Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities.
about
Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromesNovel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and proteinA survey of ovary-, testis-, and soma-biased gene expression in Drosophila melanogaster adultsAltered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathyCharacterization of a premeiotic germ cell-specific cytoplasmic protein encoded by Stra8, a novel retinoic acid-responsive geneMuscle abnormalities in Drosophila melanogaster heldup mutants are caused by missing or aberrant troponin-I isoformsA Drosophila melanogaster model of diastolic dysfunction and cardiomyopathy based on impaired troponin-T function.An actin subdomain 2 mutation that impairs thin filament regulation by troponin and tropomyosin.The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.Recovery of dominant, autosomal flightless mutants of Drosophila melanogaster and identification of a new gene required for normal muscle structure and function.An unusual metal-binding cluster found exclusively in the avian breast muscle troponin T of Galliformes and Craciformes.Genetics of the Drosophila flight muscle myofibril: a window into the biology of complex systems.Troponin T is essential for sarcomere assembly in zebrafish skeletal muscle.A direct screen identifies new flight muscle mutants on the Drosophila second chromosome.Metabolite localization in living drosophila using High Resolution Magic Angle Spinning NMRPseudo-acetylation of K326 and K328 of actin disrupts Drosophila melanogaster indirect flight muscle structure and performanceA cis-regulatory mutation in troponin-I of Drosophila reveals the importance of proper stoichiometry of structural proteins during muscle assembly.The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscleMyosin heavy chain isoforms regulate muscle function but not myofibril assembly.A cytotoxic early gene of Bacillus subtilis bacteriophage SPO1.Invertebrate muscles: muscle specific genes and proteins.The Caenorhabditis elegans UNC-87 protein is essential for maintenance, but not assembly, of bodywall muscleDevelopmental genetic analysis of troponin T mutations in striated and nonstriated muscle cells of Caenorhabditis elegans.Alterations in flight muscle ultrastructure and function in Drosophila tropomyosin mutantsCa2+-dependent muscle dysfunction caused by mutation of the Caenorhabditis elegans troponin T-1 geneA tropomyosin-2 mutation suppresses a troponin I myopathy in Drosophila.Drosophila paramyosin is important for myoblast fusion and essential for myofibril formation.Myosin light chain-2 mutation affects flight, wing beat frequency, and indirect flight muscle contraction kinetics in Drosophila.Structure and sequence of the human fast skeletal troponin T (TNNT3) gene: insight into the evolution of the gene and the origin of the developmentally regulated isoforms.Alternative splicing, muscle calcium sensitivity, and the modulation of dragonfly flight performance.Quantitative proteomics of a presymptomatic A53T alpha-synuclein Drosophila model of Parkinson disease.Distinct troponin T genes are expressed in embryonic/larval tail striated muscle and adult body wall smooth muscle of ascidian.Regulating the contraction of insect flight muscle.Assembly of thick filaments and myofibrils occurs in the absence of the myosin head.Proteasome dysfunction in cardiomyopathies.The evolutionary origin of bilaterian smooth and striated myocytes.Two functionally identical modular enhancers in Drosophila troponin T gene establish the correct protein levels in different muscle types.Aberrant splicing of an alternative exon in the Drosophila troponin-T gene affects flight muscle development.Overexpression of troponin T in Drosophila muscles causes a decrease in the levels of thin-filament proteins.Electron microscopy and three-dimensional reconstruction of native thin filaments reveal species-specific differences in regulatory strand densities.
P2860
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P2860
Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities.
description
1990 nî lūn-bûn
@nan
1990 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@ast
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@en
type
label
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@ast
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@en
prefLabel
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@ast
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@en
P2093
P1476
Drosophila melanogaster tropon ...... of myofibrillar abnormalities.
@en
P2093
P304
P356
10.1016/0022-2836(90)90390-8
P407
P577
1990-12-01T00:00:00Z