131 related articles for article (PubMed ID: 9634479)
1. Heterogeneity in the genetic basis of human complement C9 deficiency.
Witzel-Schlömp K; Hobart MJ; Fernie BA; Orren A; Würzner R; Rittner C; Kaufmann T; Schneider PM
Immunogenetics; 1998 Jul; 48(2):144-7. PubMed ID: 9634479
[No 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. 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]
4. A physical map of the human complement component C6, C7, and C9 genes.
Setién F; Alvarez V; Coto E; DiScipio RG; López-Larrea C
Immunogenetics; 1993; 38(5):341-4. PubMed ID: 8344719
[TBL] [Abstract][Full Text] [Related]
5. 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; 33(3):184-7. PubMed ID: 1672663
[TBL] [Abstract][Full Text] [Related]
6. The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure.
Witzel-Schlömp K; Späth PJ; Hobart MJ; Fernie BA; Rittner C; Kaufmann T; Schneider PM
J Immunol; 1997 May; 158(10):5043-9. PubMed ID: 9144525
[TBL] [Abstract][Full Text] [Related]
7. Phylogenetic analysis of the homologous proteins of the terminal complement complex supports the emergence of C6 and C7 followed by C8 and C9.
Mondragón-Palomino M; Piñero D; Nicholson-Weller A; Laclette JP
J Mol Evol; 1999 Aug; 49(2):282-9. PubMed ID: 10441679
[TBL] [Abstract][Full Text] [Related]
8. [The association between deficiency of terminal complement components and the occurrence of meningococcal meningitis].
Nishizaki M
Fukuoka Igaku Zasshi; 1992 May; 83(5):201-8. PubMed ID: 1612549
[TBL] [Abstract][Full Text] [Related]
9. Inherited deficiency of ninth component of complement: an increased risk of meningococcal meningitis.
Nagata M; Hara T; Aoki T; Mizuno Y; Akeda H; Inaba S; Tsumoto K; Ueda K
J Pediatr; 1989 Feb; 114(2):260-4. PubMed ID: 2915285
[No Abstract] [Full Text] [Related]
10. Meningococcal meningitis in a women with inherited deficiency of the ninth component of complement.
Fine DP; Gewurz H; Griffiss M; Lint TF
Clin Immunol Immunopathol; 1983 Sep; 28(3):413-7. PubMed ID: 6883811
[TBL] [Abstract][Full Text] [Related]
11. [C9 deficiency].
Kira R; Hara T
Ryoikibetsu Shokogun Shirizu; 2000; (32):212-4. PubMed ID: 11212695
[No Abstract] [Full Text] [Related]
12. Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes.
Hobart MJ; Fernie BA; DiScipio RG
J Immunol; 1995 May; 154(10):5188-94. PubMed ID: 7730625
[TBL] [Abstract][Full Text] [Related]
13. Nonsense mutation in exon 4 of human complement C9 gene is the major cause of Japanese complement C9 deficiency.
Kira R; Ihara K; Takada H; Gondo K; Hara T
Hum Genet; 1998 Jun; 102(6):605-10. PubMed ID: 9703418
[TBL] [Abstract][Full Text] [Related]
14. Difficulties in the ascertainment of C9 deficiency: lessons to be drawn from a compound heterozygote C9-deficient subject.
Hobart MJ; Fernie BA; Würzner R; Oldroyd RG; Harrison RA; Joysey V; Lachmann PJ
Clin Exp Immunol; 1997 Jun; 108(3):500-6. PubMed ID: 9182899
[TBL] [Abstract][Full Text] [Related]
15. [Clinical significance of C6, C7, C9 and C1-INH analysis].
Akagaki Y; Inai S
Nihon Rinsho; 1990 Feb; 48 Suppl():662-5. PubMed ID: 2113138
[No Abstract] [Full Text] [Related]
16. 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]
17. [Immunologic tests: C6, C7, C8 and C9].
Hatanaka M; Shimizu A
Nihon Rinsho; 2005 Jul; 63 Suppl 7():92-4. PubMed ID: 16111197
[No Abstract] [Full Text] [Related]
18. [Clinical findings and genetic bases of congenital complement deficiencies].
Kira R; Ihara K; Takada H; Hara J
Nihon Rinsho Meneki Gakkai Kaishi; 1999 Apr; 22(2):53-62. PubMed ID: 11126655
[TBL] [Abstract][Full Text] [Related]
19. [C6, C7, C8 and C9].
Hatanaka M; Kitano E
Nihon Rinsho; 2010 Jun; 68 Suppl 6():90-3. PubMed ID: 20942009
[No Abstract] [Full Text] [Related]
20. The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.
Rogne S; Myklebost O; Olving JH; Kyrkjebø HT; Jonassen R; Olaisen B; Gedde-Dahl T
J Med Genet; 1991 Sep; 28(9):587-90. PubMed ID: 1683409
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
