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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 1684365)

  • 1. A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes).
    Simon S; Awdeh Z; Campbell RD; Ronco P; Brink SJ; Eisenbarth GS; Yunis EJ; Alper CA
    J Clin Invest; 1991 Dec; 88(6):2142-5. PubMed ID: 1684365
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC).
    Simon S; Truedsson L; Marcus-Bagley D; Awdeh Z; Eisenbarth GS; Brink SJ; Yunis EJ; Alper CA
    Hum Immunol; 1997 Sep; 57(1):27-36. PubMed ID: 9438192
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular heterogeneity of second and fourth components of complement and their genes in systemic sclerosis and association of HLA alleles A1, B8 and DR3 with limited and DR5 with diffuse systemic sclerosis.
    Venneker GT; van den Hoogen FH; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; Boerbooms AM; de Waal LP; Bos JD; Asghar SS
    Exp Clin Immunogenet; 1998; 15(2):90-9. PubMed ID: 9691203
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT; van Meegen M; de Kok-Nazaruk M; Hulsmans RF; de Waall LP; Bos JD; Asghar SS
    Exp Clin Immunogenet; 1996; 13(2):104-11. PubMed ID: 9063702
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Studies of a C2 DNA polymorphism in RA, Felty's and normal subjects.
    Clarkson R; Sanders PA; Grennan DM
    Exp Clin Immunogenet; 1990; 7(1):64-8. PubMed ID: 1971759
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II genes.
    Truedsson L; Alper CA; Awdeh ZL; Johansen P; Sjöholm AG; Sturfelt G
    J Immunol; 1993 Nov; 151(10):5856-63. PubMed ID: 7901282
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Complement C4A, C4B and BF haplotypes in Koreans.
    Park KS; Park MH; Juji T; Tokunaga K
    Tissue Antigens; 1996 Mar; 47(3):200-5. PubMed ID: 8740769
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4.
    Hartmann D; Fremeaux-Bacchi V; Weiss L; Meyer A; Blouin J; Hauptmann G; Kazatchkine M; Uring-Lambert B
    J Clin Immunol; 1997 Mar; 17(2):176-84. PubMed ID: 9083894
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from southern Brazil: the Kaingang and the Guarani.
    Weg-Remers S; Brenden M; Schwarz E; Witzel K; Schneider PM; Guerra LK; Rehfeldt IR; Lima MT; Hartmann D; Petzl-Erler ML; de Messias IJ; Mauff G
    Hum Genet; 1997 Oct; 100(5-6):548-56. PubMed ID: 9341869
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complement genes of the major histocompatibility complex (complotypes), extended haplotypes and disease markers.
    Alper CA; Awdeh Z; Raum D; Yunis EJ
    Biochem Soc Symp; 1986; 51():19-28. PubMed ID: 3493006
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of polymorphisms in the HLA-B region with extended haplotypes.
    Egea GE; Yunis I; Spies T; Strominger J; Awdeh ZL; Alper CA; Yunis EJ
    Immunogenetics; 1991; 33(1):4-11. PubMed ID: 1671666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.
    Fasano MB; Winkelstein JA; LaRosa T; Bias WB; McLean RH
    J Clin Invest; 1992 Oct; 90(4):1180-4. PubMed ID: 1401055
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complotype genetic loci segregate more frequently with HLA-DR than with HLA-B.
    Yunis EJ; Awdeh Z; Johnson A; Suciu-Foca N; Robinson MA; Hartzman R; Raum D; Fleischnick E; Alper CA
    Immunogenetics; 1985; 21(1):25-31. PubMed ID: 3871424
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular heterogeneity of the fourth component of complement (C4) and its genes in vitiligo.
    Venneker GT; Westerhof W; de Vries IJ; Drayer NM; Wolthers BG; de Waal LP; Bos JD; Asghar SS
    J Invest Dermatol; 1992 Dec; 99(6):853-8. PubMed ID: 1469300
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic polymorphisms of HLA class III and GLO1 in Chinese Yao nationality.
    Wang C; Tian YW; Wu XW; Zhao XZ
    Gene Geogr; 1990 Apr; 4(1):29-34. PubMed ID: 2278900
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Immunogenetic markers (BF, C2, C4, 21-OH, TNF alpha, TCR beta, Ig) and insulin-dependent diabetes in the Tunisian population: serological and molecular study].
    Ben Salem M; Ghanem N; Kneissi T; Abbal M; Dugoujon JM; Ben Chibani J; Ellouze F; Lefranc G
    Ann Biol Clin (Paris); 1991; 49(7):389-96. PubMed ID: 1684890
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymorphism of the complement components in human pathology.
    Brai M; Accardo P; Bellavia D
    Ann Ital Med Int; 1994; 9(3):167-72. PubMed ID: 7946894
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Immunofixation for C2 typing: C2 allotypes in Spaniards in relation to HLA, Bf and C4.
    Regueiro JR; Arnaiz-Villena A
    Hum Genet; 1985; 71(1):58-61. PubMed ID: 3897025
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic variability of the MHC class III complement proteins C2, BF, C4A and C4B in southern Brazil.
    de Messias IT; Reis A; de Almeida PT; Mauff G
    Exp Clin Immunogenet; 1994; 11(4):192-6. PubMed ID: 7857665
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.