BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 102474)

  • 1. Combined genetic deficiency of C6 and C7 in man.
    Lachmann PJ; Hobart MJ; Woo P
    Clin Exp Immunol; 1978 Aug; 33(2):193-203. PubMed ID: 102474
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.
    Alvarez V; Coto E; Setién F; Spath PJ; López-Larrea C
    Am J Med Genet; 1995 Feb; 55(4):408-13. PubMed ID: 7762578
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular bases of combined subtotal deficiencies of C6 and C7: their effects in combination with other C6 and C7 deficiencies.
    Fernie BA; Würzner R; Orren A; Morgan BP; Potter PC; Platonov AE; Vershinina IV; Shipulin GA; Lachmann PJ; Hobart MJ
    J Immunol; 1996 Oct; 157(8):3648-57. PubMed ID: 8871666
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Genetic polymorphism of the sixth (C6) and seventh (C7) components of complement in Russian rural inhabitants of the Tomsk region].
    Kucher AN; Puzyrev VP; Ivanova OF; Khu TsIu; Siuĭ TsTs; Du ZhF
    Genetika; 1993 Nov; 29(11):1889-94. PubMed ID: 8307376
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of hereditary combined deficiency of complement components C6 and C7 in man.
    Morgan BP; Vora JP; Bennett AJ; Thomas JP; Matthews N
    Clin Exp Immunol; 1989 Mar; 75(3):396-401. PubMed ID: 2702782
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Three Japanese families with members carrying C7 silent allele (C7*Q0). Possibility for an association between C7*Q0 and C6*B.
    Nishimukai H; Kitamura H; Takeuchi Y; Shinomiya T; Tamaki Y
    Hum Hered; 1988; 38(4):246-50. PubMed ID: 3169800
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13.
    Fernie BA; Orren A; Schlesinger M; Würzner R; Platonov AE; Cooper RC; Williams YE; Hobart MJ
    Ann Hum Genet; 1997 Jul; 61(Pt 4):287-98. PubMed ID: 9365782
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Complement component C6 and C7 haplotypes associated with deficiencies of C6.
    Fernie BA; Orren A; Würzner R; Jones AM; Potter PC; Lachmann PJ; Hobart MJ
    Ann Hum Genet; 1995 Apr; 59(2):183-95. PubMed ID: 7625765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7.
    Würzner R; Rance N; Potter PC; Hendricks ML; Lachmann PJ; Orren A
    Clin Exp Immunol; 1992 Sep; 89(3):485-9. PubMed ID: 1516263
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement.
    Potter PC; Warburton C; Würzner R; Orren A; Di Scipio R
    Exp Clin Immunogenet; 1993; 10(1):38-44. PubMed ID: 7691111
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial late complement component (C6, C7) deficiency with chronic meningococcemia.
    Clough JD; Clough ML; Weinstein A; Calabrese LH; Mansfield LR; Gulick P; Gavan T; Braun WE
    Arch Intern Med; 1980 Jul; 140(7):929-33. PubMed ID: 7387302
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human C7 polymorphism: classification and association analysis with C6.
    Washio K; Tokunaga K; Omoto K; Misawa S
    Jinrui Idengaku Zasshi; 1986 Dec; 31(4):345-52. PubMed ID: 3613240
    [No Abstract]   [Full Text] [Related]  

  • 13. Molecular bases of C7 deficiency: three different defects.
    Fernie BA; Orren A; Sheehan G; Schlesinger M; Hobart MJ
    J Immunol; 1997 Jul; 159(2):1019-26. PubMed ID: 9218625
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies.
    Würzner R; Witzel-Schlömp K; Tokunaga K; Fernie BA; Hobart MJ; Orren A
    Exp Clin Immunogenet; 1998; 15(4):268-85. PubMed ID: 10072638
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structural similarities between C6 and C7 of human complement.
    Podack ER; Kolb WP; Esser AF; Müller-Eberhard HJ
    J Immunol; 1979 Sep; 123(3):1071-7. PubMed ID: 381516
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic control of C6 polymorphism and C6 deficiency in rabbits.
    Goldman MB; Cohen C; Stronski K; Bangalore S; Goldman JN
    J Immunol; 1982 Jan; 128(1):43-8. PubMed ID: 6172488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Study of genetic polymorphism of seventh complement component in two families with hereditary deficit.
    López-Larrea C; Dominguez O; Martinez-Naves E; Coto E
    Complement Inflamm; 1990; 7(2):90-4. PubMed ID: 2225795
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inherited deficiency of the sixth component of complement: a silent or null gene.
    Glass D; Raum D; Balavitch D; Kagan E; Rabson A; Schur PH; Alper CA
    J Immunol; 1978 Feb; 120(2):538-41. PubMed ID: 621392
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited deficiency of the seventh component of complement associated with nephritis. Propensity to formation of C56 and related C7-consuming activity.
    Nemerow GR; Gewurz H; Osofsky SG; Lint TF
    J Clin Invest; 1978 Jun; 61(6):1602-10. PubMed ID: 350902
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic polymorphism of complement C6 and haplotype analysis between C6 and C7 in a Japanese population.
    Nakamura S; Ooue O; Akiyama K; Abe K
    Hum Genet; 1984; 68(2):138-41. PubMed ID: 6500564
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.