Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2051-5960

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Keyword: Orthopädie

Creator: Unger, Andreas

Contributor: 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: 10.1186/s40478-017-0474-0

URN: urn:nbn:de:1111-201711179284

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:38 AM CEST

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Associated

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

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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

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Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy

Cell stress molecules in the skeletal muscle of GNE myopathy

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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

Aufsatzsammlung

Molecular chaperones

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Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins

Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure

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Bioinspirierte Titin-analoge Polymere

Dilated cardiomyopathy-mediated heart failure induces a unique skeletal muscle myopathy with inflammation

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Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function

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Other Objects (12)

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?

Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins

Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure

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?

Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins

Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure

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?

Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins

Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure

Bioinspirierte Titin-analoge Polymere

Dilated cardiomyopathy-mediated heart failure induces a unique skeletal muscle myopathy with inflammation

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