219 related articles for article (PubMed ID: 2421808)
1. High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined.
Miller BA; Salameh M; Ahmed M; Wainscoat J; Antognetti G; Orkin S; Weatherall D; Nathan DG
Blood; 1986 May; 67(5):1404-10. PubMed ID: 2421808
[TBL] [Abstract][Full Text] [Related]
2. Analysis of hemoglobin F production in Saudi Arabian families with sickle cell anemia.
Miller BA; Salameh M; Ahmed M; Olivieri N; Antognetti G; Orkin SH; Huisman TH; Nathan DG
Blood; 1987 Sep; 70(3):716-20. PubMed ID: 2441778
[TBL] [Abstract][Full Text] [Related]
3. Influence of hydroxyurea on fetal hemoglobin production in vitro.
Miller BA; Platt O; Hope S; Dover G; Nathan DG
Blood; 1987 Dec; 70(6):1824-9. PubMed ID: 2445401
[TBL] [Abstract][Full Text] [Related]
4. Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia.
Pembrey ME; Wood WG; Weatherall DJ; Perrine RP
Br J Haematol; 1978 Nov; 40(3):415-29. PubMed ID: 749927
[TBL] [Abstract][Full Text] [Related]
5. Interferon-gamma modulates fetal hemoglobin synthesis in sickle cell anemia and thalassemia.
Miller BA; Olivieri N; Hope SM; Faller DV; Perrine SP
J Interferon Res; 1990 Aug; 10(4):357-66. PubMed ID: 1700029
[TBL] [Abstract][Full Text] [Related]
6. Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia.
Miller BA; Olivieri N; Salameh M; Ahmed M; Antognetti G; Huisman TH; Nathan DG; Orkin SH
N Engl J Med; 1987 Jan; 316(5):244-50. PubMed ID: 2432426
[TBL] [Abstract][Full Text] [Related]
7. Effects of dexamethasone on fetal hemoglobin synthesis in peripheral blood erythroid burst-forming units.
Steinberg MH; Coleman MB; Garver FA; Grenett HE; Pressley A; Adams JG
Am J Hematol; 1981; 10(1):37-45. PubMed ID: 6167163
[TBL] [Abstract][Full Text] [Related]
8. Determination of the hemoglobin F program in human progenitor-derived erythroid cells.
Friedman AD; Linch DC; Miller B; Lipton JM; Javid J; Nathan DG
J Clin Invest; 1985 Apr; 75(4):1359-68. PubMed ID: 2580859
[TBL] [Abstract][Full Text] [Related]
9. Analysis of high fetal hemoglobin production in sickle cell anemia patients from the Eastern Province of Saudi Arabia.
Miller BA; Salameh M; Ahmed M; Olivieri N; Huisman TH; Orkin SH; Nathan DG
Prog Clin Biol Res; 1987; 251():415-26. PubMed ID: 2448810
[No Abstract] [Full Text] [Related]
10. A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.
Vathipadiekal V; Farrell JJ; Wang S; Edward HL; Shappell H; Al-Rubaish AM; Al-Muhanna F; Naserullah Z; Alsuliman A; Qutub HO; Simkin I; Farrer LA; Jiang Z; Luo HY; Huang S; Mostoslavsky G; Murphy GJ; Patra PK; Chui DH; Alsultan A; Al-Ali AK; Sebastiani P; Steinberg MH
Am J Hematol; 2016 Nov; 91(11):1118-1122. PubMed ID: 27501013
[TBL] [Abstract][Full Text] [Related]
11. Influence of steel factor on hemoglobin synthesis in sickle cell disease.
Miller BA; Perrine SP; Bernstein A; Lyman SD; Williams DE; Bell LL; Olivieri NF
Blood; 1992 Apr; 79(7):1861-8. PubMed ID: 1373091
[TBL] [Abstract][Full Text] [Related]
12. Fetal hemoglobin in sickle cell anemia: The Arab-Indian haplotype and new therapeutic agents.
Habara AH; Shaikho EM; Steinberg MH
Am J Hematol; 2017 Nov; 92(11):1233-1242. PubMed ID: 28736939
[TBL] [Abstract][Full Text] [Related]
13. Understanding heterogeneity of fetal hemoglobin induction through comparative analysis of F and A erythroblasts.
Khandros E; Huang P; Peslak SA; Sharma M; Abdulmalik O; Giardine BM; Zhang Z; Keller CA; Hardison RC; Blobel GA
Blood; 2020 May; 135(22):1957-1968. PubMed ID: 32268371
[TBL] [Abstract][Full Text] [Related]
14. Glycosylated hemoglobin levels in a benign form of sickle cell anemia in Saudi Arabia.
Alayash AI; Dafallah A; Al-Husayni H; Al-Ali AK; Al-Quorain A; Omer AH; Wilson MT; Bonaventura J; Cashon R
Acta Haematol; 1986; 75(3):160-4. PubMed ID: 3092532
[TBL] [Abstract][Full Text] [Related]
15. Heterogeneity in the properties of burst-forming units of erythroid lineage in sickle cell anemia: DNA synthesis and burst-promoting activity production is related to peripheral hemoglobin F levels.
Croizat H; Billett HH; Nagel RL
Blood; 1990 Feb; 75(4):1006-10. PubMed ID: 1689189
[TBL] [Abstract][Full Text] [Related]
16. The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease.
Adekile A
Med Princ Pract; 2021; 30(3):201-211. PubMed ID: 32892201
[TBL] [Abstract][Full Text] [Related]
17. Circulating cytokines response and the level of erythropoiesis in sickle cell anemia.
Croizat H; Nagel RL
Am J Hematol; 1999 Feb; 60(2):105-15. PubMed ID: 9929101
[TBL] [Abstract][Full Text] [Related]
18. A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?
Wainscoat JS; Thein SL; Higgs DR; Bell JI; Weatherall DJ; Al-Awamy BH; Serjeant GR
Br J Haematol; 1985 Jun; 60(2):261-8. PubMed ID: 2408656
[TBL] [Abstract][Full Text] [Related]
19. Peripheral blood erythroid progenitors from patients with sickle cell anemia: HPLC separation of hemoglobins and the effect of a HbF switching factor.
Rosenblum BB; Strahler JR; Hanash SM; Whitten CF; Butkunas-Puskorius R; Roberts A
Prog Clin Biol Res; 1985; 191():397-410. PubMed ID: 2413478
[TBL] [Abstract][Full Text] [Related]
20. Relationship of burst-forming-unit-erythroid progenitors and their DNA-synthesis stage to fetal hemoglobin levels in hydroxyurea-treated patients with sickle cell anemia.
Mankad VN; Baliga S; Phillips K; Shah AK; Yang YM
Am J Hematol; 1994 Aug; 46(4):259-63. PubMed ID: 7518649
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
