(Q40104574)

17 September 2017

title

Characterization of the BMPR2 5'-untranslated region and a novel mutation in pulmonary hypertension (English)

1 reference

17 September 2017

main subject

arterial hypertension

0 references

author

Rajiv Machado

series ordinal

2

1 reference

17 September 2017

5

1 reference

17 September 2017

Victoria James

3

0 references

Nicholas W Morrell

object named as

Nicholas W Morrell

series ordinal

4

0 references

author name string

Micheala A Aldred

series ordinal

1

1 reference

17 September 2017

language of work or name

English

0 references

publication date

19 July 2007

1 reference

American Journal of Respiratory and Critical Care Medicine

17 September 2017

published in

1 reference

17 September 2017

volume

176

1 reference

17 September 2017

issue

8

1 reference

17 September 2017

page(s)

819-824

1 reference

Primary pulmonary hypertension. A national prospective study

17 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

Clinical classification of pulmonary hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

Assessing protein coding region integrity in cDNA sequencing projects

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

C/T polymorphism in the 5' untranslated region of the apolipoprotein(a) gene introduces an upstream ATG and reduces in vitro translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5'-UTR of the HAMP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

Nonsense mutations in close proximity to the initiation codon fail to trigger full nonsense-mediated mRNA decay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200701-164OC

10.1164/RCCM.200701-164OC

21 January 2018

Identifiers

DOI

1 reference

17 September 2017

1 reference