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Polycystic disease of the liver
scientific article
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instance of
scholarly article
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review article
1 reference
stated in
Europe PubMed Central
title
Polycystic disease of the liver
(English)
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author name string
Gregory T Everson
series ordinal
1
0 references
Matthew R G Taylor
series ordinal
2
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R Brian Doctor
series ordinal
3
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language of work or name
English
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publication date
October 2004
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published in
Hepatology
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volume
40
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page(s)
774-82
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issue
4
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cites work
Hepatic cysts in autosomal dominant polycystic kidney disease
1 reference
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Polycystic kidney disease: The complete structure of the PKD1 gene and its protein
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Hepatic cyst infection in autosomal dominant polycystic kidney disease
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Crossref
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21 January 2018
Symptomatic hepatic cysts: percutaneous drainage and sclerosis
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Crossref
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https://api.crossref.org/works/10.1002%2FHEP.20431
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21 January 2018
Natural history of autosomal dominant polycystic kidney disease
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Combined cystic disease of the liver and kidney
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
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/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatic cystic disease in an adult polycystic kidney disease transplant population.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatic cysts in autosomal dominant polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary and acquired cystic disease of the kidney
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Is there a third gene for autosomal dominant polycystic kidney disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Survival after end-stage renal disease in autosomal dominant polycystic kidney disease: contribution of extrarenal complications to mortality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical profile of autosomal dominant polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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7 January 2021
based on heuristic
inferred from DOI database lookup
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis of the entire PKD1 gene: genetic and diagnostic implications
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Position of the Polycystic Kidney Disease 1 (PKD1) Gene Mutation Correlates with the Severity of Renal Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the human polycystic kidney disease 2 (PKD2) gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Location of mutations within the PKD2 gene influences clinical outcome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic inactivation of Pkd2 results in polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary polycystic kidney disease (adult form): a microdissection study of two cases at an early stage of the disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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/10.1002%2FHEP.1840400404
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/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional similarities of hepatic cystic and biliary epithelium: studies of fluid constituents and in vivo secretion in response to secretin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure-function relationships of the extracellular domain of the autosomal dominant polycystic kidney disease-associated protein, polycystin-1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PKD1 interacts with PKD2 through a probable coiled-coil domain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Voltage dependence and pH regulation of human polycystin-2-mediated cation channel activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin-2 is an intracellular calcium release channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin-1, the PKD1 gene product, is in a complex containing E-cadherin and the catenins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cellular localization and tissue distribution of polycystin-1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystin-1 distribution is modulated by polycystin-2 expression in mammalian cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of polycystin-2, the PKD2 gene product
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification, characterization, and localization of a novel kidney polycystin-1-polycystin-2 complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The vertebrate primary cilium is a sensory organelle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The renal cell primary cilium functions as a flow sensor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
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%2FHEP.1840400404
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/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron paramagnetic resonance reveals age-related myosin structural changes in rat skeletal muscle fibers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tubular gelatinase A (MMP-2) and its tissue inhibitors in polycystic kidney disease in the Han:SPRD rat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Matrix metalloproteinase activity in human intrahepatic biliary epithelial cell lines from patients with autosomal dominant polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Angiogenesis in autosomal-dominant polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidermal growth factor and endothelin in cyst fluid from autosomal dominant polycystic kidney disease cases: possible evidence of heterogeneity in cystogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytokines in fluids from polycystic kidneys
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polycystic liver disease: quantitation of parenchymal and cyst volumes from computed tomography images and clinical correlates of hepatic cysts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hepatic venous outflow obstruction in patients with polycystic liver disease: pathogenesis and treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intracranial aneurysms in autosomal dominant polycystic kidney disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Treatment of symptomatic congenital hepatic cysts with single-session percutaneous drainage and ethanol sclerosis: technique and outcome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adult polycystic liver disease: is fenestration the most adequate operation for long-term management?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Laparoscopic fenestration in polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Laparoscopic treatment of nonparasitic liver cysts: adequate selection of patients and surgical technique
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver resection and cyst fenestration in the treatment of severe polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver transplantation for adult polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver transplantation in patients with polycystic liver disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver transplantation for adult polycystic liver disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver transplantation for polycystic liver disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liver transplantation for polycystic liver disease--indications and outcome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.1840400404
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/HEP.20431
0 references
10.1002/HEP.1840400404
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4838372
OpenCitations bibliographic resource ID
4838372
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4838372
PubMed ID
15382167
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4838372
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