Human Pulmonary Artery Endothelial Total RNA

Product Description

Human Pulmonary Artery Endothelial Total RNA
Catalog number: B2027177
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 50 ug
Molecular Weight or Concentration: NA
Supplied as: Solution
Storage: −80°C
Keywords: HPAEC, PAEC

References:
1. Sun L, et al. N6-methyladenosine RNA modification in eukaryotic systems. Nature Reviews Molecular Cell Biology. 2019;20(4):215-226.
2. Zhou Y, et al. RNA methylations in cardiovascular diseases. Circulation Research. 2021;128(7):930-945.
3. Zeng X, et al. Altered m6A RNA methylation in pulmonary arterial hypertension. American Journal of Respiratory and Critical Care Medicine. 2021;203(5):580-592.
4. Kang H, et al. YTHDF1 facilitates hypoxic pulmonary artery smooth muscle cell proliferation. Cell Death & Disease. 2023;14(2):112.
5. Aulak KS, et al. Endothelial dysfunction and vascular remodeling in pulmonary arterial hypertension. Pulmonary Circulation. 2021;11(3):1-15.
6. Ruffenach G, et al. Inhibition of HNRNPA2B1 rescues pulmonary hypertension in rats. Science Translational Medicine. 2022;14(635):eabf6801.
7. Ismail S, et al. IGFBP-3 promotes proliferation of human pulmonary artery smooth muscle cells under hypoxia. American Journal of Physiology-Lung Cellular and Molecular Physiology. 2009;297(6):L1022-L1031.
8. Qin Y, et al. The METTL3/YTHDF2/PTEN axis regulates hypoxia-induced pulmonary artery smooth muscle cell proliferation. Biochemical and Biophysical Research Communications. 2021;554:128-134.
9. Chelladurai K, et al. EP300 and H3K27ac enrichment in remodeled pulmonary arteries. Journal of Clinical Investigation. 2022;132(11):e154321.
10. Barnes JW, et al. Cardiopulmonary dysfunction and premature death in idiopathic pulmonary arterial hypertension. Lancet Respiratory Medicine. 2019;7(8):675-688.
Human Pulmonary Artery Endothelial Total RNA

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