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المساهمون: Pulmonary medicine, ACS - Pulmonary hypertension & thrombosis, Human genetics, ACS - Atherosclerosis & ischemic syndromes, APH - Quality of Care, Gräf, Stefan [0000-0002-1315-8873], Haimel, Matthias [0000-0002-0320-0214], Bleda, Marta [0000-0002-1287-6013], Hadinnapola, Charaka [0000-0002-7794-3432], Southgate, Laura [0000-0002-2090-1450], Martin, Jennifer M [0000-0002-7697-7438], Shamardina, Olga [0000-0003-4994-2157], Aldred, Micheala [0000-0002-7390-9181], Montani, David [0000-0002-9358-6922], Prokopenko, Inga [0000-0003-1624-7457], Rhodes, Christopher J [0000-0002-4962-3204], Stein, Dan F [0000-0001-7904-832X], Toshner, Mark R [0000-0002-3969-6143], van Heel, David A [0000-0002-0637-2265], Wharton, John [0000-0001-8110-2575], Soranzo, Nicole [0000-0003-1095-3852], Lawrie, Allan [0000-0003-4192-9505], Upton, Paul D [0000-0003-2716-4921], Trembath, Richard C [0000-0003-0550-3400], Morrell, Nicholas W [0000-0001-5700-9792], Apollo - University of Cambridge Repository

المصدر: Nature Communications, Vol 9, Iss 1, Pp 1-16 (2018)
Nature Communications
Nature Communications, 9. Nature Publishing Group
Graf, S, Haimel, M, Bleda, M, Hadinnapola, C, Southgate, L, Li, W, Hodgson, J, Liu, B, Salmon, R M, Southwood, M, Machado, R D, Martin, J M, Treacy, C M, Yates, K, Daugherty, L C, Shamardina, O, Whitehorn, D, Holden, S, Aldred, M, Bogaard, H J, Church, C, Coghlan, G, Condliffe, R, Corris, P A, Danesino, C, Eyries, M, Gall, H, Ghio, S, Ghofrani, H-A, Gibbs, J S R, Girerd, B, Houweling, A C, Howard, L, Humbert, M, Kiely, D G, Kovacs, G, Ross, R V M, Moledina, S, Montani, D, Newnham, M, Olschewski, A, Olschewski, H, Peacock, A J, Pepke-Zaba, J, Prokopenko, I, Rhodes, C J, Scelsi, L, Seeger, W, Soubrier, F, Stein, D F, Suntharalingam, J, Swietlik, E M, Toshner, M R, van Heel, D A, Noordegraaf, A V, Waisfisz, Q, Wharton, J, Wort, S J, Ouwehand, W H, Soranzo, N, Lawrie, A, Upton, P D, Wilkins, M R, Trembath, R C & Morrell, N W 2018, ' Identification of rare sequence variation underlying heritable pulmonary arterial hypertension ', Nature Communications, vol. 9 . https://doi.org/10.1038/s41467-018-03672-4Test
Nature communications, vol 9, iss 1

مصطلحات موضوعية: Adult, Male, Models, Molecular, Science, Cardiovascular, Bone Morphogenetic Protein Receptors, Type II, Type II, Article, Rare Diseases, Clinical Research, Models, Transforming Growth Factor beta, MD Multidisciplinary, Genetics, polycyclic compounds, Growth Differentiation Factor 2, SOXF Transcription Factors, 2.1 Biological and endogenous factors, Humans, Familial Primary Pulmonary Hypertension, Genetic Predisposition to Disease, Aetiology, lcsh:Science, Lung, Adenosine Triphosphatases, Aquaporin 1, Base Sequence, Whole Genome Sequencing, Human Genome, Molecular, Membrane Transport Proteins, Bone Morphogenetic Protein Receptors, Prognosis, Growth Differentiation Factors, HEK293 Cells, Gene Expression Regulation, Case-Control Studies, Mutation, Female, lcsh:Q, Signal Transduction