Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46).
Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46).
复制标题
与载脂蛋白 B (B-46) 突变种相关的家族性低 β 脂蛋白血症。
DOI:
10.1056/nejm198906153202407
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发表时间:
1989
期刊:
影响因子:
--
通讯作者:
Terdiman,JF
中科院分区:
文献类型:
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作者:
Young,SG;Hubl,ST;Chappell,DA;Smith,RS;Claiborne,F;Snyder,SM;Terdiman,JF
THE two plasma forms of apolipoprotein B—B-100 and B-48 — are important proteins in mammalian lipoprotein metabolism.1Both are products of the same structural gene,2which in humans is located on chromosome 2.345Apolipoprotein B-100 is a glycoprotein containing 4536 amino acids;678910and it is synthesized by the liver.1It is an important structural protein in very-low-density lipoproteins (VLDL), which are rich in triglycerides, and low-density lipoproteins (LDL), which are rich in cholesteryl esters. Apolipoprotein B-100 is virtually the only protein component of human LDL, and it is the ligand responsible for the recognition and uptake of LDL by cellular . . .