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Human Molecular Genetics|February 8, 2017
A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell diseaseXu Zhang, Binal N Shah, Wei Zhang, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 25, 2017
Gain-of-function EGLN1 prolyl hydroxylase (PHD2 D4E:C127S) in combination with EPAS1 (HIF-2α) polymorphism lowers hemoglobin concentration in Tibetan highlandersTsewang Tashi, N Scott Reading, Tanna Wuren, et al.
Scientific Reports|September 8, 2016
Space Charge Modulated Electrical BreakdownShengtao Li, Yuanwei Zhu, Daomin Min, et al.
Medical Science Educator|October 4, 2021
Improving Medical Student Clinical Knowledge and Skills Through Influenza EducationGeorge Chen, Masooma Kazmi, Danling Chen, et al.
Optics Express|June 5, 2009
Optimization of spot pattern in indoor diffuse optical wireless local area networksDamon W K Wong, George Chen, Jianping Yao
Blood|October 19, 2017
Ruxolitinib-induced defects in DNA repair cause sensitivity to PARP inhibitors in myeloproliferative neoplasmsMargaret Nieborowska-Skorska, Silvia Maifrede, Yashodhara Dasgupta, et al.
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