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pro vyhledávání: '"Binh T. Le"'
Publikováno v:
BMJ Case Rep
Classic Bartter syndrome is a rare condition caused by mutations in the CLCNKB gene and characterised by metabolic alkalosis, hypokalaemia, hyper-reninaemia and hyperaldosteronism. Early signs and symptoms usually occur before a child’s sixth birth
Publikováno v:
BMJ Case Reports. 13:e233872
Classic Bartter syndrome is a rare condition caused by mutations in theCLCNKBgene and characterised by metabolic alkalosis, hypokalaemia, hyper-reninaemia and hyperaldosteronism. Early signs and symptoms usually occur before a child’s sixth birthda
Autor:
Binh T. Le, Jutta Veits, Ha H. Chu, Thomas C. Mettenleiter, Julia Pohl, Frank Rabenstein, Doreen M. Floss, Hoang T. Phan, Gerd Hause, Udo Conrad
Publikováno v:
Plant Biotechnology Journal. 11:582-593
Summary Reducing the cost of vaccine production is a key priority for veterinary research, and the possibility of heterologously expressing antigen in plants provides a particularly attractive means of achieving this. Here, we report the expression o