These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
143 related articles for article (PubMed ID: 6953615)
21. HLA-linked complement markers in Alzheimer's and Parkinson's disease: C4 variant (C4B2) a possible marker for senile dementia of the Alzheimer type. Nerl C; Mayeux R; O'Neill GJ Neurology; 1984 Mar; 34(3):310-4. PubMed ID: 6538270 [TBL] [Abstract][Full Text] [Related]
22. HLA A*, B*-BF* and C4 A*, B* allele associations, with special reference to BF*S07, in the Tunisian population. Helal AN; Lefranc G; Hauptmann G; Goetz J; Tongio MM; Davrinche C; Rivat C; Cavelier B; Chibani J; Chaabani H J Immunogenet; 1983 Jun; 10(3):205-8. PubMed ID: 6576063 [TBL] [Abstract][Full Text] [Related]
23. Polymorphism of BF, C2, and GLO in Japanese patients with insulin-dependent diabetes mellitus: confirmation of an increase of BF*FT. Tokunaga K; Omoto K; Juji T; Itoh T Hum Genet; 1982; 62(1):86-8. PubMed ID: 6924917 [No Abstract] [Full Text] [Related]
24. Studies of HLA, factor B (Bf), complement C2 and C4 haplotypes in type 1 diabetic and control families from northern Sweden. Hägglöf B; Holmgren G; Holmlund G; Lindblom B; Olaisen B; Teisberg P Hum Hered; 1986; 36(4):201-12. PubMed ID: 3639057 [TBL] [Abstract][Full Text] [Related]
25. HLA, complement C2, C4, properdin factor B and glyoxalase types in South Indian diabetics. Kirk RL; Ranford PR; Serjeantson SW; Thompson AR; Munirathnam Chetty SM; John L; Mohan V; Ramachandran A; Snehalatha C; Viswanathan M Diabetes Res Clin Pract; 1985 Mar; 1(1):41-7. PubMed ID: 3879724 [TBL] [Abstract][Full Text] [Related]
26. Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I. O'Neill GJ; Pollack MS; Yang SY; Levine LS; New MI; Dupont B Transplant Proc; 1979 Dec; 11(4):1713-5. PubMed ID: 316936 [No Abstract] [Full Text] [Related]
27. HLA and narcolepsy in a German population. Mueller-Eckhardt G; Meier-Ewert K; Schendel DJ; Reinecker FB; Multhoff G; Mueller-Eckhardt C Tissue Antigens; 1986 Sep; 28(3):163-9. PubMed ID: 3641479 [TBL] [Abstract][Full Text] [Related]
28. Polymorphism of properdin factor B in Japanese. Description of a rare variant and data of association with HLA and C2. Tokunaga K; Araki C; Juji T; Omoto K Hum Genet; 1982; 60(1):42-5. PubMed ID: 6918356 [TBL] [Abstract][Full Text] [Related]
30. C4 haplotypes with duplications at the C4A or C4B loci: frequency and associations with BF, C2, and HLA-A, B, C, DR alleles. Uring-Lambert B; Goetz J; Tongio MM; Mayer S; Hauptmann G Tissue Antigens; 1984 Jul; 24(1):70-2. PubMed ID: 6592795 [No Abstract] [Full Text] [Related]
31. Association between allotypes of complement components C2, BF, C4 of HLA class III and cerebral stroke. Wang C; Zhao XZ; Chen SQ; Wang ZH J Tongji Med Univ; 1992; 12(2):90-3. PubMed ID: 1433424 [TBL] [Abstract][Full Text] [Related]
32. Human MHC class III genes, BF and C4. Polymorphism, complotypes and HLA class I and II associations in the Lombardy population (Italy). De Paoli F; Cuccia Belvedere M; Martinetti M; Abbal M Gene Geogr; 1987 Aug; 1(2):121-9. PubMed ID: 3155297 [TBL] [Abstract][Full Text] [Related]
33. C4B3 allotype with a novel Ch phenotype. Skanes VM; Larsen B; Giles CM Immunogenetics; 1985; 22(6):609-16. PubMed ID: 3865894 [TBL] [Abstract][Full Text] [Related]
34. The location of C2, C4, and BF relative to HLA-B and HLA-D. Raum DD; Awdeh ZL; Glass D; Yunis E; Alper CA Immunogenetics; 1981 Mar; 12(5-6):473-83. PubMed ID: 7216322 [TBL] [Abstract][Full Text] [Related]
35. Class III alleles and high-risk MHC haplotypes in type I diabetes mellitus, Graves' disease and Hashimoto's thyroiditis. Skanes VM; Barnard J; Farid N; Marshall WH; Murphy L; Rideout D; Taylor R; Xidos G; Larsen B Mol Biol Med; 1986 Apr; 3(2):143-57. PubMed ID: 3461234 [TBL] [Abstract][Full Text] [Related]
36. Linkage of GLO with HLA in a sample of the Spanish population. Lopez-Larrea C; Bootello A; Arnaiz-Villena A Hum Genet; 1981; 57(3):317-20. PubMed ID: 6941923 [TBL] [Abstract][Full Text] [Related]
37. Association of complement alleles C4AQ0 and C4B5 with rheumatoid arthritis in Japanese patients. Takeuchi F; Mimori A; Matsuta K; Nakano K; Miyamoto T; Matsuki K; Juji T; Maeda H; Omoto K; Tokunaga K Arthritis Rheum; 1989 Jun; 32(6):691-8. PubMed ID: 2567598 [TBL] [Abstract][Full Text] [Related]
38. C4 allotypes and HLA-DR antigens in the family of a patient with C4 deficiency. Sjöholm AG; Kjellman NI; Löw B Clin Genet; 1985 Nov; 28(5):385-93. PubMed ID: 3936650 [TBL] [Abstract][Full Text] [Related]
39. Major-histocompatibility-complex extended haplotypes in membranoproliferative glomerulonephritis. Welch TR; Beischel L; Balakrishnan K; Quinlan M; West CD N Engl J Med; 1986 Jun; 314(23):1476-81. PubMed ID: 3458025 [TBL] [Abstract][Full Text] [Related]
40. Genetic polymorphisms of properdin factor B(Bf), the second component (C2), and the fourth component (C4) of complement in leprosy patients and healthy controls from Thailand. Greiner J; Weber FJ; Mauff G; Baur M Immunobiology; 1980; 158(1-2):134-8. PubMed ID: 6907169 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]