102 related articles for article (PubMed ID: 19065335)
1. The 5' regulatory region of the human fetal globin genes is a gene conversion hotspot.
Kalamaras A; Chassanidis C; Samara M; Chiotoglou I; Vamvakopoulos NK; Papadakis MN; Kollia P; Patrinos GP
Hemoglobin; 2008; 32(6):572-81. PubMed ID: 19065335
[TBL] [Abstract][Full Text] [Related]
2. Role of intergenic human gamma-delta-globin sequences in human hemoglobin switching and reactivation of fetal hemoglobin in adult erythroid cells.
Bank A; O'Neill D; Lopez R; Pulte D; Ward M; Mantha S; Richardson C
Ann N Y Acad Sci; 2005; 1054():48-54. PubMed ID: 16339651
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Variability in the fetal hemoglobin level of the normal adult.
Leonova JYe ; Kazanetz EG; Smetanina NS; Adekile AD; Efremov GD; Huisman TH
Am J Hematol; 1996 Oct; 53(2):59-65. PubMed ID: 8892728
[TBL] [Abstract][Full Text] [Related]
7. Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.
Bouva MJ; Harteveld CL; Bakker-Verweij G; van Delft P; Giordano PC
Hemoglobin; 2006; 30(3):371-7. PubMed ID: 16840228
[TBL] [Abstract][Full Text] [Related]
8. Gene order in human alpha-globin locus is required for their temporal specific expressions.
Tang Y; Wang Z; Huang Y; Liu DP; Liu G; Shen W; Tang X; Feng D; Liang CC
Genes Cells; 2006 Feb; 11(2):123-31. PubMed ID: 16436049
[TBL] [Abstract][Full Text] [Related]
9. Cluster specific regulation pattern of upstream regulatory elements in human alpha- and beta-globin gene clusters.
Tang Y; Huang Y; Shen W; Liu G; Wang Z; Tang XB; Feng DX; Liu DP; Liang CC
Exp Cell Res; 2008 Jan; 314(1):115-22. PubMed ID: 17996867
[TBL] [Abstract][Full Text] [Related]
10. Understanding mechanisms of gamma-globin gene regulation to develop strategies for pharmacological fetal hemoglobin induction.
Pace BS; Zein S
Dev Dyn; 2006 Jul; 235(7):1727-37. PubMed ID: 16607652
[TBL] [Abstract][Full Text] [Related]
11. Developmental effect of the XmnI site on Ggamma-globin gene expression among newborn Hb F-Malta-I [Ggamma117(G19)His-->Arg, CAT-->CGT] heterozygotes and adult beta+ -Thalassemia homozygotes.
Pulis S; Scerri CA; Wismayer PS; Galdies R; Wettinger SB; Felice AE
Hemoglobin; 2007; 31(1):71-82. PubMed ID: 17365007
[TBL] [Abstract][Full Text] [Related]
12. Delayed decline of gamma-globin expression in infant age associated with the presence of Ggamma-158 (C-->T) polymorphism.
Grosso M; Amendolara M; Rescigno G; Danise P; Todisco N; Izzo P; Amendola G
Int J Lab Hematol; 2008 Jun; 30(3):191-5. PubMed ID: 18479296
[TBL] [Abstract][Full Text] [Related]
13. The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A gamma-158C-->T] results from two independent gene conversion events.
Patrinos GP; Kollia P; Loutradi-Anagnostou A; Loukopoulos D; Papadakis MN
Hum Genet; 1998 Jun; 102(6):629-34. PubMed ID: 9703422
[TBL] [Abstract][Full Text] [Related]
14. Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.
Joly P; Lacan P; Garcia C; Couprie N; Francina A
Blood Cells Mol Dis; 2009; 43(1):53-7. PubMed ID: 19269866
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A new deletion in the beta globin gene cluster associated with high fetal hemoglobin production.
Camaschella C; Serra A; Gottardi E; Alfarano A; Revello D; Bertero MT; Saglio G
Prog Clin Biol Res; 1989; 316B():123-32. PubMed ID: 2482493
[No Abstract] [Full Text] [Related]
17. Organisation of the Hb 1 genes of the Antarctic skate Bathyraja eatonii: new insights into the evolution of globin genes.
Marino K; Boschetto L; de Pascale D; Cocca E
Gene; 2007 Dec; 406(1-2):199-208. PubMed ID: 17997234
[TBL] [Abstract][Full Text] [Related]
18. Mutation screening in the human epsilon-globin gene using single-strand conformation polymorphism analysis.
Papachatzopoulou A; Menounos PG; Kolonelou C; Patrinos GP
Am J Hematol; 2006 Feb; 81(2):136-8. PubMed ID: 16432873
[TBL] [Abstract][Full Text] [Related]
19. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R
Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
[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]
