These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 7739114)

  • 1. [Molecular genetics of cholesterol transport and cholesterol reverse transport disorders (familial hypercholesterolemia and CETP deficiency), and coronary heart disease].
    Mabuchi H
    Rinsho Byori; 1995 Apr; 43(4):342-6. PubMed ID: 7739114
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [New approach to pathogenesis of genetic hyperlipoproteinemias].
    Koizumi J; Inazu A; Mabuchi H
    Rinsho Byori; 1993 May; 41(5):519-26. PubMed ID: 8350515
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Progress in the diagnosis of endocrine and metabolic disorders: hyperlipidemia].
    Yamashita S
    Rinsho Byori; 1995 Nov; 43(11):1120-7. PubMed ID: 8551675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK
    Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HDL cholesterol levels in patients with molecularly defined familial hypercholesterolemia.
    Miltiadous G; Cariolou MA; Elisaf M
    Ann Clin Lab Sci; 2002; 32(1):50-4. PubMed ID: 11848618
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A low prevalence of coronary heart disease among subjects with increased high-density lipoprotein cholesterol levels, including those with plasma cholesteryl ester transfer protein deficiency.
    Moriyama Y; Okamura T; Inazu A; Doi M; Iso H; Mouri Y; Ishikawa Y; Suzuki H; Iida M; Koizumi J; Mabuchi H; Komachi Y
    Prev Med; 1998; 27(5 Pt 1):659-67. PubMed ID: 9808796
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CETP (cholesteryl ester transfer protein) promoter -1337 C>T polymorphism protects against coronary atherosclerosis in Japanese patients with heterozygous familial hypercholesterolaemia.
    Takata M; Inazu A; Katsuda S; Miwa K; Kawashiri MA; Nohara A; Higashikata T; Kobayashi J; Mabuchi H; Yamagishi M
    Clin Sci (Lond); 2006 Nov; 111(5):325-31. PubMed ID: 16822236
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical characteristics of double heterozygotes with familial hypercholesterolemia and cholesteryl ester transfer protein deficiency.
    Haraki T; Inazu A; Yagi K; Kajinami K; Koizumi J; Mabuchi H
    Atherosclerosis; 1997 Jul; 132(2):229-36. PubMed ID: 9242969
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cholesteryl ester transfer protein (CETP) deficiency and increased HDL cholesterol levels (hyperalphalipoproteinemia)].
    Inazu A; Koizumi J; Mabuchi H
    Rinsho Byori; 1996 Apr; 44(4):322-6. PubMed ID: 8847813
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetics of cholesterol transport and cholesterol reverse transport disorders (familial hypercholesterolemia and CETP deficiency) and coronary heart disease.
    Mabuchi H; Yagi K; Haraki T; Matsushita H; Inazu A; Kajinami K; Koizumi J
    Ann N Y Acad Sci; 1995 Jan; 748():333-41. PubMed ID: 7695176
    [No Abstract]   [Full Text] [Related]  

  • 11. Interaction between a common variant of the cholesteryl ester transfer protein gene and the apolipoprotein E polymorphism: effects on plasma lipids and lipoproteins in a cohort of 7-year-old children.
    Rump P; Mensink RP; Hornstra G
    Nutr Metab Cardiovasc Dis; 2002 Dec; 12(6):317-24. PubMed ID: 12669678
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic aspects of familial hypercholesterolemia and its diagnosis.
    Motulsky AG
    Arteriosclerosis; 1989; 9(1 Suppl):I3-7. PubMed ID: 2563220
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
    Wang D; Wu B; Li Y; Heng W; Zhong H; Mu Y; Wang J
    J Hum Genet; 2001; 46(3):152-4. PubMed ID: 11310584
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype of the mutant LDL receptor allele is associated with LDL particle size heterogeneity in familial hypercholesterolemia.
    Hogue JC; Lamarche B; Gaudet D; Tremblay AJ; Després JP; Gagné C; Couture P
    Atherosclerosis; 2006 Jan; 184(1):163-70. PubMed ID: 15899484
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Relationship between LDL receptor activity and development of coronary heart disease in Japanese cases with heterozygous familial hypercholesterolemia.
    Yamashita S; Kawamoto T; Ueyama Y; Funahashi T; Hara H; Hirobe K; Matsuzawa Y; Yamamoto A; Tarui S
    Artery; 1987; 15(1):24-43. PubMed ID: 3435251
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease.
    Castillo S; Reyes G; Tejedor D; Mozas P; Suarez Y; Lasuncion MA; Cenarro A; Civeira F; Alonso R; Mata P; Pocovi M;
    Hum Mutat; 2002 Dec; 20(6):477. PubMed ID: 12442279
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Identification of a novel mutation at the point of low density lipoprotein receptor gene from a subject with familial hypercholesterolemia].
    Liu YR; Tao QM; Chen JZ; Tao M; Guo XG; Shang YP; Zhu JH; Zhang FR; Zheng LR; Wang XX
    Sheng Li Xue Bao; 2004 Oct; 56(5):566-72. PubMed ID: 15497035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Taq1B polymorphism of CETP gene on lipid abnormalities in patients with type II diabetes mellitus.
    Yilmaz H; Agachan B; Karaali ZE; Isbir T
    Int J Mol Med; 2004 Jun; 13(6):889-93. PubMed ID: 15138631
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial hypercholesterolemia and coronary heart disease: a HuGE association review.
    Austin MA; Hutter CM; Zimmern RL; Humphries SE
    Am J Epidemiol; 2004 Sep; 160(5):421-9. PubMed ID: 15321838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Molecular genetic causes of familial hypercholesterolemia].
    Leren TP
    Tidsskr Nor Laegeforen; 1993 Oct; 113(26):3251-4. PubMed ID: 8236220
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.