Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2051-5960
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function ; volume:5 ; number:1 ; day:15 ; month:9 ; year:2017 ; pages:1-14 ; date:12.2017
Acta Neuropathologica Communications ; 5, Heft 1 (15.9.2017), 1-14, 12.2017
- Schlagwort
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Orthopädie
- Urheber
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Unger, Andreas
- Beteiligte Personen und Organisationen
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Beckendorf, Lisa
Böhme, Pierre
Kley, Rudolf
von Frieling-Salewsky, Marion
Lochmüller, Hanns
Schröder, Rolf
Fürst, Dieter O.
Vorgerd, Matthias
Linke, Wolfgang A.
SpringerLink (Online service)
- DOI
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10.1186/s40478-017-0474-0
- URN
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urn:nbn:de:1111-201711179284
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:38 MESZ
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Beteiligte
- Unger, Andreas
- Beckendorf, Lisa
- Böhme, Pierre
- Kley, Rudolf
- von Frieling-Salewsky, Marion
- Lochmüller, Hanns
- Schröder, Rolf
- Fürst, Dieter O.
- Vorgerd, Matthias
- Linke, Wolfgang A.
- SpringerLink (Online service)
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Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
The complexity of titin splicing pattern in human adult skeletal muscles
Urine TITIN N-fragment as a novel biomarker for critical illness myopathy: a pilot study
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
Cell stress molecules in the skeletal muscle of GNE myopathy
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Skeletal myopathy in Pompe disease: a failure of satellite cell activation?
Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure
Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins
Bioinspirierte Titin-analoge Polymere
Dilated cardiomyopathy-mediated heart failure induces a unique skeletal muscle myopathy with inflammation
Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
The complexity of titin splicing pattern in human adult skeletal muscles
Urine TITIN N-fragment as a novel biomarker for critical illness myopathy: a pilot study
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
Cell stress molecules in the skeletal muscle of GNE myopathy
Molecular chaperones
Skeletal myopathy in Pompe disease: a failure of satellite cell activation?
Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure
Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins
Bioinspirierte Titin-analoge Polymere