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Blood|June 24, 2020
Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasiaClaire L Shovlin, Ilenia Simeoni, Kate Downes, et al.
American Journal of Medical Genetics. Part A|December 14, 2021
Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformationsSrimmitha Balachandar, Tamara J Graves, Anika Shimonty, et al.
Human Mutation|September 22, 2015
Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic DefectsRajiv D Machado, Laura Southgate, Christina A Eichstaedt, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Integrative Multiomics to Dissect the Lung Transcriptional Landscape of Pulmonary Arterial HypertensionJason Hong, Brenda Wong, Christopher J Rhodes, et al.
Biorxiv : the Preprint Server for Biology|September 30, 2024
Role of Forkhead box F1 in the Pathobiology of Pulmonary Arterial HypertensionJose Gomez-Arroyo, Arjan C Houweling, Harm Jan Bogaard, et al.
Antioxidants & Redox Signaling|December 10, 2024
Alterations in Mitochondrial Function in Pulmonary Vascular DiseasesSamar Farha, Kewal Asosingh, Paul M Hassoun, et al.
Human Genetics|October 3, 2018
De novo unbalanced translocations have a complex history/aetiologyMaria Clara Bonaglia, Nehir Edibe Kurtas, Edoardo Errichiello, et al.
Human Mutation|January 24, 2006
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertensionRajiv D Machado, Micheala A Aldred, Victoria James, et al.
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