DNA polymorphisms of lipoprotein lipase gene and apolipoprotein E in Hungarian patients with familial combined hyperlipidemia

被引：0
|
作者：
Reiber, I
Szalai, C
Gógl, A
Romics, L
Császár, A
机构：
[1] St Gyorgy Hosp, Dept Med 1, Szekesfehervar, Hungary
[2] Semmelweis Univ Med, Dept Med 3, H-1085 Budapest, Hungary
[3] Heim Pal Hosp, Budapest, Hungary
来源：
ATHEROSCLEROSIS | 1998年 / 138卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
49
引用
收藏
页码：S14 / S14
页数：1
相关论文
共 50 条
  • [41] Lipoprotein lipase variant N291S is associated with hypertriglyceridemia in familial combined hyperlipidemia
    Lopez-Ruiz, A
    Martinez-Triguero, M
    Casado, M
    Jarabo, M
    Diaz-Ruiz, M
    Lopez-Gutierrez, A
    Casañ, R
    Morillas, C
    Hernandez-Mijares, A
    ATHEROSCLEROSIS SUPPLEMENTS, 2004, 5 (01) : 11 - 11
  • [42] AN APOLIPOPROTEIN B-ENRICHED LOW-DENSITY LIPOPROTEIN SUBSPECIES IN FAMILIAL COMBINED HYPERLIPIDEMIA
    KRAUSS, RM
    ALBERS, JJ
    BRUNZELL, JD
    CLINICAL RESEARCH, 1983, 31 (02): : A503 - A503
  • [43] Effects of lipoprotein lipase (LPL) and apolipoprotein E (APO E) gene polymorphisms on lipid levels: The Stanislas cohort study.
    Salah, D
    Bohnet, K
    Gueguen, R
    Siest, G
    Visvikis, S
    CLINICAL CHEMISTRY, 1997, 43 : 702 - 702
  • [44] A FREQUENTLY OCCURRING MUTATION IN THE LIPOPROTEIN-LIPASE GENE (ASN291SER) CONTRIBUTES TO THE EXPRESSION OF FAMILIAL COMBINED HYPERLIPIDEMIA
    REYMER, PWA
    GROENEMEYER, BE
    GAGNE, E
    MIAO, L
    APPELMAN, EEG
    SEIDEL, JC
    KROMHOUT, D
    BIJVOET, SM
    VANDEOEVER, K
    BRUIN, T
    HAYDEN, MR
    KASTELEIN, JJP
    HUMAN MOLECULAR GENETICS, 1995, 4 (09) : 1543 - 1549
  • [45] Apolipoprotein E gene polymorphisms in patients with migraine
    Rainero, I
    Grimaldi, LME
    Salani, G
    Valfrè, W
    Savi, L
    Rivoiro, C
    Gentile, S
    Pinessi, L
    NEUROSCIENCE LETTERS, 2002, 317 (02) : 111 - 113
  • [46] Point mutations in the genes of Lipoprotein lipase, hepatic lipase, and insulin receptor as possible susceptibility alleles in familial combined hyperlipidemia
    Jaross, W
    Gehrisch, S
    Julius, U
    Kostka, H
    Hanefeld, HM
    ATHEROSCLEROSIS, 1997, 134 (1-2) : 25 - 26
  • [47] Apolipoprotein E polymorphism influences lipid phenotypes in Chinese families with familial combined hyperlipidemia
    Pei, Wei-Dong
    Zhang, Yan-Hong
    Sun, Yu-Hua
    Gu, Yu-Chun
    Wang, Yan-Fen
    Zhang, Chao-Yang
    Zhang, Jian
    Liu, Li-Sheng
    Hui, Ru-Tai
    Liu, Yu-Qing
    Yang, Yue-Jin
    CIRCULATION JOURNAL, 2006, 70 (12) : 1606 - 1610
  • [48] ASSOCIATION BETWEEN GENETIC-VARIATION OF THE LIPOPROTEIN-LIPASE GENE AND COMBINED HYPERLIPIDEMIA
    HONG, SH
    KANG, BY
    PARK, WH
    LEE, CC
    KIM, JQ
    MOLECULES AND CELLS, 1995, 5 (05) : 481 - 485
  • [49] POINT MUTATIONS IN THE HEPATIC TRIGLYCERIDE LIPASE (HTGL) GENE IN FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL)
    GEHRISCH, S
    TESCHE, R
    KOSTKA, H
    JULIUS, U
    JAROSS, W
    CIRCULATION, 1995, 92 (08) : 2352 - 2352
  • [50] Lipoprotein phenotype and insulin resistance in familial combined hyperlipidemia
    Ascaso, JF
    Real, JT
    Merchante, A
    Rodrigo, A
    Carmena, R
    METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (12): : 1627 - 1631
12345