Genetic epidemiology of titin-truncating variants in the etiology of dilated cardiomyopathy
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1867-2469
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Genetic epidemiology of titin-truncating variants in the etiology of dilated cardiomyopathy ; day:5 ; month:5 ; year:2017 ; pages:1-17
Biophysical reviews ; (5.5.2017), 1-17
- Keyword
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Kardiovaskuläre Krankheit
- Creator
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Tabish, Ali M.
- Contributor
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Azzimato, Valerio
Alexiadis, Aris
Buyandelger, Byambajav
Knöll, Ralph
SpringerLink (Online service)
- DOI
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10.1007/s12551-017-0265-7
- URN
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urn:nbn:de:1111-201705154221
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:25 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Tabish, Ali M.
- Azzimato, Valerio
- Alexiadis, Aris
- Buyandelger, Byambajav
- Knöll, Ralph
- SpringerLink (Online service)
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Expression of truncated titin proteins in human dilated cardiomyopathy hearts and modulating role of the protein quality control machinery
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Titin: a phenotype-genotype descriptive comparison of dilated cardiomyopathy
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Circulating circRNA as biomarkers for dilated cardiomyopathy etiology
Antisense‐mediated exon skipping: a therapeutic strategy for titin‐based dilated cardiomyopathy
Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
Elucidating the role of Titin mutations and the Titin-Nexilin interaction on the pathogenesis of dilated cardiomyopathy in zebrafish
Cardiomyopathy, familial dilated
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy
The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy
Expression of truncated titin proteins in human dilated cardiomyopathy hearts and modulating role of the protein quality control machinery
Dilated cardiomyopathies and non-compaction cardiomyopathy
Titin: a phenotype-genotype descriptive comparison of dilated cardiomyopathy
Inflammatory dilated cardiomyopathy : Etiology and clinical management
Circulating circRNA as biomarkers for dilated cardiomyopathy etiology
Antisense‐mediated exon skipping: a therapeutic strategy for titin‐based dilated cardiomyopathy
Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy
Elucidating the role of Titin mutations and the Titin-Nexilin interaction on the pathogenesis of dilated cardiomyopathy in zebrafish
Cardiomyopathy, familial dilated
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy
The Assembly and Evaluation of Antisense Oligonucleotides Applied in Exon Skipping for Titin-based Mutations in Dilated Cardiomyopathy
Expression of truncated titin proteins in human dilated cardiomyopathy hearts and modulating role of the protein quality control machinery