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

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

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http://www.wikidata.org/entity/Q24338736
Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused reviewProtein Structure-Function Relationship at Work: Learning from Myopathy Mutations of the Slow Skeletal Muscle Isoform of Troponin TMyofilament incorporation determines the stoichiometry of troponin I in transgenic expression and the rescue of a null mutationIdentification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order AmishDeletion of a genomic segment containing the cardiac troponin I gene knocks down expression of the slow troponin T gene and impairs fatigue tolerance of diaphragm muscleLocalization of the two tropomyosin-binding sites of troponin TAdaptation by alternative RNA splicing of slow troponin T isoforms in type 1 but not type 2 Charcot-Marie-Tooth diseaseTroponin T core structure and the regulatory NH2-terminal variable regionTroponin T isoforms and posttranscriptional modifications: Evolution, regulation and functionDeficiency of slow skeletal muscle troponin T causes atrophy of type I slow fibres and decreases tolerance to fatigueCoexistence of cardiac troponin T variants reduces heart efficiency.Troponin T is essential for sarcomere assembly in zebrafish skeletal muscle.Differential regulation of myofilament protein isoforms underlying the contractility changes in skeletal muscle unloading.Removing the regulatory N-terminal domain of cardiac troponin I diminishes incompatibility during bacterial expression.Nonmyofilament-associated troponin T fragments induce apoptosis.TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.Elevated expression of MGb2-Ag/TRAK1 is correlated with poor prognosis in patients with colorectal cancer.
P2860

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

Item
http://www.wikidata.org/entity/Q24338736
description
2005 nî lūn-bûn
@nan
2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2005年の論文
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2005年論文
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2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
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2005年論文
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2005年论文
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name
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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type
label
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
@ast
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
@en
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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Cellular fate of truncated slo ...... ion in amish nemaline myopathy
@nl
prefLabel
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
@ast
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
@en
Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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P2860
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Cellular fate of truncated slo ...... ion in amish nemaline myopathy
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P2093
P2860
P304
P31
P3181
P356
P407
P433
P478
P577
P698
P921