125 related articles for article (PubMed ID: 9856498)
1. 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]
2. 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]
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. 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]
5. 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]
6. Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa.
Owen EP; Leisegang F; Whitelaw A; Simpson J; Baker S; Würzner R; Potter P; Orren A
S Afr Med J; 2012 May; 102(6):525-7. PubMed ID: 22668955
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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; 95(2):351-6. PubMed ID: 7508350
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Molecular basis of subtotal complement C6 deficiency. A carboxy-terminally truncated but functionally active C6.
Würzner R; Hobart MJ; Fernie BA; Mewar D; Potter PC; Orren A; Lachmann PJ
J Clin Invest; 1995 Apr; 95(4):1877-83. PubMed ID: 7535801
[TBL] [Abstract][Full Text] [Related]
20. Molecular basis for complement component 6 (C6) deficiency in rats and mice.
Bhole D; Stahl GL
Immunobiology; 2004; 209(7):559-68. PubMed ID: 15568620
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]