119 related articles for article (PubMed ID: 9703418)
21. [C9 deficiency].
Kira R; Hara T
Ryoikibetsu Shokogun Shirizu; 2000; (32):212-4. PubMed ID: 11212695
[No Abstract] [Full Text] [Related]
22. Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation.
Sugie H; Sugie Y; Ito M; Fukuda T; Nonaka I; Igarashi Y
Clin Chim Acta; 1995 Apr; 236(1):81-6. PubMed ID: 7664468
[TBL] [Abstract][Full Text] [Related]
23. Genetic basis of human complement C8 beta deficiency.
Kaufmann T; Hänsch G; Rittner C; Späth P; Tedesco F; Schneider PM
J Immunol; 1993 Jun; 150(11):4943-7. PubMed ID: 8098723
[TBL] [Abstract][Full Text] [Related]
24. Relationships between the gene and protein structure in human complement component C9.
Marazziti D; Eggertsen G; Fey GH; Stanley KK
Biochemistry; 1988 Aug; 27(17):6529-34. PubMed ID: 3219351
[TBL] [Abstract][Full Text] [Related]
25. Recurrent meningitis in a patient with congenital deficiency of the C9 component of complement. First case of C9 deficiency in Europe.
Zoppi M; Weiss M; Nydegger UE; Hess T; Späth PJ
Arch Intern Med; 1990 Nov; 150(11):2395-9. PubMed ID: 2241452
[TBL] [Abstract][Full Text] [Related]
26. High incidence of complement C9 deficiency in Koreans.
Kang HJ; Kim HS; Lee YK; Cho HC
Ann Clin Lab Sci; 2005; 35(2):144-8. PubMed ID: 15943177
[TBL] [Abstract][Full Text] [Related]
27. Molecular characterization and expression analysis of complement component C9 gene in the whitespotted bambooshark, Chiloscyllium plagiosum.
Wang Y; Xu S; Su Y; Ye B; Hua Z
Fish Shellfish Immunol; 2013 Aug; 35(2):599-606. PubMed ID: 23684808
[TBL] [Abstract][Full Text] [Related]
28. Inherited deficiency of the ninth component of complement associated with streptococcal infection.
Fujita M; Fujita T; Inai S
Acta Paediatr Jpn; 1992 Apr; 34(2):169-72. PubMed ID: 1621522
[TBL] [Abstract][Full Text] [Related]
29. Detection of the three common mutations of adeninephosphoribosyltransferase deficiency among Japanese.
Higashimoto H; Ouchi A; Kawaguchi R
Clin Chim Acta; 1995 Jan; 234(1-2):1-10. PubMed ID: 7758207
[TBL] [Abstract][Full Text] [Related]
30. Typing of the nt343C>T (R95X) allele of the C9 gene by PCR-SSP and the allele frequency of R95X in five ethnic populations.
Tsujimura R; Nishimukai H; Okiura T; Fukumori Y; Tanabe R; Orimoto C; Ueda N
Leg Med (Tokyo); 2009 Apr; 11 Suppl 1():S482-3. PubMed ID: 19261509
[TBL] [Abstract][Full Text] [Related]
31. Three nonsense mutations responsible for group A xeroderma pigmentosum.
Satokata I; Tanaka K; Miura N; Narita M; Mimaki T; Satoh Y; Kondo S; Okada Y
Mutat Res; 1992 Mar; 273(2):193-202. PubMed ID: 1372102
[TBL] [Abstract][Full Text] [Related]
32. High-incidence of C9 deficiency throughout Japan: there are no significant differences in incidence among eight areas of Japan.
Hayama K; Sugai N; Tanaka S; Lee S; Kikuchi H; Ito J; Suzuki J; Nagata Y; Kondo H; Harayama O
Int Arch Allergy Appl Immunol; 1989; 90(4):400-4. PubMed ID: 2613346
[TBL] [Abstract][Full Text] [Related]
33. Genetic bases of human complement C7 deficiency.
Nishizaka H; Horiuchi T; Zhu ZB; Fukumori Y; Volanakis JE
J Immunol; 1996 Nov; 157(9):4239-43. PubMed ID: 8892662
[TBL] [Abstract][Full Text] [Related]
34. Molecular cloning, promoter analysis and induced expression of the complement component C9 gene in the grass carp Ctenopharyngodon idella.
Li L; Chang MX; Nie P
Vet Immunol Immunopathol; 2007 Aug; 118(3-4):270-82. PubMed ID: 17604124
[TBL] [Abstract][Full Text] [Related]
35. An abnormal but functionally active complement component C9 protein found in an Irish family with subtotal C9 deficiency.
Orren A; O'Hara AM; Morgan BP; Moran AP; Würzner R
Immunology; 2003 Mar; 108(3):384-90. PubMed ID: 12603605
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. C9-R95X polymorphism in patients with neovascular age-related macular degeneration.
Nishiguchi KM; Yasuma TR; Tomida D; Nakamura M; Ishikawa K; Kikuchi M; Ohmi Y; Niwa T; Hamajima N; Furukawa K; Terasaki H
Invest Ophthalmol Vis Sci; 2012 Jan; 53(1):508-12. PubMed ID: 22190594
[TBL] [Abstract][Full Text] [Related]
39. Identification and chromosomal assignment of two heterozygous mutations in the Trp53 gene in L5178Y/Tk(+/-)-3.7.2C mouse lymphoma cells.
Clark LS; Hart DW; Vojta PJ; Harrington-Brock K; Barrett JC; Moore MM; Tindall KR
Mutagenesis; 1998 Sep; 13(5):427-34. PubMed ID: 9800187
[TBL] [Abstract][Full Text] [Related]
40. A novel mutation in the erythrocyte protein 4.2 gene of Japanese patients with hereditary spherocytosis (protein 4.2 Fukuoka).
Takaoka Y; Ideguchi H; Matsuda M; Sakamoto N; Takeuchi T; Fukumaki Y
Br J Haematol; 1994 Nov; 88(3):527-33. PubMed ID: 7819064
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
