Muscle abnormalities in Drosophila melanogaster heldup mutants are caused by missing or aberrant troponin-I isoforms
about
Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromesCaste- and development-associated gene expression in a lower termiteElevated expression of the integrin-associated protein PINCH suppresses the defects of Drosophila melanogaster muscle hypercontraction mutantsMutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathyVimar Is a Novel Regulator of Mitochondrial Fission through MiroDrosophila as a model for the identification of genes causing adult human heart disease.Myosin transducer mutations differentially affect motor function, myofibril structure, and the performance of skeletal and cardiac musclesPhysiological homology between Drosophila melanogaster and vertebrate cardiovascular systems.Identification of troponin C antagonists from a phage-displayed random peptide library.The evolutionarily conserved RNA binding protein SMOOTH is essential for maintaining normal muscle functionA 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.Determining structure/function relationships for sarcomeric myosin heavy chain by genetic and transgenic manipulation of Drosophila.Disruption of Caenorhabditis elegans muscle structure and function caused by mutation of troponin IDrosophila muscle regulation characterized by electron microscopy and three-dimensional reconstruction of thin filament mutants.Drosophila muscleblind codes for proteins with one and two tandem zinc finger motifsGalactokinase is a novel modifier of calcineurin-induced cardiomyopathy in Drosophila.Functional recovery of troponin I in a Drosophila heldup mutant after a second site mutation.Genetics of the Drosophila flight muscle myofibril: a window into the biology of complex systems.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.Suppression of muscle hypercontraction by mutations in the myosin heavy chain gene of Drosophila melanogaster.An ongoing role for structural sarcomeric components in maintaining Drosophila melanogaster muscle function and structure.Pseudo-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.Myosin heavy chain isoforms regulate muscle function but not myofibril assembly.Invertebrate muscles: muscle specific genes and proteins.The Caenorhabditis elegans UNC-87 protein is essential for maintenance, but not assembly, of bodywall muscleBoth synchronous and asynchronous muscle isoforms of projectin (the Drosophila bent locus product) contain functional kinase domains.Alterations in flight muscle ultrastructure and function in Drosophila tropomyosin mutantsA tropomyosin-2 mutation suppresses a troponin I myopathy in Drosophila.Specific myosin heavy chain mutations suppress troponin I defects in Drosophila musclesFlightin is essential for thick filament assembly and sarcomere stability in Drosophila flight musclesCharacterization of a hypercontraction-induced myopathy in Drosophila caused by mutations in Mhc.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.Slow skeletal troponin I gene transfer, expression, and myofilament incorporation enhances adult cardiac myocyte contractile function.Transcription of Drosophila troponin I gene is regulated by two conserved, functionally identical, synergistic elementsRegulating the contraction of insect flight muscle.Assembly of thick filaments and myofibrils occurs in the absence of the myosin head.
P2860
Q24531960-F237F708-9B01-48C7-9C56-C2E54B75528FQ24792797-4B83EEAB-F507-4751-8A77-1527C4B932C1Q27323931-A02357CB-29CC-4A5E-A418-008A744EC637Q28244969-91E7D06E-9584-4812-990C-9D0EA574092DQ28552681-80967305-6073-4BE6-AC31-0B56063BA0FFQ30476715-8861A439-6718-437C-9E9D-A192B5F6F896Q30481206-7A2AE2CF-A8CD-44C9-A61E-29CE25D880D7Q30500303-5BF2B1BD-A9FF-4BF3-8615-2645C21C3063Q32030884-1819E871-0519-406E-B07E-6A033BC36C1DQ33551387-57F27601-6EB8-4498-B1F8-E9FBC79E47B2Q33830492-15F577F2-9B29-40F2-9CAC-04607795CA4EQ33962858-56E05B87-8CAB-44AA-83CB-36103A84BC62Q34040305-08D945DA-B69D-4393-BC40-A09CB6597B83Q34184860-6DAE2FDA-BDBB-4438-9D89-DB4B2901CC97Q34185014-C34C1B89-41E7-4121-A0C2-D94CF157A493Q34222298-0341E395-F328-4811-8A00-1793341FFB00Q34336663-CEFB01A8-5BFE-4C8C-97C5-717DA65950EEQ34452670-B3B408EC-9B45-48AF-8335-78D532355620Q34464644-46246C95-ED30-411D-8FBA-5CCD36540A9BQ34606169-2E90E738-2C42-4F26-9162-CEFD4493DB79Q34607684-FEA1A5C2-7420-4CFA-9CDB-8F998086B86CQ34617529-B16762CF-AF6A-4EEC-B6E0-694FBDCF1E23Q35184836-AB2B3230-B3DB-474B-B12A-BFF8314DA7CDQ35545773-47E8A512-D6DA-4D08-B380-CB34F65BD1D3Q35579782-E6B3D8E8-9204-4782-AD5D-2A8D0A061CBDQ35907333-3E4D4321-0790-41DF-9382-937E3857C030Q36178999-19D6AA17-3A91-4462-BC33-B2B629A63510Q36234657-56B2E31E-0ECC-468B-A314-FB9ADB543D9FQ36235215-0833C167-3CAE-4E57-A2C9-DEB24897B9BBQ36237688-EB555B55-B702-45DE-BB8A-F4BBE4EEF718Q36285684-367ADE30-387F-4268-B057-178055CA5851Q36288309-D533132B-F212-4939-9360-F3B56DA7698BQ36293699-7A9B06B9-ECDD-45EF-B0C0-707AB154F89EQ36321914-A9697EE5-B5C1-407E-82BD-E48AAA846C48Q36325037-2C405D54-4BEC-4BEE-9887-D880B4DC1034Q36532347-B4EA1BFC-DB34-41A8-8CB9-7FA66553BE09Q36773429-4D7D06C6-7F08-4015-B4A4-D58F7A3D9D11Q36780204-52DC0CF1-1CA9-48F5-9E39-E765641C7342Q37959339-0EB33D12-070C-490B-BF7E-EC80AD6F6538Q38326007-A2261CDD-9855-498E-A26F-DA0F305127EF
P2860
Muscle abnormalities in Drosophila melanogaster heldup mutants are caused by missing or aberrant troponin-I isoforms
description
1991 nî lūn-bûn
@nan
1991 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@ast
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@en
type
label
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@ast
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@en
prefLabel
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@ast
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@en
P2860
P356
P1476
Muscle abnormalities in Drosop ...... r aberrant troponin-I isoforms
@en
P2093
P2860
P304
P356
10.1083/JCB.114.5.941
P407
P577
1991-09-01T00:00:00Z