398 related articles for article (PubMed ID: 18502179)
21. Immunoglobulin G subclasses in immunodeficiency.
Söderström T; Söderström R; Hanson LA
Ann Clin Res; 1987; 19(4):280-4. PubMed ID: 3314653
[TBL] [Abstract][Full Text] [Related]
22. Baboon immunoglobulin constant region heavy chains: identification of four IGHG genes.
Attanasio R; Jayashankar L; Engleman CN; Scinicariello F
Immunogenetics; 2002 Nov; 54(8):556-61. PubMed ID: 12439618
[TBL] [Abstract][Full Text] [Related]
23. Serum IgG subclass deficiency in ataxia-telangiectasia.
Aucouturier P; Bremard-Oury C; Griscelli C; Berthier M; Preud'homme JL
Clin Exp Immunol; 1987 May; 68(2):392-6. PubMed ID: 3652519
[TBL] [Abstract][Full Text] [Related]
24. Human immunoglobulin G and immunoglobulin G subclasses: biochemical, genetic, and clinical aspects.
Papadea C; Check IJ
Crit Rev Clin Lab Sci; 1989; 27(1):27-58. PubMed ID: 2647414
[TBL] [Abstract][Full Text] [Related]
25. Imbalanced switch of the IGHG (immunoglobulin constant heavy G chain) Gm(bfn) genes in atopic childhood asthma.
Oxelius VA
Allergy; 2000 Nov; 55(11):1063-8. PubMed ID: 11097318
[TBL] [Abstract][Full Text] [Related]
26. IgG subclass deficiency.
Preud'homme JL; Hanson LA
Immunodefic Rev; 1990; 2(2):129-49. PubMed ID: 2223061
[TBL] [Abstract][Full Text] [Related]
27. Allotypic markers.
van Loghem E
Monogr Allergy; 1986; 19():40-51. PubMed ID: 2429173
[No Abstract] [Full Text] [Related]
28. Linkage of IgA deficiency to Gm allotypes; the influence of Gm allotypes on IgA-IgG subclass deficiency.
Oxelius VA; Carlsson AM; Hammarström L; Björkander J; Hanson LA
Clin Exp Immunol; 1995 Feb; 99(2):211-5. PubMed ID: 7851013
[TBL] [Abstract][Full Text] [Related]
29. Patients with Wiskott-Aldrich syndrome have normal IgG2 levels.
Nahm MH; Blaese RM; Crain MJ; Briles DE
J Immunol; 1986 Dec; 137(11):3484-7. PubMed ID: 3782789
[TBL] [Abstract][Full Text] [Related]
30. Suppressed G2m(n) levels from IGHCG2 in IgA deficiency.
Oxelius VA
Exp Clin Immunogenet; 1996; 13(1):1-6. PubMed ID: 8854082
[TBL] [Abstract][Full Text] [Related]
31. A new look at the biological and genetic significance of rabbit heavy chain allotypes.
Mage RG
Ann Immunol (Paris); 1979; 130(2):105-14. PubMed ID: 111599
[No Abstract] [Full Text] [Related]
32. T and B markers in immunodeficiencies.
Griscelli C
Birth Defects Orig Artic Ser; 1975; 11(1):45-9. PubMed ID: 1096991
[No Abstract] [Full Text] [Related]
33. Responses of lymphocytes to Epstein-Barr virus in patients with primary immunodeficiencies.
Kondo N; Inoue R; Orii T
J Investig Allergol Clin Immunol; 1994; 4(4):182-4. PubMed ID: 7850031
[TBL] [Abstract][Full Text] [Related]
34. Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency.
Kutukculer N; Karaca NE; Demircioglu O; Aksu G
Pediatr Allergy Immunol; 2007 Mar; 18(2):167-73. PubMed ID: 17338791
[TBL] [Abstract][Full Text] [Related]
35. Molecular basis of IgG subclass deficiency.
Pan Q; Hammarström L
Immunol Rev; 2000 Dec; 178():99-110. PubMed ID: 11213812
[TBL] [Abstract][Full Text] [Related]
36. Ataxia-telangiectasia breakpoints in chromosome rearrangements reflect genes important to T and B lymphocytes.
Hecht F; Hecht BK
Kroc Found Ser; 1985; 19():189-95. PubMed ID: 3934344
[TBL] [Abstract][Full Text] [Related]
37. Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes.
Skattum L; Gullstrand B; Holmström E; Oxelius VA; Truedsson L
Clin Immunol; 2008 Oct; 129(1):123-31. PubMed ID: 18667363
[TBL] [Abstract][Full Text] [Related]
38. Molecular and serologic analysis of IgG1 deficiency caused by new forms of the constant region of the Ig H chain gene deletions.
Smith CI; Hammarström L; Henter JI; de Lange GG
J Immunol; 1989 Jun; 142(12):4514-9. PubMed ID: 2498432
[TBL] [Abstract][Full Text] [Related]
39. Gene deletion and gene duplication within the cluster of human heavy-chain genes. Selective absence of IgG sub-classes.
van Loghem E; Sukernik RI; Osipova LP; Zegers BJ; Matsumoto H; de Lange G; Lefranc G
J Immunogenet; 1980 Aug; 7(4):285-99. PubMed ID: 6778930
[TBL] [Abstract][Full Text] [Related]
40. Instability of the human immunoglobulin heavy chain constant region locus indicated by different inherited chromosomal deletions.
Lefranc MP; Lefranc G; de Lange G; Out TA; van den Broek PJ; van Nieuwkoop J; Radl J; Helal AN; Chaabani H; van Loghem E
Mol Biol Med; 1983 Sep; 1(2):207-17. PubMed ID: 6438434
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
