肌酸激酶同工酶（MPI）、丙酮酸激酶M2型（PKM2）、异柠檬酸脱氢酶（IDHM）和己糖胺酶α亚基（HEXA）定位于人类染色体15的q21至qter区域。 - Suppr

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超能文献

Localization of MPI, PKM2, IDHM, and the alpha subunit of hexosaminidase (HEXA) to the q21 leads to qter region of human chromosome 15.

作者信息

Hellkuhl B, Mayr W R, Grzeschik K H

出版信息

Cytogenet Cell Genet. 1978;22(1-6):503-5. doi: 10.1159/000131008.

DOI:10.1159/000131008

PMID:752530

Abstract

摘要

相似文献

Localization of MPI, PKM2, IDHM, and the alpha subunit of hexosaminidase (HEXA) to the q21 leads to qter region of human chromosome 15.肌酸激酶同工酶（MPI）、丙酮酸激酶M2型（PKM2）、异柠檬酸脱氢酶（IDHM）和己糖胺酶α亚基（HEXA）定位于人类染色体15的q21至qter区域。

Cytogenet Cell Genet. 1978;22(1-6):503-5. doi: 10.1159/000131008.

Assignment of the structural genes for the alpha subunit of hexosaminidase A, mannosephosphate isomerase, and pyruvate kinase to the region q22-qter of human chromosome 15.将己糖胺酶A的α亚基、甘露糖磷酸异构酶和丙酮酸激酶的结构基因定位于人类15号染色体的q22-qter区域。

Somatic Cell Genet. 1977 Nov;3(6):553-60. doi: 10.1007/BF01539065.

Regional assignment of genes for mannose phosphate isomerase, pyruvate kinase-3, and beta 2-microglobulin expression on human chromosome 15 by hybridization of cells from a t(15;22) (q14;q13.3) translocation carrier.通过对一名t(15;22)(q14;q13.3)易位携带者的细胞进行杂交，将磷酸甘露糖异构酶、丙酮酸激酶-3和β2-微球蛋白表达相关基因定位到人类15号染色体上。

Cytogenet Cell Genet. 1978;22(1-6):506-10. doi: 10.1159/000131009.

Pig gene mapping: PKM2-MPI-NP synteny.猪基因图谱：丙酮酸激酶M2-磷酸甘露糖异构酶-神经肽酶同线性

Cytogenet Cell Genet. 1981;30(1):59-62. doi: 10.1159/000131590.

The genes coding for pyruvate kinase (M2) and mannosephosphate isomerase are linked in man and mouse.编码丙酮酸激酶（M2）和甘露糖磷酸异构酶的基因在人和小鼠中是连锁的。

Cytogenet Cell Genet. 1978;22(1-6):581-4. doi: 10.1159/000131028.

Assignment of the human genes for mannose phosphate isomerase, pyruvate kinase (M2), and hexosaminidase-A to chromosome 15.将人类磷酸甘露糖异构酶、丙酮酸激酶（M2）和氨基己糖苷酶A的基因定位于15号染色体。

Cytogenet Cell Genet. 1976;16(1-5):181-3. doi: 10.1159/000130585.

Birth Defects Orig Artic Ser. 1976;12(7):181-3.

Assignment of hexosaminidase-B to chromosome 5, its segregation after diphtheria toxin selection, and the linkage of hexosaminidase-A, mannose phosphate isomerase, and pyruvate kinase (M2).己糖胺酶B定位于5号染色体、经白喉毒素选择后的分离以及己糖胺酶A、磷酸甘露糖异构酶和丙酮酸激酶（M2）的连锁关系

Birth Defects Orig Artic Ser. 1976;12(7):188-91.

Assignment of hexosaminidase-B to chromosome 5, its segregation after diphtheria toxin selection, and the linkage of hexosaminidase-A, mannose phosphate isomerase, and pyruvate kinase (M2).己糖胺酶B定位于5号染色体、经白喉毒素筛选后的分离情况以及己糖胺酶A、磷酸甘露糖异构酶和丙酮酸激酶（M2）的连锁关系

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Chromosome mapping in domestic pigs (Sus scrofa): MPI and NP located to chromosome 7.家猪（野猪）的染色体图谱：MPI和NP定位于7号染色体。

Hereditas. 1985;102(2):231-5. doi: 10.1111/j.1601-5223.1985.tb00620.x.

引用本文的文献

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.一个来自人类X染色体短臂的DNA片段，它能检测到Y染色体长臂上的一个部分同源序列。

Nucleic Acids Res. 1984 May 25;12(10):4097-109. doi: 10.1093/nar/12.10.4097.

Actin-like sequences are present on human X and Y chromosomes.肌动蛋白样序列存在于人类X和Y染色体上。

EMBO J. 1984 Aug;3(8):1803-7. doi: 10.1002/j.1460-2075.1984.tb02049.x.

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).凝血因子IX基因（B型血友病位点）在人类X染色体上的区域定位及多态性

Proc Natl Acad Sci U S A. 1984 Jan;81(2):498-502. doi: 10.1073/pnas.81.2.498.

Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome.人类Y染色体与X染色体长臂之间存在广泛的DNA序列同源性。

EMBO J. 1985 Jul;4(7):1739-43. doi: 10.1002/j.1460-2075.1985.tb03844.x.

Molecular cloning of a DNA fragment from human chromosome 14(14q11) involved in T-cell malignancies.参与T细胞恶性肿瘤的人14号染色体（14q11）DNA片段的分子克隆。

EMBO J. 1985 Dec 16;4(13A):3427-33. doi: 10.1002/j.1460-2075.1985.tb04100.x.

Interstitial deletion of chromosome 15: two cases.15号染色体间质缺失：两例报告

Hum Genet. 1988 Dec;80(4):401-4. doi: 10.1007/BF00273663.

The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene--a useful marker for human chromosome 2.人类载脂蛋白B基因基因组重组体的分离及该基因三个常见DNA多态性的定位——人类2号染色体的一个有用标记。

Hum Genet. 1986 Aug;73(4):313-9. doi: 10.1007/BF00279093.

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome.一组用于人类X染色体区域定位的X连锁序列及一组体细胞杂种的特征分析。

Hum Genet. 1986 Jan;72(1):43-9. doi: 10.1007/BF00278816.

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