ライフサイエンスコーパス: rattlesnake

1 ession in both neurotoxic and non-neurotoxic rattlesnakes.

2 ividuals in each of two species of Sistrurus rattlesnakes.

3 arning signals in response to heat-sensitive rattlesnakes.

4 structure and the deployment of rattling by rattlesnakes.

5 oted by T.H. Huxley during the voyage of the Rattlesnake (1846-1850).

6 been exploited by 2 ecological associates of rattlesnakes: (a) California ground squirrels (Spermophi

7 ows that all strata are shared between pygmy rattlesnake and garter snake, i.e., recombination was ab

8 ate its utility using datasets for Sistrurus rattlesnakes and for soybeans.

9 terodimeric neurotoxin predate the origin of rattlesnakes and were present in their last common ances

10 rox) and Eastern Diamondback (C. adamanteus) rattlesnakes ( approximately 6 mya), while a PLA2 myotox

11 We examined the tailshaker muscle of the rattlesnake because of its uniform cell properties, excl

12 of gross motor behavior in dealing with the rattlesnake, but they augmented the speed of snake recog

13 atrox was deleted from the neurotoxic Mojave rattlesnake (C. scutulatus; approximately 4 mya).

14 into phosphoribose must be purified from the rattlesnake Crotalus adamanteus venom, which is contamin

15 derived from the venom of the South American rattlesnake Crotalus durissus terrificus, has been shown

16 brain preparation of the western diamondback rattlesnake (Crotalus atrox) that allowed specific appli

17 s that also contained eastern diamond-backed rattlesnakes (Crotalus adamanteus) when the proportion o

18 high maneuverability displayed by sidewinder rattlesnakes (Crotalus cerastes) emerges from the animal

19 In particular, desert-dwelling sidewinder rattlesnakes (Crotalus cerastes) operate effectively on

20 Specifically, timber rattlesnakes (Crotalus horridus) were less likely than e

21 signals when confronting infrared-sensitive rattlesnakes (Crotalus oreganus), but tail flag without

22 d (at night using infrared lights) of Mohave rattlesnakes (Crotalus scutulatus) attempting to capture

23 an aposematic signal, the rattling sound of rattlesnakes (Crotalus viridis), has been exploited by 2

24 e found that even though most North American rattlesnakes do not produce neurotoxins, the genes of a

25 tail flagging display of the robotic models, rattlesnakes exhibited a greater shift from predatory to

26 The fibers of the shaker muscle of rattlesnakes have independently evolved similar traits,

27 s that strongly influences venom function in rattlesnakes, highlighting how gene loss can underpin ad

28 granular incline angle increases, sidewinder rattlesnakes increase the length of their body in contac

29 nd show that heteromorphic ZW chromosomes in rattlesnakes lack chromosome-wide dosage compensation.

30 m a range of distances (4.6 to 20.6 cm), and rattlesnake performance was highly variable.

31 d peptide from the venom of a South American rattlesnake, possesses potent antimicrobial, antitumor,

32 ontrol squirrels were presented with a caged rattlesnake pre- and postsurgery.

33 vioral excitability during encounters with a rattlesnake predator.

34 Rattlesnakes produce a sustained, high-frequency warning

35 n the burrowing owl's defensive hiss and the rattlesnake's rattling reflects both exaptation and adap

36 e of evolutionary strata on garter and pygmy rattlesnake sex chromosomes where recombination was abol

37 ineages in the endangered Eastern Massasauga Rattlesnake (Sistrurus catenatus).

38 m proteins from 254 adult eastern massasauga rattlesnakes (Sistrurus c. catenatus) collected from 10

39 Maximum velocity and acceleration of some rattlesnake strikes fell within the range of reported la

40 protein from the venom of the South American rattlesnake that functions as a potent agonist of the pl

41 rm a transcriptome analysis in boa and pygmy rattlesnake to establish baseline levels of sex-biased e

42 By comparing human and rattlesnake TRPA1 channels, we have identified two porta

43 Sidewinder rattlesnakes used two distinct turning methods, which we

44 f crotamines (highly toxic peptides found in rattlesnake venom) supports their homology, even though

45 Here, human antimicrobial peptide hBD-2 and rattlesnake venom-toxin crotamine were compared in phylo

46 d either Crotalus atrox (Western diamondback rattlesnake) venom (CV) or isolated C. atrox phospholipa

47 in both garter snakes (Colubridae) and pygmy rattlesnake (Viperidae).

48 from genomic DNA from four taxa of Sistrurus rattlesnakes which feed on different prey.

49 The authors tested this hypothesis in rattlesnakes within a predatory context by unilaterally