The Vfl1 Protein in Chlamydomonas localizes in a rotationally asymmetric pattern at the distal ends of the basal bodies
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LRRC50, a conserved ciliary protein implicated in polycystic kidney diseaseLoss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesiaA novel multifunctional factor involved in trans-splicing of chloroplast introns in Chlamydomonas.Basal body structure and composition in the apicomplexans Toxoplasma and PlasmodiumThe evolution of land plant ciliaThe awesome power of dikaryons for studying flagella and basal bodies in Chlamydomonas reinhardtiiKatanin localization requires triplet microtubules in Chlamydomonas reinhardtiiA dynein light intermediate chain, D1bLIC, is required for retrograde intraflagellar transport.The transcriptional regulator CzcR modulates antibiotic resistance and quorum sensing in Pseudomonas aeruginosaTCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.CEP290 tethers flagellar transition zone microtubules to the membrane and regulates flagellar protein content.Three-dimensional organization of basal bodies from wild-type and delta-tubulin deletion strains of Chlamydomonas reinhardtiiThe DPY-30 domain and its flanking sequence mediate the assembly and modulation of flagellar radial spoke complexes.FAP20 is an inner junction protein of doublet microtubules essential for both the planar asymmetrical waveform and stability of flagella in ChlamydomonasSite-specific basal body duplication in Chlamydomonas.DRC3 connects the N-DRC to dynein g to regulate flagellar waveform.The LF1 gene of Chlamydomonas reinhardtii encodes a novel protein required for flagellar length control.Bld10p, a novel protein essential for basal body assembly in Chlamydomonas: localization to the cartwheel, the first ninefold symmetrical structure appearing during assemblyFlagellar length control system: testing a simple model based on intraflagellar transport and turnoverAn evolutionarily conserved coiled-coil protein implicated in polycystic kidney disease is involved in basal body duplication and flagellar biogenesis in Trypanosoma bruceiMembrane fusion triggers rapid degradation of two gamete-specific, fusion-essential proteins in a membrane block to polygamy in Chlamydomonas.HA-tagging of putative flagellar proteins in Chlamydomonas reinhardtii identifies a novel protein of intraflagellar transport complex B.Epsilon-tubulin is an essential component of the centriole.Centrosome reduction during gametogenesis and its significance.Oda5p, a novel axonemal protein required for assembly of the outer dynein arm and an associated adenylate kinase.NPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone.Targeting Toxoplasma tubules: tubulin, microtubules, and associated proteins in a human pathogenThe green microalga Chlamydomonas reinhardtii has a single ω-3 fatty acid desaturase that localizes to the chloroplast and impacts both plastidic and extraplastidic membrane lipids.Molecular map of the Chlamydomonas reinhardtii nuclear genomeElucidation of basal body and centriole functions in Chlamydomonas reinhardtii.The Chlamydomonas cell cycle.Defective flagellar assembly and length regulation in LF3 null mutants in Chlamydomonas.Mining the Giardia genome and proteome for conserved and unique basal body proteins.Chlamydomonas reinhardtii hydin is a central pair protein required for flagellar motility.The Uni2 phosphoprotein is a cell cycle regulated component of the basal body maturation pathway in Chlamydomonas reinhardtii.A flagellar A-kinase anchoring protein with two amphipathic helices forms a structural scaffold in the radial spoke complex.The conserved plant sterility gene HAP2 functions after attachment of fusogenic membranes in Chlamydomonas and Plasmodium gametesThe UNI1 and UNI2 genes function in the transition of triplet to doublet microtubules between the centriole and cilium in Chlamydomonas.Molecular architecture of the centriole proteome: the conserved WD40 domain protein POC1 is required for centriole duplication and length control.PF15p is the chlamydomonas homologue of the Katanin p80 subunit and is required for assembly of flagellar central microtubules.
P2860
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P2860
The Vfl1 Protein in Chlamydomonas localizes in a rotationally asymmetric pattern at the distal ends of the basal bodies
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
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name
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@ast
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@en
type
label
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@ast
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@en
prefLabel
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@ast
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@en
P2093
P2860
P356
P1476
The Vfl1 Protein in Chlamydomo ...... istal ends of the basal bodies
@en
P2093
C D Silflow
M Borodovsky
P A Lefebvre
P2860
P356
10.1083/JCB.153.1.63
P407
P577
2001-04-01T00:00:00Z