Infantile restrictive cardiomyopathy : cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: PLoS ONE, 15, 3, Article e0229227, S. e0229227-1-e0229227-20
- Ereignis
-
Veröffentlichung
- (wo)
-
Bochum
- (wer)
-
Ruhr-Universität Bochum
- (wann)
-
2020
- Urheber
-
Cimiotti, Diana
Fujita-Becker, Setsuko
Möhner, Desirée Martha
Smolina, Natalia
Budde, Heidi
Wies, Aline
Morgenstern, Janine
Gudkova, Alexandra
Sejersen, Thomas
Sjöberg, Gunnar
Mügge, Andreas
Nowaczyk, Marc Michael
Reusch, Peter
Pfitzer, Gabriele
Stehle, Robert
Schröder, Rasmus R.
Mannherz, Hans Georg
Kostareva, Anna
Jaquet, Kornelia
- URN
-
urn:nbn:de:hbz:294-76819
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:50 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Cimiotti, Diana
- Fujita-Becker, Setsuko
- Möhner, Desirée Martha
- Smolina, Natalia
- Budde, Heidi
- Wies, Aline
- Morgenstern, Janine
- Gudkova, Alexandra
- Sejersen, Thomas
- Sjöberg, Gunnar
- Mügge, Andreas
- Nowaczyk, Marc Michael
- Reusch, Peter
- Pfitzer, Gabriele
- Stehle, Robert
- Schröder, Rasmus R.
- Mannherz, Hans Georg
- Kostareva, Anna
- Jaquet, Kornelia
- Ruhr-Universität Bochum
Entstanden
- 2020
Ähnliche Objekte (12)
Genetic insights into primary restrictive cardiomyopathy
Overexpression of human BAG3P209L in mice causes restrictive cardiomyopathy
Genetic restrictive cardiomyopathy: causes and consequences : an integrative approach
The desmin mutation DES-c.735G>C causes severe restrictive cardiomyopathy by inducing in-frame skipping of exon-3
Australia: Restrictive trade policy
Germany: Restrictive stabillsation programme
Verschlußsache TN 2, TN 3 und TN 4
Metabolic cardiomyopathy
Metabolic cardiomyopathy
Restrictive cardiomyopathy is caused by a novel homozygous desmin \(\it (DES)\) mutation p.Y122H leading to a severe filament assembly defect
Masculine identity and restrictive emotionality
Embedding non-restrictive relative clauses
Genetic insights into primary restrictive cardiomyopathy
Overexpression of human BAG3P209L in mice causes restrictive cardiomyopathy
Genetic restrictive cardiomyopathy: causes and consequences : an integrative approach
The desmin mutation DES-c.735G>C causes severe restrictive cardiomyopathy by inducing in-frame skipping of exon-3
Australia: Restrictive trade policy
Germany: Restrictive stabillsation programme
Verschlußsache TN 2, TN 3 und TN 4
Metabolic cardiomyopathy
Metabolic cardiomyopathy
Restrictive cardiomyopathy is caused by a novel homozygous desmin \(\it (DES)\) mutation p.Y122H leading to a severe filament assembly defect
Masculine identity and restrictive emotionality
Embedding non-restrictive relative clauses
Genetic insights into primary restrictive cardiomyopathy
Overexpression of human BAG3P209L in mice causes restrictive cardiomyopathy
Genetic restrictive cardiomyopathy: causes and consequences : an integrative approach
The desmin mutation DES-c.735G>C causes severe restrictive cardiomyopathy by inducing in-frame skipping of exon-3
Australia: Restrictive trade policy
Germany: Restrictive stabillsation programme
Verschlußsache TN 2, TN 3 und TN 4
Metabolic cardiomyopathy
Metabolic cardiomyopathy
Restrictive cardiomyopathy is caused by a novel homozygous desmin \(\it (DES)\) mutation p.Y122H leading to a severe filament assembly defect
Masculine identity and restrictive emotionality