| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0735-1097(03)00491-1 |
| P698 | PubMed publication ID | 12821254 |
| P50 | author | Derliz Mereles | Q47114678 |
| Bart J. Janssen | Q54568136 | ||
| Gabriel Miltenberger-Miltenyi | Q56441245 | ||
| Ekkehard Grünig | Q114404293 | ||
| Albrecht von Hippel | Q114512146 | ||
| Karlin Arnold | Q114512147 | ||
| Hugo A. Katus | Q27929168 | ||
| Horst Olschewski | Q39684611 | ||
| Marius M Hoeper | Q41143674 | ||
| P2093 | author name string | Claus R Bartram | |
| Rolf Koehler | |||
| Jörg Winkler | |||
| William Nichols | |||
| Michael Pauciulo | |||
| Wolfgang Kübler | |||
| Matthias Rindermann | |||
| P2860 | cites work | Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension | Q55670914 |
| Stress Doppler echocardiography for identification of susceptibility to high altitude pulmonary edema | Q57113288 | ||
| Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32 | Q59674443 | ||
| Abnormal Pulmonary Artery Pressure Response in Asymptomatic Carriers of Primary Pulmonary Hypertension Gene | Q61767006 | ||
| Pulmonary artery pressure and oxygen consumption measurement during supine bicycle exercise | Q68256506 | ||
| Primary pulmonary hypertension | Q71957743 | ||
| Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32 | Q73437866 | ||
| Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33 | Q73536845 | ||
| TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS | Q76612865 | ||
| Functional analysis of bone morphogenetic protein type II receptor mutations underlying primary pulmonary hypertension | Q24298704 | ||
| BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension | Q34043809 | ||
| Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia. | Q34085780 | ||
| Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene | Q34142690 | ||
| Is the serotonin transporter involved in the pathogenesis of pulmonary hypertension? | Q34650342 | ||
| Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family | Q35559673 | ||
| Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptor | Q43952396 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | primary pulmonary hypertension | Q18554794 |
| P304 | page(s) | 2237-2244 | |
| P577 | publication date | 2003-06-01 | |
| P1433 | published in | Journal of the American College of Cardiology | Q2984355 |
| P1476 | title | Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31 | |
| P478 | volume | 41 |
| Q36940790 | Eisenmenger syndrome and atrial septal defect: nature or nurture? |
| Q35118881 | Identification of a new intronic BMPR2-mutation and early diagnosis of heritable pulmonary arterial hypertension in a large family with mean clinical follow-up of 12 years |
| Q51760564 | Molecular effects of loss of BMPR2 signaling in smooth muscle in a transgenic mouse model of PAH. |
| Q52997994 | Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension. |
| Q37033842 | Potassium channels in the regulation of pulmonary artery smooth muscle cell proliferation and apoptosis: pharmacotherapeutic implications |
| Q36023813 | The biological "scrabble" of pulmonary arteriovenous malformations: considerations in the setting of cavopulmonary surgery |
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