Pages that link to "Q35197101"
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The following pages link to Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes (Q35197101):
Displaying 50 items.
- Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy (Q24296437) (← links)
- A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies (Q26738818) (← links)
- Arrhythmogenic cardiomyopathy (Q26753099) (← links)
- Titin-based tension in the cardiac sarcomere: molecular origin and physiological adaptations (Q26996063) (← links)
- Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease (Q27024037) (← links)
- Mutations with pathogenic potential in proteins located in or at the composite junctions of the intercalated disk connecting mammalian cardiomyocytes: a reference thesaurus for arrhythmogenic cardiomyopathies and for Naxos and Carvajal diseases (Q27024101) (← links)
- Importance of genetic evaluation and testing in pediatric cardiomyopathy (Q27024601) (← links)
- Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy (Q27310698) (← links)
- Arrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders (Q28069859) (← links)
- The genetic background of arrhythmogenic right ventricular cardiomyopathy (Q28074493) (← links)
- Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy (Q28246696) (← links)
- The ARVD/C genetic variants database: 2014 update (Q28256845) (← links)
- Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy (Q28287122) (← links)
- Exploration of pathomechanisms triggered by a single-nucleotide polymorphism in titin's I-band: the cardiomyopathy-linked mutation T2580I. (Q30393558) (← links)
- Single molecule force spectroscopy on titin implicates immunoglobulin domain stability as a cardiac disease mechanism. (Q30425614) (← links)
- S-glutathionylation of cryptic cysteines enhances titin elasticity by blocking protein folding (Q30576327) (← links)
- Update on Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C). (Q33162846) (← links)
- SCN5A mutation in Chinese patients with arrhythmogenic right ventricular dysplasia (Q33163606) (← links)
- Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes (Q33167672) (← links)
- The electrocardiographic manifestations of arrhythmogenic right ventricular dysplasia (Q33695854) (← links)
- Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy (Q33812341) (← links)
- Arrhythmogenic cardiomyopathy: diagnosis, genetic background, and risk management (Q33906065) (← links)
- A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy. (Q34429834) (← links)
- Arrhythmogenic right ventricular cardiomyopathy (ARVC): cardiovascular magnetic resonance update (Q34465268) (← links)
- Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins (Q34628389) (← links)
- Cardiac titin and heart disease (Q34721100) (← links)
- Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges (Q34780116) (← links)
- Mechanotransduction in cardiac hypertrophy and failure (Q35376847) (← links)
- Prevalence of Titin Truncating Variants in General Population (Q35877860) (← links)
- Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy (Q38639057) (← links)
- A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy (Q36405878) (← links)
- Genetic mutations and mechanisms in dilated cardiomyopathy (Q36497170) (← links)
- Almanac 2011: cardiomyopathies. The national society journals present selected research that has driven recent advances in clinical cardiology (Q36587026) (← links)
- Titin is a major human disease gene (Q36675841) (← links)
- Role of Titin Missense Variants in Dilated Cardiomyopathy (Q36836249) (← links)
- Rare coding TTN variants are associated with electrocardiographic QT interval in the general population (Q37019258) (← links)
- The expression of Lamin A mutant R321X leads to endoplasmic reticulum stress with aberrant Ca2 handling. (Q37370789) (← links)
- Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy (Q37433690) (← links)
- Genetics and genetic testing of dilated cardiomyopathy: a new perspective. (Q37863505) (← links)
- Pathophysiology of arrhythmogenic cardiomyopathy (Q37962327) (← links)
- Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C): A Review of Molecular and Clinical Literature (Q37994613) (← links)
- Arrhythmogenic right ventricular cardiomyopathy: an update on pathophysiology, genetics, diagnosis, and risk stratification (Q38046512) (← links)
- Genetic testing in the contemporary diagnosis of cardiomyopathy (Q38058475) (← links)
- Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D). (Q38119176) (← links)
- Genetics in dilated cardiomyopathy (Q38125766) (← links)
- Desmosomes in the heart: a review of clinical and mechanistic analyses (Q38206258) (← links)
- A rising titan: TTN review and mutation update (Q38224878) (← links)
- Arrhythmogenic cardiomyopathy: a disease of intercalated discs (Q38262612) (← links)
- Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy (Q38268280) (← links)
- The research venture in arrhythmogenic right ventricular cardiomyopathy: a paradigm of translational medicine (Q38338091) (← links)