(Q24304085)

GOA release 2020-03-11

muscle filament sliding

1 reference

GOA release 2020-03-11

dilated cardiomyopathy

1 reference

1 reference

Hugh Christian Watkins

9

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Jens Mogensen

object named as

Jens Mogensen

5

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author name string

Mahmooda Mirza

1

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Steven Marston

2

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Ruth Willott

3

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Christopher Ashley

4

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William McKenna

6

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Paul Robinson

7

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Charles Redwood

Journal of Biological Chemistry

8

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language of work or name

English

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publication date

5 August 2005

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published in

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volume

280

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issue

31

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page(s)

28498-506

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cites work

Isometric tension and mutant myosin heavy chain content in single skeletal myofibers from hypertrophic cardiomyopathy patients

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Effect of Hypertrophic Cardiomyopathy Mutations in Human Cardiac Muscle α -tropomyosin (Asp175Asn and Glu180Gly) on the Regulatory Properties of Human Cardiac Troponin Determined by in vitro Motility Assay

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

In vitro motility analysis of thin filaments from failing and non-failing human heart: troponin from failing human hearts induces slower filament sliding and higher Ca(2+) sensitivity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Functional defects in troponin and the systems biology of heart failure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

A simple method for automatic tracking of actin filaments in the motility assay.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

The 14-fold periodicity in alpha-tropomyosin and the interaction with actin.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Molecular polarity in tropomyosin-troponin T co-crystals

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

The failing human heart

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Functional analysis of human cardiac troponin by the in vitro motility assay: comparison of adult, foetal and failing hearts

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

The Genetic Basis for Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

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/10.1074%2FJBC.M412281200

7 January 2021

Separation and characterization of the two functional regions of troponin involved in muscle thin filament regulation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Regulatory properties of recombinant tropomyosins containing 5-hydroxytryptophan: Ca2+-binding to troponin results in a conformational change in a region of tropomyosin outside the troponin binding site

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Factors contributing to troponin exchange in myofibrils and in solution

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Cardiac and skeletal myopathies: can genotype explain phenotype?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Random walks with thin filaments: application of in vitro motility assay to the study of actomyosin regulation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Structure of the core domain of human cardiac troponin in the Ca(2+)-saturated form

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Troponin I and troponin T interact with troponin C to produce different Ca2+-dependent effects on actin-tropomyosin filament motility

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Ca(2+)-regulated structural changes in troponin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Deciphering the design of the tropomyosin molecule

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Regulatory properties of the NH2- and COOH-terminal domains of troponin T. ATPase activation and binding to troponin I and troponin C

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Mapping the interacting regions between troponins T and C. Binding of TnT and TnI peptides to TnC and NMR mapping of the TnT-binding site on TnC

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Folding and function of the troponin tail domain. Effects of cardiomyopathic troponin T mutations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Different functional properties of troponin T mutants that cause dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Cardiomyopathic tropomyosin mutations that increase thin filament Ca2+ sensitivity and tropomyosin N-domain flexibility

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Identification of a functionally critical protein kinase C phosphorylation residue of cardiac troponin T

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Ca2+-induced rolling of tropomyosin in muscle thin filaments: the alpha- and beta-band hypothesis revisited

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Many roads lead to a broken heart: the genetics of dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Is depressed myocyte contractility centrally involved in heart failure?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

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/10.1074%2FJBC.M412281200

7 January 2021

Effects of calcium, inorganic phosphate, and pH on isometric force in single skinned cardiomyocytes from donor and failing human hearts

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M412281200

7 January 2021

Identifiers

DOI

10.1074/JBC.M412281200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

15923195

1 reference

Consolidated OpenCitations Corpus – April 2017