213 related articles for article (PubMed ID: 8598197)
1. Role of the duplicated CCAAT box region in gamma-globin gene regulation and hereditary persistence of fetal haemoglobin.
Ronchi A; Berry M; Raguz S; Imam A; Yannoutsos N; Ottolenghi S; Grosveld F; Dillon N
EMBO J; 1996 Jan; 15(1):143-9. PubMed ID: 8598197
[TBL] [Abstract][Full Text] [Related]
2. A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin.
Berry M; Grosveld F; Dillon N
Nature; 1992 Aug; 358(6386):499-502. PubMed ID: 1379347
[TBL] [Abstract][Full Text] [Related]
3. Regulation of embryonic/fetal globin genes by nuclear hormone receptors: a novel perspective on hemoglobin switching.
Filipe A; Li Q; Deveaux S; Godin I; Roméo PH; Stamatoyannopoulos G; Mignotte V
EMBO J; 1999 Feb; 18(3):687-97. PubMed ID: 9927428
[TBL] [Abstract][Full Text] [Related]
4. Increased gamma-globin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor.
Martin DI; Tsai SF; Orkin SH
Nature; 1989 Mar; 338(6214):435-8. PubMed ID: 2467208
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of the human fetal-to-adult globin switching.
Katsube T; Fucharoen S; Tojo H; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():212-20. PubMed ID: 8629109
[TBL] [Abstract][Full Text] [Related]
6. DNA-protein interactions in the proximal zeta-globin promoter: identification of novel CCACCC- and CCAAT-binding proteins.
Sabath DE; Koehler KM; Yang WQ; Phan V; Wilson J
Blood Cells Mol Dis; 1998 Jun; 24(2):183-98. PubMed ID: 9642099
[TBL] [Abstract][Full Text] [Related]
7. Sites I and II upstream of the A gamma globin gene bind nuclear factors and affect gene expression.
Lloyd JA; Lee RF; Menon AG; Lingrel JB
Prog Clin Biol Res; 1989; 316A():139-48. PubMed ID: 2480607
[TBL] [Abstract][Full Text] [Related]
8. HMG-I binds to GATA motifs: implications for an HPFH syndrome.
Magis W; Martin DI
Biochem Biophys Res Commun; 1995 Sep; 214(3):927-33. PubMed ID: 7575565
[TBL] [Abstract][Full Text] [Related]
9. An erythroid-specific DNA binding factor mediates increased gamma-globin expression in hereditary persistence of fetal hemoglobin (HPFH).
Martin DI; Orkin SH
Prog Clin Biol Res; 1989; 316A():217-28. PubMed ID: 2480608
[No Abstract] [Full Text] [Related]
10. Use of the hereditary persistence of fetal hemoglobin 2 enhancer to increase the expression of oncoretrovirus vectors for human gamma-globin.
Fragkos M; Anagnou NP; Tubb J; Emery DW
Gene Ther; 2005 Nov; 12(21):1591-600. PubMed ID: 15944728
[TBL] [Abstract][Full Text] [Related]
11. Juxtaposition of the HPFH2 enhancer is not sufficient to reactivate the gamma-globin gene in adult erythropoiesis.
Xiang P; Han H; Barkess G; Olave I; Fang X; Yin W; Stamatoyannopoulos G; Li Q
Hum Mol Genet; 2005 Oct; 14(20):3047-56. PubMed ID: 16155112
[TBL] [Abstract][Full Text] [Related]
12. Developmental specificity of recruitment of TBP to the TATA box of the human gamma-globin gene.
Duan ZJ; Fang X; Rohde A; Han H; Stamatoyannopoulos G; Li Q
Proc Natl Acad Sci U S A; 2002 Apr; 99(8):5509-14. PubMed ID: 11960008
[TBL] [Abstract][Full Text] [Related]
13. Human fetal-to-adult globin gene switching in transgenic mice: persistent expression of the G gamma-globin gene in the Japanese HPFH.
Katsube T; Tojo H; Sakaguchi T; Fukumaki Y
Biochem Biophys Res Commun; 1993 Jul; 194(1):246-52. PubMed ID: 7687430
[TBL] [Abstract][Full Text] [Related]
14. Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice.
Anagnou NP; Perez-Stable C; Gelinas R; Costantini F; Liapaki K; Constantopoulou M; Kosteas T; Moschonas NK; Stamatoyannopoulos G
J Biol Chem; 1995 Apr; 270(17):10256-63. PubMed ID: 7537267
[TBL] [Abstract][Full Text] [Related]
15. A region upstream of the human delta-globin gene shows a stage-specific interaction with globin promoters in erythroid cell lines.
Vitale M; Calzolari R; Di Marzo R; Acuto S; Maggio A
Blood Cells Mol Dis; 2001; 27(5):874-81. PubMed ID: 11783950
[TBL] [Abstract][Full Text] [Related]
16. Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobin.
Gumucio DL; Rood KL; Gray TA; Riordan MF; Sartor CI; Collins FS
Mol Cell Biol; 1988 Dec; 8(12):5310-22. PubMed ID: 2468996
[TBL] [Abstract][Full Text] [Related]
17. Altered binding to the gamma-globin promoter of two erythroid specific nuclear proteins in different HPFH syndromes.
Ottolenghi S; Mantovani R; Nicolis S; Ronchi A; Malgaretti N; Giglioni B; Gilman J
Prog Clin Biol Res; 1989; 316A():229-36. PubMed ID: 2480609
[No Abstract] [Full Text] [Related]
18. Sequences of G gamma, A gamma, and beta genes of the Greek (A gamma) HPFH mutant: evidence for a distal CCAAT box mutation in the A gamma gene.
Gelinas R; Yagi M; Endlich B; Lotshaw C; Kazazian HH; Stamatoyannopoulos G
Prog Clin Biol Res; 1985; 191():125-39. PubMed ID: 2413469
[TBL] [Abstract][Full Text] [Related]
19. Comparative studies of nondeletional HPFH gamma-globin gene promoters.
Motum PI; Lindeman R; Harvey MP; Trent RJ
Exp Hematol; 1993 Jul; 21(7):852-8. PubMed ID: 7686501
[TBL] [Abstract][Full Text] [Related]
20. Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster.
de Andrade TG; Peterson KR; Cunha AF; Moreira LS; Fattori A; Saad ST; Costa FF
Blood Cells Mol Dis; 2006; 37(2):82-90. PubMed ID: 16952470
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
