β-半乳糖苷酶缺乏型粘脂贮积症：体细胞杂种中神经氨酸酶的互补研究 - Suppr

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超能文献

beta-Galactosidase deficient-type mucolipidosis: a complementation study of neuraminidase in somatic cell hybrids.

作者信息

Kato T, Okada S, Yutaka T, Inui K, Yabuuchi H, Chiyo H, Furuyama J I, Okada Y

出版信息

Biochem Biophys Res Commun. 1979 Nov 14;91(1):114-7. doi: 10.1016/0006-291x(79)90590-4.

DOI:10.1016/0006-291x(79)90590-4

PMID:518612

Abstract

摘要

相似文献

beta-Galactosidase deficient-type mucolipidosis: a complementation study of neuraminidase in somatic cell hybrids.β-半乳糖苷酶缺乏型粘脂贮积症：体细胞杂种中神经氨酸酶的互补研究

Biochem Biophys Res Commun. 1979 Nov 14;91(1):114-7. doi: 10.1016/0006-291x(79)90590-4.

Human beta-galactosidase and alpha-neuraminidase deficient mucolipidosis: genetic complementation analysis of the neuraminidase deficiency.人类β-半乳糖苷酶和α-神经氨酸酶缺乏型黏脂贮积症：神经氨酸酶缺乏的遗传互补分析

Hum Genet. 1982;60(2):158-62. doi: 10.1007/BF00569704.

The complementation of beta-galactosidase in fused cells of mucolipidosis II with another variants of beta-galactosidase deficiency using new single cell enzyme assay.利用新型单细胞酶检测法，在黏脂贮积症II型融合细胞中β-半乳糖苷酶与β-半乳糖苷酶缺乏的其他变体之间的互补作用。

Biochem Biophys Res Commun. 1979 May 28;88(2):559-62. doi: 10.1016/0006-291x(79)92084-9.

Oligosaccharide and ganglioside neuraminidase activities of mucolipidosis I (sialidosis) and mucolipidosis II (I-cell disease) fibroblasts.黏脂贮积症I型（唾液酸沉积症）和黏脂贮积症II型（I-细胞病）成纤维细胞的寡糖和神经节苷脂神经氨酸酶活性

Eur J Biochem. 1979 Jun;97(1):113-8. doi: 10.1111/j.1432-1033.1979.tb13091.x.

Genetic heterogeneity in human neuraminidase deficiency.人类神经氨酸酶缺乏症中的遗传异质性。

Nature. 1980 Jun 12;285(5765):500-2. doi: 10.1038/285500a0.

Adult mucolipidosis with beta-galactosidase and neuraminidase deficiencies.伴有β-半乳糖苷酶和神经氨酸酶缺乏的成人粘脂贮积症

J Neurol Sci. 1980 May;46(2):245-54. doi: 10.1016/0022-510x(80)90083-0.

Adult type GMl-gangliosidosis: a complementation study on somatic cell hybrids.成人型GM1-神经节苷脂贮积症：体细胞杂种的互补研究。

Brain Dev. 1979;1(2):83-6. doi: 10.1016/s0387-7604(79)80014-5.

Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblasts.通过与溶酶体酶缺陷型人成纤维细胞杂交纠正I-细胞缺陷。

Am J Hum Genet. 1980 Jul;32(4):519-28.

[Studies on sialidosis and mucolipidosis. Properties of neuraminidase in cultured skin fibroblasts].[涎酸沉积症和粘脂贮积症的研究。培养皮肤成纤维细胞中神经氨酸酶的特性]

Biochim Biophys Acta. 1982 Sep 7;706(2):212-20. doi: 10.1016/0167-4838(82)90489-7.

Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders.唾液酸沉积症和半乳糖唾液酸沉积症：与神经氨酸酶缺乏症相关的两个基因的染色体定位

Proc Natl Acad Sci U S A. 1986 Mar;83(6):1817-21. doi: 10.1073/pnas.83.6.1817.

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Characterization of human placental neuraminidases. Stability, substrate specificity and molecular weight.人胎盘神经氨酸酶的特性：稳定性、底物特异性及分子量

Biochem J. 1982 Aug 1;205(2):345-51. doi: 10.1042/bj2050345.

Hum Genet. 1982;60(2):158-62. doi: 10.1007/BF00569704.

Combined deficiency of beta-galactosidase and neuraminidase: three affected siblings in a French family.

J Inherit Metab Dis. 1981;4(4):221-3. doi: 10.1007/BF02263656.

Diagnosis of Tay-Sachs disease using radiolabelled chondroitin 6-sulphate-derived trisaccharides.

J Inherit Metab Dis. 1983;6(3):135-6. doi: 10.1007/BF01800749.

A severe infantile sialidosis (beta-galactosidase-alpha-neuraminidase deficiency) mimicking GM1-gangliosidosis type 1.一种酷似1型GM1神经节苷脂贮积症的严重婴儿唾液酸沉积症（β-半乳糖苷酶-α-神经氨酸酶缺乏症）

Eur J Pediatr. 1983 Sep;140(4):295-8. doi: 10.1007/BF00442667.

Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.异染性脑白质营养不良和多种硫酸酯酶缺乏症成纤维细胞的体细胞杂种中芳基硫酸酯酶A的互补作用。

Proc Natl Acad Sci U S A. 1980 Oct;77(10):6166-70. doi: 10.1073/pnas.77.10.6166.

Genetic analysis of liver neuraminidase isozymes in Rattus norvegicus: independent control of NEU-1 and NEU-2 phenotypes.褐家鼠肝脏神经氨酸酶同工酶的遗传分析：NEU-1和NEU-2表型的独立控制

Genetics. 1986 Sep;114(1):247-58. doi: 10.1093/genetics/114.1.247.

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