Yamamura T - Search Results

1

Homozygous familial hypercholesterolemia mutant with a defect in internalization of low density lipoprotein.

Miyake Y, Tajima S, Yamamura T, Yamamoto A. Miyake Y, et al. Among authors: yamamura t. Proc Natl Acad Sci U S A. 1981 Aug;78(8):5151-5. doi: 10.1073/pnas.78.8.5151. Proc Natl Acad Sci U S A. 1981. PMID: 6272292 Free PMC article.

2

A point mutation of low-density-lipoprotein receptor causing rapid degradation of the receptor.

Miyake Y, Tajima S, Funahashi T, Yamamura T, Yamamoto A. Miyake Y, et al. Among authors: yamamura t. Eur J Biochem. 1992 Nov 15;210(1):1-7. doi: 10.1111/j.1432-1033.1992.tb17383.x. Eur J Biochem. 1992. PMID: 1446662 Free article.

3

Clinical features of familial hypercholesterolemia.

Yamamoto A, Kamiya T, Yamamura T, Yokoyama S, Horiguchi Y, Funahashi T, Kawaguchi A, Miyake Y, Beppu S, Ishikawa K, et al. Yamamoto A, et al. Among authors: yamamura t. Arteriosclerosis. 1989 Jan-Feb;9(1 Suppl):I66-74. Arteriosclerosis. 1989. PMID: 2912433

4

Rate of cholesteryl ester transfer between high and low density lipoproteins in human serum and a case with decreased transfer rate in association with hyperalphalipoproteinemia.

Kurasawa T, Yokoyama S, Miyake Y, Yamamura T, Yamamoto A. Kurasawa T, et al. Among authors: yamamura t. J Biochem. 1985 Dec;98(6):1499-508. doi: 10.1093/oxfordjournals.jbchem.a135418. J Biochem. 1985. PMID: 3867663 Free article.

5

A Japanese family with high density lipoprotein deficiency.

Ohtaki S, Nakagawa H, Kida N, Nakamura H, Tsuda K, Yokoyama S, Yamamura T, Tajima S, Yamamoto A. Ohtaki S, et al. Among authors: yamamura t. Atherosclerosis. 1983 Oct;49(1):79-88. doi: 10.1016/0021-9150(83)90009-6. Atherosclerosis. 1983. PMID: 6651915

6

Common mutations in the low-density-lipoprotein-receptor gene causing familial hypercholesterolemia in the Japanese population.

Maruyama T, Miyake Y, Tajima S, Harada-Shiba M, Yamamura T, Tsushima M, Kishino B, Horiguchi Y, Funahashi T, Matsuzawa Y, et al. Maruyama T, et al. Among authors: yamamura t. Arterioscler Thromb Vasc Biol. 1995 Oct;15(10):1713-8. doi: 10.1161/01.atv.15.10.1713. Arterioscler Thromb Vasc Biol. 1995. PMID: 7583548

7

A novel point mutation in a splice acceptor site of intron 1 of the human low density lipoprotein receptor gene which causes severe hypercholesterolemia: an unexpected absence of exon skipping. Mutations in brief no. 139. Online.

Maruyama T, Miyake Y, Yamamura T, Tajima S, Funahashi T, Matsuzawa Y, Yamamoto A. Maruyama T, et al. Among authors: yamamura t. Hum Mutat. 1998;11(6):480-1. doi: 10.1002/(SICI)1098-1004(1998)11:6<480::AID-HUMU11>3.0.CO;2-W. Hum Mutat. 1998. PMID: 10200052

8

Low density lipoprotein (LDL) binding affinity for the LDL receptor in hyperlipoproteinemia.

Toyota Y, Yamamura T, Miyake Y, Yamamoto A. Toyota Y, et al. Among authors: yamamura t. Atherosclerosis. 1999 Nov 1;147(1):77-86. doi: 10.1016/s0021-9150(99)00166-5. Atherosclerosis. 1999. PMID: 10525128

9

Site-directed mutagenesis of an apolipoprotein E mutant, apo E5(Glu3----Lys) and its binding to low density lipoprotein receptors.

Dong LM, Yamamura T, Tajima S, Yamamoto A. Dong LM, et al. Among authors: yamamura t. Biochem Biophys Res Commun. 1992 Sep 16;187(2):1180-6. doi: 10.1016/0006-291x(92)91321-g. Biochem Biophys Res Commun. 1992. PMID: 1530612

10

Risk factors for atherosclerotic vascular diseases with special reference to the relationship between apolipoprotein E mutations and hyperlipidemia.

Yamamoto A, Yamamura T, Tajima S. Yamamoto A, et al. Among authors: yamamura t. Ann N Y Acad Sci. 1990;598:58-65. doi: 10.1111/j.1749-6632.1990.tb42276.x. Ann N Y Acad Sci. 1990. PMID: 2248462 No abstract available.

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