A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India. (Q54345908)

28 May 2018

title

A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India. (English)

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28 May 2018

hypertrophic cardiomyopathy

main subject

India

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familial hypertrophic cardiomyopathy

inferred from title

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Tabrez A Mohammad

6

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Hampapathalu A Nagarajaram

7

object named as

Hampapathalu A Nagarajaram

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28 May 2018

author name string

Murali D Bashyam

1

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28 May 2018

Guroji Purushotham

2

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28 May 2018

Ajay K Chaudhary

3

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28 May 2018

Katika Madhumohan Rao

4

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28 May 2018

Vishal Acharya

5

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28 May 2018

Vuppaladadhiam Hariram

8

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28 May 2018

Calambur Narasimhan

9

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28 May 2018

publication date

29 September 2011

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28 May 2018

Molecular and Cellular Biochemistry

published in

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28 May 2018

volume

360

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issue

1-2

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28 May 2018

page(s)

373-382

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28 May 2018

https://scigraph.springernature.com/pub.10.1007/s11010-011-1077-x

exact match

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cites work

Hypertrophic cardiomyopathy: a systematic review

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Causes of sudden death in competitive athletes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Sarcomeric proteins and inherited cardiomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Progression of left ventricular hypertrophy and the angiotensin-converting enzyme gene polymorphism in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

EMBOSS: the European Molecular Biology Open Software Suite

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Comparative protein modelling by satisfaction of spatial restraints

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Main-chain bond lengths and bond angles in protein structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Assessment of protein models with three-dimensional profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

GROMACS: fast, flexible, and free

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Myosin binding protein C interaction with actin: characterization and mapping of the binding site

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Identification of novel interactions between domains of Myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Cardiomyopathy: a systematic review of disease-causing mutations in myosin heavy chain 7 and their phenotypic manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Nonsense-mediated decay: linking a basic cellular process to human disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Mutations profile in Chinese patients with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

Genotype, phenotype: upstairs, downstairs in the family of cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

ACE I/D polymorphism in Indian patients with hypertrophic cardiomyopathy and dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11010-011-1077-X

The MYH7 p.R787H mutation causes hypertrophic cardiomyopathy in two unrelated families

21 January 2018

1 reference

12 December 2020

Lack of association of polymorphisms of the angiotensin converting enzyme and angiotensinogen genes with nonfamilial hypertrophic or dilated cardiomyopathy

1 reference

12 December 2020

Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics

1 reference

12 December 2020

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

1 reference

12 December 2020

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

1 reference

12 December 2020

Mistyping ACE heterozygotes

1 reference

12 December 2020

Impact of renin-angiotensin system polymorphisms on development of systolic dysfunction in hypertrophic cardiomyopathy. Evidence from a study of genotyped patients

1 reference

12 December 2020

Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.

1 reference

12 December 2020

10.1007/S11010-011-1077-X

Identifiers

DOI

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28 May 2018

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28 May 2018