Ultrastructural and molecular analyses of homozygous-viable Drosophila melanogaster muscle mutants indicate there is a complex pattern of myosin heavy-chain isoform distribution.
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Myosin functional domains encoded by alternative exons are expressed in specific thoracic muscles of DrosophilaThe evolutionarily conserved RNA binding protein SMOOTH is essential for maintaining normal muscle functionMapping interactions between myosin relay and converter domains that power muscle function.Complete sequence of the Drosophila nonmuscle myosin heavy-chain transcript: conserved sequences in the myosin tail and differential splicing in the 5' untranslated sequenceA Drosophila model of dominant inclusion body myopathy type 3 shows diminished myosin kinetics that reduce muscle power and yield myofibrillar defects.Recovery of dominant, autosomal flightless mutants of Drosophila melanogaster and identification of a new gene required for normal muscle structure and function.Mutating the converter-relay interface of Drosophila myosin perturbs ATPase activity, actin motility, myofibril stability and flight abilityDetermining structure/function relationships for sarcomeric myosin heavy chain by genetic and transgenic manipulation of Drosophila.Arrest is a regulator of fiber-specific alternative splicing in the indirect flight muscles of DrosophilaAdult myogenesis in Drosophila melanogaster can proceed independently of myocyte enhancer factor-2Green fluorescent protein tagging Drosophila proteins at their native genomic loci with small P elementsDifferential requirements for Myocyte Enhancer Factor-2 during adult myogenesis in DrosophilaAlternative relay and converter domains tune native muscle myosin isoform function in Drosophila.Myosin heavy chain isoforms regulate muscle function but not myofibril assembly.A Drosophila model for mito-nuclear diseases generated by an incompatible interaction between tRNA and tRNA synthetase.Muscle-specific accumulation of Drosophila myosin heavy chains: a splicing mutation in an alternative exon results in an isoform substitution.Alternative S2 hinge regions of the myosin rod differentially affect muscle function, myofibril dimensions and myosin tail length.Transcriptional regulation of the Drosophila melanogaster muscle myosin heavy-chain geneInvertebrate muscles: muscle specific genes and proteins.Transformation of Drosophila melanogaster with the wild-type myosin heavy-chain gene: rescue of mutant phenotypes and analysis of defects caused by overexpression.Specific myosin heavy chain mutations suppress troponin I defects in Drosophila musclesA Failure to Communicate: MYOSIN RESIDUES INVOLVED IN HYPERTROPHIC CARDIOMYOPATHY AFFECT INTER-DOMAIN INTERACTION.Extradenticle and homothorax control adult muscle fiber identity in Drosophila.Alternative relay domains of Drosophila melanogaster myosin differentially affect ATPase activity, in vitro motility, myofibril structure and muscle function.Crossveinless and the TGFbeta pathway regulate fiber number in the Drosophila adult jump muscleAn embryonic myosin converter domain influences Drosophila indirect flight muscle stretch activation, power generation and flight.Analysis of Drosophila paramyosin: identification of a novel isoform which is restricted to a subset of adult muscles.Inhibition of distinct steps in the adipocyte differentiation pathway in 3T3 T mesenchymal stem cells by dimethyl sulphoxide (DMSO).Absence of the Drosophila jump muscle actin Act79B is compensated by up-regulation of Act88F.Myosin storage myopathy mutations yield defective myosin filament assembly in vitro and disrupted myofibrillar structure and function in vivo.Bendless alters thoracic musculature in Drosophila.Five Alternative Myosin Converter Domains Influence Muscle Power, Stretch Activation, and Kinetics.Polarization-resolved microscopy reveals a muscle myosin motor-independent mechanism of molecular actin ordering during sarcomere maturation.Prolonged cross-bridge binding triggers muscle dysfunction in a model of myosin-based hypertrophic cardiomyopathy
P2860
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P2860
Ultrastructural and molecular analyses of homozygous-viable Drosophila melanogaster muscle mutants indicate there is a complex pattern of myosin heavy-chain isoform distribution.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Ultrastructural and molecular ...... vy-chain isoform distribution.
@en
type
label
Ultrastructural and molecular ...... vy-chain isoform distribution.
@en
prefLabel
Ultrastructural and molecular ...... vy-chain isoform distribution.
@en
P2093
P356
P1433
P1476
Ultrastructural and molecular ...... vy-chain isoform distribution.
@en
P2093
Bernstein SI
Collier VL
O'Donnell PT
P304
P356
10.1101/GAD.3.8.1233
P577
1989-08-01T00:00:00Z