Cardiopulmonary phenotype associated with human PHD2 mutation.

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Therapeutic targeting of the HIF oxygen-sensing pathway: Lessons learned from clinical studies.The PHD1 oxygen sensor in health and disease.

P2860

Q39291945-6AB55F45-887B-4AEC-BFAC-5DC168BAD3DE Q50050250-5843E14C-5713-40F0-BA10-B462C9DA8143

P2860

Cardiopulmonary phenotype associated with human PHD2 mutation.

Item

http://www.wikidata.org/entity/Q42291369

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Cardiopulmonary phenotype associated with human PHD2 mutation.

@en

Cardiopulmonary phenotype associated with human PHD2 mutation.

@nl

type

Item

label

Cardiopulmonary phenotype associated with human PHD2 mutation.

@en

Cardiopulmonary phenotype associated with human PHD2 mutation.

@nl

prefLabel

Cardiopulmonary phenotype associated with human PHD2 mutation.

@en

Cardiopulmonary phenotype associated with human PHD2 mutation.

@nl

P1476

Cardiopulmonary phenotype associated with human PHD2 mutation.

@en

P2093

George M Balanos

http://www.w3.org/2001/XMLSchema#string

Keith L Dorrington

http://www.w3.org/2001/XMLSchema#string

Peter A Robbins

http://www.w3.org/2001/XMLSchema#string

P2860

HIFalpha targeted for VHL-mediated destruction by proline hydroxylation: implications for O2 sensing

C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation

Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension

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

Cardiopulmonary function in two human disorders of the hypoxia-inducible factor (HIF) pathway: von Hippel-Lindau disease and HIF-2alpha gain-of-function mutation

Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation

Mutation of von Hippel-Lindau tumour suppressor and human cardiopulmonary physiology

Differential function of the prolyl hydroxylases PHD1, PHD2, and PHD3 in the regulation of hypoxia-inducible factor

Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations.

Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.

P31

scholarly article

case report

P356

10.14814/PHY2.13224

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Thomas G Smith

Nick P Talbot

Patrick H Maxwell

P577

2017-04-01T00:00:00Z

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P698

28400504

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P932

5392514

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Cardiopulmonary phenotype associated with human PHD2 mutation.

about

P2860

P2860

Cardiopulmonary phenotype associated with human PHD2 mutation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P50

P577

P698

P932