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Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
title
Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia
(English)
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
main subject
Nephronophthisis 1 (juvenile) homolog (human)
1 reference
stated in
GOA release 2020-03-11
NIMA (never in mitosis gene a)-related expressed kinase 8
1 reference
stated in
GOA release 2020-03-11
Inversin
1 reference
stated in
GOA release 2020-03-11
Nephronophthisis 4 (juvenile) homolog (human)
1 reference
stated in
GOA release 2020-03-11
Nephronophthisis 3 (adolescent)
1 reference
stated in
GOA release 2020-03-11
author name string
Dai Shiba
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
Danielle K. Manning
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
Hisashi Koga
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
David R. Beier
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
Takahiko Yokoyama
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
publication date
1 February 2010
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
published in
Cytoskeleton
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
volume
67
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
issue
2
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
page(s)
112–119
1 reference
stated in
PubMed
PubMed ID
20169535
retrieved
31 January 2017
cites work
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of intraflagellar transport protein IFT52 identifies basal body transitional fibers as the docking site for IFT particles
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The ciliary necklace. A ciliary membrane specialization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nephronophthisis-associated ciliopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sentan: a novel specific component of the apical structure of vertebrate motile cilia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NIMA-related kinases defective in murine models of polycystic kidney diseases localize to primary cilia and centrosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of inv, a gene that controls left/right asymmetry and kidney development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nek8 regulates the expression and localization of polycystin-1 and polycystin-2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of NPHP2 and NPHP3 in infantile nephronophthisis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary cilia in normal and pathological tissues
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reversal of left-right asymmetry: a situs inversus mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FCM.20428
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/CM.20428
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2150783
OpenCitations bibliographic resource ID
2150783
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2150783
PubMed ID
20169535
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2150783
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