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 *

115 related articles for article (PubMed ID: 18258526)

  • 1. Absence of apolipoprotein B-3500 mutation in Turkish patients with coronary and cerebrovascular atherosclerosis.
    Eroğlu Z; Selvi N; Kosova B; Biray C; Kumral E; Topçuoğlu N; Kayikçioğlu M
    Anadolu Kardiyol Derg; 2008 Feb; 8(1):7-9. PubMed ID: 18258526
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Apolipoprotein B gene polymorphisms in people in the east Mediterranean area of Turkey.
    Tamer L; Tanriverdi K; Ercan B; Unlu A; Sucu N; Pekdemir H; Atik U
    East Mediterr Health J; 2004; 10(1-2):125-30. PubMed ID: 16201717
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.
    Shen H; Damcott CM; Rampersaud E; Pollin TI; Horenstein RB; McArdle PF; Peyser PA; Bielak LF; Post WS; Chang YP; Ryan KA; Miller M; Rumberger JA; Sheedy PF; Shelton J; O'Connell JR; Shuldiner AR; Mitchell BD
    Arch Intern Med; 2010 Nov; 170(20):1850-5. PubMed ID: 21059979
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cholesterol ester transfer protein, apolipoprotein E and lipoprotein lipase genotypes in patients with coronary artery disease in the Turkish population.
    Isbir T; Yilmaz H; Agachan B; Karaali ZE
    Clin Genet; 2003 Sep; 64(3):228-34. PubMed ID: 12919138
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients.
    Cefalù AB; Barbagallo CM; Sesti E; Caldarella R; Polizzi F; Marino G; Noto D; Rolleri M; Travali S; Scalisi G; Notarbartolo A; Corsini A; Bertolini S; Averna MR
    Clin Exp Med; 2001 Sep; 1(3):151-4. PubMed ID: 11833852
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diagnosis of families with familial hypercholesterolaemia and/or Apo B-100 defect by means of DNA analysis of LDL-receptor gene mutations.
    Widhalm K; Dirisamer A; Lindemayr A; Kostner G
    J Inherit Metab Dis; 2007 Apr; 30(2):239-47. PubMed ID: 17347910
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Importance of lipid ratios for predicting intracranial atherosclerotic stenosis.
    Yang WS; Li R; Shen YQ; Wang XC; Liu QJ; Wang HY; Li Q; Yao GE; Xie P
    Lipids Health Dis; 2020 Jul; 19(1):160. PubMed ID: 32622367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of clinical diagnosis criteria of familial ligand defective apoB 100 and lipoprotein phenotype comparison between LDL receptor gene mutations affecting ligand-binding domain and the R3500Q mutation of the apoB gene in patients from a South European population.
    Ejarque I; Real JT; Martinez-Hervas S; Chaves FJ; Blesa S; Garcia-Garcia AB; Millan E; Ascaso JF; Carmena R
    Transl Res; 2008 Mar; 151(3):162-7. PubMed ID: 18279815
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Screening for mutations in apolipoprotein B genes in a group of patients with hyperlipoproteinemia].
    Grombiríková H; Freiberger T; Kuhrová V; Soska V; Nedomová K
    Cas Lek Cesk; 2001 Jan; 140(1):18-21. PubMed ID: 11242979
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of apolipoprotein E gene polymorphism with ischemic stroke involving large-vessel disease and its relation to serum lipid levels.
    Saidi S; Slamia LB; Ammou SB; Mahjoub T; Almawi WY
    J Stroke Cerebrovasc Dis; 2007; 16(4):160-6. PubMed ID: 17689412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.
    van der Hoek YY; Lingenhel A; Kraft HG; Defesche JC; Kastelein JJ; Utermann G
    J Clin Invest; 1997 May; 99(9):2269-73. PubMed ID: 9151801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial defective apolipoprotein B-100: detection and haplotype analysis of the Arg(3500)-->Gln mutation in hyperlipidemic Chinese.
    Teng YN; Pan JP; Chou SC; Tai DY; Lee-Chen GJ
    Atherosclerosis; 2000 Oct; 152(2):385-90. PubMed ID: 10998466
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Serum low density lipoprotein cholesterol level and cholesterol absorption efficiency are influenced by apolipoprotein B and E polymorphism and by the FH-Helsinki mutation of the low density lipoprotein receptor gene in familial hypercholesterolemia.
    Gylling H; Aalto-Setälä K; Kontula K; Miettinen TA
    Arterioscler Thromb; 1991; 11(5):1368-75. PubMed ID: 1911722
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the apolipoprotein (apo) B-100 receptor-binding region: detection of apo B-100 (Arg3500-->Trp) associated with two new haplotypes and evidence that apo B-100 (Glu3405-->Gln) diminishes receptor-mediated uptake of LDL.
    Fisher E; Scharnagl H; Hoffmann MM; Kusterer K; Wittmann D; Wieland H; Gross W; März W
    Clin Chem; 1999 Jul; 45(7):1026-38. PubMed ID: 10388479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Impact of Genetic Defects on Coronary Atherosclerosis among Turkish Cypriots.
    Conkbayir C; Fahrioglu Yamaci R; Gencer P; Barin B; Yucel G; Yildiz CE; Ugurlucan M; Basak AN
    Heart Surg Forum; 2017 Oct; 20(5):E223-E229. PubMed ID: 29087287
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases.
    Brugger D; Schuster H; Zöllner N
    Eur J Med Res; 1996 May; 1(8):383-6. PubMed ID: 9360938
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK.
    Wenham PR; Henderson BG; Penney MD; Ashby JP; Rae PW; Walker SW
    Atherosclerosis; 1997 Mar; 129(2):185-92. PubMed ID: 9105560
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patients.
    Ceska R; Vrablík M; Horínek A
    Physiol Res; 2000; 49 Suppl 1():S125-30. PubMed ID: 10984082
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA polymorphisms of the apolipoprotein B gene (XbaI, EcoRI, and MspI RFLPs) in Norwegians at risk of atherosclerosis and healthy controls.
    Delghandi M; Thangarajah R; Nilsen M; Grimsgaard S; Bønaa KH; Tonstad S; Jørgensen L
    Acta Cardiol; 1999 Aug; 54(4):215-25. PubMed ID: 10511898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of platelet-activating factor acetylhydrolase gene polymorphism with premature coronary artery disease in Turkish patients.
    Sekuri C; Cam FS; Tengiz I; Ercan E; Bayturan O; Berdeli A
    Anadolu Kardiyol Derg; 2006 Jun; 6(2):132-4. PubMed ID: 16766276
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.