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pro vyhledávání: '"Renae Mayer"'
Autor:
Santosh L. Saraf, Patrick Kelly, Frans A. Kuypers, Patricia Schroeder, Eric Q. Wu, Sanjeev Forsyth, Theodosia A. Kalfa, Renae Mayer, Marilyn J. Telen, Punam Malik, Mark Lerman, Luke R. Smart, Jeremie H. Estepp, Kimberly Cruz, Maria D. Ribadeneira, R. Clark Brown
Publikováno v:
Blood. 136:19-20
I NTRODUCTION: The hallmark of sickle cell disease (SCD) is hemoglobin S (HbS) polymerization upon deoxygenation, resulting in red blood cell (RBC) sickling, oxidative damage, membrane damage, hemolysis, cell adhesion, and vaso-occlusion. Exacerbatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1cf42e524e00d46570afb00e1e37038
https://doi.org/10.1182/blood-2020-134269
https://doi.org/10.1182/blood-2020-134269
