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Peter Meinke

Showing results (31-40 of 51) with videos related to

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Human Molecular Genetics|October 25, 2022
Metabolic, fibrotic and splicing pathways are all altered in Emery-Dreifuss muscular dystrophy spectrum patients to differing degreesJose I de Las Heras, Vanessa Todorow, Lejla Krečinić-Balić, et al.
BMC Musculoskeletal Disorders|September 21, 2021
Influence of IGF-I serum concentration on muscular regeneration capacity in patients with sarcopeniaStefanie Jarmusch, Lisa Baber, Martin Bidlingmaier, et al.
BMC Neurology|June 26, 2021
Late-onset neuromuscular disorders in the differential diagnosis of sarcopeniaFabian Hofmeister, Lisa Baber, Uta Ferrari, et al.
Experimental Gerontology|November 28, 2020
Type-2 muscle fiber atrophy is associated with sarcopenia in elderly men with hip fractureFabiana Tanganelli, Peter Meinke, Fabian Hofmeister, 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.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Elimination of myotonia improves myopathy in a muscleblind knockout model of myotonic dystrophyMatthew T Sipple, Sakura A Hamazaki, Vanessa Todorow, 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.
Plos One|November 12, 2014
NET23/STING promotes chromatin compaction from the nuclear envelopePoonam Malik, Nikolaj Zuleger, Jose I de las Heras, 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.
Aging Clinical and Experimental Research|November 9, 2023
11-beta-hydroxysteroid dehydrogenase type 1 (HSD11B1) gene expression in muscle is linked to reduced skeletal muscle index in sarcopenic patientsSabine Schluessel, Wei Zhang, Hanna Nowotny, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|October 25, 2022
Metabolic, fibrotic and splicing pathways are all altered in Emery-Dreifuss muscular dystrophy spectrum patients to differing degreesJose I de Las Heras, Vanessa Todorow, Lejla Krečinić-Balić, et al.
BMC Musculoskeletal Disorders|September 21, 2021
Influence of IGF-I serum concentration on muscular regeneration capacity in patients with sarcopeniaStefanie Jarmusch, Lisa Baber, Martin Bidlingmaier, et al.
BMC Neurology|June 26, 2021
Late-onset neuromuscular disorders in the differential diagnosis of sarcopeniaFabian Hofmeister, Lisa Baber, Uta Ferrari, et al.
Experimental Gerontology|November 28, 2020
Type-2 muscle fiber atrophy is associated with sarcopenia in elderly men with hip fractureFabiana Tanganelli, Peter Meinke, Fabian Hofmeister, 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.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Elimination of myotonia improves myopathy in a muscleblind knockout model of myotonic dystrophyMatthew T Sipple, Sakura A Hamazaki, Vanessa Todorow, 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.
Plos One|November 12, 2014
NET23/STING promotes chromatin compaction from the nuclear envelopePoonam Malik, Nikolaj Zuleger, Jose I de las Heras, 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.
Aging Clinical and Experimental Research|November 9, 2023
11-beta-hydroxysteroid dehydrogenase type 1 (HSD11B1) gene expression in muscle is linked to reduced skeletal muscle index in sarcopenic patientsSabine Schluessel, Wei Zhang, Hanna Nowotny, et al.
Pageof 6