(Q55670914)

English

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

scientific journal published in 2000

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scholarly article

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

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primary pulmonary hypertension

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based on heuristic

inferred from title

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author name string

K B Lane

2

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R D Machado

3

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M W Pauciulo

4

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J R Thomson

5

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J A Phillips

6

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J E Loyd

7

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W C Nichols

8

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R C Trembath

9

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language of work or name

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publication date

September 2000

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Nature Genetics

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26

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1

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81-4

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Primary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

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inferred from DOI database lookup

Primary pulmonary hypertension

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https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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Primary pulmonary hypertension. A national prospective study

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https://api.crossref.org/works/10.1038%2F79226

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

inferred from DOI database lookup

Two distinct transmembrane serine/threonine kinases from Drosophila melanogaster form an activin receptor complex

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

inferred from DOI database lookup

Disruption of transforming growth factor beta signaling by a mutation that prevents transphosphorylation within the receptor complex.

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

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Bone morphogenetic protein receptor complexes on the surface of live cells: a new oligomerization mode for serine/threonine kinase receptors

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1038%2F79226

7 January 2021

based on heuristic

inferred from DOI database lookup

Human type II receptor for bone morphogenic proteins (BMPs): extension of the two-kinase receptor model to the BMPs

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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Cloning and characterization of a human type II receptor for bone morphogenetic proteins

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

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cDNA cloning and genomic organization of the mouse BMP type II receptor

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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The molecular basis of genetic dominance

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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Primary pulmonary hypertension: the pressure rises for a gene.

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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HNPCC associated with germline mutation in the TGF-beta type II receptor gene.

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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Monoclonal endothelial cell proliferation is present in primary but not secondary pulmonary hypertension

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

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LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

1 reference

https://api.crossref.org/works/10.1038%2F79226

7 January 2021

based on heuristic

inferred from DOI database lookup

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364a4be169a519e321d39480cf9c951a807556f8

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