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The Journal of Biological Chemistry|July 14, 2000
A mechanism of membrane neutral lipid acquisition by the microsomal triglyceride transfer proteinJ Read, T A Anderson, P J Ritchie, et al.Atherosclerosis|January 1, 1988
Characterization of genetic markers in the 3' end of the apo B gene and their use in family and population studiesK Jenner, A Sidoli, M Ball, et al.Atherosclerosis|April 1, 1991
Variation at the apo AI/CIII/AIV gene complex is associated with elevated plasma levels of apo CIIIC C Shoulders, P J Harry, L Lagrost, et al.The Journal of Clinical Investigation|September 1, 1985
Deoxyribonucleic acid polymorphism in the apolipoprotein A-1-C-III gene cluster. Association with hypertriglyceridemiaA Rees, J Stocks, C R Sharpe, et al.Human Genetics|November 1, 1996
Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school childrenC C Shoulders, T T Grantham, J D North, et al.Prenatal Diagnosis|February 19, 1998
The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22-24)K E Heath, L A Luong, J V Leonard, et al.Human Molecular Genetics|December 1, 1993
Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer proteinC C Shoulders, D J Brett, J D Bayliss, et al.American Journal of Human Genetics|December 1, 1995
Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemiaT M Narcisi, C C Shoulders, S A Chester, et al.The Journal of Biological Chemistry|January 23, 1999
A common binding site on the microsomal triglyceride transfer protein for apolipoprotein B and protein disulfide isomeraseP Bradbury, C J Mann, S Köchl, et al.Cell|October 1, 1980
The structure and evolution of the human beta-globin gene familyA Efstratiadis, J W Posakony, T Maniatis, et al.Pageof 4