A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis (Q24536498)

6

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author name string

Melanie J Percy

1

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Quan Zhao

2

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Adrian Flores

3

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Claire Harrison

4

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Terence R J Lappin

5

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Mary Frances McMullin

Proceedings of the National Academy of Sciences of the United States of America

7

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language of work or name

English

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publication date

17 January 2006

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published in

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volume

103

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page(s)

654-9

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issue

3

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cites work

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27 September 2017

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30 May 2018

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30 May 2018

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29 November 2018

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Mutations in the VHL gene in sporadic apparently congenital polycythemia

29 November 2018

1 reference

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The transcriptional activity of the APP intracellular domain-Fe65 complex is inhibited by activation of the NF-kappaB pathway

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16407130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16407130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Erythrocytosis and the Chuvash von Hippel‐Lindau mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16407130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0508423103

1 reference

3875348

ADS bibcode

2006PNAS..103..654P

0 references

3875348

1 reference

1 reference

1 reference