胎儿血红蛋白遗传性持续存在。纯合子及合并β地中海贫血时胎儿血红蛋白的异质性。 - Suppr

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超能文献

Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia.

作者信息

Huisman T H, Schroeder W A, Charache S, Bethlenfalvay N C, Bouver N, Shelton J R, Shelton J B, Apell G

出版信息

N Engl J Med. 1971 Sep 23;285(13):711-6. doi: 10.1056/NEJM197109232851303.

DOI:10.1056/NEJM197109232851303

PMID:5571129

Abstract

摘要

相似文献

Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia.胎儿血红蛋白遗传性持续存在。纯合子及合并β地中海贫血时胎儿血红蛋白的异质性。

N Engl J Med. 1971 Sep 23;285(13):711-6. doi: 10.1056/NEJM197109232851303.

Hemoglobin heterogeneity.

N Engl J Med. 1971 Sep 23;285(13):746-7. doi: 10.1056/NEJM197109232851308.

The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions.β地中海贫血中胎儿血红蛋白异质性的现状：统一地中海贫血及相关病症中一些观察结果的尝试。

Ann N Y Acad Sci. 1974;232(0):107-24. doi: 10.1111/j.1749-6632.1974.tb20576.x.

Chemical heterogeneity of foetal haemoglobin in the Lepore haemoglobinopathy.

Br J Haematol. 1974 Jun;27(2):319-29. doi: 10.1111/j.1365-2141.1974.tb06799.x.

Nature of foetal haemoglobin in F-thalassaemia.F地中海贫血中胎儿血红蛋白的性质

Br J Haematol. 1971 Dec;21(6):633-42. doi: 10.1111/j.1365-2141.1971.tb02726.x.

Gamma-chain heterogeneity of fetal hemoglobin in nonblack beta- and delta beta- thalassemia and HPFH heterozygotes and homozygotes.非黑人β-地中海贫血、δβ-地中海贫血以及遗传性胎儿血红蛋白持续存在症杂合子和纯合子中胎儿血红蛋白的γ链异质性

Am J Hematol. 1982 Jun;12(4):367-82. doi: 10.1002/ajh.2830120408.

Heterogeneity of fetal hemoglobin among Israel families with beta-thalassemia.

Isr J Med Sci. 1973 Sep-Oct;9(9):1464-8.

Homozygous delta-thalassemia first discovered in Japanese family with hereditary persistence of fetal hemoglobin.

Blood. 1971 Jun;37(6):706-15.

A homozygote for the Hb G type of foetal haemoglobin in India: a study of two Indian and four Negro families.印度一名胎儿血红蛋白Hb G类型的纯合子：对两个印度家庭和四个黑人家庭的研究。

Br J Haematol. 1972 Oct;23(4):403-17. doi: 10.1111/j.1365-2141.1972.tb07075.x.

Delta-beta-thalassaemia in a Chinese family.一个中国家庭中的δ-β地中海贫血

Br J Haematol. 1972 Oct;23(4):393-402. doi: 10.1111/j.1365-2141.1972.tb07074.x.

引用本文的文献

Manipulation of Developmental Gamma-Globin Gene Expression: an Approach for Healing Hemoglobinopathies.调控发育性γ-珠蛋白基因表达：治疗血红蛋白病的一种方法。

Mol Cell Biol. 2020 Dec 21;41(1). doi: 10.1128/MCB.00253-20.

Genome editing using CRISPR-Cas9 to create the HPFH genotype in HSPCs: An approach for treating sickle cell disease and β-thalassemia.使用CRISPR-Cas9进行基因组编辑以在造血干细胞中创建HPFH基因型：一种治疗镰状细胞病和β地中海贫血的方法。

Proc Natl Acad Sci U S A. 2016 Sep 20;113(38):10661-5. doi: 10.1073/pnas.1612075113. Epub 2016 Sep 6.

Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain.三种类型胎儿血红蛋白遗传性持续存在的分子基础异质性以及γ链的Gγ和Aγ类型的相对合成

Biochem Genet. 1984 Feb;22(1-2):21-35. doi: 10.1007/BF00499284.

Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant.Gγ(β)+遗传性胎儿血红蛋白持续存在症和一种中国Aγ遗传性胎儿血红蛋白持续存在症变体中γ-δ-β-珠蛋白区域的限制性内切酶图谱分析

Am J Hum Genet. 1983 Jul;35(4):611-20.

The G and A hemoglobin chains during human fetal development.人类胎儿发育过程中的G和A血红蛋白链。

Am J Hum Genet. 1973 May;25(3):271-6.

Beta-thalassemia in the American Negro.美国黑人中的β地中海贫血

J Clin Invest. 1973 Jun;52(6):1453-9. doi: 10.1172/JCI107319.

Fetal and embryonic haemoglobins.胎儿血红蛋白和胚胎血红蛋白。

J Med Genet. 1973 Mar;10(1):50-64. doi: 10.1136/jmg.10.1.50.

Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.一个捷克斯洛伐克家庭中，β0地中海贫血（移码密码子38/39；-C）和非缺失型瑞士型遗传性胎儿血红蛋白持续存在症（核苷酸-110处A→C，Gγ）的复合杂合性。

Ann Hematol. 1991 Aug;63(2):111-5. doi: 10.1007/BF01707283.

A note on the inheritance of the hereditary persistence of fetal haemoglobin and the delta-chain variant Hb-A2'.关于胎儿血红蛋白遗传性持续存在及δ链变体Hb - A2'遗传方式的注释

J Med Genet. 1976 Feb;13(1):62-3. doi: 10.1136/jmg.13.1.62.

Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.胎儿血红蛋白的遗传性持续存在、β地中海贫血与血红蛋白δ-β基因座：更多家族数据及遗传学解释

Am J Hum Genet. 1975 Mar;27(2):140-54.

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