Rare variants in genes encoding MuRF1 and MuRF2 are modifiers of hypertrophic cardiomyopathy. (Q33907456)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24865491%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

title

Rare variants in genes encoding MuRF1 and MuRF2 are modifiers of hypertrophic cardiomyopathy (English)

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19 March 2020

8

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19 March 2020

author name string

Ming Su

1

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19 March 2020

Jizheng Wang

2

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19 March 2020

Lianming Kang

3

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19 March 2020

Yilu Wang

4

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19 March 2020

Yubao Zou

5

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19 March 2020

Xinxing Feng

6

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19 March 2020

Dong Wang

7

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19 March 2020

Xianliang Zhou

9

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19 March 2020

Rutai Hui

10

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19 March 2020

Lei Song

11

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19 March 2020

language of work or name

English

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publication date

26 May 2014

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International Journal of Molecular Sciences

19 March 2020

published in

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19 March 2020

volume

15

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19 March 2020

issue

6

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19 March 2020

page(s)

9302-9313

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Creative Commons Attribution 4.0 International

19 March 2020

copyright license

start time

26 May 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Human molecular genetic and functional studies identify TRIM63, encoding Muscle RING Finger Protein 1, as a novel gene for human hypertrophic cardiomyopathy.

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Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history

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The ubiquitin ligase MuRF1 protects against cardiac ischemia/reperfusion injury by its proteasome-dependent degradation of phospho-c-Jun.

5 July 2018

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Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice

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Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hypertrophic cardiomyopathy

5 July 2018

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Cooperative control of striated muscle mass and metabolism by MuRF1 and MuRF2.

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Crossref

https://api.crossref.org/works/10.3390%2FIJMS15069302

A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy

21 January 2018

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Does p.Q247X in TRIM63 cause human hypertrophic cardiomyopathy?

21 January 2018

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Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

21 January 2018

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Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24865491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24865491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hypertrophic cardiomyopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24865491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3390/IJMS15069302

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24865491%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24865491%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

PubMed publication ID

24865491

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24865491%20AND%20SRC:MED&resulttype=core&format=json