95 related articles for article (PubMed ID: 21035360)
1. Molecular identification of the novel Gγ-β hybrid hemoglobin: Hb Gγ-β Ulsan (Gγ through 13; β from 19).
Kim SY; Lee SH; Cho SI; Song SH; Hattori Y; Park SK; Song J; Choi Y; Yang M; Park H; Kim SR; Seong MW; Kim JY; Cho HI; Park SS
Blood Cells Mol Dis; 2010 Dec; 45(4):276-9. PubMed ID: 21035360
[TBL] [Abstract][Full Text] [Related]
2. Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.
Lou JW; Li Q; Wei XF; Huang JW; Xu XM
Hemoglobin; 2010; 34(4):343-53. PubMed ID: 20642332
[TBL] [Abstract][Full Text] [Related]
3. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer.
Sangkitporn SK; Eksiri L; Sangnoi A; Duangruang S; Dumbua A; Rattanakittisophon K; Sangkitporn S
Int J Lab Hematol; 2009 Oct; 31(5):521-7. PubMed ID: 18498386
[TBL] [Abstract][Full Text] [Related]
6. Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families.
Voruganti I; Eng B; Waye JS
Hemoglobin; 2009; 33(6):422-7. PubMed ID: 19958187
[TBL] [Abstract][Full Text] [Related]
7. Axolotl hemoglobin: cDNA-derived amino acid sequences of two alpha globins and a beta globin from an adult Ambystoma mexicanum.
Shishikura F; Takeuchi HA; Nagai T
Comp Biochem Physiol B Biochem Mol Biol; 2005 Nov; 142(3):258-68. PubMed ID: 16143550
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic variation in mouse beta globin cysteine content modifies glutathione metabolism: implications for the use of mouse models.
Hempe JM; Ory-Ascani J; Hsia D
Exp Biol Med (Maywood); 2007 Mar; 232(3):437-44. PubMed ID: 17327478
[TBL] [Abstract][Full Text] [Related]
10. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
[TBL] [Abstract][Full Text] [Related]
11. Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster.
Lee ST; Yoo EH; Kim JY; Kim JW; Ki CS
Br J Haematol; 2010 Jan; 148(1):154-60. PubMed ID: 19807730
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes].
Chen JF; Long GF; Lin WX; Chen P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181
[TBL] [Abstract][Full Text] [Related]
14. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
[TBL] [Abstract][Full Text] [Related]
15. Comprehensive and efficient HBB mutation analysis for detection of beta-hemoglobinopathies in a pan-ethnic population.
Chan OT; Westover KD; Dietz L; Zehnder JL; Schrijver I
Am J Clin Pathol; 2010 May; 133(5):700-7. PubMed ID: 20395516
[TBL] [Abstract][Full Text] [Related]
16. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC
Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
[TBL] [Abstract][Full Text] [Related]
17. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
Lemsaddek W; Picanço I; Seuanes F; Mahmal L; Benchekroun S; Khattab M; Nogueira P; Osório-Almeida L
Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of a beta-globin gene deletion of 1357 bp in a Taiwanese beta-thalassemia carrier.
Huang CH; Chang YY; Chen CH; Ko TM
Hemoglobin; 2008; 32(5):498-504. PubMed ID: 18932076
[TBL] [Abstract][Full Text] [Related]
20. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
