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The von Hippel-Lindau Chuvash mutation promotes pulmonary hypertension and fibrosis in mice

The von Hippel-Lindau Chuvash mutation promotes pulmonary hypertension and fibrosis in mice

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2827942

The von Hippel-Lindau Chuvash mutation promotes pulmonary hypertension and fibrosis in mice

About this item

Full title

The von Hippel-Lindau Chuvash mutation promotes pulmonary hypertension and fibrosis in mice

Publisher

United States: American Society for Clinical Investigation

Journal title

The Journal of clinical investigation, 2010-03, Vol.120 (3), p.827-839

Language

English

Formats

Publication information

Publisher

United States: American Society for Clinical Investigation

More information

Scope and Contents

Contents

Mutation of the von Hippel-Lindau (VHL) tumor suppressor protein at codon 200 (R200W) is associated with a disease known as Chuvash polycythemia. In addition to polycythemia, Chuvash patients have pulmonary hypertension and increased respiratory rates, although the pathophysiological basis of these symptoms is unclear. Here we sought to address thi...

Alternative Titles

Full title

The von Hippel-Lindau Chuvash mutation promotes pulmonary hypertension and fibrosis in mice

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2827942

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2827942

Other Identifiers

ISSN

0021-9738

E-ISSN

1558-8238

DOI

10.1172/JCI36362

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