Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tova Morad"'
Autor:
Sali Usher, Tova Morad, Elena Keren-Tardai, Hava Peretz, Hanna Shalev, Ayala Lagziel, Daniel Landau, Tong Zhang, Gavin Blackburn, David Levartovsky, David G. Watson, Victoria Greenshpun, Meirav Shtauber-Naamati
Publikováno v:
Metabolomics. 8:951-959
Classical xanthinuria is a rare inherited metabolic disorder caused by either isolated xanthine dehydrogenase (XDH) deficiency (type I) or combined XDH and aldehyde oxidase (AO) deficiency (type II). XDH and AO are evolutionary related enzymes that s
Publikováno v:
International Journal of Gynecological Cancer. 19:1300-1302
Hypothesis: To assess the frequency distribution of the CYP1A1 and CYP2D6 gene polymorphisms in Israeli Jewish women with cervical cancer. Methods: Forty-three Israeli Jewish women with cervical cancer and 123 healthy Israeli Jewish women were assess
Autor:
Moshe Leshno, Laurie Blendis, Tova Morad, Eli Brazowski, Ran Oren, Hava Peretz, Yoav Lurie, Zamir Halpern, Elisheva Grynberg, Sigal Fishman, Guy Rosner
Publikováno v:
Liver international : official journal of the International Association for the Study of the Liver. 26(3)
Objective: Previous studies have demonstrated that CYP2D6 polymorphism is associated with liver cirrhosis. The aim of the present study was to find out whether CYP2D6 n 4, the poor metabolizer allele can predict fibrosis progression rate. Methods: Se