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Review 1. Treating sickle cell disease by targeting HbS polymerization.

Authors: William A Eaton; H Franklin Bunn
Journal: Blood Date: 2017-04-06 Impact factor: 22.113

2. FT-4202, an oral PKR activator, has potent antisickling effects and improves RBC survival and Hb levels in SCA mice.

Authors: Archana Shrestha; Mengna Chi; Kimberly Wagner; Astha Malik; Jennifer Korpik; Adam Drake; Keertik Fulzele; Sylvie Guichard; Punam Malik
Journal: Blood Adv Date: 2021-05-11

Review 3. Therapeutic strategies to alter the oxygen affinity of sickle hemoglobin.

Authors: Martin K Safo; Gregory J Kato
Journal: Hematol Oncol Clin North Am Date: 2014-01-21 Impact factor: 3.722

4. Erythrocyte Hb-S concentration. An important factor in the low oxygen affinity of blood in sickle cell anemia.

Authors: M Seakins; W N Gibbs; P F Milner; J F Bertles
Journal: J Clin Invest Date: 1973-02 Impact factor: 14.808

Review 5. New developments in anti-sickling agents: can drugs directly prevent the polymerization of sickle haemoglobin in vivo?

Authors: Esther Oder; Martin K Safo; Osheiza Abdulmalik; Gregory J Kato
Journal: Br J Haematol Date: 2016-09-08 Impact factor: 6.998

6. Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.

Authors: Sharon E Cox; Julie Makani; Charles R Newton; Andrew M Prentice; Fenella J Kirkham
Journal: ISRN Hematol Date: 2013-04-03

6 in total