HSPB7 interacts with dimerized FLNC and its absence results in progressive myopathy in skeletal muscles
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
HSPB7 interacts with dimerized FLNC and its absence results in progressive myopathy in skeletal muscles
Authors
Keywords
-
Journal
JOURNAL OF CELL SCIENCE
Volume 129, Issue 8, Pages 1661-1670
Publisher
The Company of Biologists
Online
2016-03-01
DOI
10.1242/jcs.179887
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Drosophila small heat shock protein CryAB ensures structural integrity of developing muscles, and proper muscle and heart performance
- (2015) I. Wojtowicz et al. DEVELOPMENT
- Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients
- (2015) Sophie Garnier et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
- Neuropathy- and myopathy-associated mutations in human small heat shock proteins: Characteristics and evolutionary history of the mutation sites
- (2014) Rainer Benndorf et al. MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
- Cellular Mechanotransduction Relies on Tension-Induced and Chaperone-Assisted Autophagy
- (2013) Anna Ulbricht et al. CURRENT BIOLOGY
- Small heat shock proteins Hspb7 and Hspb12 regulate early steps of cardiac morphogenesis
- (2013) Gabriel E. Rosenfeld et al. DEVELOPMENTAL BIOLOGY
- Small heat shock proteins are necessary for heart migration and laterality determination in zebrafish
- (2013) Jamie L. Lahvic et al. DEVELOPMENTAL BIOLOGY
- Filamins in Mechanosensing and Signaling
- (2012) Ziba Razinia et al. Annual Review of Biophysics
- Association of Plasma Concentration of Small Heat Shock Protein B7 With Acute Coronary Syndrome
- (2012) Te-Fa Chiu et al. CIRCULATION JOURNAL
- A persistent level of Cisd2 extends healthy lifespan and delays aging in mice
- (2012) Chia-Yu Wu et al. HUMAN MOLECULAR 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
- HSPB1, HSPB6, HSPB7 and HSPB8 Protect against RhoA GTPase-Induced Remodeling in Tachypaced Atrial Myocytes
- (2011) Lei Ke et al. PLoS One
- Common Variants in HSPB7 and FRMD4B Associated With Advanced Heart Failure
- (2010) Thomas P. Cappola et al. Circulation-Cardiovascular Genetics
- Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance
- (2010) Verena Arndt et al. CURRENT BIOLOGY
- HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones
- (2010) Michel J. Vos et al. HUMAN MOLECULAR GENETICS
- Proteomic profiling of x-linked muscular dystrophy
- (2010) Caroline Lewis et al. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
- Filamins in cell signaling, transcription and organ development
- (2010) Alex-Xianghua Zhou et al. TRENDS IN CELL BIOLOGY
- Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy
- (2010) Klaus Stark et al. PLoS Genetics
- Structural and Functional Diversities between Members of the Human HSPB, HSPH, HSPA, and DNAJ Chaperone Families†
- (2008) Michel J. Vos et al. BIOCHEMISTRY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search