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

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Acta Neuropathologica Communications 5 (2017).

Keyword: -
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Event: Veröffentlichung

(where): Erlangen

(who): Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)

(when): 2017

Creator: Unger, Andreas
Beckendorf, Lisa
Böhme, Pierre
Kley, Rudolf
Frieling-Salewsky, Marion von
Lochmüller, Hanns
Schröder, Rolf
Fürst, Dieter O.
Vorgerd, Matthias
Linke, Wolfgang A.

URN: urn:nbn:de:bvb:29-opus4-88783

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:28 AM CEST

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Associated

Unger, Andreas
Beckendorf, Lisa
Böhme, Pierre
Kley, Rudolf
Frieling-Salewsky, Marion von
Lochmüller, Hanns
Schröder, Rolf
Fürst, Dieter O.
Vorgerd, Matthias
Linke, Wolfgang A.
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)

Time of origin

2017

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

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

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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

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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

Cell stress molecules in the skeletal muscle of GNE myopathy

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

Aufsatzsammlung

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

Hochschulschrift

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

Cell stress molecules in the skeletal muscle of GNE myopathy

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

Aufsatzsammlung

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

Hochschulschrift

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

Cell stress molecules in the skeletal muscle of GNE myopathy

Tropomyosin 3 (TPM3) function in skeletal muscle and in 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

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

Cell stress molecules in the skeletal muscle of GNE myopathy

Tropomyosin 3 (TPM3) function in skeletal muscle and in 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

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

Cell stress molecules in the skeletal muscle of GNE myopathy

Tropomyosin 3 (TPM3) function in skeletal muscle and in 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

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

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