The biochemistry of familial hypercholesterolaemia.
作者信息
Myant N B
出版信息
Biochem Soc Trans. 1976;4(4):580-4. doi: 10.1042/bst0040580.
PMID:187482
Abstract
摘要
相似文献
1
The biochemistry of familial hypercholesterolaemia.
Biochem Soc Trans. 1976;4(4):580-4. doi: 10.1042/bst0040580.
2
Familial hypercholesterolemia: unraveling a genetic receptor disease.
Trans Assoc Am Physicians. 1977;90:91-108.
3
Familial hypercholesterolemia: A genetic defect in the low-density lipoprotein receptor.家族性高胆固醇血症：低密度脂蛋白受体的一种基因缺陷。
N Engl J Med. 1976 Jun 17;294(25):1386-90. doi: 10.1056/NEJM197606172942509.
4
The metabolic lesion in familial hypercholesterolaemia.
Expos Annu Biochim Med. 1977;33:39-52.
5
The LDL receptor and HMG-CoA reductase--two membrane molecules that regulate cholesterol homeostasis.
Curr Top Cell Regul. 1985;26:3-15. doi: 10.1016/b978-0-12-152826-3.50008-5.
6
Use of fibroblast culture to diagnose and genotype familial hypercholesterolaemia.利用成纤维细胞培养诊断家族性高胆固醇血症并进行基因分型。
Ann Nutr Metab. 1982;26(4):240-7. doi: 10.1159/000176569.
7
Regulation of lipid synthesis by low density lipoproteins in cultured skin fibroblasts in homozygous familial hypercholesterolemia.纯合子家族性高胆固醇血症患者培养的皮肤成纤维细胞中低密度脂蛋白对脂质合成的调节作用
Biochim Biophys Acta. 1977 Jun 22;487(3):445-57. doi: 10.1016/0005-2760(77)90215-6.
8
Use of mutant fibroblasts in the analysis of the regulation of cholesterol metabolism in human cells.突变成纤维细胞在人类细胞胆固醇代谢调节分析中的应用。
J Cell Physiol. 1975 Apr;85(2 Pt 2 Suppl 1):425-36. doi: 10.1002/jcp.1040850409.
9
Human mutations affecting the low density lipoprotein pathway.
Curr Concepts Nutr. 1979;8:173-8.
10
[Homozygote familial hypercholesterinemia. Pathophysiology and genetic control of cholesterol metabolism].
Med Klin. 1978 Jun 9;73(23):849-54.
Zotero 插件