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人皮肤来源的组织培养中的胱硫醚合酶:同型胱氨酸尿症中的酶缺陷。

Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria.

作者信息

Uhlendorf B W, Mudd S H

出版信息

Science. 1968 May 31;160(3831):1007-9. doi: 10.1126/science.160.3831.1007.

Abstract

Fibroblasts derived from normal human skin and from cells in amniotic fluid and grown in tissue culture have cystathionine synthase activity. Skin from homocystinuric patients gives rise to fibroblast lines with normal activities of methionine-activating enzyme, but with very low or undetectable cystathionine synthase activity. Thus, the enzyme lesion in homocystinuria is demonstrable in readily available human cells. Neither cystathionine synthase nor methionine-activating enzyme could be detected in intact normal skin.

摘要

从正常人皮肤以及羊水细胞中获取并在组织培养中生长的成纤维细胞具有胱硫醚合酶活性。同型胱氨酸尿症患者的皮肤产生的成纤维细胞系,其蛋氨酸激活酶活性正常,但胱硫醚合酶活性非常低或无法检测到。因此,在容易获取的人类细胞中可以证明同型胱氨酸尿症中的酶缺陷。在完整的正常皮肤中既检测不到胱硫醚合酶也检测不到蛋氨酸激活酶。

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