Ca(2 )-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy. (Q33894656)

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5 December 2019

title

Ca(2 )-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy (English)

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5 December 2019

1

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5 December 2019

author name string

Q-W Lu

2

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5 December 2019

K Harada

3

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5 December 2019

F Takahashi-Yanaga

4

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5 December 2019

R Minakami

5

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5 December 2019

M Ohta

6

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5 December 2019

T Sasaguri

7

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5 December 2019

I Ohtsuki

8

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5 December 2019

language of work or name

English

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publication date

2 January 2002

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5 December 2019

number of pages

6

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Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

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5 December 2019

volume

99

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5 December 2019

issue

2

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5 December 2019

page(s)

913-918

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Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy

5 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

5 July 2018

1 reference

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The molecular genetic basis for hypertrophic cardiomyopathy

5 July 2018

1 reference

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Invited Review: pathophysiology of cardiac muscle contraction and relaxation as a result of alterations in thin filament regulation

5 July 2018

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

5 July 2018

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Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

5 July 2018

1 reference

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Animal models of hypertrophic cardiomyopathy

5 July 2018

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Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2 ) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein

5 July 2018

1 reference

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Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

5 July 2018

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Functional consequences of the deletion mutation deltaGlu160 in human cardiac troponin T

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Effects of missense mutations Phe110Ile and Glu244Asp in human cardiac troponin T on force generation in skinned cardiac muscle fibers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Desmin mutation responsible for idiopathic dilated cardiomyopathy

5 July 2018

1 reference

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Functional consequences of a carboxyl terminal missense mutation Arg278Cys in human cardiac troponin T

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

The causes of dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Calcium ion and muscle contraction

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

5 July 2018

1 reference

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Regulatory and cytoskeletal proteins of vertebrate skeletal muscle.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop

5 July 2018

1 reference

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Replacement of troponin components in myofibrils

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Two genetically expressed troponin T fragments representing alpha and beta isoforms exhibit functional differences

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

The calcium and magnesium binding sites on troponin and their role in the regulation of myofibrillar adenosine triphosphatase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Ca2 binding to cardiac troponin C in the myofilament lattice and its relation to the myofibrillar ATPase activity.

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.022628899

Idiopathic Dilated Cardiomyopathy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.022628899

Ca2 -sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=117405

Ca2 sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy

29 October 2018

1 reference

12 December 2020

Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathy

1 reference

12 December 2020

Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy

1 reference

12 December 2020

In Vitro Recombination and Mutagenesis of DNA: SOEing Together Tailor-Made Genes

1 reference

12 December 2020

Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Abnormal contractile function in transgenic mice expressing a familial hypertrophic cardiomyopathy-linked troponin T (I79N) mutation

1 reference

12 December 2020

Effects of troponin T mutations in familial hypertrophic cardiomyopathy on regulatory functions of other troponin subunits

1 reference

12 December 2020

Chymotryptic subfragments of troponin T from rabbit skeletal muscle. Interaction with tropomyosin, troponin I and troponin C

1 reference

12 December 2020

Ca2 - and Sr2 -sensitivity of the ATPase activity of rabbit skeletal myofibrils: effect of the complete substitution of troponin C with cardiac troponin C, calmodulin, and parvalbumins

1 reference

12 December 2020

Effect of different troponin T-tropomyosin combinations on thin filament activation

1 reference

12 December 2020

Effect of Myosin Cross-Bridge Interaction with Actin on the Ca2 -Binding Properties of Troponin C in Fast Skeletal Myofibrils1

1 reference

12 December 2020

Replacement of three troponin components with cardiac troponin components within single glycerinated skeletal muscle fibers

1 reference

12 December 2020

Effect of removal and reconstitution of troponins C and I on the Ca(2 )-activated tension development of single glycerinated rabbit skeletal muscle fibers

1 reference

12 December 2020

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

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12 December 2020

Identifiers

DOI

10.1073/PNAS.022628899

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11773635 AND SRC:MED&resulttype=core&format=json

5 December 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11773635 AND SRC:MED&resulttype=core&format=json

5 December 2019

PubMed publication ID

11773635

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11773635 AND SRC:MED&resulttype=core&format=json