65 related articles for article (PubMed ID: 2482504)
1. Point mutations or polymorphisms? A sequence analysis of the enhancer 3' to the A gamma-globin gene.
Cohen CJ; Penny L; Forget BG
Prog Clin Biol Res; 1989; 316B():395-401. PubMed ID: 2482504
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
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. Sequence variations in the 3' A gamma enhancer are silent polymorphisms.
Ragusa A; Lombardo M; Lombardo T; Beldjord C; Nagel RL; Elion J; Labie D; Krishnamoorthy R
Prog Clin Biol Res; 1989; 316B():409-17. PubMed ID: 2482506
[No Abstract] [Full Text] [Related]
7. G gamma-196 C-->T, A gamma-201 C-->T: two novel mutations in the promoter region of the gamma-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece.
Tasiopoulou M; Boussiou M; Sinopoulou K; Moraitis G; Loutradi-Anagnostou A; Karababa P
Blood Cells Mol Dis; 2008; 40(3):320-2. PubMed ID: 18096417
[TBL] [Abstract][Full Text] [Related]
8. Construction of vectors to study expression of wild type and non deletion HPFH gamma globin genes.
Rixon MW; Miller AD; Gelinas RE
Prog Clin Biol Res; 1987; 251():391-400. PubMed ID: 2448809
[No Abstract] [Full Text] [Related]
9. A gamma globin gene with G gamma-like promoter in a benin sickle cell anemia haplotype associated with elevated fetal hemoglobin.
Mishima N; Gilman JG; Huey LO; Milner PF
Prog Clin Biol Res; 1989; 316B():403-8. PubMed ID: 2482505
[No Abstract] [Full Text] [Related]
10. Two mutations in the locus control region hypersensitivity site-2 (5' HS-2) of haplotype 19 beta s chromosomes alter binding of trans-acting factors.
Morgan JC; Scott DF; Lanclos KD
Am J Hematol; 1996 Jan; 51(1):12-8. PubMed ID: 8571932
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Disorders of the synthesis of human fetal hemoglobin.
Manca L; Masala B
IUBMB Life; 2008 Feb; 60(2):94-111. PubMed ID: 18379999
[TBL] [Abstract][Full Text] [Related]
13. Three novel polymorphisms in the beta globin gene.
Nadkarni A; Sakaguchi T; Gorakshakar A; Phanasgaonkar S; Colah R; Mohanty D; Kiyama R
Am J Hematol; 2005 Oct; 80(2):161-3. PubMed ID: 16184579
[TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of unknown beta-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with beta-thalassemias and beta-globin variants.
Chinchang W; Viprakasit V; Pung-Amritt P; Tanphaichitr VS; Yenchitsomanus PT
Clin Biochem; 2005 Nov; 38(11):987-96. PubMed ID: 16139831
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterisation of Vietnamese HPFH.
Motum PI; Hamilton TJ; Lindeman R; Le H; Trent RJ
Hum Mutat; 1993; 2(3):179-84. PubMed ID: 7689901
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Nucleotide variation regulates the level of enhancement by hypersensitive site 2 of the beta-globin locus control region.
Ofori-Acquah SF; Lalloz MR; Layton DM
Blood Cells Mol Dis; 2001; 27(5):803-11. PubMed ID: 11783943
[TBL] [Abstract][Full Text] [Related]
18. The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene.
Oner R; Kutlar F; Gu LH; Huisman TH
Blood; 1991 Mar; 77(5):1124-5. PubMed ID: 1704803
[No Abstract] [Full Text] [Related]
19. A novel DNA polymorphism of the human A gamma-globin gene (A gamma-588, A-->G) is linked with the XMN / polymorphism (G gamma-158, C-->T).
Patrinos GP; Loutradi-Anagnostou A; Papadakis MN
Hemoglobin; 1995; 19(6):419-23. PubMed ID: 8718702
[No Abstract] [Full Text] [Related]
20. An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells.
Feingold EA; Penny LA; Nienhuis AW; Forget BG
Genomics; 1999 Oct; 61(1):15-23. PubMed ID: 10512676
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
