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Results: 1-15 |
Results: 15
HETEROZYGOUS MUTATIONS IN THE LIPOPROTEIN-LIPASE GENE CONTRIBUTE TO CHYLOMICRONEMIA IN THE ADULT
Authors: NEVIN DN DEEB SS HAYDEN MR BRUNZELL JD
Citation: Dn. Nevin et al., HETEROZYGOUS MUTATIONS IN THE LIPOPROTEIN-LIPASE GENE CONTRIBUTE TO CHYLOMICRONEMIA IN THE ADULT, Journal of investigative medicine, 44(1), 1996, pp. 180-180
PARAOXONASE GENOTYPES, LIPOPROTEIN-LIPASE ACTIVITY, AND HDL
Authors: NEVIN DN ZAMBON A FURLONG CE RICHTER RJ HUMBERT R HOKANSON JE BRUNZELL JD
Citation: Dn. Nevin et al., PARAOXONASE GENOTYPES, LIPOPROTEIN-LIPASE ACTIVITY, AND HDL, Arteriosclerosis, thrombosis, and vascular biology, 16(10), 1996, pp. 1243-1249
2 NOVEL APOLIPOPROTEIN-A-IV VARIANTS IN INDIVIDUALS WITH FAMILIAL COMBINED HYPERLIPIDEMIA AND DIMINISHED LEVELS OF LIPOPROTEIN-LIPASE ACTIVITY
Authors: DEEB SS NEVIN DN IWASAKI L BRUNZELL JD
Citation: Ss. Deeb et al., 2 NOVEL APOLIPOPROTEIN-A-IV VARIANTS IN INDIVIDUALS WITH FAMILIAL COMBINED HYPERLIPIDEMIA AND DIMINISHED LEVELS OF LIPOPROTEIN-LIPASE ACTIVITY, Human mutation, 8(4), 1996, pp. 319-325
A MUTATION IN THE PROMOTER OF THE LIPOPROTEIN-LIPASE (LPL) GENE IN A PATIENT WITH FAMILIAL COMBINED HYPERLIPIDEMIA AND LOW LPL ACTIVITY (VOL 92, PG 4462, 1995)
Authors: YANG WS NEVIN DN PENG RL BRUNZELL JD DEEB SS
Citation: Ws. Yang et al., A MUTATION IN THE PROMOTER OF THE LIPOPROTEIN-LIPASE (LPL) GENE IN A PATIENT WITH FAMILIAL COMBINED HYPERLIPIDEMIA AND LOW LPL ACTIVITY (VOL 92, PG 4462, 1995), Proceedings of the National Academy of Sciences of the United Statesof America, 93(1), 1996, pp. 524-524
A NOVEL A-]G MUTATION IN INTRON-I OF THE HEPATIC LIPASE GENE LEADS TOALTERNATIVE SPLICING RESULTING IN ENZYME DEFICIENCY
Authors: BRAND K DUGI KA BRUNZELL JD NEVIN DN SANTAMARINAFOJO S
Citation: K. Brand et al., A NOVEL A-]G MUTATION IN INTRON-I OF THE HEPATIC LIPASE GENE LEADS TOALTERNATIVE SPLICING RESULTING IN ENZYME DEFICIENCY, Journal of lipid research, 37(6), 1996, pp. 1213-1223
REGULATORY MUTATIONS IN THE HUMAN LIPOPROTEIN-LIPASE GENE IN PATIENTSWITH FAMILIAL COMBINED HYPERLIPIDEMIA AND CORONARY-ARTERY DISEASE
Authors: YANG WS NEVIN DN IWASAKI L PENG RL BROWN BG BRUNZELL JD DEEB SS
Citation: Ws. Yang et al., REGULATORY MUTATIONS IN THE HUMAN LIPOPROTEIN-LIPASE GENE IN PATIENTSWITH FAMILIAL COMBINED HYPERLIPIDEMIA AND CORONARY-ARTERY DISEASE, Journal of lipid research, 37(12), 1996, pp. 2627-2637
A MUTATION IN THE PROMOTER OF THE LIPOPROTEIN-LIPASE (LPL) GENE IN A PATIENT WITH FAMILIAL COMBINED HYPERLIPIDEMIA AND LOW LPL ACTIVITY
Authors: YANG WS NEVIN DN PENG RL BRUNZELL JD DEEB SS
Citation: Ws. Yang et al., A MUTATION IN THE PROMOTER OF THE LIPOPROTEIN-LIPASE (LPL) GENE IN A PATIENT WITH FAMILIAL COMBINED HYPERLIPIDEMIA AND LOW LPL ACTIVITY, Proceedings of the National Academy of Sciences of the United Statesof America, 92(10), 1995, pp. 4462-4466
THE LPL GENE IN INDIVIDUALS WITH FAMILIAL COMBINED HYPERLIPIDEMIA ANDDECREASED LPL ACTIVITY
