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3 ric evaluation of the cobra venom (Naja naja naja) group IA phospholipase A 2 (GIA PLA 2) was carried
4 ified from the venom of Naja naja (CVFn) and Naja haje (CVFh) and compared them to those for two C3b-
10 three residues on the alpha-neurotoxin from Naja mossambica mossambica (Lys27, Arg33, and Lys47) and
11 report here on a short alpha-neurotoxin from Naja mossambica mossambica (NmmI) that, similar to other
12 rge reversal mutations on the three loops of Naja mossambica mossambica alpha-toxin, Lys(27) --> Glu,
14 lcholine bilayers by phospholipase A(2) from Naja mossambica mossambica venom is accompanied by destr
15 a recombinant DNA-derived alpha-neurotoxin (Naja mossambica mossambica, NmmI) and mouse muscle nAChR
16 Bb) made with CVF purified from the venom of Naja naja (CVFn) and Naja haje (CVFh) and compared them
17 e A2 (PLA2) from the venom of Chinese cobra (Naja naja atra) has high activity on zwitterionic membra
19 piscivorus, acidic PLA(2) from the venom of Naja naja atra, human group IIa and V PLA(2)s, and the C
23 spectrometric evaluation of the cobra venom (Naja naja naja) group IA phospholipase A 2 (GIA PLA 2) w
24 er) are exposed to PLA2 isolated from cobra (Naja naja naja) venom at varying enzyme concentrations.
25 , we report that both porcine pancreatic and Naja naja PLA2s, in a dose-dependent manner, stimulate d
26 nAChR affinity purified on alpha-cobratoxin (Naja naja siamensis) columns and extracted using sinapin
27 ng the different sPLA(2)s tested, bee venom, Naja naja, and porcine and human pancreatic PLA(2)s all
28 se (NN) purified from the venom of the snake Naja nigricollis nigricollis, cleaves human factor V at
29 ents with alpha-conotoxin ImI and a chimeric Naja oxiana alpha-neurotoxin indicating that the major r
31 variants in some plants (e.g., aquatic genus Najas) potentially reflect ecological adaptations to fac
32 rom Dendroaspis species and selected African Naja species was performed based on custom-made high-den
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