Cargando…

Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases

BACKGROUND: Cardiomyopathies are a heterogeneous group of heart muscle disorders and are classified as 1) Hypertrophic Cardiomyopathy (HCM) 2) Dilated cardiomyopathy (DCM) 3) Restrictive cardiomyopathy (RCM) and 4) Arrhythmogenic right ventricular dysplasia (ARVD) as per WHO classification, of which...

Descripción completa

Detalles Bibliográficos
Autores principales:	Annapurna, S. D., Reena, T. R., Nallari, Pratibha, Calambur, Narasimhan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications 2007
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168158/ https://www.ncbi.nlm.nih.gov/pubmed/21957345 http://dx.doi.org/10.4103/0971-6866.34706

Ejemplares similares

An In Silico Analysis of Troponin I Mutations in Hypertrophic Cardiomyopathy of Indian Origin
por: Ramachandran, Gayatri, et al.
Publicado: (2013)

Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy
por: Tanjore, Reena, et al.
Publicado: (2010)

High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians
por: Rani, Deepa Selvi, et al.
Publicado: (2012)

A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family with Dilated Cardiomyopathy (FDCM)
por: Rani, Deepa Selvi, et al.
Publicado: (2014)

Novel mutations in arrhythmogenic right ventricular cardiomyopathy from Indian population
por: Pamuru, Pranathi Rao, et al.
Publicado: (2011)

Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy
por: Rani, Deepa Selvi, et al.
Publicado: (2021)

Clinical Picture Of Arrhythmogenic Right Ventricular Dysplasia / Cardiomyopathy Patients From Indian Origin
por: Maithili, DVN, et al.
Publicado: (2009)

Cardiac Troponin I and T as Prognostic Markers in Cats with Hypertrophic Cardiomyopathy
por: Langhorn, R., et al.
Publicado: (2014)

Diagnostic utility of cardiac troponin I in cats with hypertrophic cardiomyopathy
por: Hori, Yasutomo, et al.
Publicado: (2018)

Linkage analysis of three families with arrythmogenic right ventricular cardiomyopathy in India
por: Dokuparthi, Maithili V.N., et al.
Publicado: (2009)

Plasma Cardiac Troponin I Concentration and Cardiac Death in Cats with Hypertrophic Cardiomyopathy
por: Borgeat, K., et al.
Publicado: (2014)

Correlations between cardiac troponin I and nonsustained ventricular tachycardia in hypertrophic obstructive cardiomyopathy
por: Liu, Limin, et al.
Publicado: (2020)

Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy
por: Fahed, Akl C., et al.
Publicado: (2020)

Mutational analysis of SCN5A gene in long QT syndrome
por: Qureshi, Sameera Fatima, et al.
Publicado: (2015)

Mechanisms of Arrhythmogenicity of Hypertrophic Cardiomyopathy-Associated Troponin T (TNNT2) Variant I79N
por: Shafaattalab, Sanam, et al.
Publicado: (2021)

Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy
por: Fujita, Etsuko, et al.
Publicado: (2013)

Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylation()
por: Messer, Andrew E., et al.
Publicado: (2016)

Reversed Septal Curvature Is Associated with Elevated Troponin Level in Hypertrophic Cardiomyopathy
por: Rajtar-Salwa, Renata, et al.
Publicado: (2020)

Hypertrophic Cardiomyopathy Mutations of Troponin Reveal Details of Striated Muscle Regulation
por: Chalovich, J. M., et al.
Publicado: (2022)

Atrial natriuretic peptide gene - a potential biomarker for long QT syndrome
por: Qureshi, Sameera Fatima, et al.
Publicado: (2014)

The genetics of hypertrophic cardiomyopathy
por: Akhtar, Mohammed, et al.
Publicado: (2018)

Cardiac Troponin and Tropomyosin: Structural and Cellular Perspectives to Unveil the Hypertrophic Cardiomyopathy Phenotype
por: Marques, Mayra de A., et al.
Publicado: (2016)

Elevation of high‐sensitivity cardiac troponin T and left ventricular remodelling in hypertrophic cardiomyopathy
por: Kubo, Toru, et al.
Publicado: (2020)

Evaluation of a sensitive cardiac troponin I assay as a screening test for the diagnosis of hypertrophic cardiomyopathy in cats
por: Hertzsch, S., et al.
Publicado: (2019)

Association of diet with left ventricular wall thickness, troponin I and IGF‐1 in cats with subclinical hypertrophic cardiomyopathy
por: van Hoek, Ingrid, et al.
Publicado: (2020)

Cardiac troponin I in healthy Norwegian Forest Cat, Birman and domestic shorthair cats, and in cats with hypertrophic cardiomyopathy
por: Hanås, Sofia, et al.
Publicado: (2022)

Familial Hypertrophic Cardiomyopathy Related Cardiac Troponin C L29Q Mutation Alters Length-Dependent Activation and Functional Effects of Phosphomimetic Troponin I*
por: Li, Alison Y., et al.
Publicado: (2013)

Unexpected high troponin T and I values in a child with hypertrophic cardiomyopathy and acute chest pain: a case report
por: van Avezaath, Lisanne K, et al.
Publicado: (2023)

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
por: van den Wijngaard, A., et al.
Publicado: (2011)

Genotype–phenotype correlation in long QT syndrome families
por: Qureshi, Sameera Fatima, et al.
Publicado: (2015)

Gene database for the development of genetic testing for hypertrophic cardiomyopathy
por: Silas, Justin Carlus, et al.
Publicado: (2014)

Electrophysiological and Structural Remodeling of the Atria in a Mouse Model of Troponin-I Mutation Linked Hypertrophic Cardiomyopathy: Implications for Atrial Fibrillation
por: Lim, Wei-Wen, et al.
Publicado: (2021)

Clinical findings using echocardiography and plasma cardiac troponin I and pathological findings in dogs with hypertrophic cardiomyopathy: A retrospective study
por: Ando, Takeki, et al.
Publicado: (2023)

Differentiation of infiltrative cardiomyopathy from hypertrophic cardiomyopathy using high-sensitivity cardiac troponin T: a case-control study
por: Kubo, Toru, et al.
Publicado: (2015)

Sexual dimorphism in cardiac transcriptome associated with a troponin C murine model of hypertrophic cardiomyopathy
por: Dieseldorff Jones, Karissa M., et al.
Publicado: (2020)

Anomalous structural dynamics of minimally frustrated residues in cardiac troponin C triggers hypertrophic cardiomyopathy
por: Marques, Mayra A., et al.
Publicado: (2021)

Haplotypes of NOS3 Gene Polymorphisms in Dilated Cardiomyopathy
por: Matsa, Lova Satyanarayana, et al.
Publicado: (2013)

Hypertrophic Cardiomyopathy: An Overview of Genetics and Management
por: Teekakirikul, Polakit, et al.
Publicado: (2019)

Genetic Testing in Patients with Hypertrophic Cardiomyopathy
por: Bonaventura, Jiri, et al.
Publicado: (2021)

Genetic and Molecular Mechanisms of Hypertrophic Cardiomyopathy
por: Chou, Chun, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_p7kq18qcitg0omjs6hn7cgqah9