Overall Architecture of the Intraflagellar Transport (IFT)-B Complex Containing Cluap1/IFT38 as an Essential Component of the IFT-B Peripheral Subcomplex.
SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins.
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Annotation inferences using phylogenetic trees
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.
Combined Automated Annotation using Multiple IEA Methods
Assembly of the anterograde IFT train
The retrograde IFT train dissociates
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.
Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella.
IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome.
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.
The anterograde IFT train dissociates
Assembly of the retrograde IFT train
Deep research report on IFT52 (Falcon)
Intrinsic heterogeneity of primary cilia revealed through spatial proteomics.