(Q83275688)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21259275%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Slow cardiac myosin regulatory light chain 2 (MYL2) was down-expressed in chronic heart failure patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21259275%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

main subject

chronic heart failure

1 reference

Yuanhong Li

1

1 reference

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20 January 2020

Gang Wu

2

1 reference

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20 January 2020

Qizhu Tang

3

1 reference

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20 January 2020

Congxin Huang

4

1 reference

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20 January 2020

Hong Jiang

5

1 reference

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20 January 2020

Lisong Shi

6

1 reference

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20 January 2020

Xin Tu

7

1 reference

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20 January 2020

Jinqi Huang

8

1 reference

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20 January 2020

Xiaoqing Zhu

9

1 reference

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20 January 2020

Hongli Wang

10

1 reference

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20 January 2020

publication date

10 December 2010

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20 January 2020

1 reference

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20 January 2020

volume

34

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20 January 2020

issue

1

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20 January 2020

page(s)

30-34

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21259275%20AND%20SRC:MED&resulttype=core&format=json

Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation

20 January 2020

cites work

1 reference

12 December 2020

Hypertrophic cardiomyopathy: a systematic review

1 reference

12 December 2020

Phosphorylation of the regulatory light chains of myosin affects Ca2+ sensitivity of skeletal muscle contraction

1 reference

12 December 2020

Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

A point mutation in the regulatory light chain reduces the step size of skeletal muscle myosin

1 reference

12 December 2020

1 reference

12 December 2020

The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a common gene expression signature in dilated cardiomyopathy across independent microarray studies

1 reference

12 December 2020

Shared genetic causes of cardiac hypertrophy in children and adults

1 reference

12 December 2020

A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy

1 reference

12 December 2020

Heart failure: targeting transcriptional and post-transcriptional control mechanisms of hypertrophy for treatment.

1 reference

12 December 2020

Molecular mechanisms underlying the transition of cardiac hypertrophy to heart failure

1 reference

12 December 2020

ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2008 of the European Society of Cardiology

1 reference

12 December 2020

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy

1 reference

12 December 2020

Global gene expression profiling in the failing myocardium

1 reference

12 December 2020

Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.

1 reference

12 December 2020

Identification of genes related to heart failure using global gene expression profiling of human failing myocardium

1 reference

12 December 2020

Interaction of a conserved peptide domain in recombinant human ventricular myosin light chain-2 with myosin heavy chain

1 reference

12 December 2020

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

1 reference

12 December 2020

Identifiers

DOI

10.1002/CLC.20832

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21259275%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21259275%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

21259275

1 reference