人类中苹果酸氧化还原酶脱羧基因定位于6号染色体，肽酶B和乳酸脱氢酶B基因定位于12号染色体。 - Suppr

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超能文献

Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man.

作者信息

Chen T R, McMorris F A, Creagan R, Ricciuti F, Tischfield J, Ruddle F

出版信息

Am J Hum Genet. 1973 Mar;25(2):200-7.

PMID:4689040

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1762508/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1dc/1762508/398ecb66466c/ajhg00447-0088-a.jpg

相似文献

Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man.人类中苹果酸氧化还原酶脱羧基因定位于6号染色体，肽酶B和乳酸脱氢酶B基因定位于12号染色体。

Am J Hum Genet. 1973 Mar;25(2):200-7.

Genetic analysis with man-mouse somatic cell hybrids. Linkage between human lactate dehydrogenase A and B and peptidase B.用人-鼠体细胞杂种进行基因分析。人乳酸脱氢酶A和B与肽酶B之间的连锁关系。

Nature. 1970 Jul 18;227(5255):251-7. doi: 10.1038/227251a0.

Linkage relationships of seventeen human gene loci as determined by man--mouse somatic cell hybrids.通过人-小鼠体细胞杂种确定的17个人类基因位点的连锁关系。

Nat New Biol. 1971 Jul 21;232(29):69-73. doi: 10.1038/newbio232069a0.

Localization of human gene loci using spontaneous chromosome rearrangements in human-Chinese hamster somatic cell hybrids.利用人-中国仓鼠体细胞杂种中的自发染色体重排对人类基因座进行定位。

Am J Hum Genet. 1975 Sep;27(5):595-608.

[Gene localization in the chimpanzee (Pan troglodytes). Comparison with the factor mapping of man (Homo sapiens)].[黑猩猩（Pan troglodytes）的基因定位。与人类（Homo sapiens）的因子定位比较]

Ann Genet. 1975 Sep;18(3):169-77.

Genetics of human-mouse somatic cell hybrids: linkage of human genes for isocitrate dehydrogenase and malate dehydrogenase.人-小鼠体细胞杂种的遗传学：异柠檬酸脱氢酶和苹果酸脱氢酶的人类基因连锁

Biochem Genet. 1972 Dec;7(3):193-204. doi: 10.1007/BF00484817.

Loss of human genetic markers in man--Chinese hamster somatic cell hybrids.人类遗传标记在人-中国仓鼠体细胞杂种中的丢失

Nat New Biol. 1971 Nov 3;234(44):20-4. doi: 10.1038/newbio234020a0.

Assignment of genes to human chromosomes by somatic cell genetics.

Birth Defects Orig Artic Ser. 1973 Jan;9(1):188-93.

Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids. Assignment of PGM3 to chromosome C6 and regional mapping of the PGD, PGM1 and pep-C genes on chromosome A1.通过对人-中国仓鼠体细胞杂种的研究进行人类染色体上基因的定位。将磷酸葡萄糖变位酶3（PGM3）定位于6号染色体C组，并对1号染色体A组上的磷酸葡萄糖脱氢酶（PGD）、磷酸葡萄糖变位酶1（PGM1）和羧肽酶C（pep-C）基因进行区域定位。

Humangenetik. 1973 Dec 10;20(3):195-202. doi: 10.1007/BF00385730.

Assignment of three human genes to chromosomes (LDH-A to 11, TK to 17, and IDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids (thymidine kinase-lactate dehydrogenase A-isocitrate dehydrogenase-C-11, E-17, and F-20 chromosomes).将三个人类基因定位到染色体上（乳酸脱氢酶A基因定位于11号染色体，胸苷激酶基因定位于17号染色体，异柠檬酸脱氢酶基因定位于20号染色体），以及在体细胞杂种中人类与小鼠染色体之间发生易位的证据（胸苷激酶 - 乳酸脱氢酶A - 异柠檬酸脱氢酶 - C - 11号染色体、E - 17号染色体和F - 20号染色体）。

Proc Natl Acad Sci U S A. 1972 Feb;69(2):510-4. doi: 10.1073/pnas.69.2.510.

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The Rasgrf1-repeat sequence (D9Ncvs53) maps between Mod1 and Rbp1 on mouse chromosome 9 and may define a putative imprinted region.Rasgrf1重复序列（D9Ncvs53）定位于小鼠9号染色体上的Mod1和Rbp1之间，可能界定一个假定的印记区域。

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Immunogenetics. 1981;14(3-4):231-40. doi: 10.1007/BF00342192.

