Weisgraber KH - Search Results

1

Genetic defects in lipoprotein metabolism. Elevation of atherogenic lipoproteins caused by impaired catabolism.

Mahley RW, Weisgraber KH, Innerarity TL, Rall SC Jr. Mahley RW, et al. Among authors: weisgraber kh. JAMA. 1991 Jan 2;265(1):78-83. doi: 10.1001/jama.265.1.78. JAMA. 1991. PMID: 1845776 Review.

2

Two apolipoprotein E5 variants illustrate the importance of the position of additional positive charge on receptor-binding activity.

Wardell MR, Rall SC Jr, Schaefer EJ, Kane JP, Weisgraber KH. Wardell MR, et al. Among authors: weisgraber kh. J Lipid Res. 1991 Mar;32(3):521-8. J Lipid Res. 1991. PMID: 1648586 Free article.

3

The functional characteristics of a human apolipoprotein E variant (cysteine at residue 142) may explain its association with dominant expression of type III hyperlipoproteinemia.

Horie Y, Fazio S, Westerlund JR, Weisgraber KH, Rall SC Jr. Horie Y, et al. Among authors: weisgraber kh. J Biol Chem. 1992 Jan 25;267(3):1962-8. J Biol Chem. 1992. PMID: 1730728 Free article.

4

Isolation and characterization of plasma lipoproteins of common marmoset monkey. Comparison of effects of control and atherogenic diets.

Crook D, Weisgraber KH, Boyles JK, Mahley RW. Crook D, et al. Among authors: weisgraber kh. Arteriosclerosis. 1990 Jul-Aug;10(4):633-47. doi: 10.1161/01.atv.10.4.633. Arteriosclerosis. 1990. PMID: 2114868

5

Atherogenic lipoproteins resulting from genetic defects of apolipoproteins B and E.

Weisgraber KH, Innerarity TL, Rall SC Jr, Mahley RW. Weisgraber KH, et al. Ann N Y Acad Sci. 1990;598:37-48. doi: 10.1111/j.1749-6632.1990.tb42274.x. Ann N Y Acad Sci. 1990. PMID: 2248450 Review.

6

Apolipoprotein C-I modulates the interaction of apolipoprotein E with beta-migrating very low density lipoproteins (beta-VLDL) and inhibits binding of beta-VLDL to low density lipoprotein receptor-related protein.

Weisgraber KH, Mahley RW, Kowal RC, Herz J, Goldstein JL, Brown MS. Weisgraber KH, et al. J Biol Chem. 1990 Dec 25;265(36):22453-9. J Biol Chem. 1990. PMID: 2266137 Free article.

7

Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.

Innerarity TL, Mahley RW, Weisgraber KH, Bersot TP, Krauss RM, Vega GL, Grundy SM, Friedl W, Davignon J, McCarthy BJ. Innerarity TL, et al. Among authors: weisgraber kh. J Lipid Res. 1990 Aug;31(8):1337-49. J Lipid Res. 1990. PMID: 2280177 Free article. Review.

8

Type III hyperlipoproteinemia associated with apolipoprotein E phenotype E3/3. Structure and genetics of an apolipoprotein E3 variant.

Rall SC Jr, Newhouse YM, Clarke HR, Weisgraber KH, McCarthy BJ, Mahley RW, Bersot TP. Rall SC Jr, et al. Among authors: weisgraber kh. J Clin Invest. 1989 Apr;83(4):1095-101. doi: 10.1172/JCI113988. J Clin Invest. 1989. PMID: 2539388 Free PMC article.

9

Site-specific mutagenesis of human apolipoprotein E. Receptor binding activity of variants with single amino acid substitutions.

Lalazar A, Weisgraber KH, Rall SC Jr, Giladi H, Innerarity TL, Levanon AZ, Boyles JK, Amit B, Gorecki M, Mahley RW, et al. Lalazar A, et al. Among authors: weisgraber kh. J Biol Chem. 1988 Mar 15;263(8):3542-5. J Biol Chem. 1988. PMID: 2831187 Free article.

10

Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.

Weisgraber KH, Innerarity TL, Newhouse YM, Young SG, Arnold KS, Krauss RM, Vega GL, Grundy SM, Mahley RW. Weisgraber KH, et al. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9758-62. doi: 10.1073/pnas.85.24.9758. Proc Natl Acad Sci U S A. 1988. PMID: 3200853 Free PMC article.

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