慢性戈谢病：白细胞葡萄糖脑苷脂酶的耐热性与某些临床参数的关系 - Suppr

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超能文献

Chronic Gaucher's disease: heat-resistance of leukocyte glucocerebrosidase in relation to some clinical parameters.

作者信息

Klibansky C, Hoffman J, Zaizov R, Matoth Y, Pinkhas J, de Vries A

出版信息

Biomedicine. 1973 Aug 10;19(8):345-8.

PMID:4774111

Abstract

摘要

相似文献

Chronic Gaucher's disease: heat-resistance of leukocyte glucocerebrosidase in relation to some clinical parameters.慢性戈谢病：白细胞葡萄糖脑苷脂酶的耐热性与某些临床参数的关系

Biomedicine. 1973 Aug 10;19(8):345-8.

Gaucher's disease, chronic adult type: a comparative study of glucocerebroside and methylumbelliferyl-glucopyranoside cleaving potency in leukocytes.戈谢病，慢性成人型：白细胞中葡萄糖脑苷脂和甲基伞形酮基 - 吡喃葡萄糖苷裂解能力的比较研究

Biomedicine. 1974 Jan;20(1):24-30.

Clinical and biochemical aspects of chronic Gaucher's disease.慢性戈谢病的临床和生化特征

Isr J Med Sci. 1974 Dec;10(12):1523-9.

[Laboratory diagnosis of Gaucher's disease. Value of leukocyte beta-glucosidase determination].[戈谢病的实验室诊断。白细胞β-葡萄糖苷酶测定的价值]

Nouv Presse Med. 1972 Jun 3;1(23):1579-81.

The diagnosis of the adult type of Gaucher's disease and its carrier state by demonstration of deficiency of beta-glucosidase activity in peripheral blood leukocytes.通过检测外周血白细胞中β-葡萄糖苷酶活性缺乏来诊断成人型戈谢病及其携带者状态。

J Lab Clin Med. 1970 Nov;76(5):747-55.

Infantile Gaucher's disease: glucocerebrosidase deficiency in peripheral blood leukocytes and cultured fibroblasts.婴儿型戈谢病：外周血白细胞和培养的成纤维细胞中葡萄糖脑苷脂酶缺乏

Neuropadiatrie. 1975 Nov;6(4):377-82. doi: 10.1055/s-0028-1091678.

Neuropathic Gaucher's disease with normal 4-methylumbelliferyl-beta-glucosidase activity in the liver.肝脏中4-甲基伞形酮基-β-葡萄糖苷酶活性正常的神经性戈谢病。

Pediatr Res. 1977 May;11(5):641-6. doi: 10.1203/00006450-197705000-00004.

[Glucocerebrosidase deficiency and tentative identification of heterozygous carriers in a family with Gaucher's disease type I (author's transl)].1型戈谢病患者家系中的葡萄糖脑苷脂酶缺乏及杂合子携带者的初步鉴定（作者译）

Klin Wochenschr. 1974 Dec 15;52(24):1177-8. doi: 10.1007/BF01466738.

Leukocyte glucocerebrosidase deficiency diagnostic in adult Gaucher's disease with negative bone marrow biopsy. Some properties of the enzyme in leukocytes and spleen.成人戈谢病白细胞葡萄糖脑苷脂酶缺乏症诊断：骨髓活检阴性。白细胞和脾脏中该酶的一些特性。

Eur J Clin Invest. 1974 Apr;4(2):101-7. doi: 10.1111/j.1365-2362.1974.tb00379.x.

The occurrence of beta-glucocerebrosidase activity in the glucocerebroside-rich deposits of Gaucher's disease.β-葡萄糖脑苷脂酶活性在戈谢病富含葡萄糖脑苷脂的沉积物中的出现。

Arch Biochem Biophys. 1974 Jan;160(1):162-7. doi: 10.1016/s0003-9861(74)80022-6.

引用本文的文献

Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single "Gaucher gene".使用单细胞微量分析技术对戈谢病进行互补分析。单一“戈谢基因”的证据。

Hum Genet. 1983;65(2):112-6. doi: 10.1007/BF00286645.

Genetic heterogeneity in Gaucher disease.戈谢病中的基因异质性。

J Med Genet. 1986 Aug;23(4):319-22. doi: 10.1136/jmg.23.4.319.

Properties of beta-glucosidase in cultured skin fibroblasts from controls and patients with Gaucher disease.对照人群和戈谢病患者培养的皮肤成纤维细胞中β-葡萄糖苷酶的特性

Am J Hum Genet. 1978 Jul;30(4):346-58.

Gaucher disease: isolation and comparison of normal and mutant glucocerebrosidase from human spleen tissue.戈谢病：从人脾脏组织中分离并比较正常和突变的葡萄糖脑苷脂酶

Proc Natl Acad Sci U S A. 1978 Aug;75(8):3970-3. doi: 10.1073/pnas.75.8.3970.

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