Fibroblast culture and inherited neurological diseases.
作者信息
Stewart G
出版信息
Proc R Soc Med. 1971 Feb;64(2):185-6.
Abstract
摘要
相似文献
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Fibroblast culture and inherited neurological diseases.成纤维细胞培养与遗传性神经疾病
Proc R Soc Med. 1971 Feb;64(2):185-6.
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[Changes in acid phosphatase activity induced by vitamin A in cultures of fibroblasts from a patient with mucopolysaccharidosis].
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The self-associating property of fibroblast proteoheparan sulphate.成纤维细胞蛋白聚糖硫酸酯的自缔合特性。
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The tissue culture detection of corrective factor activity for Hurler fibroblasts.对Hurler成纤维细胞校正因子活性的组织培养检测
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The genetic secrets of the humble fibroblast.普通成纤维细胞的基因奥秘。
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Measurement of the ratio of lactate to pyruvate in skin fibroblast cultures.皮肤成纤维细胞培养物中乳酸与丙酮酸比率的测定。
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Effects of gadolinium-based magnetic resonance imaging contrast agents on human skin in organ culture and human skin fibroblasts.钆基磁共振成像造影剂对器官培养中的人体皮肤及人体皮肤成纤维细胞的影响。
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本文引用的文献
1
Properties of galactosemic cells in culture.培养中的半乳糖血症细胞的特性。
Biochem Biophys Res Commun. 1960 Nov;3:518-24. doi: 10.1016/0006-291x(60)90167-4.
2
Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria.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。
Science. 1968 May 31;160(3831):1007-9. doi: 10.1126/science.160.3831.1007.
3
Hurler's syndrome: deficiency of a specific beta galactosidase isoenzyme.胡勒氏综合征：一种特定β-半乳糖苷酶同工酶缺乏症。
Science. 1969 Aug 8;165(3893):611-3. doi: 10.1126/science.165.3893.611.
4
Hurler's syndrome: demonstration of an inherited disorder of connective tissue in cell culture.胡勒氏综合征：细胞培养中一种遗传性结缔组织疾病的证明。
Science. 1965 Aug 27;149(3687):987-9. doi: 10.1126/science.149.3687.987.
5
Glycolipid and mucopolysaccharide abnormality in fibroblasts of fabry's disease.法布里病成纤维细胞中的糖脂和粘多糖异常。
Science. 1969 Jun 27;164(3887):1522-3. doi: 10.1126/science.164.3887.1522.
6
Generalized gangliosidosis: impaired cleavage of galactose from a mucopolysaccharide and a glycoprotien.全身性神经节苷脂沉积症：从黏多糖和糖蛋白中半乳糖的裂解受损。
Science. 1969 Feb 28;163(3870):946-7. doi: 10.1126/science.163.3870.946.
7
The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.黏多糖贮积症Ⅰ型（胡尔勒氏综合征）和黏多糖贮积症Ⅱ型（亨特氏综合征）中的缺陷：黏多糖降解异常。
Proc Natl Acad Sci U S A. 1968 Jun;60(2):699-706. doi: 10.1073/pnas.60.2.699.
8
Limitations of metachromasia as a diagnostic aid in pediatrics.异染性作为儿科诊断辅助手段的局限性。
N Engl J Med. 1969 Nov 13;281(20):1108-11. doi: 10.1056/NEJM196911132812009.
9
Acid mucopolysaccharides in cultured human fibroblasts.培养的人成纤维细胞中的酸性粘多糖
Lancet. 1969 Oct 18;2(7625):838-41. doi: 10.1016/s0140-6736(69)92289-2.
10
Cultivated amniotic-fluid cells and fibroblasts derived from families with cystic fibrosis.来自囊性纤维化家族的培养羊水细胞和成纤维细胞。
Lancet. 1969 Jul 12;2(7611):84-5. doi: 10.1016/s0140-6736(69)92393-9.
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