(Q24291970)

Troponin C1, slow skeletal and cardiac type

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

troponin I binding

1 reference

hypertrophic cardiomyopathy

GOA release 2020-03-11

1 reference

familial hypertrophic cardiomyopathy

inferred from title

1 reference

F Takahashi-Yanaga

1

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S Morimoto

2

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K Harada

3

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R Minakami

4

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F Shiraishi

5

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M Ohta

6

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Q W Lu

7

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T Sasaguri

8

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I Ohtsuki

Journal of Molecular and Cellular Cardiology

9

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language of work or name

English

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publication date

December 2001

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published in

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volume

33

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page(s)

2095-107

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issue

12

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cites work

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Role of troponin I isoform switching in determining the pH sensitivity of Ca(2+) regulation in developing rabbit cardiac muscle.

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Mapping of a second actin-tropomyosin and a second troponin C binding site within the C terminus of troponin I, and their importance in the Ca2+-dependent regulation of muscle contraction

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

A new and convenient colorimetric determination of inorganic orthophosphate and its application to the assay of inorganic pyrophosphatase

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Effects of a non-divalent cation binding mutant of myosin regulatory light chain on tension generation in skinned skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Regulatory and cytoskeletal proteins of vertebrate skeletal muscle.

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Fluorescent probes attached to Cys 35 or Cys 84 in cardiac troponin C are differentially sensitive to Ca(2+)-dependent events in vitro and in situ

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Proton-magnetic-resonance studies on the interaction of rabbit skeletal-muscle troponin I with troponin C and actin

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

The role of the NH(2)- and COOH-terminal domains of the inhibitory region of troponin I in the regulation of skeletal muscle contraction

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Roles of troponin isoforms in pH dependence of contraction in rabbit fast and slow skeletal and cardiac muscles

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Effect of Arg145Gly mutation in human cardiac troponin I on the ATPase activity of cardiac myofibrils

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Replacement of troponin components in myofibrils

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Sensitivity of Actomyosin ATPase to Calcium and Strontium Ions. Effect of Hybrid Troponins1

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Recent advances in the molecular genetics of hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1006%2FJMCC.2001.1473

7 January 2021