(Q28300361)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17476457%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

title

Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17476457%20AND%20SRC:MED&resulttype=core&format=json

hypertrophic cardiomyopathy

30 December 2019

main subject

1 reference

2

1 reference

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30 December 2019

Hiroshi Takeshima

8

1 reference

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30 December 2019

author name string

Yoshihisa Matsushita

1

1 reference

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30 December 2019

Hiroshi Kasanuki

3

1 reference

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30 December 2019

Makoto Nishibatake

4

1 reference

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30 December 2019

Yachiyo Kurihara

5

1 reference

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30 December 2019

Atsushi Ikeda

6

1 reference

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30 December 2019

Rumiko Matsuoka

9

1 reference

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30 December 2019

Naoyuki Kamatani

7

1 reference

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30 December 2019

language of work or name

English

0 references

publication date

3 May 2007

1 reference

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Journal of Human Genetics

30 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17476457%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

volume

52

1 reference

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30 December 2019

issue

6

1 reference

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30 December 2019

page(s)

543-548

1 reference

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https://scigraph.springernature.com/pub.10.1007/s10038-007-0149-y

30 December 2019

exact match

0 references

cites work

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-007-0149-Y

Junctophilins: a novel family of junctional membrane complex proteins

21 January 2018

1 reference

12 December 2020

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

1 reference

12 December 2020

Structural analysis of muscle development: transverse tubules, sarcoplasmic reticulum, and the triad

1 reference

12 December 2020

Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human

1 reference

12 December 2020

Characterization of human junctophilin subtype genes

1 reference

12 December 2020

Functional uncoupling between Ca2+ release and afterhyperpolarization in mutant hippocampal neurons lacking junctophilins

1 reference

12 December 2020

Mutations profile in Chinese patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Deficiency of triad junction and contraction in mutant skeletal muscle lacking junctophilin type 1.

1 reference

12 December 2020

Store-operated Ca2+ entry uncoupled with ryanodine receptor and junctional membrane complex in heart muscle cells.

1 reference

12 December 2020

Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy

1 reference

12 December 2020

Ryanodine receptor/Ca2+ release channels and their regulation by endogenous effectors

1 reference

12 December 2020

Motor discoordination in mutant mice lacking junctophilin type 3

1 reference

12 December 2020

Effect of trifluoroethanol on protein secondary structure: an NMR and CD study using a synthetic actin peptide

1 reference

12 December 2020

Hypertrophic cardiomyopathy: a systematic review

1 reference

12 December 2020

Abnormal junctional membrane structures in cardiac myocytes expressing ectopic junctophilin type 1

1 reference

12 December 2020

Regional location of a novel yes-related proto-oncogene, syn, on human chromosome 6 at band q21

1 reference

12 December 2020

Junctophilin-mediated channel crosstalk essential for cerebellar synaptic plasticity.

1 reference

12 December 2020

Hypertrophic cardiomyopathy

1 reference

12 December 2020

Persistence of the alpha-helix stop signal in the S-peptide in trifluoroethanol solutions

1 reference

12 December 2020

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

1 reference

12 December 2020

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Ryanodine receptors of striated muscles: a complex channel capable of multiple interactions

1 reference

12 December 2020

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion

1 reference

12 December 2020

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.

1 reference

12 December 2020

The endoplasmic reticulum: a multifunctional signaling organelle

1 reference

12 December 2020

Coexpression of junctophilin type 3 and type 4 in brain

1 reference

12 December 2020

Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing

1 reference

12 December 2020

10.1007/S10038-007-0149-Y

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

4752771

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17476457%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

4752771

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

4752771