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
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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In: Acta Neuropathologica Communications 5 (2017).
- Schlagwort
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Orthopädie
- Ereignis
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Veröffentlichung
- (wo)
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Erlangen
- (wer)
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Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
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2017
- Urheber
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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
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urn:nbn:de:bvb:29-opus4-88783
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:28 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- 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)
Entstanden
- 2017
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Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
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Urine TITIN N-fragment as a novel biomarker for critical illness myopathy: a pilot study
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Age-dependent loss of Crls1 causes myopathy and skeletal muscle regeneration failure
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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
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Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy
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