170 related articles for article (PubMed ID: 10072638)
1. 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]
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 component C6: protein typing.
Geserick G; Schröder H; Correns A
Exp Clin Immunogenet; 1998; 15(4):286-90. PubMed ID: 10072639
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
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; 89(3):485-9. PubMed ID: 1516263
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. [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]
12. 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; 38(4):246-50. PubMed ID: 3169800
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Combined genetic deficiency of C6 and C7 in man.
Lachmann PJ; Hobart MJ; Woo P
Clin Exp Immunol; 1978 Aug; 33(2):193-203. PubMed ID: 102474
[TBL] [Abstract][Full Text] [Related]
15. [Genetic polymorphism of the sixth (C6) and seventh (C7) components of complement in Russian rural inhabitants of the Tomsk region].
Kucher AN; Puzyrev VP; Ivanova OF; Khu TsIu; Siuĭ TsTs; Du ZhF
Genetika; 1993 Nov; 29(11):1889-94. PubMed ID: 8307376
[TBL] [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. 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; 75(3):396-401. PubMed ID: 2702782
[TBL] [Abstract][Full Text] [Related]
18. Human C7 polymorphism: classification and association analysis with C6.
Washio K; Tokunaga K; Omoto K; Misawa S
Jinrui Idengaku Zasshi; 1986 Dec; 31(4):345-52. PubMed ID: 3613240
[No Abstract] [Full Text] [Related]
19. Inherited deficiencies of the late-acting complement components other than C9 found among healthy blood donors.
Inai S; Akagaki Y; Moriyama T; Fukumori Y; Yoshimura K; Ohnoki S; Yamaguchi H
Int Arch Allergy Appl Immunol; 1989; 90(3):274-9. PubMed ID: 2592116
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
