(Q47589236)

4 February 2018

title

BMPR2 mutations have short lifetime expectancy in primary pulmonary hypertension (English)

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4 February 2018

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3

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4 February 2018

Juha Kere

10

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4 February 2018

Richard C Trembath

14

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4 February 2018

Morag Dixon

object named as

Morag Dixon

7

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Tarja Laitinen

15

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Tarja Laitinen

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4 February 2018

Markku Kupari

12

object named as

Markku Kupari

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4 February 2018

author name string

Marja Sankelo

1

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4 February 2018

Julia A Flanagan

2

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4 February 2018

Rachel Harrison

4

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4 February 2018

Nung Rudarakanchana

5

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4 February 2018

Nicholas Morrell

6

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4 February 2018

Maija Halme

8

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4 February 2018

Hannu Puolijoki

9

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4 February 2018

Outi Elomaa

11

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4 February 2018

Anne Räisänen-Sokolowski

13

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4 February 2018

publication date

1 August 2005

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4 February 2018

published in

Human Mutation

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4 February 2018

volume

26

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4 February 2018

issue

2

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4 February 2018

page(s)

119-124

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4 February 2018

Genetic basis of pulmonary arterial hypertension: current understanding and future directions

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

Primary pulmonary hypertension. A national prospective study

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.20200

Primary pulmonary hypertension in Israel: a national survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

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/10.1002%2FHUMU.20200

7 January 2021

Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Evidence of founder mutations in Finnish BRCA1 and BRCA2 families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Cloning of a novel type II serine/threonine kinase receptor through interaction with the type I transforming growth factor-beta receptor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Human population genetics: lessons from Finland

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

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/10.1002%2FHUMU.20200

7 January 2021

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

The mode of bone morphogenetic protein (BMP) receptor oligomerization determines different BMP-2 signaling pathways.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Founding mutations and Alu-mediated recombination in hereditary colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

The ever-increasing complexity of TGF-beta signaling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

Primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20200

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/10.1002%2FHUMU.20200

7 January 2021

Identifiers

DOI

10.1002/HUMU.20200

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4 February 2018

PubMed ID

15965979

1 reference

4 February 2018