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English
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
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scholarly article
1 reference
stated in
PubMed
PubMed ID
15231740
retrieved
26 November 2016
title
Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport
(English)
1 reference
stated in
PubMed
PubMed ID
15231740
retrieved
26 November 2016
main subject
Caenorhabditis elegans
0 references
BBSome
1 reference
stated in
Gene Ontology release 2020-05-02
Gene Ontology ID
GO:0034464
Tetratricopeptide repeat protein 8 CELE_T25F10.5
1 reference
stated in
GOA release 2020-03-11
Bardet-Biedl syndrome 1 protein homolog CELE_Y105E8A.5
1 reference
stated in
GOA release 2020-03-11
Bardet-Biedl syndrome 7 protein homolog CELE_Y75B8A.12
1 reference
stated in
GOA release 2020-03-11
author
Nicholas Katsanis
series ordinal
15
0 references
Stephen R Wicks
object named as
Stephen R Wicks
series ordinal
17
0 references
Lynne Quarmby
object named as
Lynne M Quarmby
series ordinal
16
0 references
Moe R Mahjoub
object named as
Moe R Mahjoub
series ordinal
5
0 references
Jose Badano
object named as
Jose L Badano
series ordinal
7
0 references
Oliver E Blacque
object named as
Oliver E Blacque
series ordinal
1
0 references
Michel R Leroux
series ordinal
18
object named as
Michel R Leroux
0 references
author name string
Michael J Reardon
series ordinal
2
0 references
Chunmei Li
series ordinal
3
0 references
Jonathan McCarthy
series ordinal
4
0 references
Stephen J Ansley
series ordinal
6
0 references
Allan K Mah
series ordinal
8
0 references
Philip L Beales
series ordinal
9
0 references
William S Davidson
series ordinal
10
0 references
Robert C Johnsen
series ordinal
11
0 references
Mark Audeh
series ordinal
12
0 references
Ronald H A Plasterk
series ordinal
13
0 references
David L Baillie
series ordinal
14
0 references
language of work or name
English
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publication date
1 July 2004
0 references
published in
Genes & Development
0 references
volume
18
0 references
page(s)
1630-42
0 references
issue
13
0 references
cites work
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
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Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis
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Protein particles in Chlamydomonas flagella undergo a transport cycle consisting of four phases
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Intraflagellar transport
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Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
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The tetratricopeptide repeat: a structural motif mediating protein-protein interactions
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Hedgehog signalling in the mouse requires intraflagellar transport proteins
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Loss of the Tg737 protein results in skeletal patterning defects
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An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons
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Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella
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The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination
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The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance
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Localization of intraflagellar transport protein IFT52 identifies basal body transitional fibers as the docking site for IFT particles
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Mutant sensory cilia in the nematode Caenorhabditis elegans
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Intraflagellar transport (IFT) cargo: IFT transports flagellar precursors to the tip and turnover products to the cell body
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Intraflagellar Transport
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PubMed Central
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XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans
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Mutations in MKKS cause Bardet-Biedl syndrome
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A novel WD40 protein, CHE-2, acts cell-autonomously in the formation of C. elegans sensory cilia.
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27 September 2017
Analysis of osm-6, a gene that affects sensory cilium structure and sensory neuron function in Caenorhabditis elegans
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27 September 2017
CHE-3, a cytosolic dynein heavy chain, is required for sensory cilia structure and function in Caenorhabditis elegans.
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30 May 2018
Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation.
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28 November 2018
The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443524
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28 November 2018
The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans
1 reference
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PubMed Central
reference URL
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28 November 2018
Intraflagellar transport in the unicellular green alga, Chlamydomonas reinhardtii
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15231740
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1101/GAD.1194004
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1552405
OpenCitations bibliographic resource ID
1552405
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1552405
PMCID
443524
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1552405
PubMed ID
15231740
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1552405
ResearchGate publication ID
8476495
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