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Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.

作者信息

Wood W G, Clegg J B, Weatherall D J

出版信息

Br J Haematol. 1979 Dec;43(4):509-20. doi: 10.1111/j.1365-2141.1979.tb03784.x.

DOI:10.1111/j.1365-2141.1979.tb03784.x
PMID:93487
Abstract
摘要

相似文献

1
Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.胎儿血红蛋白遗传性持续存在（HPFH）与δβ地中海贫血
Br J Haematol. 1979 Dec;43(4):509-20. doi: 10.1111/j.1365-2141.1979.tb03784.x.
2
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.β-珠蛋白基因簇中两种不同疾病的相互作用与血红蛋白F产量增加相关：一种新型缺失型（G）γ+（（A）γδβ）（0）-地中海贫血和一种δ（0）-胎儿血红蛋白遗传性持续决定因素。
Blood. 1991 Feb 15;77(4):861-7.
3
delta beta-Thalassemia and HPFH.δβ地中海贫血和遗传性胎儿血红蛋白持续增多症
Birth Defects Orig Artic Ser. 1982;18(7):65-7.
4
Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia.希腊遗传性胎儿血红蛋白持续存在症中Gγ血红蛋白F的出现：β地中海贫血杂合子和复合杂合子的分析
Br J Haematol. 1979 Dec;43(4):521-36. doi: 10.1111/j.1365-2141.1979.tb03785.x.
5
Delta beta thalassemia and hereditary persistence of fetal hemoglobin.δ地中海贫血与胎儿血红蛋白遗传性持续存在
Hematol Oncol Clin North Am. 1991 Jun;5(3):399-422.
6
beta Thalassemia associated with increased HB F production. Evidence for the existence of a heterocellular hereditary persistence of fetal hemoglobin (HPFH) determinant linked to beta thalassemia in a southern Italian population.与血红蛋白F（HB F）生成增加相关的β地中海贫血。在意大利南部人群中存在与β地中海贫血相关的胎儿血红蛋白（HPFH）决定簇异细胞遗传性持续存在的证据。
Hemoglobin. 1981;5(1):1-17. doi: 10.3109/03630268108996907.
7
Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.非缺失型胎儿血红蛋白遗传性持续存在与δβ地中海贫血的复合杂合性
Am J Hematol. 2008 Sep;83(9):760. doi: 10.1002/ajh.21243.
8
Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.异细胞遗传性胎儿血红蛋白持续存在症、β（+）地中海贫血和δβ（0）地中海贫血的关联：血液学和分子学方面
J Med Genet. 1984 Aug;21(4):263-7. doi: 10.1136/jmg.21.4.263.
9
Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH).胎儿血红蛋白遗传性持续存在（HPFH）中珠蛋白基因缺失的物理图谱分析。
Nucleic Acids Res. 1980 Apr 11;8(7):1521-34. doi: 10.1093/nar/8.7.1521.
10
Globin gene deletion in HPFH, delta (o) beta (o) thalassaemia and Hb Lepore disease.遗传性胎儿血红蛋白持续增多症、δ（0）β（0）地中海贫血和血红蛋白 Lepore 病中的珠蛋白基因缺失。
Nature. 1979 Apr 12;278(5705):654-7. doi: 10.1038/278654a0.

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Identification of a rare [γ(γδβ)] -thalassemia using tandem mass spectrometry.应用串联质谱技术鉴定罕见的 [γ(γδβ)] -地中海贫血。
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Disruption of the MBD2-NuRD complex but not MBD3-NuRD induces high level HbF expression in human adult erythroid cells.破坏 MBD2-NuRD 复合物而不是 MBD3-NuRD 可在人类成红细胞中诱导高水平的 HbF 表达。
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Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia-Current Status and Perspectives in Fetal Hemoglobin Reactivation.
治疗β地中海贫血和镰状细胞贫血的天然疗法——胎儿血红蛋白再激活的现状与展望
Int Sch Res Notices. 2014 Oct 2;2014:123257. doi: 10.1155/2014/123257. eCollection 2014.
4
HIF prolyl hydroxylase inhibition results in endogenous erythropoietin induction, erythrocytosis, and modest fetal hemoglobin expression in rhesus macaques.低氧诱导因子脯氨酰羟化酶抑制导致恒河猴内源性促红细胞生成素诱导、红细胞增多以及胎儿血红蛋白适度表达。
Blood. 2007 Sep 15;110(6):2140-7. doi: 10.1182/blood-2007-02-073254. Epub 2007 Jun 8.
5
Genetic and molecular diversity in nondeletion Hb H disease.非缺失型血红蛋白H病的遗传和分子多样性。
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5833-7. doi: 10.1073/pnas.78.9.5833.
6
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.Gγβ⁺遗传性胎儿血红蛋白持续存在：黏粒克隆及Gγ基因5'端特定突变的鉴定
Proc Natl Acad Sci U S A. 1984 Aug;81(15):4894-8. doi: 10.1073/pnas.81.15.4894.
7
Delta beta (F)-thalassaemia in Sardinia.撒丁岛的δβ（F）-地中海贫血
J Med Genet. 1982 Jun;19(3):184-92. doi: 10.1136/jmg.19.3.184.
8
Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?δβ地中海贫血与胎儿血红蛋白DNA遗传性持续存在的分子比较：调控区域的证据？
Proc Natl Acad Sci U S A. 1982 Apr;79(7):2347-51. doi: 10.1073/pnas.79.7.2347.
9
Interaction of alpha- and delta beta o- thalassaemia: haematological features and globin chain synthesis analysis.α和δβ地中海贫血的相互作用：血液学特征及珠蛋白链合成分析
J Med Genet. 1981 Feb;18(1):40-2. doi: 10.1136/jmg.18.1.40.
10
Molecular characterization of a novel form of (A gamma delta beta)zero-thalassemia deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism.
Nucleic Acids Res. 1988 Jul 11;16(13):6057-66. doi: 10.1093/nar/16.13.6057.