TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships. - Wikidata - wikimedia - TriplyDB

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

http://www.wikidata.org/entity/Q37666010

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Protein Structure-Function Relationship at Work: Learning from Myopathy Mutations of the Slow Skeletal Muscle Isoform of Troponin T Long-term, but not short-term high-fat diet induces fiber composition changes and impaired contractile force in mouse fast-twitch skeletal muscle.Deep RNA sequencing of pectoralis muscle transcriptomes during late-term embryonic to neonatal development in indigenous Chinese duck breeds.What to do when you question cardiac troponin values.Identification of a Gene Encoding Slow Skeletal Muscle Troponin T as a Novel Marker for Immortalization of Retinal Pigment Epithelial Cells.A One Health Approach to Hypertrophic Cardiomyopathy.Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.Passive Stretch Induces Structural and Functional Maturation of Engineered Heart Muscle as Predicted by Computational Modeling.Aerobic exercise preconception and during pregnancy enhances oxidative capacity in the hindlimb muscles of mice offspring.HIC2 regulates isoform switching during maturation of the cardiovascular system.Troponin through the looking-glass: emerging roles beyond regulation of striated muscle contraction.Cell-type-resolved alternative splicing patterns in mouse liver.

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TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

http://www.wikidata.org/entity/Q37666010

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 13 January 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

@en

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

@nl

type

label

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

@en

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

@nl

prefLabel

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

@en

TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

@nl

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J.GENE.2016.01.006

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TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.

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Bin Wei

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J-P Jin

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P2860

Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused review

A novel nemaline myopathy in the Amish caused by a mutation in troponin T1

A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin

Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype

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

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

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

Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy

Raf-1: a novel cardiac troponin T kinase

MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods

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1-13

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scholarly article

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10.1016/J.GENE.2016.01.006

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