Polycystic disease of the liver (Q28283470)

Hepatic cysts in autosomal dominant polycystic kidney disease

Europe PubMed Central

title

Polycystic disease of the liver (English)

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author name string

Gregory T Everson

series ordinal

1

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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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issue

4

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page(s)

774-82

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cites work

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Polycystic kidney disease: The complete structure of the PKD1 gene and its protein

21 January 2018

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Hepatic cyst infection in autosomal dominant polycystic kidney disease

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Symptomatic hepatic cysts: percutaneous drainage and sclerosis

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Natural history of autosomal dominant polycystic kidney disease

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Combined cystic disease of the liver and kidney

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Risk factors for the development of hepatic cysts in autosomal dominant polycystic kidney disease

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7 January 2021

Hepatic cystic disease in an adult polycystic kidney disease transplant population.

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7 January 2021

Hepatic cysts in autosomal dominant polycystic kidney disease

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7 January 2021

Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group

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7 January 2021

Hereditary and acquired cystic disease of the kidney

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7 January 2021

Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes

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7 January 2021

Is there a third gene for autosomal dominant polycystic kidney disease?

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7 January 2021

Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis

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7 January 2021

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

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7 January 2021

Survival after end-stage renal disease in autosomal dominant polycystic kidney disease: contribution of extrarenal complications to mortality

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Clinical profile of autosomal dominant polycystic liver disease

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Mutation analysis of the entire PKD1 gene: genetic and diagnostic implications

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7 January 2021

Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease

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7 January 2021

Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype.

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7 January 2021

The Position of the Polycystic Kidney Disease 1 (PKD1) Gene Mutation Correlates with the Severity of Renal Disease

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7 January 2021

Autosomal dominant polycystic kidney disease

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7 January 2021

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

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7 January 2021

Mutations of the human polycystic kidney disease 2 (PKD2) gene

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7 January 2021

Location of mutations within the PKD2 gene influences clinical outcome.

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7 January 2021

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

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7 January 2021

Somatic inactivation of Pkd2 results in polycystic kidney disease

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7 January 2021

The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage

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7 January 2021

Hereditary polycystic kidney disease (adult form): a microdissection study of two cases at an early stage of the disease

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7 January 2021

Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease

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https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Structure-function relationships of the extracellular domain of the autosomal dominant polycystic kidney disease-associated protein, polycystin-1.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

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

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

PKD1 interacts with PKD2 through a probable coiled-coil domain

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Voltage dependence and pH regulation of human polycystin-2-mediated cation channel activity

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystin-2 is an intracellular calcium release channel

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Cellular localization and tissue distribution of polycystin-1

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystin-1 distribution is modulated by polycystin-2 expression in mammalian cells

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Identification, characterization, and localization of a novel kidney polycystin-1-polycystin-2 complex

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

The vertebrate primary cilium is a sensory organelle

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Defects in cholangiocyte fibrocystin expression and ciliary structure in the PCK rat.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

The renal cell primary cilium functions as a flow sensor

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Electron paramagnetic resonance reveals age-related myosin structural changes in rat skeletal muscle fibers

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Tubular gelatinase A (MMP-2) and its tissue inhibitors in polycystic kidney disease in the Han:SPRD rat

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Matrix metalloproteinase activity in human intrahepatic biliary epithelial cell lines from patients with autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Angiogenesis in autosomal-dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Epidermal growth factor and endothelin in cyst fluid from autosomal dominant polycystic kidney disease cases: possible evidence of heterogeneity in cystogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Cytokines in fluids from polycystic kidneys

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Polycystic liver disease: quantitation of parenchymal and cyst volumes from computed tomography images and clinical correlates of hepatic cysts

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Hepatic venous outflow obstruction in patients with polycystic liver disease: pathogenesis and treatment

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Intracranial aneurysms in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Treatment of symptomatic congenital hepatic cysts with single-session percutaneous drainage and ethanol sclerosis: technique and outcome

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Adult polycystic liver disease: is fenestration the most adequate operation for long-term management?

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Laparoscopic fenestration in polycystic liver disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Laparoscopic treatment of nonparasitic liver cysts: adequate selection of patients and surgical technique

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Liver resection and cyst fenestration in the treatment of severe polycystic liver disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Liver transplantation for adult polycystic liver disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Liver transplantation in patients with polycystic liver disease.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Liver transplantation for adult polycystic liver disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Liver transplantation for polycystic liver disease.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Liver transplantation for polycystic liver disease--indications and outcome

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840400404

7 January 2021

Identifiers

DOI

10.1002/HEP.20431

0 references

10.1002/HEP.1840400404

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

15382167

1 reference

Consolidated OpenCitations Corpus – April 2017