BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 12653841)

  • 1. Restricted genetic defects underlie human complement C6 deficiency.
    Dragon-Durey MA; Fremeaux-Bacchi V; Blouin J; Barraud D; Fridman WH; Kazatchkine MD
    Clin Exp Immunol; 2003 Apr; 132(1):87-91. PubMed ID: 12653841
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular defects leading to human complement component C6 deficiency in an African-American family.
    Zhu ZB; Totemchokchyakarn K; Atkinson TP; Volanakis JE
    Clin Exp Immunol; 1998 Jan; 111(1):91-6. PubMed ID: 9472666
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High prevalence of complement component C6 deficiency among African-Americans in the south-eastern USA.
    Zhu Z; Atkinson TP; Hovanky KT; Boppana SB; Dai YL; Densen P; Go RC; Jablecki JS; Volanakis JE
    Clin Exp Immunol; 2000 Feb; 119(2):305-10. PubMed ID: 10632667
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular bases for inherited human complement component C6 deficiency in two unrelated individuals.
    Nishizaka H; Horiuchi T; Zhu ZB; Fukumori Y; Nagasawa K; Hayashi K; Krumdieck R; Cobbs CG; Higuchi M; Yasunaga S; Niho Y; Volanakis JE
    J Immunol; 1996 Mar; 156(6):2309-15. PubMed ID: 8690922
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The molecular basis of C6 deficiency in the western Cape, South Africa.
    Hobart MJ; Fernie BA; Fijen KA; Orren A
    Hum Genet; 1998 Oct; 103(4):506-12. PubMed ID: 9856498
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complement component C6 deficiency in a Spanish family: implications for clinical and molecular diagnosis.
    Moya-Quiles MR; Bernardo-Pisa MV; Martínez P; Gimeno L; Bosch A; Salgado G; Martínez-Banaclocha H; Eguia J; Campillo JA; Muro M; Vidal-Bugallo JB; Alvarez-López MR; García-Alonso AM
    Gene; 2013 May; 521(1):204-6. PubMed ID: 23537992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deficiency of the sixth component of complement and susceptibility to Neisseria meningitidis infections: studies in 10 families and five isolated cases.
    Orren A; Potter PC; Cooper RC; du Toit E
    Immunology; 1987 Oct; 62(2):249-53. PubMed ID: 3679285
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family.
    Parham KL; Roberts A; Thomas A; Würzner R; Henderson HE; Potter PC; Morgan BP; Orren A
    Mol Immunol; 2007 Apr; 44(10):2756-60. PubMed ID: 17257682
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism.
    Ikinciogullari A; Tekin M; Dogu F; Reisli I; Tanir G; Yi Z; Garrison N; Brilliant MH; Babacan E
    Eur J Pediatr; 2005 Mar; 164(3):177-9. PubMed ID: 15565285
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects.
    Orren A
    Clin Exp Immunol; 2000 Feb; 119(2):255-8. PubMed ID: 10632659
    [No Abstract]   [Full Text] [Related]  

  • 11. Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans.
    Orren A; Owen EP; Henderson HE; van der Merwe L; Leisegang F; Stassen C; Potter PC
    Clin Exp Immunol; 2012 Mar; 167(3):459-71. PubMed ID: 22288589
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human deficiency of the sixth component of complement in a patient with meningococcal meningitis and no haemostasis abnormality.
    Kernbaum S; Bastin R; Wautier JL; Bure A; Gougerot M; Peltier AP
    Biomedicine; 1980; 33(6):197-201. PubMed ID: 6783144
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Molecular defects of the C7 gene in two patients with complement C7 deficiency.
    Barroso S; Rieubland C; José álvarez A; López-Trascasa M; Bart PA; Núñez-Roldán A; Sánchez B
    Immunology; 2006 Jun; 118(2):257-60. PubMed ID: 16771861
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary complement deficiency and lupus: report of four Tunisian cases.
    Kallel-Sellami M; Baili-Klila L; Zerzeri Y; Laadhar L; Blouin J; Abdelmalek R; Fremeaux-Bacchi V; Zitouni M; Makni S
    Ann N Y Acad Sci; 2007 Jun; 1108():197-202. PubMed ID: 17893986
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.
    Owen EP; Würzner R; Leisegang F; Rizkallah P; Whitelaw A; Simpson J; Thomas AD; Harris CL; Giles JL; Hellerud BC; Mollnes TE; Morgan BP; Potter PC; Orren A
    Mol Immunol; 2015 Mar; 64(1):170-6. PubMed ID: 25534848
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prevalence of congenital or acquired complement deficiency in patients with sporadic meningococcal disease.
    Ellison RT; Kohler PF; Curd JG; Judson FN; Reller LB
    N Engl J Med; 1983 Apr; 308(16):913-6. PubMed ID: 6835295
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Recurrent meningococcal meningitis associated with complement C6 deficiency (author's transl)].
    Avril MF; Lebas J; Autran B; Modai J
    Nouv Presse Med; 1981 Oct; 10(37):3057-9. PubMed ID: 7290963
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The role of complement in anti-bacterial defence.
    D'Amelio R; Biselli R
    Ann Ital Med Int; 1994; 9(3):173-7. PubMed ID: 7946895
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 114(3):355-61. PubMed ID: 9844043
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.