1.A new molecular defect in the lecithin: cholesterol acyltransferase (LCAT) gene associated with fish eye disease.

作　　者：C Contacos ;D R Sullivan ;K A Rye 等

出　　处：JLR Papers In Press. 1996 ;37(1):35-44.

出版社：American Society for Biochemistry and Molecular Biology

文章 ID：192687738

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2.Normolipemic dysbetalipoproteinemia and hyperlipoproteinemia type III in subjects homozygous for a rare genetic apolipoprotein E variant (apoE1).

作　　者：A Steinmetz ;N Assefbarkhi ;C Eltze 等

出　　处：JLR Papers In Press. 1990 ;31(6):1005-1013.

出版社：American Society for Biochemistry and Molecular Biology

文章 ID：192686581

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3.Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45-->Asn), in a Turkish patient.

作　　者：S Lüttmann ;A von Eckardstein ;W Wei 等

出　　处：JLR Papers In Press. 1994 ;35(8):1431-1440.

出版社：American Society for Biochemistry and Molecular Biology

文章 ID：192687450

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4.A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

作　　者：H Funke ;A von Eckardstein ;P H Pritchard 等

出　　处：Proceedings of the National Academy of Sciences. 1991 ;88(11):4855-4859.doi:10.1073/pnas.88.11.4855

出版社：The National Academy of Sciences of the United States of America

文章 ID：200599571

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	G Assmann	4篇
	H Funke	4篇
	A von Eckardstein	2篇
	A Pies	1篇
	A Steinmetz	1篇

	C Contacos	1篇
	C Droste	1篇
	C Eltze	1篇
	D R Sullivan	1篇
	E Köhler	1篇
	H Kaffarnik	1篇
	J J Albers	1篇
	J J Kastelein	1篇
	K A Rye	1篇
	K Ehlenz	1篇
	N Assefbarkhi	1篇
	P H Pritchard	1篇
	R W Mahley	1篇
	S Lüttmann	1篇
	W Wei	1篇

	心理学	3篇
	自然科学总论	1篇

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	JLR Papers In Press	3篇
	Proceedings of the National Academy of Sciences	1篇

	1996	1篇
	1994	1篇
	1991	1篇
	1990	1篇