Functional interactions between unlinked muscle genes within haploinsufficient regions of the Drosophila genome.
about
Elevated expression of the integrin-associated protein PINCH suppresses the defects of Drosophila melanogaster muscle hypercontraction mutantsMuscle abnormalities in Drosophila melanogaster heldup mutants are caused by missing or aberrant troponin-I isoformsIfm(2)2 is a myosin heavy chain allele that disrupts myofibrillar assembly only in the indirect flight muscle of Drosophila melanogasterGenetic feminization of the thoracic nervous system disrupts courtship song in male Drosophila melanogaster.The alpha glycerophosphate cycle in Drosophila melanogaster V. molecular analysis of alpha glycerophosphate dehydrogenase and alpha glycerophosphate oxidase mutants.Co-localization to chromosome bands 99E1-3 of the Drosophila melanogaster myosin light chain-2 gene and a haplo-insufficient locus that affects flight behaviorA tripartite interaction among alleles of Notch, Delta, and Enhancer of split during imaginal development of Drosophila melanogaster.Dominant maternal-effect mutations causing embryonic lethality in Caenorhabditis elegans.Genetic analysis of the Shaker gene complex of Drosophila melanogaster.Two types of genetic interaction implicate the whirligig gene of Drosophila melanogaster in microtubule organization in the flagellar axoneme.The generation and genetic analysis of suppressors of lethal mutations in the Caenorhabditis elegans rol-3(V) gene.Recovery of dominant, autosomal flightless mutants of Drosophila melanogaster and identification of a new gene required for normal muscle structure and function.Interactions of polyhomeotic with Polycomb group genes of Drosophila melanogaster.Analysis of dominant mutations affecting muscle excitation in Caenorhabditis elegansA molecularly defined duplication set for the X chromosome of Drosophila melanogaster.Epistatic interactions between smell-impaired loci in Drosophila melanogaster.The haplolethal region at the 16F gene cluster of Drosophila melanogaster: structure and functionA direct screen identifies new flight muscle mutants on the Drosophila second chromosome.A Kalman-filter based approach to identification of time-varying gene regulatory networks.A cis-regulatory mutation in troponin-I of Drosophila reveals the importance of proper stoichiometry of structural proteins during muscle assembly.Molecular genetics of Drosophila alpha-actinin: mutant alleles disrupt Z disc integrity and muscle insertionsThe generation of chromosomal deletions to provide extensive coverage and subdivision of the Drosophila melanogaster genomeTransformation of Drosophila melanogaster with the wild-type myosin heavy-chain gene: rescue of mutant phenotypes and analysis of defects caused by overexpression.Ca2+-dependent muscle dysfunction caused by mutation of the Caenorhabditis elegans troponin T-1 geneSpecific myosin heavy chain mutations suppress troponin I defects in Drosophila musclesIdentification of the essential protein domains for Mib2 function during the development of the Drosophila larval musculature and adult flight muscles.Characterization of a hypercontraction-induced myopathy in Drosophila caused by mutations in Mhc.Perturbations of Drosophila alpha-actinin cause muscle paralysis, weakness, and atrophy but do not confer obvious nonmuscle phenotypes.Interacting proteins identified by genetic interactions: a missense mutation in alpha-tubulin fails to complement alleles of the testis-specific beta-tubulin gene of Drosophila melanogaster.Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophyAberrant splicing of an alternative exon in the Drosophila troponin-T gene affects flight muscle development.Characterization of the mus308 gene in Drosophila melanogaster.Properties of a class of genes required for ray morphogenesis in Caenorhabditis elegans.Abnormal muscle development in the heldup3 mutant of Drosophila melanogaster is caused by a splicing defect affecting selected troponin I isoforms.The Caenorhabditis elegans spe-6 gene is required for major sperm protein assembly and shows second site non-complementation with an unlinked deficiency.A Unique Phenotype in Heterozygotes of the Auxin-Insensitive Mutant of Tomato, diageotropica.Drosophila model of Meier-Gorlin syndrome based on the mutation in a conserved C-Terminal domain of Orc6.
P2860
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P2860
Functional interactions between unlinked muscle genes within haploinsufficient regions of the Drosophila genome.
description
1988 nî lūn-bûn
@nan
1988 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Functional interactions betwee ...... ions of the Drosophila genome.
@ast
Functional interactions betwee ...... ions of the Drosophila genome.
@en
type
label
Functional interactions betwee ...... ions of the Drosophila genome.
@ast
Functional interactions betwee ...... ions of the Drosophila genome.
@en
prefLabel
Functional interactions betwee ...... ions of the Drosophila genome.
@ast
Functional interactions betwee ...... ions of the Drosophila genome.
@en
P2860
P1433
P1476
Functional interactions betwee ...... gions of the Drosophila genome
@en
P2093
P2860
P304
P407
P577
1988-05-01T00:00:00Z