(Q35103361)

6 August 2017

title

Biliary dysgenesis in the PCK rat, an orthologous model of autosomal recessive polycystic kidney disease (English)

1 reference

autosomal recessive polycystic kidney

6 August 2017

main subject

0 references

author name string

Tatyana V Masyuk

1

1 reference

6 August 2017

Bing Q Huang

2

1 reference

6 August 2017

Anatoliy I Masyuk

3

1 reference

6 August 2017

Erik L Ritman

4

1 reference

6 August 2017

Vicente E Torres

5

1 reference

6 August 2017

Xiaofang Wang

6

1 reference

6 August 2017

Peter C Harris

7

1 reference

6 August 2017

Nicholas F Larusso

8

1 reference

6 August 2017

language of work or name

English

0 references

publication date

1 November 2004

1 reference

The American Journal of Pathology

6 August 2017

published in

1 reference

6 August 2017

volume

165

1 reference

6 August 2017

issue

5

1 reference

6 August 2017

page(s)

1719-1730

1 reference

describes a project that uses

6 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1618661/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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

9 July 2018

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

9 July 2018

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9 July 2018

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

9 July 2018

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9 July 2018

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

9 July 2018

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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

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Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

9 July 2018

1 reference

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

9 July 2018

1 reference

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9 July 2018

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9 July 2018

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9 July 2018

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

9 July 2018

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Caloric restriction improves thermotolerance and reduces hyperthermia-induced cellular damage in old rats.

9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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

9 July 2018

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27 September 2018

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27 September 2018

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A new mouse model for autosomal recessive polycystic kidney disease

27 September 2018

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

27 September 2018

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27 September 2018

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27 September 2018

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7 January 2021

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Murine models of polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Murine autosomal recessive polycystic kidney disease with multiorgan involvement induced by the cpk gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Germline and somatic loss of function of the mouse cpk gene causes biliary ductal pathology that is genetically modulated

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Renal and biliary abnormalities in a new murine model of autosomal recessive polycystic kidney disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Characterization of a novel polycystic kidney rat model with accompanying polycystic liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

In vivo quantification of ageing changes in the rat liver from early juvenile to senescent life

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963427-X

Quantification and longitudinal trends of kidney, renal cyst, and renal parenchyma volumes in autosomal dominant polycystic kidney disease

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15509540

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Development of autosomal recessive polycystic kidney disease in BALB/c-cpk/cpk mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15509540

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)63427-X

1 reference

6 August 2017

1 reference

6 August 2017

1 reference