Overall Architecture of the Intraflagellar Transport (IFT)-B Complex Containing Cluap1/IFT38 as an Essential Component of the IFT-B Peripheral Subcomplex.
Combined Automated Annotation using Multiple IEA Methods
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Assembly of the anterograde IFT train
The retrograde IFT train dissociates
Annotation inferences using phylogenetic trees
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Characterization of the intraflagellar transport complex B core: direct interaction of the IFT81 and IFT74/72 subunits.
Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors.
Biochemically validated structural model of the 15-subunit intraflagellar transport complex IFT-B.
The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base.
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella.
Assembly of the retrograde IFT train
The anterograde IFT train dissociates
Proteomic analysis of cerebrospinal fluid extracellular vesicles: a comprehensive dataset.
Deep research report on IFT172 (Falcon)
Intrinsic heterogeneity of primary cilia revealed through spatial proteomics.
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome.