169 related articles for article (PubMed ID: 2462941)
1. An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.
Stoming TA; Stoming GS; Lanclos KD; Fei YJ; Altay C; Kutlar F; Huisman TH
Blood; 1989 Jan; 73(1):329-33. PubMed ID: 2462941
[TBL] [Abstract][Full Text] [Related]
2. The Australian type of nondeletional G gamma-HPFH has a C-->G substitution at nucleotide -114 of the G gamma gene.
Motum PI; Deng ZM; Huong L; Trent RJ
Br J Haematol; 1994 Jan; 86(1):219-21. PubMed ID: 7516698
[TBL] [Abstract][Full Text] [Related]
3. Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobin.
Toma S; Tenorio M; Oakley M; Thein SL; Clark BE
Hemoglobin; 2014; 38(1):67-9. PubMed ID: 24144231
[TBL] [Abstract][Full Text] [Related]
4. G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis.
Coleman MB; Adams JG; Steinberg MH; Plonczynski MW; Harrell AH; Castro O; Winter WP
Am J Hematol; 1993 Feb; 42(2):186-90. PubMed ID: 7679879
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. A short review of human gamma-globin gene anomalies.
Huisman TH
Acta Haematol; 1987; 78(2-3):80-4. PubMed ID: 2446459
[TBL] [Abstract][Full Text] [Related]
8. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
Ottolenghi S; Giglioni B; Taramelli R; Comi P; Mazza U; Saglio G; Camaschella C; Izzo P; Cao A; Galanello R; Gimferrer E; Baiget M; Gianni AM
Proc Natl Acad Sci U S A; 1982 Apr; 79(7):2347-51. PubMed ID: 6179097
[TBL] [Abstract][Full Text] [Related]
9. %Hb A2, %Hb F, %G gamma values and the haplotypes in the beta-globin gene cluster in Japanese adults with elevated Hb F.
Shimizu K; Keino H
Hum Hered; 1992; 42(4):222-30. PubMed ID: 1380945
[TBL] [Abstract][Full Text] [Related]
10. The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin.
Camaschella C; Oggiano L; Sampietro M; Gottardi E; Alfarano A; Pistidda P; Dore F; Taramelli R; Ottolenghi S; Longinotti M
Blood; 1989 May; 73(7):1999-2002. PubMed ID: 2469505
[TBL] [Abstract][Full Text] [Related]
11. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.
Losekoot M; Fodde R; Gerritsen EJ; van de Kuit I; Schreuder A; Giordano PC; Vossen JM; Bernini LF
Blood; 1991 Feb; 77(4):861-7. PubMed ID: 1704267
[TBL] [Abstract][Full Text] [Related]
12. Identical mutations in the paralogous human γ-globin genes leading to hemoglobin variants and nondeletional hereditary persistence of fetal hemoglobin.
Papachatzopoulou A; Patrinos GP
Hemoglobin; 2011; 35(2):135-41. PubMed ID: 21417570
[TBL] [Abstract][Full Text] [Related]
13. The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin.
Efremov DG; Dimovski AJ; Huisman TH
Blood; 1994 Jun; 83(11):3350-5. PubMed ID: 7514907
[TBL] [Abstract][Full Text] [Related]
14. Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFH.
Winichagoon P; Fucharoen S; Wilairat P; Chihara K; Fukumaki Y
Br J Haematol; 1994 Aug; 87(4):797-804. PubMed ID: 7527242
[TBL] [Abstract][Full Text] [Related]
15. An A gamma globin promoter (four base-pair deletion) mutant shows linked polymorphic changes throughout the A gamma gene.
Harvey MP; Motum P; Lindeman R; Trent RJ
Exp Hematol; 1992 Mar; 20(3):320-3. PubMed ID: 1373683
[TBL] [Abstract][Full Text] [Related]
16. Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoter.
Ottolenghi S; Nicolis S; Taramelli R; Malgaretti N; Mantovani R; Comi P; Giglioni B; Longinotti M; Dore F; Oggiano L
Blood; 1988 Mar; 71(3):815-7. PubMed ID: 2449927
[TBL] [Abstract][Full Text] [Related]
17. Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure.
Yang KG; Stoming TA; Fei YJ; Liang S; Wong SC; Masala B; Huang RB; Wei ZP; Huisman TH
Blood; 1988 May; 71(5):1414-7. PubMed ID: 2451950
[TBL] [Abstract][Full Text] [Related]
18. A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH.
Surrey S; Delgrosso K; Malladi P; Schwartz E
Blood; 1988 Mar; 71(3):807-10. PubMed ID: 2449926
[TBL] [Abstract][Full Text] [Related]
19. Molecular basis of hereditary persistence of fetal hemoglobin.
Forget BG
Ann N Y Acad Sci; 1998 Jun; 850():38-44. PubMed ID: 9668525
[TBL] [Abstract][Full Text] [Related]
20. Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
Wilcox I; Boettger K; Greene L; Malek A; Davis L; Steinberg MH; Luo HY; Chui DH
Am J Hematol; 2009 Jan; 84(1):55-8. PubMed ID: 19006227
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
