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[Mutation processes in the formation of hemoglobin variants].

作者信息

Vogel F, Röhrborn G

出版信息

Humangenetik. 1965;1(7):635-50.

PMID:5869486
Abstract
摘要

相似文献

1
[Mutation processes in the formation of hemoglobin variants].[血红蛋白变体形成中的突变过程]
Humangenetik. 1965;1(7):635-50.
2
Point mutations and human hemoglobin variants.点突变与人类血红蛋白变体。
Humangenetik. 1969;8(1):1-26. doi: 10.1007/BF00286751.
3
Study of abnormal hemoglobin in Ehime, Japan: two structural variants of hemoglobin A (Hb I and Hb J Iran) and structural and synthetic variants of delta chain.
Jinrui Idengaku Zasshi. 1984 Sep;29(3):335-51. doi: 10.1007/BF01871249.
4
[Fetal hemoglobin. I. Quantitative analysis of amino acids of crystallized human fetal hemoglobin and various technical devices].[胎儿血红蛋白。I. 结晶人胎儿血红蛋白氨基酸的定量分析及各种技术手段]
Boll Soc Ital Biol Sper. 1955 Mar-Apr;31(3-4):328-30.
5
Amino-acids and proteins in haemoglobin formation; tryptophan.
Biochem J. 1947;41(3):382-8.
6
[THE GENE AND ITS ACTION].[基因及其作用]
Ber Zusammenkunft Dtsch Ophthalmol Ges. 1964;65:18-27.
7
Quantitative immunological studies on single amino acid substitution in human hemoglobin: demonstration of specific antibodies to multiple sites.
Immunochemistry. 1974 Jan;11(1):21-7. doi: 10.1016/0019-2791(74)90338-3.
8
The structure of goat hemoglobins. 3. Hemoglobin D, a beta chain variant with one apparet amino acid substitution (21 Asp--His).山羊血红蛋白的结构。3. 血红蛋白D,一种具有一个明显氨基酸取代(21位天冬氨酸→组氨酸)的β链变体。
Arch Biochem Biophys. 1968 Sep 20;127(1):398-405. doi: 10.1016/0003-9861(68)90242-7.
9
Detection of neutral amino acid substitutions in proteins.蛋白质中中性氨基酸取代的检测。
Proc Natl Acad Sci U S A. 1985 Nov;82(22):7646-50. doi: 10.1073/pnas.82.22.7646.
10
[HEREDITARY DISEASES AND NUCLEIC ACIDS].
Sogo Igaku. 1963 Dec;20:853-60.

引用本文的文献

1
Recurrent mutations in the factor IX gene: founder effect or repeat de novo events. Investigation of the German haemophilia B population and review of de novo mutations.凝血因子IX基因的复发性突变:奠基者效应还是反复的从头事件。对德国B型血友病患者群体的调查及对从头突变的综述。
Hum Genet. 1993 Aug;92(1):40-8. doi: 10.1007/BF00216143.
2
Two further cases of mutation R1947X in the NF1 gene: screening for a relatively common recurrent mutation.
Hum Genet. 1995 Sep;96(3):361-3. doi: 10.1007/BF00210425.
3
Nonrandomness of point mutation as reflected in nucleotide substitutions in pseudogenes and its evolutionary implications.假基因中核苷酸替换所反映的点突变的非随机性及其进化意义。

本文引用的文献

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The reaction of mono- and di-functional alkylating agents with nucleic acids.单官能和双官能烷基化剂与核酸的反应。
Biochem J. 1961 Sep;80(3):496-503. doi: 10.1042/bj0800496.
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HUMAN HAEMOGLOBINS.人类血红蛋白
J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.
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THE EVOLUTION OF HEMOGLOBIN.血红蛋白的进化
J Mol Evol. 1984;21(1):58-71. doi: 10.1007/BF02100628.
4
Hemoglobin E: distribution and population dynamics.血红蛋白E:分布与群体动态
Humangenetik. 1967;3(3):189-234. doi: 10.1007/BF00273124.
5
Point mutations and human hemoglobin variants.点突变与人类血红蛋白变体。
Humangenetik. 1969;8(1):1-26. doi: 10.1007/BF00286751.
6
[Cytogenetic study of a kinship with Fabry-Anderson syndrome (angiokeratoma corporis diffusion universale)].[法布里 - 安德森综合征(全身性弥漫性血管角质瘤)亲缘关系的细胞遗传学研究]
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1969;179(2):118-37. doi: 10.1007/BF00410378.
7
Evidence on the mechanism of spontaneous mutations from human haemoglobin variants and some other proteins.
Humangenetik. 1972;16(1):71-6. doi: 10.1007/BF00393989.
8
Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes.脊椎动物基因组中胞嘧啶甲基化与CpG二核苷酸的命运
Hum Genet. 1989 Sep;83(2):181-8. doi: 10.1007/BF00286715.
9
Use of Chou-Fasman amino acid conformational parameters to analyze the organization of the genetic code and to construct protein genealogies.使用周氏-法斯曼氨基酸构象参数分析遗传密码的组织并构建蛋白质谱系。
J Mol Evol. 1977 Sep 20;10(1):7-47. doi: 10.1007/BF01796133.
10
Higher frequencies of transitions among point mutations.点突变之间转换的频率更高。
J Mol Evol. 1977 Apr 29;9(2):159-80. doi: 10.1007/BF01732746.
Sci Am. 1965 May;212:110-8. doi: 10.1038/scientificamerican0565-110.
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PHYSICAL CHANGES AND MUTAGENESIS.物理变化与诱变作用
J Cell Comp Physiol. 1964 Oct;64:SUPPL 1:51-68.
5
ACRIDINE MUTAGENS AND DNA STRUCTURE.吖啶诱变剂与DNA结构
J Cell Comp Physiol. 1964 Oct;64:SUPPL 1:1-18.
6
REACTION OF SOME MUTAGENIC AND CARCINOGENIC COMPOUNDS WITH NUCLEIC ACIDS.
J Cell Comp Physiol. 1964 Oct;64:SUPPL 1:111-27.
7
[The structure of normal adult human hemoglobins].[正常成人血红蛋白的结构]
Hoppe Seylers Z Physiol Chem. 1961 Sep 20;325:283-6. doi: 10.1515/bchm2.1961.325.1.283.
8
Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin.人类血红蛋白中的基因突变:正常血红蛋白与镰状细胞血红蛋白的化学差异。
Nature. 1957 Aug 17;180(4581):326-8. doi: 10.1038/180326a0.
9
A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin.正常人类血红蛋白和镰状细胞贫血血红蛋白中珠蛋白的特定化学差异。
Nature. 1956 Oct 13;178(4537):792-4. doi: 10.1038/178792a0.
10
Abnormal haemoglobins and the genetic code.异常血红蛋白与遗传密码
Nature. 1965 Jul 17;207(994):259-61. doi: 10.1038/207259a0.