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pro vyhledávání: '"Hannah Szafraniec"'
Autor:
Athena C. Geisness, Melissa Azul, Dillon Williams, Hannah Szafraniec, Daniel C. De Souza, John M. Higgins, David K. Wood
Publikováno v:
Haematologica, Vol 107, Iss 6 (2021)
Sickle cell disease (SCD) is characterized by sickle hemoglobin (HbS) which polymerizes under deoxygenated conditions to form a stiff, sickled erythrocyte. The dehydration of sickle erythrocytes increases intracellular HbS concentration and the prope
Externí odkaz:
https://doaj.org/article/2c9bacc87031420c84daa30f5d0874b2
Autor:
David K. Wood, Dillon Williams, Melissa Azul, Daniel C. De Souza, John M. Higgins, Hannah Szafraniec, Athena C Geisness
Publikováno v:
Haematologica. 107(6)
Sickle cell disease (SCD) is characterized by sickle hemoglobin (HbS) which polymerizes under deoxygenated conditions to form a stiff, sickled erythrocyte. The dehydration of sickle erythrocytes increases intracellular HbS concentration and the prope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0cae496d97ebb8fa1dc30d0c814e944
https://pubmed.ncbi.nlm.nih.gov/34706495
https://pubmed.ncbi.nlm.nih.gov/34706495