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Journal Abstract Search

287 related items for PubMed ID: 7691111

  • 1.
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  • 2. Complement C6 and C7 DNA polymorphisms analysed by PCR in seven ethnic groups and characterisation of the C6 MspI RFLP.
    Fernie BA, Finlay A, Price D, Chan E, Orren A, Joysey VC, Joysey KA, Hobart MJ.
    Exp Clin Immunogenet; 1996; 13(2):92-103. PubMed ID: 9063701
    [Abstract] [Full Text] [Related]

  • 3. 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 13; 55(4):408-13. PubMed ID: 7762578
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  • 4. C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP).
    Fernie BA, Hobart MJ, Delbridge G, Potter PC, Orren A, Lachmann PJ.
    Clin Exp Immunol; 1994 Feb 13; 95(2):351-6. PubMed ID: 7508350
    [Abstract] [Full Text] [Related]

  • 5. 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 13; 61(Pt 4):287-98. PubMed ID: 9365782
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  • 6. 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 13; 89(3):485-9. PubMed ID: 1516263
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  • 8. [Polymorphism MI detected through the enzyme MspI in the study of congenital protein C deficiency].
    Soria JM, Ibáñez I, Fontcuberta J, Borrell M, Estivill X, Sala N.
    Med Clin (Barc); 1992 Nov 21; 99(17):649-52. PubMed ID: 1280311
    [Abstract] [Full Text] [Related]

  • 9. 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 21; 59(2):183-95. PubMed ID: 7625765
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  • 12. Xbal 16- plus 9-kilobase DNA restriction fragments identify a mutant allele for debrisoquin hydroxylase: report of a family study.
    Evans WE, Relling MV.
    Mol Pharmacol; 1990 May 21; 37(5):639-42. PubMed ID: 1971090
    [Abstract] [Full Text] [Related]

  • 13. 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 May 21; 38(4):246-50. PubMed ID: 3169800
    [Abstract] [Full Text] [Related]

  • 14. A MspI restriction fragment length polymorphism at the ovine locus for 2',3'-cyclic-nucleotide 3'-phosphohydrolase.
    Penty JM, Tou HM, Hill DF.
    Anim Genet; 1991 May 21; 22(2):196. PubMed ID: 1716426
    [No Abstract] [Full Text] [Related]

  • 15. Carrier detection in severe (type III) von Willebrand disease using two intragenic restriction fragment length polymorphisms.
    Bahnak BR, Lavergne JM, Verweij CL, Rothschild C, Pannekoek H, Larrieu MJ, Meyer D.
    Thromb Haemost; 1988 Oct 31; 60(2):178-81. PubMed ID: 2905841
    [Abstract] [Full Text] [Related]

  • 16. MspI polymorphism at the human complement component C6 gene (C6).
    Coto E, Domínguez O, Martínez-Naves E, Setién F, Gutiérrez V, López-Larrea C.
    Nucleic Acids Res; 1991 Jan 11; 19(1):194. PubMed ID: 1707160
    [No Abstract] [Full Text] [Related]

  • 17. Combined genetic deficiency of C6 and C7 in man.
    Lachmann PJ, Hobart MJ, Woo P.
    Clin Exp Immunol; 1978 Aug 11; 33(2):193-203. PubMed ID: 102474
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  • 18. 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 15; 157(8):3648-57. PubMed ID: 8871666
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 120(2):538-41. PubMed ID: 621392
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