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[Cystic liver diseases. Genetics and cell biology]
scientific article published on 01 August 2005
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
review article
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stated in
Europe PubMed Central
title
[Cystic liver diseases. Genetics and cell biology]
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
main subject
cell biology
1 reference
based on heuristic
inferred from title
author name string
Chantal Housset
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
publication date
1 August 2005
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
published in
Gastroenterologie Clinique et Biologique
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
volume
29
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
issue
8-9
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
page(s)
861-869
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
cites work
Polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adult polycystic liver and kidney diseases are separate entities
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical profile of autosomal dominant polycystic liver disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Risk factors for the development of hepatic cysts in autosomal dominant polycystic kidney disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
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inferred from DOI database lookup
The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. The European Polycystic Kidney Disease Consortium
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
From cilia to cyst.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystic liver disease is genetically heterogeneous: clinical and linkage studies in eight Finnish families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft für Pädiatrische, Nephrologie
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in cholangiocyte fibrocystin expression and ciliary structure in the PCK rat.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Phosphomannose isomerase deficiency as a cause of congenital hepatic fibrosis and protein-losing enteropathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital hepatic fibrosis-is it really a matter of "a spoonful of sugar?"
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Renal and biliary abnormalities in a new murine model of autosomal recessive polycystic kidney disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effective treatment of an orthologous model of autosomal dominant polycystic kidney disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Alfa and beta estrogen receptors and the biliary tree
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystic disease of the liver
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986361-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0399-8320(05)86361-4
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
PubMed ID
16294159
1 reference
stated in
Europe PubMed Central
PubMed ID
16294159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 January 2020
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