(Q35860406)

10 August 2017

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title

Cystic kidney diseases: all roads lead to the cilium (English)

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10 August 2017

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Qihong Zhang

1

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10 August 2017

Patrick D Taulman

series ordinal

2

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10 August 2017

Bradley K Yoder

series ordinal

3

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10 August 2017

language of work or name

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1 August 2004

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10 August 2017

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10 August 2017

19

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10 August 2017

225-230

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

10 August 2017

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Molecular genetics and pathogenesis of autosomal dominant polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Congenital murine polycystic kidney disease. I. The ontogeny of tubular cyst formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Calcium signalling--an overview

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Cardiovascular, skeletal, and renal defects in mice with a targeted disruption of the Pkd1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Localization of 5-HT(6) receptors at the plasma membrane of neuronal cilia in the rat brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

The bld1 mutation identifies the Chlamydomonas osm-6 homolog as a gene required for flagellar assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Turning on and turning off the sense of smell.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Identification and characterization of polycystin-2, the PKD2 gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Polycystic kidney disease: primary extracellular matrix abnormality or defective cellular differentiation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Positional cloning of jcpk/bpk locus of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Chlamydomonas kinesin-II-dependent intraflagellar transport (IFT): IFT particles contain proteins required for ciliary assembly in Caenorhabditis elegans sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Elevated c-myc protooncogene expression in autosomal recessive polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Oral-facial-digital syndrome type 1 is another dominant polycystic kidney disease: clinical, radiological and histopathological features of a new kindred.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Characterization of the OFD1/Ofd1 genes on the human and mouse sex chromosomes and exclusion of Ofd1 for the Xpl mouse mutant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Murine models of polycystic kidney disease: molecular and therapeutic insights

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Selective targeting of somatostatin receptor 3 to neuronal cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Genetics and pathogenesis of polycystic kidney disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Exploring the molecular basis of Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Polycystin-2 is an intracellular calcium release channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

The pck rat: a new model that resembles human autosomal dominant polycystic kidney and liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

An inherited kidney disease of mice resembling human nephronophthisis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Polycystic kidney disease: etiology, pathogenesis, and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Two populations of node monocilia initiate left-right asymmetry in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Mechanisms of Ca(2+)-dependent transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Cloning of inv, a gene that controls left/right asymmetry and kidney development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

A proteomic analysis of human cilia: identification of novel components

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Intraflagellar transport and cilia-dependent diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

The ion channel polycystin-2 is required for left-right axis determination in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Mutant sensory cilia in the nematode Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Bending the MDCK cell primary cilium increases intracellular calcium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Removal of the MDCK cell primary cilium abolishes flow sensing

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

PKD1 interacts with PKD2 through a probable coiled-coil domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

The sensory cilium of retinal rods is analogous to the transitional zone of motile cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Distinct subcellular expression of endogenous polycystin-2 in the plasma membrane and Golgi apparatus of MDCK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Molecular analysis of neurotransmitter release

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Ca2+-dependent cell signaling through calmodulin-activated protein phosphatase and protein kinases minireview series

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Expression of primary cilia in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Apoptosis and loss of renal tissue in polycystic kidney diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Molecular cloning, cDNA sequence analysis, and chromosomal localization of mouse Pkd2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00003.2004

10.1152/PHYSIOL.00003.2004

21 January 2018

Identifiers

DOI

1 reference

10 August 2017

1 reference