Now showing items 1-2 of 2

    • Skewed X chromosome inactivation in blood cells of women with scleroderma 

      Özbalkan, Z.; Baǧişlar, S.; Kiraz, S.; Akyerli, C. B.; Özer H. T. E.; Yavuz, Ş.; Birlik, A. M.; Çalgüneri, M.; Özçelik, T. (John Wiley & Sons, Inc., 2005)
      Objective. Scleroderma (SSc) is an autoimmune disease of unknown etiology. The disease is 3-8 times more frequent in women than in men. The role of X chromosome inactivation (XCI) in the predisposition of women to autoimmunity ...
    • Survey of factor V leiden and prothrombin gene mutations in systemic lupus erythematosus 

      Topaloglu, R.; Akıerli, C.; Bakkaloglu, A.; Aydıntug, O.; Ozen, S.; Besbas, N.; Ozcelik, T. (Springer-Verlag, 2001)
      The two most common hereditary risk factors for thrombosis are factor V Leiden mutation and a prothrombin gene mutation. There is indeed a thrombotic tendency in patients with systemic lupus erythematosis (SLE) and it is ...