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1            The reconstitutable apoprotein of Crotalus adamanteus L-amino acid oxidase was prepared us
2 ribose must be purified from the rattlesnake Crotalus adamanteus venom, which is contaminated with pr
3  predators-eastern diamondback rattlesnakes (Crotalus adamanteus) and coyotes (Canis latrans).
4 ntained eastern diamond-backed rattlesnakes (Crotalus adamanteus) when the proportion of evergreen fo
5 cluding the eastern diamondback rattlesnake (Crotalus adamanteus), undergo correlated changes in diet
6 e (n = 23) eastern diamondback rattlesnakes (Crotalus adamanteus; EDBs) for one year, and demonstrate
7 lidae) polyvalent (equine origin) and either Crotalus atrox (Western diamondback rattlesnake) venom (
8 egrin-like/cysteine-rich (DC) domains of the Crotalus atrox hemorrhagic metalloproteinase atrolysin A
9                      Phospholipase A(2) from Crotalus atrox hydrolyzes all of the phospholipids that
10 chrome bc(1) (EC 1.10.2.2) by digestion with Crotalus atrox phospholipase A(2).
11  removed from each complex by digestion with Crotalus atrox phospholipase A2, i.e., each delipidated
12 s study was to evaluate preconditioning with Crotalus atrox venom (Cv-PC) as potential preventive the
13                                  The dimeric Crotalus atrox venom PLA2 is part of the secreted phosph
14 VMPs) in the Western Diamondback rattlesnake Crotalus atrox which possesses the largest known battery
15 lineages leading to the Western Diamondback (Crotalus atrox) and Eastern Diamondback (C. adamanteus)
16 tion of the western diamondback rattlesnake (Crotalus atrox) that allowed specific application of mul
17 enes in the Western Diamondback rattlesnake (Crotalus atrox) through a number of single gene and mult
18 rabidopsis thaliana, Drosphila melanogaster, Crotalus atrox, and Xenopus laevis have recently been sh
19               We describe the interaction of Crotalus atrox-secreted phospholipase A2 (sPLA2) with gi
20 ce of thrombin, arvin, or a snake venom from Crotalus atrox.
21 tracked free-ranging sidewinder rattlesnakes Crotalus cerastes to their selected ambush sites and rec
22 bility displayed by sidewinder rattlesnakes (Crotalus cerastes) emerges from the animal's ability to
23 ar, desert-dwelling sidewinder rattlesnakes (Crotalus cerastes) operate effectively on inclined granu
24 omys merriami and the sidewinder rattlesnake Crotalus cerastes, and from the Negev Desert in the Midd
25                                       SVP of Crotalus duressus terrificus (SVP I) was found to be the
26 ontent on the initial hydrolytic activity of Crotalus durissus terrificus venom phospholipase A2 (sPL
27 Convulxin (CVX), a C-type snake protein from Crotalus durissus terrificus venom, is the quintessentia
28 2(CB)), a protein isolated from the venom of Crotalus durissus terrificus was previously shown to pos
29  the venom of the South American rattlesnake Crotalus durissus terrificus, has been shown to be a cel
30           Specifically, timber rattlesnakes (Crotalus horridus) were less likely than expected by cha
31  SVMP family expanded and diversified in the Crotalus lineage.
32 main of the venom of the American pit viper, Crotalus molossus molossus as the targeting moiety and a
33 confronting infrared-sensitive rattlesnakes (Crotalus oreganus), but tail flag without augmenting inf
34 naturally occurring rattlesnake hybrid zone (Crotalus scutulatus x viridis).
35 ing infrared lights) of Mohave rattlesnakes (Crotalus scutulatus) attempting to capture Merriam's kan
36     Genomic analyses of several rattlesnake (Crotalus) species revealed the SVMP family massively exp
37 sly described using phosphodiesterase I from Crotalus venom after the cleavage processes.
38  signal, the rattling sound of rattlesnakes (Crotalus viridis), has been exploited by 2 ecological as
39 el genome assembly of a prairie rattlesnake (Crotalus viridis), together with Hi-C, RNA-seq, and whol