Focal segmental glomerulosclerosis with heterozygous apolipoprotein E5 (Glu3Lys)-Reference-Cited by-同舟云学术

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Focal segmental glomerulosclerosis with heterozygous apolipoprotein E5 (Glu3Lys)

Published:2018-05-08 Issue:2 Volume:7 Page:225-228
ISSN:2192-4449
Container-title:CEN Case Reports
language:en
Short-container-title:CEN Case Rep

Author:

Sasaki Masaru,Yasuno Tetsuhiko,Ito Kenji,Matsunaga Akira,Hisano Satoshi,Abe Yasuhiro,Miyake Katsuhisa,Masutani Kosuke,Nakashima Hitoshi,Saito Takao

Publisher

Springer Science and Business Media LLC

Subject

General Earth and Planetary Sciences,General Environmental Science

Link

http://link.springer.com/article/10.1007/s13730-018-0331-4/fulltext.html

Reference13 articles.

1. Matsunaga A, Sasaki J, Moriyama K, et al. Population frequency of apolipoprotein E5 (Glu3→Lys) and E7 (Glu244→Lys, Glu245→Lys) variants in western Japan. Clin Genet. 1995;48:93–9.

2. Dong LM, Yamamura T, Yamamoto A. Enhanced binding activity of an apolipoprotein E mutant, APO E5, to LDL receptors on human fibroblasts. Biochem Biophys Res Commun. 1990;168:409–14.

3. Dong LM, Yamamura T, Tajima S, Yamamoto A. Site-directed mutagenesis of an apolipoprotein E mutant, apo E5(Glu3→Lys) and its binding to low density lipoprotein receptors. Biochem Biophys Res Commun. 1992;187:1180–6.

4. Kodera H, Mizutani Y, Sugiyama S, et al. A case of lipoprotein glomerulopathy with ApoE Chicago and ApoE (Glu3Lys) treated with fenofibrate. Case Rep Nephrol Dial. 2017;7(2):112–20.

5. Takasaki S, Matsunaga A, Joh K, Saito T. A case of lipoprotein glomerulopathy with a rare apolipoprotein E isoform combined with neurofibromatosis type I. CEN Case Rep. 2018;7(1):127–31.

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