Somatic Inactivation of Pkd2 Results in Polycystic Kidney Disease (Q74502174)

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11 November 2019

title

Somatic inactivation of Pkd2 results in polycystic kidney disease (English)

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11 November 2019

Somatic Inactivation of Pkd2 Results in Polycystic Kidney Disease (English)

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https://api.crossref.org/works/10.1016/S0092-8674(00)81570-6

polycystic kidney disease

19 December 2024

main subject

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G. Wu

1

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V. D'Agati

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Y. Cai

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G. Markowitz

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J. H. Park

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D. M. Reynolds

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H. Hou

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W. Edelmann

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S. Somlo

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publication date

1 April 1998

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11 November 2019

17 April 1998

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9568711

http://www.cell.com/article/S0092867400815706/pdf

19 December 2024

language of work or name

English

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work available at URL

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11 November 2019

volume

93

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issue

2

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page(s)

177-188

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Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium)

11 November 2019

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

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Polycystic kidney disease: primary extracellular matrix abnormality or defective cellular differentiation?

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Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

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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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Identification and localization of polycystin, the PKD1 gene product

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Autosomal dominant polycystic kidney disease: neoplasia in disguise?

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Characterization of the Exon Structure of the Polycystic Kidney Disease 2 Gene (PKD2)

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Pathophysiology of Tamm-Horsfall protein

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

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Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein

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

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Changes in the glycosylation pattern during embryonic development of mouse kidney as revealed with lectin conjugates

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A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

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The sea urchin sperm receptor for egg jelly is a modular protein with extensive homology to the human polycystic kidney disease protein, PKD1.

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Identifiers

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11 November 2019

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