Plectin isoform P1b and P1d deficiencies differentially affect mitochondrial morphology and function in skeletal muscle
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Plectin isoform P1b and P1d deficiencies differentially affect mitochondrial morphology and function in skeletal muscle
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 24, Issue 16, Pages 4530-4544
Publisher
Oxford University Press (OUP)
Online
2015-05-28
DOI
10.1093/hmg/ddv184
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mitochondrial membrane potential is regulated by vimentin intermediate filaments
- (2015) Ivan S. Chernoivanenko et al. FASEB JOURNAL
- Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex
- (2015) Katarzyna B. Gostyńska et al. HUMAN MOLECULAR GENETICS
- Chemical chaperone ameliorates pathological protein aggregation in plectin-deficient muscle
- (2014) Lilli Winter et al. JOURNAL OF CLINICAL INVESTIGATION
- Neuromuscular synapse integrity requires linkage of acetylcholine receptors to postsynaptic intermediate filament networks via rapsyn–plectin 1f complexes
- (2014) Eva Mihailovska et al. MOLECULAR BIOLOGY OF THE CELL
- Keeping mitochondria in shape: a matter of life and death
- (2013) Luca Scorrano EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
- Mechanosensing through focal adhesion-anchored intermediate filaments
- (2013) Martin Gregor et al. FASEB JOURNAL
- From Structure to Function: Mitochondrial Morphology, Motion and Shaping in Vascular Smooth Muscle
- (2013) John G. McCarron et al. JOURNAL OF VASCULAR RESEARCH
- Mechanisms of Mitochondrial Fission and Fusion
- (2013) A. M. van der Bliek et al. Cold Spring Harbor Perspectives in Biology
- Linking cytoarchitecture to metabolism: sarcolemma-associated plectin affects glucose uptake by destabilizing microtubule networks in mdx myofibers
- (2013) Marianne Raith et al. Skeletal Muscle
- The many faces of plectin and plectinopathies: pathology and mechanisms
- (2012) Lilli Winter et al. ACTA NEUROPATHOLOGICA
- Myasthenic syndrome caused by plectinopathy
- (2011) D. Selcen et al. NEUROLOGY
- Mutation in Exon 1f of PLEC, Leading to Disruption of Plectin Isoform 1f, Causes Autosomal-Recessive Limb-Girdle Muscular Dystrophy
- (2010) Hulya Gundesli et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE
- (2010) RA Maselli et al. CLINICAL GENETICS
- Plectin isoform 1b mediates mitochondrion–intermediate filament network linkage and controls organelle shape
- (2008) Lilli Winter et al. JOURNAL OF CELL BIOLOGY
- Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms
- (2008) Patryk Konieczny et al. JOURNAL OF CELL BIOLOGY
- Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells
- (2008) Andrey V Kuznetsov et al. Nature Protocols
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started