Manfred S. Wehnert

Greifswald, MV, Germany

Last Updated: 09/26/2026

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Found 15 publications

Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere.

Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere.

Journal: The Journal of biological chemistry

Published: September 05, 2023

A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism.

A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism.

Journal: EBioMedicine

Published: October 14, 2019

Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology.

Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology.

Journal: Neuromuscular disorders : NMD

Published: July 20, 2016

Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells.

Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells.

Journal: Nucleus (Austin, Tex.)

Published: March 05, 2015

Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics.

Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics.

Journal: Aging

Published: October 18, 2014

Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy.

Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy.

Journal: Neuromuscular disorders : NMD

Published: July 28, 2014

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization.

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization.

Journal: PLoS genetics

Published: October 02, 2013

Contribution of SUN1 mutations to the pathomechanism in muscular dystrophies.

Contribution of SUN1 mutations to the pathomechanism in muscular dystrophies.

Journal: Human mutation

Published: August 01, 2013

New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update.

New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update.

Journal: European journal of human genetics : EJHG

Published: July 02, 2013

Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C.

Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C.

Journal: Aging

Published: June 28, 2013

Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation.

Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation.

Journal: Neuromuscular disorders : NMD

Published: November 09, 2012

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution.

Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution.

Journal: Cell cycle (Georgetown, Tex.)

Published: September 01, 2012

Showing 1-12 of 15

Last Updated: 09/26/2026