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2. Unique Cardio‐metabolic Consequences of Superimposed Sustained and Intermittent Hypoxia

5. Hypoxic Pulmonary Vasoconstriction in Isolated Mouse Lungs

6. Upregulation of G protein‐couple receptor 68 (GPCR68) in pulmonary artery smooth muscle cells from animals and humans with pulmonary hypertension

7. Decreased MicroRNA‐153 Promotes Endothelial‐to‐Mesenchymal Transition in Idiopathic Pulmonary Arterial Hypertension

8. Using Pulmonary Angiogram to Estimate Vascular Remodeling in Mice

9. Calcium Homeostasis Modulator (CALHM1/2) and Pulmonary Arterial Hypertension

12. Overactivation of Ca 2+ /Calmodulin‐Dependent Protein Kinase IV and IIδ Contributes to Enhancing Pulmonary Arterial Smooth Muscle Cell Proliferation in Patients with Idiopathic Pulmonary Arterial Hypertension

16. Different Pattern of ATP‐mediated Increases in [Ca 2+ ] cyt Contributes to ATP‐induced Increase in Bcl‐2/Bax Ratio in Lung Cancer Cells But Not in Normal Control Cells

17. MiR‐17~92 promotes hypoxia‐induced pulmonary hypertension by regulating proliferation and contraction of pulmonary arterial smooth muscle cells (LB779)

18. SGLT inhibitors attenuate NO‐dependent vascular relaxation in mouse pulmonary artery (677.3)

19. Shear stress enhance intracellular Ca 2+ in PASMC from patients with idiopathic pulmonary arterial hypertension (1090.13)

20. The crucial role of calcium sensing receptor for hypoxia‐induced pulmonary arterial hypertension in mice (889.2)

22. microRNA 29b is upregulated in pulmonary artery smooth muscle cells from patients with idiopathic pulmonary arterial hypertension and inhibits K+ channel expression and function

25. Kinins and Kinin Receptors in Pulmonary Vasoconstriction and Vascular Remodeling

27. Selectively upregulated microRNAs in pulmonary artery smooth muscle cells from patients with idiopathic pulmonary arterial hypertension

30. Role of STIM1 in Coronary Endothelial Cell Dysfunction in Type 1 Diabetic Mice

33. Electrophysiological characterization of cells isolated from endarterectomized tissue from patients with chronic thromboembolic pulmonary hypertension (CTEPH)

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