BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 1912089)

  • 1. Rapid diagnosis of familial defective apolipoprotein B-100.
    Geisel J; Schleifenbaum T; Weisshaar B; Oette K
    Eur J Clin Chem Clin Biochem; 1991 Jun; 29(6):395-9. PubMed ID: 1912089
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A robust strategy for screening and confirmation of familial defective apolipoprotein B-100.
    Mamotte CD; van Bockxmeer FM
    Clin Chem; 1993 Jan; 39(1):118-21. PubMed ID: 8380363
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Allele-specific and asymmetric polymerase chain reaction amplification in combination: a one step polymerase chain reaction protocol for rapid diagnosis of familial defective apolipoprotein B-100.
    Schuster H; Rauh G; Müller S; Keller C; Wolfram G; Zöllner N
    Anal Biochem; 1992 Jul; 204(1):22-5. PubMed ID: 1514690
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Application of PCR site-directed mutagenesis for a rapid and accurate detection of mutation 3500 (Arg-->Gln) of human apolipoprotein B-100.
    Richard P; de Zulueta MP; Weill F; Cassaigne A; Iron A
    Mol Cell Probes; 1994 Jun; 8(3):257-60. PubMed ID: 7969202
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis.
    Kotze MJ; Langenhoven E; Peeters AV; Theart L; Oosthuizen CJ
    Mol Cell Probes; 1994 Dec; 8(6):513-8. PubMed ID: 7700273
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol.
    Hämäläinen T; Palotie A; Aalto-Setälä K; Kontula K; Tikkanen MJ
    Atherosclerosis; 1990 Jun; 82(3):177-83. PubMed ID: 2375782
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene.
    Bednarska-Makaruk M; Bisko M; Pulawska MF; Hoffman-Zacharska D; Rodo M; Roszczynko M; Solik-Tomassi A; Broda G; Polakowska M; Pytlak A; Wehr H
    Eur J Hum Genet; 2001 Nov; 9(11):836-42. PubMed ID: 11781700
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100.
    Ludwig EH; McCarthy BJ
    Am J Hum Genet; 1990 Oct; 47(4):712-20. PubMed ID: 1977310
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: a French multicenter study.
    Viola S; Benlian P; Morali A; Dobbelaere D; Lacaille F; Rieu D; Ginies JL; Maurage C; Meyer M; Lachaux A; Larchet M; Lenearts C; Goulet O; Sarles J; Mouterde O; Girardet JP;
    J Pediatr Gastroenterol Nutr; 2001 Aug; 33(2):122-6. PubMed ID: 11568510
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detecting familial defective apolipoprotein B-100: three molecular scanning methods compared.
    Henderson BG; Wenham PR; Ashby JP; Blundell G
    Clin Chem; 1997 Sep; 43(9):1630-4. PubMed ID: 9299944
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rapid diagnosis of familial defective apolipoprotein B-100 by Amplification Refractory Mutation System.
    Wenham PR; Newton CR; Houlston RS; Price WH
    Clin Chem; 1991 Nov; 37(11):1983-7. PubMed ID: 1934475
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and Wales.
    Wenham PR; Bloomfield P; Blundell G; Penney MD; Rae PW; Walker SW
    Ann Clin Biochem; 1996 Sep; 33 ( Pt 5)():443-50. PubMed ID: 8888978
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of familial defective apolipoprotein B-100 among patients clinically diagnosed with heterozygous familial hypercholesterolemia in maritime Canada.
    Morash B; Guernsey DL; Tan MH; Dempsey G; Nassar BA
    Clin Biochem; 1994 Aug; 27(4):265-72. PubMed ID: 8001287
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel truncated apolipoprotein B (apo B55) in a patient with familial hypobetalipoproteinemia and atypical retinitis pigmentosa.
    Talmud PJ; Converse C; Krul E; Huq L; McIlwaine GG; Series JJ; Boyd P; Schonfeld G; Dunning A; Humphries S
    Clin Genet; 1992 Aug; 42(2):62-70. PubMed ID: 1424233
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele.
    Abdel-Wareth LO; Pimstone SN; Lagarde JP; Raisonnier A; Benlian P; Pritchard H; Hayden MR; Frohlich JJ
    Atherosclerosis; 1997 Dec; 135(2):181-5. PubMed ID: 9430367
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of DNA analysis for differential diagnosis of familial hypercholesterolemia and familial defect of apolipoprotein b-100].
    Krapivner SR; Malyshev PP; Rozhkova TA; Potaraus AB; Kukharchuk VV; Bochkov VN
    Ter Arkh; 2000; 72(4):9-12. PubMed ID: 10833789
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Improved detection of familial defective apolipoprotein B-100 by restriction-site-introducing polymerase chain reaction.
    Geisel J; Schleifenbaum T; Weisshaar B; Oette K
    Clin Chem; 1993 Sep; 39(9):2026-7. PubMed ID: 8375096
    [No Abstract]   [Full Text] [Related]  

  • 19. Using mutagenic polymerase chain reaction primers to detect carriers of familial defective apolipoprotein B-100.
    Motti C; Funke H; Rust S; Dergunov A; Assmann G
    Clin Chem; 1991 Oct; 37(10 Pt 1):1762-6. PubMed ID: 1680583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid detection of 3500Q and 3531 mutations and MspI polymorphism in exon 26 at the apolipoprotein B gene.
    Cavalli SA; Hirata MH; Hirata RD
    J Clin Lab Anal; 2001; 15(1):35-9. PubMed ID: 11170232
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.