(Q47069413)

4 January 2018

title

Functional characterization of the C. elegans nephrocystins NPHP-1 and NPHP-4 and their role in cilia and male sensory behaviors (English)

1 reference

4 January 2018

Polycystin-2 CELE_Y73F8A.1

main subject

Caenorhabditis elegans

0 references

1 reference

Nephrocystin-1-like protein CELE_M28.7

GOA release 2020-03-11

1 reference

NePHronoPhthisis (human kidney disease) homolog CELE_R13H4.1

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Andrew R Jauregui

series ordinal

1

1 reference

4 January 2018

Maureen M Barr

series ordinal

2

1 reference

4 January 2018

language of work or name

English

0 references

publication date

1 May 2005

1 reference

4 January 2018

Experimental Cell Research

published in

1 reference

4 January 2018

volume

305

1 reference

4 January 2018

issue

2

1 reference

4 January 2018

page(s)

333-342

1 reference

4 January 2018

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

1 reference

Intraflagellar transport and cilia-dependent renal disease: the ciliary hypothesis of polycystic kidney disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The autosomal recessive polycystic kidney disease protein is localized to primary cilia, with concentration in the basal body area

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

A proteomic analysis of human cilia: identification of novel components

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Intraflagellar transport and cilia-dependent diseases.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

7 January 2021

Intraflagellar Transport

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

New insights: nephronophthisis-medullary cystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The Structure of the Nervous System of the Nematode Caenorhabditis elegans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The Caenorhabditis elegans male: Postembryonic development of nongonadal structures

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Sensory regulation of male mating behavior in Caenorhabditis elegans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

A polycystic kidney-disease gene homologue required for male mating behaviour in C. elegans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Mutant sensory cilia in the nematode Caenorhabditis elegans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Green fluorescent protein as a marker for gene expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

C. elegans responds to chemical repellents by integrating sensory inputs from the head and the tail

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Systematic functional analysis of the Caenorhabditis elegans genome using RNAi

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Chemosensory neurons with overlapping functions direct chemotaxis to multiple chemicals in C. elegans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Nephrocystin interacts with Pyk2, p130(Cas), and tensin and triggers phosphorylation of Pyk2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

Crk-associated substrate p130(Cas) interacts with nephrocystin and both proteins localize to cell-cell contacts of polarized epithelial cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

The left-right determinant Inversin is a component of node monocilia and other 9+0 cilia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2005.01.008

10.1016/J.YEXCR.2005.01.008

7 January 2021

Identifiers

DOI

1 reference

4 January 2018

1 reference

4 January 2018