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Familial lecithin:cholesterol acyltransferase deficiency. Studies on lipid composition and morphology of tissues.

作者信息

Stokke K T, Bjerve K S, Blomhoff J P, Oystese B, Flatmark A, Norum K R, Gjone E

出版信息

Scand J Clin Lab Invest Suppl. 1974;137:93-100.

PMID:4367608
Abstract
摘要

相似文献

1
Familial lecithin:cholesterol acyltransferase deficiency. Studies on lipid composition and morphology of tissues.家族性卵磷脂：胆固醇酰基转移酶缺乏症。组织脂质成分与形态学研究。
Scand J Clin Lab Invest Suppl. 1974;137:93-100.
2
Familial lecithin:cholesterol acyltransferase deficiency. Ultrastructural studies on lipid deposition and tissue reactions.家族性卵磷脂：胆固醇酰基转移酶缺乏症。脂质沉积和组织反应的超微结构研究。
Scand J Clin Lab Invest Suppl. 1974;137:135-46.
3
Familial plasma lecithin: cholesterol acyltransferase (LCAT) deficiency. Ultrastructural aspects of a new syndrome with particular reference to lesions in the kidneys and the spleen.家族性血浆卵磷脂：胆固醇酰基转移酶（LCAT）缺乏症。一种新综合征的超微结构特征，特别提及肾脏和脾脏的病变。
Acta Pathol Microbiol Scand A. 1973 Sep;81(5):681-97.
4
Familial lecithin:cholesterol acyltransferase deficiency--a clinical survey.
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5
Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members.家族性卵磷脂：胆固醇酰基转移酶缺乏症。挪威第三个有两名患病成员的家族报告。
Scand J Clin Lab Invest Suppl. 1974;137:101-5.
6
Lipid and lipoprotein abnormalities in liver disease: the possible role of lecithin: cholesterol acyltransferase deficiency.
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7
Familial lecithin: cholesterol acyltransferase deficiency. Study of two new patients and their close relatives.家族性卵磷脂：胆固醇酰基转移酶缺乏症。两名新患者及其近亲的研究。
Acta Med Scand. 1970 Oct;188(4):323-6.
8
The influence of plasma from patients with familial plasma lecithin: cholesterol acyltransferase deficiency on the lipid pattern of erythrocytes.
Scand J Clin Lab Invest. 1968;22(2):94-8. doi: 10.3109/00365516809160951.
9
Ocular manifestations in familial lecithin: cholesterol acyltransferase deficiency.家族性卵磷脂：胆固醇酰基转移酶缺乏症的眼部表现。
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10
Apolipoproteins and lipoprotein families in familial lecithin: cholesterol acyltransferase deficiency.
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Indian J Clin Biochem. 2011 Jan;26(1):57-61. doi: 10.1007/s12291-010-0096-9. Epub 2010 Dec 29.
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Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature.由于新的功能丧失突变导致的纯合子卵磷脂：胆固醇酰基转移酶（LCAT）缺乏症，并对文献进行回顾。
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AAV8-mediated long-term expression of human LCAT significantly improves lipid profiles in hCETP;Ldlr(+/-) mice.腺相关病毒 8 介导的人卵磷脂胆固醇酰基转移酶的长期表达显著改善了 hCETP;Ldlr(+/-) 小鼠的脂质谱。
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Effect of recombinant human lecithin cholesterol acyltransferase infusion on lipoprotein metabolism in mice.重组人卵磷脂胆固醇酰基转移酶输注对小鼠脂蛋白代谢的影响。
J Pharmacol Exp Ther. 2010 Oct;335(1):140-8. doi: 10.1124/jpet.110.169540. Epub 2010 Jul 6.