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PUBMED FOR HANDHELDS

Journal Abstract Search


406 related items for PubMed ID: 30610955

  • 1.
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  • 2. Autophagy contributes to BMP type 2 receptor degradation and development of pulmonary arterial hypertension.
    Gomez-Puerto MC, van Zuijen I, Huang CJ, Szulcek R, Pan X, van Dinther MA, Kurakula K, Wiesmeijer CC, Goumans MJ, Bogaard HJ, Morrell NW, Rana AA, Ten Dijke P.
    J Pathol; 2019 Nov; 249(3):356-367. PubMed ID: 31257577
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  • 3. Beraprost Upregulates KV Channel Expression and Function via EP4 Receptor in Pulmonary Artery Smooth Muscle Cells Obtained from Rats with Hypoxia-Induced Pulmonary Hypertension.
    Tian H, Fan F, Geng J, Deng J, Tian H.
    J Vasc Res; 2019 Nov; 56(4):204-214. PubMed ID: 31189158
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  • 5. Glycyrrhizin, inhibitor of high mobility group box-1, attenuates monocrotaline-induced pulmonary hypertension and vascular remodeling in rats.
    Yang PS, Kim DH, Lee YJ, Lee SE, Kang WJ, Chang HJ, Shin JS.
    Respir Res; 2014 Nov 25; 15():148. PubMed ID: 25420924
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  • 6. CCL5 deficiency rescues pulmonary vascular dysfunction, and reverses pulmonary hypertension via caveolin-1-dependent BMPR2 activation.
    Nie X, Tan J, Dai Y, Liu Y, Zou J, Sun J, Ye S, Shen C, Fan L, Chen J, Bian JS.
    J Mol Cell Cardiol; 2018 Mar 25; 116():41-56. PubMed ID: 29374556
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  • 7. HIMF (Hypoxia-Induced Mitogenic Factor) Signaling Mediates the HMGB1 (High Mobility Group Box 1)-Dependent Endothelial and Smooth Muscle Cell Crosstalk in Pulmonary Hypertension.
    Lin Q, Fan C, Gomez-Arroyo J, Van Raemdonck K, Meuchel LW, Skinner JT, Everett AD, Fang X, Macdonald AA, Yamaji-Kegan K, Johns RA.
    Arterioscler Thromb Vasc Biol; 2019 Dec 25; 39(12):2505-2519. PubMed ID: 31597444
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  • 11. MiR-23a regulates the proliferation and migration of human pulmonary artery smooth muscle cells (HPASMCs) through targeting BMPR2/Smad1 signaling.
    Zhang Y, Peng B, Han Y.
    Biomed Pharmacother; 2018 Jul 25; 103():1279-1286. PubMed ID: 29864909
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  • 12. Selenoprotein P Promotes the Development of Pulmonary Arterial Hypertension: Possible Novel Therapeutic Target.
    Kikuchi N, Satoh K, Kurosawa R, Yaoita N, Elias-Al-Mamun M, Siddique MAH, Omura J, Satoh T, Nogi M, Sunamura S, Miyata S, Saito Y, Hoshikawa Y, Okada Y, Shimokawa H.
    Circulation; 2018 Aug 07; 138(6):600-623. PubMed ID: 29636330
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  • 14. Upregulation of Angiomotin-Like 2 Ameliorates Experimental Pulmonary Arterial Hypertension by Inactivating YAP1 Signaling.
    Deng J, Yang G, Zhong N, Liang L, Chen H.
    J Cardiovasc Pharmacol; 2024 Sep 01; 84(3):356-369. PubMed ID: 39027975
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  • 18. Dihydroartemisinin Attenuates Pulmonary Hypertension Through Inhibition of Pulmonary Vascular Remodeling in Rats.
    Tang M, Wang R, Feng P, Dong Q, Chen W, Zhao Y, Li A, Li H, Chen J, Huang W.
    J Cardiovasc Pharmacol; 2020 Sep 01; 76(3):337-348. PubMed ID: 32569012
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  • 19. Network of MicroRNAs Mediate Translational Repression of Bone Morphogenetic Protein Receptor-2: Involvement in HIV-Associated Pulmonary Vascular Remodeling.
    Chinnappan M, Mohan A, Agarwal S, Dalvi P, Dhillon NK.
    J Am Heart Assoc; 2018 Feb 25; 7(5):. PubMed ID: 29478969
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  • 20. HMGB1 is mechanistically essential in the development of experimental pulmonary hypertension.
    Dai M, Xiao R, Cai L, Ge T, Zhu L, Hu Q.
    Am J Physiol Cell Physiol; 2019 Feb 01; 316(2):C175-C185. PubMed ID: 30517029
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