MYBPH acts as modifier of cardiac hypertrophy in hypertrophic cardiomyopathy (HCM) patients. (Q53152120)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26969327%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

title

MYBPH acts as modifier of cardiac hypertrophy in hypertrophic cardiomyopathy (HCM) patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26969327%20AND%20SRC:MED&resulttype=core&format=json

hypertrophic cardiomyopathy

10 March 2020

main subject

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7

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10 March 2020

Jomien Mouton

1

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10 March 2020

author name string

L van der Merwe

2

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10 March 2020

A Goosen

3

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10 March 2020

M Revera

4

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10 March 2020

P A Brink

5

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10 March 2020

J C Moolman-Smook

6

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10 March 2020

publication date

11 March 2016

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10 March 2020

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10 March 2020

volume

135

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issue

5

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10 March 2020

page(s)

477-483

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Haploview: analysis and visualization of LD and haplotype maps

10 March 2020

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A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy

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Splice site prediction in Arabidopsis thaliana pre-mRNA by combining local and global sequence information

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Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

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Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

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The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events

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Heritability of cardiovascular and personality traits in 6,148 Sardinians

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Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy

21 January 2018

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Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history

21 January 2018

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Rare variants in genes encoding MuRF1 and MuRF2 are modifiers of hypertrophic cardiomyopathy.

21 January 2018

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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

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Transesophageal Echocardiography

21 January 2018

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21 January 2018

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12 December 2020

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

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12 December 2020

Ascribing novel functions to the sarcomeric protein, myosin binding protein H (MyBPH) in cardiac sarcomere contraction.

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12 December 2020

10.1007/S00439-016-1649-7

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26969327%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1 reference