Defining the locus of origin of a genetically determined electrophoretic variant of a multilocus enzyme system; the Calcutta-1 of human LDH system is a B-locus variant.确定多基因座酶系统中一种由遗传决定的电泳变异体的起源位点；人类乳酸脱氢酶系统的加尔各答-1是一种B基因座变异体。

Hum Genet. 1981;57(3):290-5. doi: 10.1007/BF00278947.

Linkage of the structural gene for uroporphyrinogen I synthase to markers on mouse chromosome 9 in a cross between feral and inbred mice.野生小鼠与近交系小鼠杂交中，尿卟啉原I合酶结构基因与小鼠9号染色体上标记的连锁关系。

Biochem Genet. 1982 Aug;20(7-8):703-10. doi: 10.1007/BF00483967.

Genetic manipulation by means of microcell-mediated transfer of normal human chromosomes into recipient mouse cells.通过微细胞介导将正常人染色体转移到受体小鼠细胞中进行基因操作。

Proc Natl Acad Sci U S A. 1980 Sep;77(9):5394-8. doi: 10.1073/pnas.77.9.5394.

Localization of a gene which complements branched-chain amino acid transaminase deficiency to the short arm of human chromosome 12.一个可弥补支链氨基酸转氨酶缺陷的基因在人类12号染色体短臂上的定位。

Hum Genet. 1984;66(2-3):206-11. doi: 10.1007/BF00286602.

Estimation of the gene frequency of lactate dehydrogenase subunit deficiencies.乳酸脱氢酶亚基缺乏症基因频率的估计。

Am J Hum Genet. 1984 Nov;36(6):1204-14.

A null mutation at the mouse Phosphoglucomutase-1 locus and a new locus Pgm-3.小鼠磷酸葡萄糖变位酶-1基因座的无效突变及一个新基因座Pgm-3。

Biochem Genet. 1981 Jun;19(5-6):599-615. doi: 10.1007/BF00484629.

本文引用的文献

VIRUS-CELL INTERACTION WITH A TUMOR-PRODUCING VIRUS.病毒与致瘤病毒的细胞相互作用

Proc Natl Acad Sci U S A. 1960 Mar;46(3):365-70. doi: 10.1073/pnas.46.3.365.

SELECTION OF HYBRIDS FROM MATINGS OF FIBROBLASTS IN VITRO AND THEIR PRESUMED RECOMBINANTS.体外成纤维细胞交配产生的杂种及其假定重组体的选择

Science. 1964 Aug 14;145(3633):709-10. doi: 10.1126/science.145.3633.709.

Nature. 1970 Jul 18;227(5255):251-7. doi: 10.1038/227251a0.

Genetic analysis with man-mouse somatic cell hybrids. Linkage between human lactate dehydrogenase B and peptidase B genes.用人-鼠体细胞杂种进行基因分析。人类乳酸脱氢酶B基因与肽酶B基因之间的连锁关系。

Nature. 1970 Jul 18;227(5255):248-51. doi: 10.1038/227248a0.

Human-mouse hybrid cell lines containing partial complements of human chromosomes and functioning human genes.含有部分人类染色体互补物和功能性人类基因的人-鼠杂交细胞系。

Proc Natl Acad Sci U S A. 1967 Sep;58(3):1104-11. doi: 10.1073/pnas.58.3.1104.

Starch gel electrophoretic phenotypes of mouse times human somatic cell hybrids and mouse isozyme polymorphisms.小鼠与人类体细胞杂种的淀粉凝胶电泳表型及小鼠同工酶多态性

In Vitro. 1971 Nov-Dec;7(3):120-31. doi: 10.1007/BF02617955.

Evidence for ancient tetraploidy and conservation of linkage groups in mammalian chromosomes.

Nature. 1972 Aug 25;238(5365):455-7. doi: 10.1038/238455a0.

Genetics of somatic mammalian cells: lethal antigens as genetic markers for study of human linkage groups.哺乳动物体细胞遗传学：致死抗原作为研究人类连锁群的遗传标记。

Proc Natl Acad Sci U S A. 1971 Dec;68(12):3102-6. doi: 10.1073/pnas.68.12.3102.

Controlled production of proliferating somatic cell hybrids.增殖性体细胞杂种的可控生产。

J Cell Biol. 1970 Apr;45(1):74-82. doi: 10.1083/jcb.45.1.74.

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.人类中期染色体的24种荧光模式——鉴别特征与变异性

Hereditas. 1972;67(1):89-102. doi: 10.1111/j.1601-5223.1971.tb02363.x.

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