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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 ater movement and larger home ranges than RH rattlesnakes across behavioral seasons.
8 ows that all strata are shared between pygmy rattlesnake and garter snake, i.e., recombination was ab
9 venom regulatory architecture in the prairie rattlesnake and identify cis-regulatory sequences (enhan
10 ate its utility using datasets for Sistrurus rattlesnakes and for soybeans.
11 terodimeric neurotoxin predate the origin of rattlesnakes and were present in their last common ances
12 rox) and Eastern Diamondback (C. adamanteus) rattlesnakes ( approximately 6 mya), while a PLA2 myotox
13     We examined the tailshaker muscle of the rattlesnake because of its uniform cell properties, excl
14  of gross motor behavior in dealing with the rattlesnake, but they augmented the speed of snake recog
15 atrox was deleted from the neurotoxic Mojave rattlesnake (C. scutulatus; approximately 4 mya).
16 fanged venomous snakes in North America: the rattlesnakes, copperheads, cantils, and cottonmouths.
17 n has further shaped the SVMP complex within rattlesnakes, creating both fusion genes and substantial
18 into phosphoribose must be purified from the rattlesnake Crotalus adamanteus venom, which is contamin
19 oteinases (SVMPs) in the Western Diamondback rattlesnake Crotalus atrox which possesses the largest k
20 oo rat Dipodomys merriami and the sidewinder rattlesnake Crotalus cerastes, and from the Negev Desert
21 derived from the venom of the South American rattlesnake Crotalus durissus terrificus, has been shown
22           We tracked free-ranging sidewinder rattlesnakes Crotalus cerastes to their selected ambush
23 us snakes, including the eastern diamondback rattlesnake (Crotalus adamanteus), undergo correlated ch
24 brain preparation of the western diamondback rattlesnake (Crotalus atrox) that allowed specific appli
25 s 31 tandem genes in the Western Diamondback rattlesnake (Crotalus atrox) through a number of single
26 hromosome-level genome assembly of a prairie rattlesnake (Crotalus viridis), together with Hi-C, RNA-
27                  Genomic analyses of several rattlesnake (Crotalus) species revealed the SVMP family
28 North American predators-eastern diamondback rattlesnakes (Crotalus adamanteus) and coyotes (Canis la
29 s that also contained eastern diamond-backed rattlesnakes (Crotalus adamanteus) when the proportion o
30 or adult female (n = 23) eastern diamondback rattlesnakes (Crotalus adamanteus; EDBs) for one year, a
31 high maneuverability displayed by sidewinder rattlesnakes (Crotalus cerastes) emerges from the animal
32    In particular, desert-dwelling sidewinder rattlesnakes (Crotalus cerastes) operate effectively on
33                         Specifically, timber rattlesnakes (Crotalus horridus) were less likely than e
34  signals when confronting infrared-sensitive rattlesnakes (Crotalus oreganus), but tail flag without
35 d (at night using infrared lights) of Mohave rattlesnakes (Crotalus scutulatus) attempting to capture
36  an aposematic signal, the rattling sound of rattlesnakes (Crotalus viridis), has been exploited by 2
37                                              Rattlesnakes did not face ambush directions that offered
38                                           NH rattlesnakes displayed greater movement and larger home
39 e found that even though most North American rattlesnakes do not produce neurotoxins, the genes of a
40 tail flagging display of the robotic models, rattlesnakes exhibited a greater shift from predatory to
41                                          The rattlesnakes have heat sensing organs (pits) and the kan
42           The fibers of the shaker muscle of rattlesnakes have independently evolved similar traits,
43 s that strongly influences venom function in rattlesnakes, highlighting how gene loss can underpin ad
44 ament and syndromes in a naturally occurring rattlesnake hybrid zone (Crotalus scutulatus x viridis).
45 ply these to a dataset of 118 genomes from a rattlesnake hybrid zone.
46 granular incline angle increases, sidewinder rattlesnakes increase the length of their body in contac
47 The eastern massasauga (Sistrurus catenatus) rattlesnake is listed as Federally Threatened in the Uni
48 nd show that heteromorphic ZW chromosomes in rattlesnakes lack chromosome-wide dosage compensation.
49 ence the angular orientation of free-ranging rattlesnakes once they have selected an ambush site.
50 m a range of distances (4.6 to 20.6 cm), and rattlesnake performance was highly variable.
51 ns (MNs) in the body and tail spinal cord of rattlesnakes possess fundamentally different physiologic
52 d peptide from the venom of a South American rattlesnake, possesses potent antimicrobial, antitumor,
53 ontrol squirrels were presented with a caged rattlesnake pre- and postsurgery.
54 vioral excitability during encounters with a rattlesnake predator.
55                                              Rattlesnakes produce a sustained, high-frequency warning
56                                              Rattlesnakes provide a unique opportunity to investigate
57 n the burrowing owl's defensive hiss and the rattlesnake's rattling reflects both exaptation and adap
58 e of evolutionary strata on garter and pygmy rattlesnake sex chromosomes where recombination was abol
59                               New results in rattlesnakes show that shifting a motor neuron's tempora
60 osome-level genome assembly of an endangered rattlesnake (Sistrurus catenatus) combined with whole ge
61 ineages in the endangered Eastern Massasauga Rattlesnake (Sistrurus catenatus).
62 m proteins from 254 adult eastern massasauga rattlesnakes (Sistrurus c. catenatus) collected from 10
63 ses the simplest and most toxic venom of any rattlesnake species, to determine whether the simple ven
64    Maximum velocity and acceleration of some rattlesnake strikes fell within the range of reported la
65 protein from the venom of the South American rattlesnake that functions as a potent agonist of the pl
66 rm a transcriptome analysis in boa and pygmy rattlesnake to establish baseline levels of sex-biased e
67       Here, we use whole-genome data from 68 rattlesnakes to test hypotheses about the factors that d
68                       By comparing human and rattlesnake TRPA1 channels, we have identified two porta
69                                 For example, rattlesnakes use infrared (IR) radiation to detect warm
70                                   Sidewinder rattlesnakes used two distinct turning methods, which we
71  time series gene expression analyses of the rattlesnake venom gland in comparison with several non-v
72 f crotamines (highly toxic peptides found in rattlesnake venom) supports their homology, even though
73  Here, human antimicrobial peptide hBD-2 and rattlesnake venom-toxin crotamine were compared in phylo
74 o the production of the simplest, most toxic rattlesnake venom.
75 d either Crotalus atrox (Western diamondback rattlesnake) venom (CV) or isolated C. atrox phospholipa
76 in both garter snakes (Colubridae) and pygmy rattlesnake (Viperidae).
77 from genomic DNA from four taxa of Sistrurus rattlesnakes which feed on different prey.
78    Here, we sequence the genome of the Tiger Rattlesnake, which possesses the simplest and most toxic
79        The authors tested this hypothesis in rattlesnakes within a predatory context by unilaterally
80                              We identify the rattlesnake Z Chromosome, including the recombining pseu