K Shumaker, Joachim Köser, et al.
Human Mutation|December 31, 2013
Contribution of SUN1 mutations to the pathomechanism in muscular dystrophiesPing Li, Peter Meinke, Le Thi Thanh Huong, et al.
Journal of Molecular Endocrinology|June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophyRene Cortese, Florian Eckhardt, Marianne Volleth, et al.
Archives of Gynecology and Obstetrics|May 13, 2008
Restrictive dermopathy: a rare laminopathyMarc Thill, Thuy Duong Nguyen, Manfred Wehnert, et al.
Biochimica Et Biophysica Acta|June 16, 2009
Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutationsLindsay J Emerson, Mark R Holt, Matthew A Wheeler, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Neurology|May 31, 2007
What message does the nuclear envelope hold?Hanns Lochmüller, Manfred Wehnert
Neuromuscular Disorders : NMD|June 11, 2013
Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutationMatthias Türk, Manfred Wehnert, Rolf Schröder, et al.
Neuromuscular Disorders : NMD|May 16, 2006
Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium compositionIan Holt, Thi Man Nguyen, Manfred Wehnert, et al.
Experimental Cell Research|May 16, 2009
Nuclear protein import is reduced in cells expressing nuclear envelopathy-causing lamin A mutantsAlbert Busch, Tilman Kiel, Wolfgang-M Heupel, et al.
European Journal of Cell Biology|July 11, 2009
Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA geneSebastian Kandert, Manfred Wehnert, Clemens R Müller, et al.
Nucleus (Austin, Tex.)|October 11, 2011
Distinct association of the nuclear pore protein Nup153 with A- and B-type laminsTeiba Al-Haboubi, Dale K Shumaker, Joachim Köser, et al.
Human Mutation|December 31, 2013
Contribution of SUN1 mutations to the pathomechanism in muscular dystrophiesPing Li, Peter Meinke, Le Thi Thanh Huong, et al.
Journal of Molecular Endocrinology|June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophyRene Cortese, Florian Eckhardt, Marianne Volleth, et al.
Archives of Gynecology and Obstetrics|May 13, 2008
Restrictive dermopathy: a rare laminopathyMarc Thill, Thuy Duong Nguyen, Manfred Wehnert, et al.
Biochimica Et Biophysica Acta|June 16, 2009
Defects in cell spreading and ERK1/2 activation in fibroblasts with lamin A/C mutationsLindsay J Emerson, Mark R Holt, Matthew A Wheeler, et al.
Pageof 5