Stephanou C, Menzel S, Philipsen S, Kountouris P
Int J Mol Sci. 2024; 25(21).
PMID: 39518961
PMC: 11546522.
DOI: 10.3390/ijms252111408.
Lessard S, Rimmele P, Ling H, Moran K, Vieira B, Lin Y
Sci Rep. 2024; 14(1):24298.
PMID: 39414860
PMC: 11484757.
DOI: 10.1038/s41598-024-74716-7.
Zhang X, Xia F, Zhang X, Blumenthal R, Cheng X
J Mol Biol. 2023; 436(7):168343.
PMID: 37924864
PMC: 11185177.
DOI: 10.1016/j.jmb.2023.168343.
Rosanwo T, Bauer D
Mol Ther. 2021; 29(11):3163-3178.
PMID: 34628053
PMC: 8571174.
DOI: 10.1016/j.ymthe.2021.10.002.
Romito M, Rai R, Thrasher A, Cavazza A
Emerg Top Life Sci. 2021; 3(3):289-299.
PMID: 33523137
PMC: 7288986.
DOI: 10.1042/ETLS20180147.
Therapeutic gene editing strategies using CRISPR-Cas9 for the β-hemoglobinopathies.
Papizan J, Porter S, Sharma A, Pruett-Miller S
J Biomed Res. 2020; 35(2):115-134.
PMID: 33349624
PMC: 8038529.
DOI: 10.7555/JBR.34.20200096.
Post-Transcriptional Genetic Silencing of to Treat Sickle Cell Disease.
Esrick E, Lehmann L, Biffi A, Achebe M, Brendel C, Ciuculescu M
N Engl J Med. 2020; 384(3):205-215.
PMID: 33283990
PMC: 7962145.
DOI: 10.1056/NEJMoa2029392.
Sickle cell disease in the era of precision medicine: looking to the future.
Steinberg M, Kumar S, Murphy G, Vanuytsel K
Expert Rev Precis Med Drug Dev. 2020; 4(6):357-367.
PMID: 33015364
PMC: 7531762.
DOI: 10.1080/23808993.2019.1688658.
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease.
Adekile A
Med Princ Pract. 2020; 30(3):201-211.
PMID: 32892201
PMC: 8280415.
DOI: 10.1159/000511342.
Fetal hemoglobin in sickle cell anemia.
Steinberg M
Blood. 2020; 136(21):2392-2400.
PMID: 32808012
PMC: 7685210.
DOI: 10.1182/blood.2020007645.
and induction of fetal hemoglobin with a reversible and selective DNMT1 inhibitor.
Gilmartin A, Groy A, Gore E, Atkins C, Long E, Montoute M
Haematologica. 2020; 106(7):1979-1987.
PMID: 32586904
PMC: 8252945.
DOI: 10.3324/haematol.2020.248658.
Health outcomes and services in children with sickle cell trait, sickle cell anemia, and normal hemoglobin.
Reeves S, Jary H, Gondhi J, Kleyn M, Dombkowski K
Blood Adv. 2019; 3(10):1574-1580.
PMID: 31101648
PMC: 6538867.
DOI: 10.1182/bloodadvances.2018028043.
Metformin induces FOXO3-dependent fetal hemoglobin production in human primary erythroid cells.
Zhang Y, Paikari A, Sumazin P, Ginter Summarell C, Crosby J, Boerwinkle E
Blood. 2018; 132(3):321-333.
PMID: 29884740
PMC: 6053951.
DOI: 10.1182/blood-2017-11-814335.
A phased SNP-based classification of sickle cell anemia HBB haplotypes.
Shaikho E, Farrell J, Alsultan A, Qutub H, Al-Ali A, Figueiredo M
BMC Genomics. 2017; 18(1):608.
PMID: 28800727
PMC: 5553663.
DOI: 10.1186/s12864-017-4013-y.
Fetal hemoglobin in sickle cell anemia: The Arab-Indian haplotype and new therapeutic agents.
Habara A, Shaikho E, Steinberg M
Am J Hematol. 2017; 92(11):1233-1242.
PMID: 28736939
PMC: 5647233.
DOI: 10.1002/ajh.24872.
Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.
Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell J, Al-Rubaish A, Al-Muhanna F
Am J Hematol. 2016; 91(6):E308-11.
PMID: 27185208
PMC: 4874527.
DOI: 10.1002/ajh.24368.
Sickle Cell Disease in Central India: A Potentially Severe Syndrome.
Jain D, Warthe V, Dayama P, Sarate D, Colah R, Mehta P
Indian J Pediatr. 2016; 83(10):1071-6.
PMID: 27053181
DOI: 10.1007/s12098-016-2081-7.
Sickle Cell Disease: Reappraisal of the Role of Foetal Haemoglobin Levels in the Frequency of Vaso-Occlusive Crisis.
Antwi-Boasiako C, Frimpong E, Ababio G, Dzudzor B, Ekem I, Gyan B
Ghana Med J. 2015; 49(2):102-6.
PMID: 26339094
PMC: 4549825.
DOI: 10.4314/gmj.v49i2.7.
Genomic approaches to identifying targets for treating β hemoglobinopathies.
Ngo D, Steinberg M
BMC Med Genomics. 2015; 8:44.
PMID: 26215470
PMC: 4517356.
DOI: 10.1186/s12920-015-0120-2.
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
Sebastiani P, Farrell J, Alsultan A, Wang S, Edward H, Shappell H
Blood Cells Mol Dis. 2015; 54(3):224-30.
PMID: 25703683
PMC: 4341902.
DOI: 10.1016/j.bcmd.2015.01.001.
