Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31 (Q57824372)

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5 November 2019

title

Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31 (English)

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primary pulmonary hypertension

5 November 2019

main subject

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Gabriel Miltenberger-Miltenyi

inferred from title

author

5

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5 November 2019

Derliz Mereles

6

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5 November 2019

Horst Olschewski

10

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5 November 2019

Marius M Hoeper

11

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5 November 2019

13

Hugo A Katus

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5 November 2019

2

Ekkehard Grünig

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5 November 2019

3

Albrecht von Hippel

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5 November 2019

7

Karlin Arnold

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5 November 2019

16

Bart Janssen

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5 November 2019

author name string

Matthias Rindermann

1

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5 November 2019

Rolf Koehler

4

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5 November 2019

Michael Pauciulo

8

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5 November 2019

William Nichols

9

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5 November 2019

Jörg Winkler

12

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5 November 2019

Wolfgang Kübler

14

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5 November 2019

Claus R Bartram

15

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5 November 2019

language of work or name

English

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publication date

1 June 2003

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Journal of the American College of Cardiology

5 November 2019

published in

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5 November 2019

volume

41

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issue

12

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5 November 2019

page(s)

2237-2244

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Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Functional analysis of bone morphogenetic protein type II receptor mutations underlying primary pulmonary hypertension

1 reference

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7 January 2021

Abnormal Pulmonary Artery Pressure Response in Asymptomatic Carriers of Primary Pulmonary Hypertension Gene

1 reference

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7 January 2021

Primary pulmonary hypertension

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7 January 2021

Stress Doppler echocardiography for identification of susceptibility to high altitude pulmonary edema

1 reference

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7 January 2021

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Is the serotonin transporter involved in the pathogenesis of pulmonary hypertension?

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900491-1

7 January 2021

Pulmonary artery pressure and oxygen consumption measurement during supine bicycle exercise

1 reference

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7 January 2021

10.1016/S0735-1097(03)00491-1

Identifiers

DOI

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5 November 2019

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