Zobrazeno 1 - 3
of 3
pro vyhledávání: '"C R, Weiler"'
Publikováno v:
Mayo Clinic Proceedings. 82:1541-1549
Publikováno v:
Journal of Inherited Metabolic Disease. 28:181-186
Smith-Lemli-Opitz syndrome is a rare autosomal recessive disorder characterized by multiple congenital anomalies and various degrees of cognitive deficits. This condition results from a deficiency of 7-dehydrocholesterol reductase, a critical step in
Publikováno v:
Tissue antigens. 55(4)
We investigated the immune response to the German cockroach (Blattella germanica), and one of its major antigens, Blattella germanica group 5 (Bla g 5), in a double-transgenic, double-knockout mouse expressing human HLA-DQ8, HLA-DQ6 and CD4 molecules