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Titlebook: Cysteine Proteases of Pathogenic Organisms; Mark W. Robinson,John P. Dalton Book 2011 The Editor(s) (if applicable) and The Author(s), und

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樓主: 貪吃的人
31#
發(fā)表于 2025-3-26 23:27:20 | 只看該作者
Cathepsins B1 and B2 of , SPP., Bird Schistosomes Causing Cercarial Dermatitis,re able to penetrate, transform and then migrate as schistosomula in nonspecific hosts (e.g., mouse, man). Peptidases are among the key molecules produced by these schistosomes that enable parasite invasion and survival within the host and include cysteine peptidases such as cathepsins B1 and B2. Th
32#
發(fā)表于 2025-3-27 04:06:36 | 只看該作者
Proteases in Blood-Feeding Nematodes and Their Potential as Vaccine Candidates,f host protein for nutrients, evasion of host immune responses and for internal processes such as tissue catabolism and apoptosis. For these broad reasons they have been examined as possible parasite control targets. Blood-feeding nematodes such as the barber-pole worm . that infect sheep and goats
33#
發(fā)表于 2025-3-27 07:09:32 | 只看該作者
34#
發(fā)表于 2025-3-27 10:38:08 | 只看該作者
35#
發(fā)表于 2025-3-27 15:25:57 | 只看該作者
Cystatins of Parasitic Organisms,ntly of the type 2 cystatins. Recently, a wealth of information on these molecules and their activities has been described. Parasite cystatins are shown to have dual functions via interaction with both parasite and host proteases. Thereby, parasite cystatins are not only essentially involved in the
36#
發(fā)表于 2025-3-27 17:58:18 | 只看該作者
https://doi.org/10.1007/978-1-4419-8414-2Cysteine; Dalton; Organism; Pathogenic; Protease; Robinson
37#
發(fā)表于 2025-3-27 23:31:26 | 只看該作者
38#
發(fā)表于 2025-3-28 02:20:52 | 只看該作者
39#
發(fā)表于 2025-3-28 07:04:56 | 只看該作者
40#
發(fā)表于 2025-3-28 11:02:49 | 只看該作者
Studies in the History of Philosophy of Mindracterized of these proteases are the falcipains, a family of four papain-family enzymes. Falcipain-2 and falcipain-3 act in concert with other proteases to hydrolyze host erythrocyte hemoglobin in the parasite food vacuole. Disruption of the falcipain-2 gene led to a transient block in hemoglobin h
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