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125 related items for PubMed ID: 7625765

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 Apr; 38(4):246-50. PubMed ID: 3169800
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  • 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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  • 6. 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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  • 7. 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 Jul 13; 10(1):38-44. PubMed ID: 7691111
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  • 9. 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 13; 75(3):396-401. PubMed ID: 2702782
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  • 10. C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish.
    O'Hara AM, Fernie BA, Moran AP, Williams YE, Connaughton JJ, Orren A, Hobart MJ.
    Clin Exp Immunol; 1998 Dec 13; 114(3):355-61. PubMed ID: 9844043
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  • 11. 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 Dec 13; 7(2):90-4. PubMed ID: 2225795
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  • 12. Molecular bases of C7 deficiency: three different defects.
    Fernie BA, Orren A, Sheehan G, Schlesinger M, Hobart MJ.
    J Immunol; 1997 Jul 15; 159(2):1019-26. PubMed ID: 9218625
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  • 13. 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 15; 95(2):351-6. PubMed ID: 7508350
    [Abstract] [Full Text] [Related]

  • 14. DNA polymorphisms of the complement C6 and C7 genes.
    Fernie BA, Würzner R, Unsworth DJ, Tuxworth RI, Hobart MJ.
    Ann Hum Genet; 1995 Apr 15; 59(2):163-81. PubMed ID: 7625764
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  • 15. 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 Apr 15; 68(2):138-41. PubMed ID: 6500564
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  • 16. 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 Apr 15; 15(4):268-85. PubMed ID: 10072638
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  • 17. Family study on the polymorphisms of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analyses.
    Tokunaga K, Dewald G, Omoto K, Juji T.
    Am J Hum Genet; 1986 Sep 15; 39(3):414-9. PubMed ID: 3766543
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  • 18. The molecular basis of C6 deficiency in the western Cape, South Africa.
    Hobart MJ, Fernie BA, Fijen KA, Orren A.
    Hum Genet; 1998 Oct 15; 103(4):506-12. PubMed ID: 9856498
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  • 19. DNA polymorphisms and linkage relationship of the human complement component C6, C7, and C9 genes.
    Coto E, Martínez-Naves E, Domínguez O, DiScipio RG, Urra JM, López-Larrea C.
    Immunogenetics; 1991 Oct 15; 33(3):184-7. PubMed ID: 1672663
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  • 20. 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 Oct 15; 13(2):92-103. PubMed ID: 9063701
    [Abstract] [Full Text] [Related]

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