Abstract: A method for managing the security of a client device in a mobile device management system (MDMS) comprises receiving a security policy at a client device, applying the security policy on the client device, determining an occurrence of a security policy event, determining a violation based on the occurrence of the security policy event and applying different security controls based on predefined elapsed times on the client device.

Abstract: Embodiments of the invention described herein provide approaches relating generally to location position management of mobile devices. Specifically, a policy-based mobile device management system (MDMS) is provided for determining a location of a mobile device based on the user's access history information and controlling the mobile device based on the location.

Abstract: A use of vivapain-4 (VX-4), which is a cysteine protease of Plasmodium vivax, showing pH-dependent switching of substrate specificity, is provided. More specifically, a method of treating a parasitic disease caused by Plasmodium vivax by inhibiting VX-4; a method of screening a protease inhibitor acting on VX-4, wherein the protease inhibitor is useful as an anti-malarial agent acting on Plasmodium species, for example, Plasmodium vivax; and a method of identifying the activity of VX-4, are provided.

Abstract: This invention is directed to an isolated DNA sequence encoding an antigen of Taenia solium metacestodes. A 10 kDa antigen of Taenia solium metacestodes (TSM) has been shown to be specific for immunodiagnosis of Neurocysticercosis (NCC), which is an important cause of neurological disease worldwide. This invention discloses a method of cloning a cDNA library encoding a 10 kDa protein from Taenia solium metacestodes. The cloned cDNA contained a 258 bp complete open reading frame, encoding an 86 amino acid protein with a calculated molecular weight of 9,582 Da. It showed 73% homology with a 10 kDa antigen of T. crassiceps. The recombinant protein was expressed bacterially as a fusion protein at a high level. A recombinant TSM antigen prepared according: to this invention is useful in detecting neurocysticerocosis disease. In immunoblot with purified recombinant protein, 97% of sera from active NCC showed strong reactivity while 14% of sera from chronic calcified NCC were weekly positive.