Authors: NEVIN DN BRUNZELL JD DEEB SS
Citation: Dn. Nevin et al., THE LPL GENE IN INDIVIDUALS WITH FAMILIAL COMBINED HYPERLIPIDEMIA ANDDECREASED LPL ACTIVITY, Arteriosclerosis and thrombosis, 14(6), 1994, pp. 869-873
APOLIPOPROTEIN-B AND A 2ND MAJOR GENE LOCUS CONTRIBUTE TO PHENOTYPIC VARIATION OF SPONTANEOUS HYPERCHOLESTEROLEMIA IN PIGS
Authors: AIELLO RJ NEVIN DN EBERT DL UELMEN PJ KAISER ME MACCLUER JW BLANGERO J DYER TD ATTIE AD
Citation: Rj. Aiello et al., APOLIPOPROTEIN-B AND A 2ND MAJOR GENE LOCUS CONTRIBUTE TO PHENOTYPIC VARIATION OF SPONTANEOUS HYPERCHOLESTEROLEMIA IN PIGS, Arteriosclerosis and thrombosis, 14(3), 1994, pp. 409-419
EVIDENCE THAT CENTRAL OBESITY MODULATES GENETIC EXPRESSION OF LOW-DENSITY-LIPOPROTEIN SUBCLASS PHENOTYPE-B
Authors: NEVIN DN SCHWARTZ RS BRUNZELL JD
Citation: Dn. Nevin et al., EVIDENCE THAT CENTRAL OBESITY MODULATES GENETIC EXPRESSION OF LOW-DENSITY-LIPOPROTEIN SUBCLASS PHENOTYPE-B, Diabetes, 43, 1994, pp. 10000035-10000035
DETERMINATION OF PIG APOLIPOPROTEIN-B GENOTYPE BY GENE AMPLIFICATION AND RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS
Authors: KAISER ME NEVIN DN STURLEY SL PURTELL C ATTIE AD
Citation: Me. Kaiser et al., DETERMINATION OF PIG APOLIPOPROTEIN-B GENOTYPE BY GENE AMPLIFICATION AND RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS, Animal genetics, 24(2), 1993, pp. 117-120
NUCLEOTIDE-SEQUENCE ENCODING THE CARBOXYL-TERMINAL HALF OF APOLIPOPROTEIN-B FROM SPONTANEOUSLY HYPERCHOLESTEROLEMIC PIGS
Authors: PURTELL C MAEDA N EBERT DL KAISER M LUNDKATZ S STURLEY SL KODOYIANNI V GRUNWALD K NEVIN DN AIELLO RJ ATTIE AD
Citation: C. Purtell et al., NUCLEOTIDE-SEQUENCE ENCODING THE CARBOXYL-TERMINAL HALF OF APOLIPOPROTEIN-B FROM SPONTANEOUSLY HYPERCHOLESTEROLEMIC PIGS, Journal of lipid research, 34(8), 1993, pp. 1323-1335
NUCLEOTIDE-SEQUENCE ENCODING THE CARBOXYL-TERMINAL HALF OF APOLIPOPROTEIN-B FROM SPONTANEOUSLY HYPERCHOLESTEROLEMIC PIGS (VOL 34, PG 1323, 1993)
Authors: PURTELL C MAEDA N EBERT DL KAISER M LUNDKATZ S STURLEY SL KODOYIANNI V GRUNDWALD K NEVIN DN AIELLO RJ ATTIE AD
Citation: C. Purtell et al., NUCLEOTIDE-SEQUENCE ENCODING THE CARBOXYL-TERMINAL HALF OF APOLIPOPROTEIN-B FROM SPONTANEOUSLY HYPERCHOLESTEROLEMIC PIGS (VOL 34, PG 1323, 1993), Journal of lipid research, 34(10), 1993, pp. 1832-1832
ALTERNATIVE SPLICING - A NOVEL MECHANISM LEADING TO DEFICIENCY OF HEPATIC LIPASE
Authors: BRAND K DUGI KA BRUNZELL JD NEVIN DN BREWER HB SANTAMARINAFOJO S
Citation: K. Brand et al., ALTERNATIVE SPLICING - A NOVEL MECHANISM LEADING TO DEFICIENCY OF HEPATIC LIPASE, Circulation, 88(4), 1993, pp. 178-178
METABOLIC ASSOCIATIONS IN INSULIN-RESISTANCE SYNDROME - EFFECT OF WEIGHT PERTURBATION
Authors: NEVIN DN SCHWARTZ RS KAHN SE BRUNZELL JD
Citation: Dn. Nevin et al., METABOLIC ASSOCIATIONS IN INSULIN-RESISTANCE SYNDROME - EFFECT OF WEIGHT PERTURBATION, Circulation, 88(4), 1993, pp. 455-455
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