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6. GBT440 increases haemoglobin oxygen affinity, reduces sickling and prolongs RBC half-life in a murine model of sickle cell disease. Oksenberg D; Dufu K; Patel MP; Chuang C; Li Z; Xu Q; Silva-Garcia A; Zhou C; Hutchaleelaha A; Patskovska L; Patskovsky Y; Almo SC; Sinha U; Metcalf BW; Archer DR Br J Haematol; 2016 Oct; 175(1):141-53. PubMed ID: 27378309 [TBL] [Abstract][Full Text] [Related]
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11. Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes. Brittenham GM; Schechter AN; Noguchi CT Blood; 1985 Jan; 65(1):183-9. PubMed ID: 3965046 [TBL] [Abstract][Full Text] [Related]
12. GBT440 Inhibits Sickling of Sickle Cell Trait Blood Under Dufu K; Lehrer-Graiwer J; Ramos E; Oksenberg D Hematol Rep; 2016 Sep; 8(3):6637. PubMed ID: 27757216 [TBL] [Abstract][Full Text] [Related]
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15. Simultaneous polymerization and adhesion under hypoxia in sickle cell disease. Papageorgiou DP; Abidi SZ; Chang HY; Li X; Kato GJ; Karniadakis GE; Suresh S; Dao M Proc Natl Acad Sci U S A; 2018 Sep; 115(38):9473-9478. PubMed ID: 30190429 [TBL] [Abstract][Full Text] [Related]
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19. Sulfated non-anticoagulant heparin derivative modifies intracellular hemoglobin, inhibits cell sickling in vitro, and prolongs survival of sickle cell mice under hypoxia. Abdulmalik O; Darwish NHE; Muralidharan-Chari V; Taleb MA; Mousa SA Haematologica; 2022 Feb; 107(2):532-540. PubMed ID: 33567814 [TBL] [Abstract][Full Text] [Related]
20. Established and experimental treatments for sickle cell disease. De Franceschi L; Corrocher R Haematologica; 2004 Mar; 89(3):348-56. PubMed ID: 15020275 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]