(Q36047287)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

review article

1 reference

title

A mechanistic approach to inherited polycystic kidney disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Bradley P Dixon

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

author name string

John J Bissler

series ordinal

1

1 reference

11 August 2017

Bradley P Dixon

series ordinal

2

1 reference

11 August 2017

publication date

18 February 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

page(s)

558-566

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00467-004-1665-z

8 January 2020

exact match

0 references

cites work

Modification of the composition of polycystin-1 multiprotein complexes by calcium and tyrosine phosphorylation

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00467-004-1665-Z

Mutation and cancer: statistical study of retinoblastoma

21 January 2018

1 reference

12 December 2020

A cross sectional study of renal involvement in tuberous sclerosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Murine models of polycystic kidney disease: molecular and therapeutic insights

1 reference

12 December 2020

The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I.

1 reference

12 December 2020

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cen

1 reference

12 December 2020

Polycystin-1, the PKD1 gene product, is in a complex containing E-cadherin and the catenins

1 reference

12 December 2020

In vitro modulation of cyst formation by a novel tyrosine kinase inhibitor.

1 reference

12 December 2020

The renal cell primary cilium functions as a flow sensor

1 reference

12 December 2020

Uromodulin (Tamm-Horsfall glycoprotein): a renal ligand for lymphokines

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetics. The land between Mendelian and multifactorial inheritance

1 reference

12 December 2020

PKD1 induces p21(waf1) and regulation of the cell cycle via direct activation of the JAK-STAT signaling pathway in a process requiring PKD2

1 reference

12 December 2020

Reversed polarity of Na(+) -K(+) -ATPase: mislocation to apical plasma membranes in polycystic kidney disease epithelia

1 reference

12 December 2020

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

1 reference

12 December 2020

Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Basolateral chloride transporters in autosomal dominant polycystic kidney disease

1 reference

12 December 2020

Cardiac defects and renal failure in mice with targeted mutations in Pkd2

1 reference

12 December 2020

Effective treatment of an orthologous model of autosomal dominant polycystic kidney disease

1 reference

12 December 2020

Bending the primary cilium opens Ca2+-sensitive intermediate-conductance K+ channels in MDCK cells

1 reference

12 December 2020

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Reduced cell motility and enhanced focal adhesion contact formation in cells from FAK-deficient mice

1 reference

12 December 2020

Expression of the beta2-subunit and apical localization of Na+-K+-ATPase in metanephric kidney.

1 reference

12 December 2020

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology

1 reference

12 December 2020

Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

1 reference

12 December 2020

Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor

1 reference

12 December 2020

Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13 in renal cyst cells supports a loss-of-function model for cyst pathogenesis

1 reference

12 December 2020

Identification of human uromodulin as the Tamm-Horsfall urinary glycoprotein

1 reference

12 December 2020

Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene

1 reference

12 December 2020

Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis

1 reference

12 December 2020

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

1 reference

12 December 2020

Decreased amiloride-sensitive Na+absorption in collecting duct principal cells isolated from BPK ARPKD mice

1 reference

12 December 2020

Bcl-2 overexpression prevents apoptosis-induced Madin-Darby canine kidney simple epithelial cyst formation

1 reference

12 December 2020

The PKD1 gene product, "polycystin-1," is a tyrosine-phosphorylated protein that colocalizes with alpha2beta1-integrin in focal clusters in adherent renal epithelia

1 reference

12 December 2020

DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease

1 reference

12 December 2020

Functional analysis of PKD1 transgenic lines reveals a direct role for polycystin-1 in mediating cell-cell adhesion

1 reference

12 December 2020

Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome

1 reference

12 December 2020

Histogenesis of the renal cysts in adult (autosomal dominant) polycystic kidney disease: a histochemical study.

1 reference

12 December 2020

Inhibition of renal cystic disease development and progression by a vasopressin V2 receptor antagonist

1 reference

12 December 2020

Compromised cytoarchitecture and polarized trafficking in autosomal dominant polycystic kidney disease cells

1 reference

12 December 2020

Primary cilia in normal and pathological tissues

1 reference

12 December 2020

Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Removal of the MDCK cell primary cilium abolishes flow sensing

1 reference

12 December 2020

10.1007/S00467-004-1665-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15719257%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference