Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? (Q28264798)

Europe PubMed Central

title

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? (English)

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author

Michelle S Parvatiyar

4

object named as

Michelle S Parvatiyar

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author name string

Ruth H Willott

1

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Aldrin V Gomes

2

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Audrey N Chang

3

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Jose Renato Pinto

5

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James D Potter

Journal of Molecular and Cellular Cardiology

6

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language of work or name

English

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publication date

May 2010

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published in

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volume

48

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issue

5

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page(s)

882-92

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cites work

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7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Phenotypic differences between electrocardiographic and echocardiographic determination of hypertrophic cardiomyopathy in genetically affected subjects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Frequency of cardiac troponin I mutations in families with hypertrophic cardiomyopathy in China

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Late-onset hypertrophic cardiomyopathy caused by a mutation in the cardiac troponin T gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Low prevalence of cardiac troponin T mutations in a Greek hypertrophic cardiomyopathy cohort

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

inferred from DOI database lookup

7 January 2021

based on heuristic

Ca2 -sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.YJMCC.2009.10.031

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YJMCC.2009.10.031

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

19914256

1 reference

Consolidated OpenCitations Corpus – April 2017