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Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
title
Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis
(English)
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
main subject
cilium assembly
0 references
Dynein 2 intermediate chain 1
1 reference
stated in
GOA release 2020-03-11
Dynein 2 intermediate chain 2
1 reference
stated in
GOA release 2020-03-11
Dynein light chain LC8-type 1
1 reference
stated in
GOA release 2020-03-11
Dynein cytoplasmic 2 heavy chain 1
1 reference
stated in
GOA release 2020-03-11
Tctex1 domain containing 2
1 reference
stated in
GOA release 2020-03-11
dynein light chain binding
1 reference
stated in
GOA release 2020-03-11
short rib – polydactyly syndrome
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polydactyly
1 reference
based on heuristic
inferred from title
author
Harish Dharmarajan
object named as
Harish Dharmarajan
series ordinal
6
0 references
Julian P Whitelegge
series ordinal
9
object named as
Julian P. Whitelegge
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
author name string
Ankur A. Gholkar
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Silvia Senese
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Yu-Chen Lo
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Joseph Capri
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
William J. Deardorff
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Ely Contreras
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Emmanuelle Hodara
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Peter K. Jackson
series ordinal
10
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
Jorge Z. Torres
series ordinal
11
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
publication date
1 January 2015
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
published in
Cell Cycle
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stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
volume
14
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stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
page(s)
1116–1125
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stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
issue
7
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stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
cites work
An intriguing shift occurs in the novel protein phosphatase 1 binding partner, TCTEX1D4: evidence of positive selection in a pika model
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PubMed Central
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TCTEX1D4, a novel protein phosphatase 1 interactor: connecting the phosphatase to the microtubule network
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16 March 2017
The spinocerebellar ataxia-associated gene Tau tubulin kinase 2 controls the initiation of ciliogenesis
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PubMed Central
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The STARD9/Kif16a kinesin associates with mitotic microtubules and regulates spindle pole assembly
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Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome
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Cep164, a novel centriole appendage protein required for primary cilium formation
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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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Rhodopsin's carboxy-terminal cytoplasmic tail acts as a membrane receptor for cytoplasmic dynein by binding to the dynein light chain Tctex-1
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A dynein light chain is essential for the retrograde particle movement of intraflagellar transport (IFT)
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Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy
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Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60
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Non-repair pathways for minimizing protein isoaspartyl damage in the yeast Saccharomyces cerevisiae
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Striated rootlet and nonfilamentous forms of rootletin maintain ciliary function
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Ciliary disorder of the skeleton
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MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement
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Chlamydomonas FAP133 is a dynein intermediate chain associated with the retrograde intraflagellar transport motor
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Piecing together a ciliome
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4614626
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3 June 2018
Genome-wide transcriptional analysis of flagellar regeneration in Chlamydomonas reinhardtii identifies orthologs of ciliary disease genes
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PubMed Central
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3 June 2018
Analysis of xbx genes in C. elegans
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Robust method for proteome analysis by MS/MS using an entire translated genome: demonstration on the ciliome of Tetrahymena thermophila
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Crossref
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21 January 2018
Identifiers
DOI
10.4161/15384101.2014.985066
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
PMCID
4614626
0 references
PubMed ID
25830415
1 reference
stated in
PubMed
PubMed ID
25830415
retrieved
14 February 2017
ResearchGate publication ID
274400964
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