Myofibrillar instability exacerbated by acute exercise in filaminopathy
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Myofibrillar instability exacerbated by acute exercise in filaminopathy
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 24, Issue 25, Pages 7207-7220
Publisher
Oxford University Press (OUP)
Online
2015-10-16
DOI
10.1093/hmg/ddv421
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The toxic effect of R350P mutant desmin in striated muscle of man and mouse
- (2014) Christoph S. Clemen et al. ACTA NEUROPATHOLOGICA
- Aciculin interacts with filamin C and Xin and is essential for myofibril assembly, remodeling and maintenance
- (2014) S. Molt et al. JOURNAL OF CELL SCIENCE
- Automated phenotyping and advanced data mining exemplified in rats transgenic for Huntington's disease
- (2014) Yvonne K. Urbach et al. JOURNAL OF NEUROSCIENCE METHODS
- Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
- (2014) Rafael Valdés-Mas et al. Nature Communications
- Cellular Mechanotransduction Relies on Tension-Induced and Chaperone-Assisted Autophagy
- (2013) Anna Ulbricht et al. CURRENT BIOLOGY
- Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling
- (2013) Stefan Eulitz et al. MOLECULAR BIOLOGY OF THE CELL
- Filamin C-related myopathies: pathology and mechanisms
- (2012) Dieter O. Fürst et al. ACTA NEUROPATHOLOGICA
- Pathophysiology of protein aggregation and extended phenotyping in filaminopathy
- (2012) Rudolf A. Kley et al. BRAIN
- Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy
- (2012) Avnika A. Ruparelia et al. HUMAN MOLECULAR GENETICS
- A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients
- (2012) Rudolf A. Kley et al. MOLECULAR & CELLULAR PROTEOMICS
- Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy
- (2011) Rachael M. Duff et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacro
- (2011) Misato Fujita et al. DEVELOPMENTAL BIOLOGY
- Novel interactions of ankyrins-G at the costameres: The muscle-specific Obscurin/Titin-Binding-related Domain (OTBD) binds plectin and filamin C
- (2011) Yimingjiang Maiweilidan et al. EXPERIMENTAL CELL RESEARCH
- Selective Hippocampal Neurodegeneration in Transgenic Mice Expressing Small Amounts of Truncated A Is Induced by Pyroglutamate-A Formation
- (2011) A. Alexandru et al. JOURNAL OF NEUROSCIENCE
- Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency
- (2011) V. Guergueltcheva et al. NEUROLOGY
- Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy
- (2011) Montse Olivé et al. NEUROMUSCULAR DISORDERS
- Myofibrillar myopathies
- (2011) Duygu Selcen NEUROMUSCULAR DISORDERS
- Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance
- (2010) Verena Arndt et al. CURRENT BIOLOGY
- The sarcomeric Z-disc component myopodin is a multiadapter protein that interacts with filamin and α-actinin
- (2010) Anja Linnemann et al. EUROPEAN JOURNAL OF CELL BIOLOGY
- A novel heterozygous deletion–insertion mutation (2695–2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family
- (2010) Xinghua Luan et al. NEUROMUSCULAR DISORDERS
- Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study
- (2009) Kristl G. Claeys et al. ACTA NEUROPATHOLOGICA
- Myofibrillar Myopathies: A Clinical and Myopathological Guide
- (2009) Rolf Schröder et al. BRAIN PATHOLOGY
- In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy
- (2008) Alexey Shatunov et al. EUROPEAN JOURNAL OF HUMAN GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started