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2. Identification of the low density lipoprotein receptor-binding site in apolipoprotein B100 and the modulation of its binding activity by the carboxyl terminus in familial defective apo-B100. Boren J; Lee I; Zhu W; Arnold K; Taylor S; Innerarity TL J Clin Invest; 1998 Mar; 101(5):1084-93. PubMed ID: 9486979 [TBL] [Abstract][Full Text] [Related]
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12. Identification of the principal proteoglycan-binding site in LDL. A single-point mutation in apo-B100 severely affects proteoglycan interaction without affecting LDL receptor binding. Borén J; Olin K; Lee I; Chait A; Wight TN; Innerarity TL J Clin Invest; 1998 Jun; 101(12):2658-64. PubMed ID: 9637699 [TBL] [Abstract][Full Text] [Related]
13. The binding of very low density lipoprotein remnants to the low density lipoprotein receptor in familial defective apolipoprotein B-100. Maher VM; Gallagher JJ; Myant NB Atherosclerosis; 1993 Aug; 102(1):51-61. PubMed ID: 8257452 [TBL] [Abstract][Full Text] [Related]
14. Isolation of allele-specific, receptor-binding-defective low density lipoproteins from familial defective apolipoprotein B-100 subjects. Arnold KS; Balestra ME; Krauss RM; Curtiss LK; Young SG; Innerarity TL J Lipid Res; 1994 Aug; 35(8):1469-76. PubMed ID: 7989871 [TBL] [Abstract][Full Text] [Related]
16. Ability of the LDL receptor from several animal species to recognize the human apo B binding domain: studies with LDL from familial defective apo B-100. Corsini A; Mazzotti M; Villa A; Maggi FM; Bernini F; Romano L; Romano C; Fumagalli R; Catapano AL Atherosclerosis; 1992 Mar; 93(1-2):95-103. PubMed ID: 1596308 [TBL] [Abstract][Full Text] [Related]
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18. Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100. Rauh G; Schuster H; Fischer J; Keller C; Wolfram G; Zöllner N Klin Wochenschr; 1991 May; 69(7):320-4. PubMed ID: 2067318 [TBL] [Abstract][Full Text] [Related]
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