BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

274 related articles for article (PubMed ID: 7962342)

  • 1. Molecular screening of the lipoprotein lipase gene in hypertriglyceridemic members of familial noninsulin-dependent diabetes mellitus families.
    Elbein SC; Yeager C; Kwong LK; Lingam A; Inoue I; Lalouel JM; Wilson DE
    J Clin Endocrinol Metab; 1994 Nov; 79(5):1450-6. PubMed ID: 7962342
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and non-insulin-dependent diabetes.
    Wilson DE; Hata A; Kwong LK; Lingam A; Shuhua J; Ridinger DN; Yeager C; Kaltenborn KC; Iverius PH; Lalouel JM
    J Clin Invest; 1993 Jul; 92(1):203-11. PubMed ID: 8325986
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel mutations of the lipoprotein lipase gene associated with hypertriglyceridemia in members of type 2 diabetic pedigrees.
    Hu Y; Ren Y; Luo RZ; Mao X; Li X; Cao X; Guan L; Chen X; Li J; Long Y; Zhang X; Tian H
    J Lipid Res; 2007 Aug; 48(8):1681-8. PubMed ID: 17476032
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia.
    Evans D; Arzer J; Aberle J; Beil FU
    Atherosclerosis; 2011 Feb; 214(2):386-90. PubMed ID: 21159338
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.
    Yang T; Pang CP; Tsang MW; Lam CW; Poon PM; Chan LY; Wu XQ; Tomlinson B; Baum L
    Hum Mutat; 2003 Apr; 21(4):453. PubMed ID: 12655575
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23.
    Hölzl B; Kraft HG; Wiebusch H; Sandhofer A; Patsch J; Sandhofer F; Paulweber B
    J Lipid Res; 2000 May; 41(5):734-41. PubMed ID: 10787434
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heterozygosity for Asn291-->Ser mutation in the lipoprotein lipase gene in two Finnish pedigrees: effect of hyperinsulinemia on the expression of hypertriglyceridemia.
    Syvänne M; Antikainen M; Ehnholm S; Tenkanen H; Lahdenperä S; Ehnholm C; Taskinen MR
    J Lipid Res; 1996 Apr; 37(4):727-38. PubMed ID: 8732773
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic screening of the lipoprotein lipase gene for mutations in Chinese subjects with or without hypertriglyceridemia.
    Yang Y; Mu Y; Zhao Y; Liu X; Zhao L; Wang J; Xie Y
    J Genet Genomics; 2007 May; 34(5):381-91. PubMed ID: 17560523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants.
    Kassner U; Salewsky B; Wühle-Demuth M; Szijarto IA; Grenkowitz T; Binner P; März W; Steinhagen-Thiessen E; Demuth I
    Eur J Hum Genet; 2015 Sep; 23(9):1259-61. PubMed ID: 25585702
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A missense (Asp250----Asn) mutation in the lipoprotein lipase gene in two unrelated families with familial lipoprotein lipase deficiency.
    Ishimura-Oka K; Semenkovich CF; Faustinella F; Goldberg IJ; Shachter N; Smith LC; Coleman T; Hide WA; Brown WV; Oka K
    J Lipid Res; 1992 May; 33(5):745-54. PubMed ID: 1619366
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.
    Wilson DE; Emi M; Iverius PH; Hata A; Wu LL; Hillas E; Williams RR; Lalouel JM
    J Clin Invest; 1990 Sep; 86(3):735-50. PubMed ID: 2394828
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hyperinsulinemia and abdominal obesity affect the expression of hypertriglyceridemia in heterozygous familial lipoprotein lipase deficiency.
    Julien P; Vohl MC; Gaudet D; Gagné C; Lévesque G; Després JP; Cadelis F; Brun LD; Nadeau A; Ven Murthy MR
    Diabetes; 1997 Dec; 46(12):2063-8. PubMed ID: 9392497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A compound heterozygote for a novel missense mutation (G105R) in exon 3 and a missense mutation (D204E) in exon 5 of the lipoprotein lipase gene in a Japanese infant with hyperchylomicronaemia.
    Ikeda Y; Goji K; Takagi A
    Clin Sci (Lond); 2000 Dec; 99(6):569-78. PubMed ID: 11099402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia.
    Pasalić D; Jurcić Z; Stipancić G; Ferencak G; Leren TP; Djurovic S; Stavljenić-Rukavina A
    Clin Chim Acta; 2004 May; 343(1-2):179-84. PubMed ID: 15115692
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent.
    Minnich A; Kessling A; Roy M; Giry C; DeLangavant G; Lavigne J; Lussier-Cacan S; Davignon J
    J Lipid Res; 1995 Jan; 36(1):117-24. PubMed ID: 7706936
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Newly identified missense mutation reduces lipoprotein lipase activity in Taiwanese patients with hypertriglyceridemia.
    Kao JT; Hsiao WH; Yu CJ; Chiang FT
    J Formos Med Assoc; 1999 Sep; 98(9):606-12. PubMed ID: 10560236
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel nonsense mutation in exon 1 and a transition in intron 3 of the lipoprotein lipase gene.
    Nakamura T; Suehiro T; Yasuoka N; Yamamoto M; Ito H; Yamano T; Hashimoto K
    J Atheroscler Thromb; 1996; 3(1):17-24. PubMed ID: 9225235
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes.
    Weinstock PH; Bisgaier CL; Aalto-Setälä K; Radner H; Ramakrishnan R; Levak-Frank S; Essenburg AD; Zechner R; Breslow JL
    J Clin Invest; 1995 Dec; 96(6):2555-68. PubMed ID: 8675619
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial lipoprotein lipase (LPL) deficiency: a catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy.
    Mailly F; Palmen J; Muller DP; Gibbs T; Lloyd J; Brunzell J; Durrington P; Mitropoulos K; Betteridge J; Watts G; Lithell H; Angelico F; Humphries SE; Talmud PJ
    Hum Mutat; 1997; 10(6):465-73. PubMed ID: 9401010
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mutation-function analysis in the lipoprotein lipase gene of Chinese patients with hypertriglyceridemic type 2 diabetes].
    Yang T; Lam CW; Tsang MW; Chan LY; Poon PM; Huang SZ; Pang CP
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Apr; 25(2):134-41. PubMed ID: 12905705
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.