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Manfred Wehnert

Showing results (21-30 of 41) with videos related to

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Human Molecular Genetics|April 22, 2005
Altered pre-lamin A processing is a common mechanism leading to lipodystrophyCristina Capanni, Elisabetta Mattioli, Marta Columbaro, et al.
Annals of Neurology|December 29, 2004
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeriaJanbernd Kirschner, Thomas Brune, Manfred Wehnert, et al.
Experimental Cell Research|November 5, 2003
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcriptionCristina Capanni, Vittoria Cenni, Elisabetta Mattioli, et al.
Plos Genetics|September 12, 2014
Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organizationPeter Meinke, Elisabetta Mattioli, Farhana Haque, et al.
Pediatric Endocrinology Reviews : PER|January 24, 2006
Progeria: a new kind of Laminopathy-- report of the First European Symposium on Progeria and creation of EURO-Progeria, a European Consortium on Progeria and related disordersThomas Brune, Gisele Bonne, Jonas Denecke, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophyPeter Meinke, Peter Schneiderat, Vlastimil Srsen, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophyMichal Vytopil, Enzo Ricci, Antonio Dello Russo, et al.
Aging|June 28, 2013
Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435CSven Starke, Peter Meinke, Daria Camozzi, et al.
Journal of Cellular Biochemistry|July 27, 2007
Pre-Lamin A processing is linked to heterochromatin organizationGiovanna Lattanzi, Marta Columbaro, Elisabetta Mattioli, et al.
Cell Cycle (Georgetown, Tex.)|December 4, 2010
Prelamin A processing and functional effects in restrictive dermopathyMarta Columbaro, Elisabetta Mattioli, Elisa Schena, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|April 22, 2005
Altered pre-lamin A processing is a common mechanism leading to lipodystrophyCristina Capanni, Elisabetta Mattioli, Marta Columbaro, et al.
Annals of Neurology|December 29, 2004
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeriaJanbernd Kirschner, Thomas Brune, Manfred Wehnert, et al.
Experimental Cell Research|November 5, 2003
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcriptionCristina Capanni, Vittoria Cenni, Elisabetta Mattioli, et al.
Plos Genetics|September 12, 2014
Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organizationPeter Meinke, Elisabetta Mattioli, Farhana Haque, et al.
Pediatric Endocrinology Reviews : PER|January 24, 2006
Progeria: a new kind of Laminopathy-- report of the First European Symposium on Progeria and creation of EURO-Progeria, a European Consortium on Progeria and related disordersThomas Brune, Gisele Bonne, Jonas Denecke, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophyPeter Meinke, Peter Schneiderat, Vlastimil Srsen, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophyMichal Vytopil, Enzo Ricci, Antonio Dello Russo, et al.
Aging|June 28, 2013
Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435CSven Starke, Peter Meinke, Daria Camozzi, et al.
Journal of Cellular Biochemistry|July 27, 2007
Pre-Lamin A processing is linked to heterochromatin organizationGiovanna Lattanzi, Marta Columbaro, Elisabetta Mattioli, et al.
Cell Cycle (Georgetown, Tex.)|December 4, 2010
Prelamin A processing and functional effects in restrictive dermopathyMarta Columbaro, Elisabetta Mattioli, Elisa Schena, et al.
Pageof 5