人-中国仓鼠体细胞杂种中人己糖胺酶A和B的独立缺失 - Suppr | 超能文献

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1

Independent loss of human hexosaminidases A and B in man-chinese hamster somatic cell hybrids.人-中国仓鼠体细胞杂种中人己糖胺酶A和B的独立缺失

Humangenetik. 1973 Apr 16;18(2):171-4. doi: 10.1007/BF00291485.

2

Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybrids.利用人-中国仓鼠细胞杂交体对桑德霍夫病中残余己糖胺酶活性的表征。

Hum Genet. 1977 Dec 23;39(3):315-9. doi: 10.1007/BF00295426.

3

Characterization of beta-D-N-acetylhexosaminidase isoenzymes in man-Chinese hamster somatic cell hybrids.

Am J Hum Genet. 1977 Jan;29(1):14-23.

4

[Genetic study of GM2 gangliosidosis (Tay-Sachs and Sandhoff) by the study of the hexosaminidases of the Sandhoff-rodents hybrids (mouse and hamster)].通过对桑德霍夫啮齿动物杂种（小鼠和仓鼠）的己糖胺酶研究进行GM2神经节苷脂沉积症（泰-萨克斯病和桑德霍夫病）的遗传学研究

Ann Genet. 1975 Sep;18(3):163-8.

5

Synteny relationship between the human loci for hexosaminidase-a, mannose phosphate isomerase, and pyruvate kinase-3 studied in man-Chinese hamster somatic cell hybrids.在中国仓鼠体细胞杂种中研究的人己糖胺酶 - a、磷酸甘露糖异构酶和丙酮酸激酶 - 3基因座之间的同线性关系。

Cytogenet Cell Genet. 1975;14(3-6):455-7. doi: 10.1159/000130406.

6

Enzyme electrophoresis on cellulose acetate gel. II. Zymogram patterns in man-Chinese hamster somatic cell hybrids.醋酸纤维素凝胶上的酶电泳。II. 人 - 中国仓鼠体细胞杂种中的酶谱模式。

Humangenetik. 1974;25(3):189-201. doi: 10.1007/BF00281426.

7

A study of hexosaminadases in interspecific hybrids and in GM2 gangliosidosis with a discussion on their genetic control.种间杂种和GM2神经节苷脂沉积症中己糖胺酶的研究及其遗传控制的讨论

Ann Hum Genet. 1975 Jul;39(1):111-23. doi: 10.1111/j.1469-1809.1975.tb00112.x.

8

Probable existence of hexosaminidase C locus located on chromosome 7 in man.人类7号染色体上可能存在己糖胺酶C基因座。

C R Acad Hebd Seances Acad Sci D. 1974 Mar 25;278(13):1761-4.

9

[Reconstruction of hexosaminidase isoenzymes during hybridization of fibroblasts from Tay-Sachs and Sandhoff diseases].[在泰-萨克斯病和桑德霍夫病成纤维细胞杂交过程中己糖胺酶同工酶的重建]

Biull Eksp Biol Med. 1984 Jan;97(1):83-6.

10

Genetics of somatic mammalian cells: demonstration of a human esterase activator gene linked to the adeB gene.体细胞哺乳动物细胞遗传学：证明一个与adeB基因相连的人类酯酶激活基因。

Proc Natl Acad Sci U S A. 1972 Nov;69(11):3273-7. doi: 10.1073/pnas.69.11.3273.

引用本文的文献

1

Ganglioside storage diseases: an updated review.神经节苷脂贮积病：最新综述

Ital J Neurol Sci. 1981 Aug;2(3):219-26. doi: 10.1007/BF02335401.

2

On the molecular basis of Sandhoff's disease.关于桑德霍夫病的分子基础。

Humangenetik. 1973;20(2):167-70. doi: 10.1007/BF00284854.

3

Enzyme electrophoresis on cellulose acetate gel. II. Zymogram patterns in man-Chinese hamster somatic cell hybrids.醋酸纤维素凝胶上的酶电泳。II. 人 - 中国仓鼠体细胞杂种中的酶谱模式。

本文引用的文献

1

Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase component.泰-萨克斯病：普遍缺乏β-D-N-乙酰己糖胺酶成分。

Science. 1969 Aug 15;165(3894):698-700. doi: 10.1126/science.165.3894.698.

2

Deficient hexozaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.在一例特殊的泰-萨克斯病中，己糖胺酶活性缺乏，同时在内脏器官中额外储存了肾糖苷脂。

Life Sci. 1968 Mar 15;7(6):283-8. doi: 10.1016/0024-3205(68)90024-6.

3

N-Acetyl-beta-glucosaminidases in human spleen.