These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. A Combined Targeted and Whole Exome Sequencing Approach Identified Novel Candidate Genes Involved in Heritable Pulmonary Arterial Hypertension. Barozzi C; Galletti M; Tomasi L; De Fanti S; Palazzini M; Manes A; Sazzini M; Galiè N Sci Rep; 2019 Jan; 9(1):753. PubMed ID: 30679663 [TBL] [Abstract][Full Text] [Related]
13. SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension. Wang TM; Wang SS; Xu YJ; Zhao CM; Qiao XH; Yang CX; Liu XY; Yang YQ Int Heart J; 2021 May; 62(3):566-574. PubMed ID: 33952808 [TBL] [Abstract][Full Text] [Related]
14. Clinical characteristics and survival of Chinese patients diagnosed with pulmonary arterial hypertension who carry BMPR2 or EIF2KAK4 variants. Zeng Q; Yang H; Liu B; Ma Y; Liu Z; Chen Q; Li W; Luo Q; Zhao Z; Zhou Z; Xiong C BMC Pulm Med; 2020 May; 20(1):150. PubMed ID: 32471403 [TBL] [Abstract][Full Text] [Related]
15. Genetics dictating therapeutic decisions in pediatric pulmonary hypertension? A case report suggesting we are getting closer. Stevens L; Colglazier E; Parker C; Amin EK; Nawaytou H; Teitel D; Reddy VM; Welch CL; Chung WK; Fineman JR Pulm Circ; 2022 Jan; 12(1):e12033. PubMed ID: 35506084 [TBL] [Abstract][Full Text] [Related]
16. ATP13A3 is a major component of the enigmatic mammalian polyamine transport system. Hamouda NN; Van den Haute C; Vanhoutte R; Sannerud R; Azfar M; Mayer R; Cortés Calabuig Á; Swinnen JV; Agostinis P; Baekelandt V; Annaert W; Impens F; Verhelst SHL; Eggermont J; Martin S; Vangheluwe P J Biol Chem; 2021; 296():100182. PubMed ID: 33310703 [TBL] [Abstract][Full Text] [Related]
17. Loss-of-function variants in Yigit G; Sheffer R; Daana M; Li Y; Kaygusuz E; Mor-Shakad H; Altmüller J; Nürnberg P; Douiev L; Kaulfuss S; Burfeind P; Wollnik B; Brockmann K J Med Genet; 2022 Jun; 59(6):549-553. PubMed ID: 34172529 [TBL] [Abstract][Full Text] [Related]
18. A rare homozygous missense GDF2 (BMP9) mutation causing PAH in siblings: Does BMP10 status contribute? Upton P; Richards S; Bates A; Niederhoffer KY; Morrell NW; Christian S Am J Med Genet A; 2023 Jan; 191(1):228-233. PubMed ID: 36259599 [TBL] [Abstract][Full Text] [Related]
19. Genetic and functional analyses of TBX4 reveal novel mechanisms underlying pulmonary arterial hypertension. Yoshida Y; Uchida K; Kodo K; Shibata H; Furutani Y; Nakayama T; Sakai S; Nakanishi T; Takahashi T; Yamagishi H J Mol Cell Cardiol; 2022 Oct; 171():105-116. PubMed ID: 35914404 [TBL] [Abstract][Full Text] [Related]
20. Biallelic variants in the calpain regulatory subunit Postma AV; Rapp CK; Knoflach K; Volk AE; Lemke JR; Ackermann M; Regamey N; Latzin P; Celant L; Jansen SMA; Bogaard HJ; Ilgun A; Alders M; van Spaendonck-Zwarts KY; Jonigk D; Klein C; Gräf S; Kubisch C; Houweling AC; Griese M Genet Med Open; 2023; 1(1):100811. PubMed ID: 38230350 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]