ライフサイエンスコーパス: snout

1 resented simultaneously on both sides of the snout.

2 delivered to a cold-sensitive region of the snout.

3 row or 3 caudal whiskers on each side of the snout.

4 ned array of whiskers and sinus hairs on the snout.

5 tribution of whiskers and sinus hairs on the snout.

6 sed along the representation of the glabrous snout.

7 ystacial vibrissae, lower jaw, and glaborous snout.

8 ic projections from whiskers on the rodent's snout.

9 nd transverse compression of the spinosaurid snout.

10 d by cleft palate and short limbs, tail, and snout.

11 ls that corresponded to the vibrissae on the snout.

12 fields were often small, especially for the snout.

13 showed fully penetrant cleft lips and short snouts.

14 s compared to taxa with broader, more robust snouts.

15 resulted in relatively longer hindlimbs and snouts.

16 tems, approaching the physical limits (mouse snout ~10 mm).

17 this Bauplan, possessing an extremely blunt snout, a tall, rounded skull, an anteriorly shifted jaw

18 nnosaurini and the smaller, gracile, shallow-snouted Alioramini as highly derived eutyrannosaurian si

19 the placement of the nares on the top of the snout and a "fish-trap"-type dentition.

20 d to representing the perioral hairs and the snout and also that neurons within this representation h

21 restrial diapsid reptiles, including a short snout and body trunk.

22 In addition, like in other dinosaurs, its snout and lower jaw show large cranial fenestrae.

23 aging, bioluminescence being detected in the snout and lungs of infected mice after nasal inoculation

24 ed during the Jurassic, before the elongated snout and other fish-eating adaptations in the skull.

25 ere tuned to the distance between the animal snout and the contralateral wall, with monotonic, unimod

26 ical relevance of orienting movements of the snout and the whiskers in these animals.

27 trusion, the proximodistal shortening of the snout and widening of the hard palate is common to brach

28 FKO mice exhibit shortened snouts and wide-set eyes that become apparent at postnat

29 feeding strikes occur (above the end of the snout), and permits syngnathid fish to approach highly s

30 strictly synchronous and symmetric about the snout, and it is thought to be controlled by a brainstem

31 found in some non-ocular tissues, i.e. ears, snout, and limbs of embryos of E13.5 and E14.5 but was n

32 taining dermal lesions appeared on the ears, snout, and perianal regions of transgenic mice by the ag

33 hing tubular structures with pseudo-apocrine snouts, and either totally absent (2/2, 50%) or rare (2/

34 y and toughness of the distal portion of the snout are characterized.

35 The most prominent defects in FKO snouts are (1) a lack of growth within the frontonasal s

36 electrical stimulation of the contralateral snout as well as changes in DC-coupled potential were mo

37 ected populations of the invasive eucalyptus snout beetle, Gonipterus platensis (Coleoptera: Curculio

38 m Mongolia seem to indicate a divergent long-snouted body plan among some derived tyrannosaurids, but

39 s and fatty acid synthesis in juvenile blunt snout bream.

40 bility, and paedomorphic skulls with reduced snouts but enlarged eyes and brains.

41 tes that Alioramus is a small, gracile, long-snouted carnivore that deviates from other tyrannosaurid

42 own feeding ecology for both African slender-snouted crocodile and alligator, and suggest that the sp

43 s: two longistrine taxa, the African slender-snouted crocodile Mecistops cataphractus and the Indian

44 Results show that African slender-snouted crocodile skulls are more resistant to bending t

45 determined from the ratio of tusk length to snout dimensions.

46 er fragment showed expression in the cornea, snout, dorsal fin, and tail fin of 3-day-old zebrafish l

47 ceptionally small eyes relative to the body, snout ending with crura with a large internasal space, h

48 rn weevil (Curculio Linnaeus, 1758) rostrum (snout) exhibits remarkable flexibility and toughness der

49 m of craniofacial defects, including shorter snout, expansion of the facial midline, cleft lip, exten

50 and crusts occurred predominantly around the snout, eyes, and on ears.

51 us), which rub each other's clitorises using snouts, flippers, or flukes(3).

52 ies and Food, Atrophic Rhinitis: a System of Snout Grading, 1978).

53 Such an early burst of facial (i.e., snout) growth resembles that of young crocodilians.(7) H

54 contingent upon the presence of the animal's snout in a nosepoke apparatus at the target time, as an

55 study, with an unexpected separation of the snout in upper and lower sub-modules and the presence of

56 tion of running or upon the insertion of the snout into the food cup.

57 length (P < 0.05) and face width relative to snout length (P < 0.01) were present in the 44-cM region

58 sults confirmed QTLs, determining that short snout length (P < 0.05) and face width relative to snout

59 variance in relative limb length and 33% of snout length across species.

60 ignificant logarithm-of-odds (LOD) score for snout length on mouse chromosome 12 at 44 centimorgan (c

61 ation between the larval period and limb and snout lengths, mirroring the effects of within-species p

62 y traits including male pregnancy, elongated snouts, loss of teeth, and dermal bony armor.

63 rences in phylogenetically conserved traits (snout morphology and body size) were consistently linked

64 Alioramus individuals, showing that the long-snouted morphology was not a transient juvenile conditio

65 or the synchronization of vibrissa, pad, and snout movements, as well as for the bilateral synchroniz

66 s devoted to representation of the glaborous snout, mystacial vibrissae, lower jaw, and oral cavity (

67 J (short snout/wide face) and C57BL/6J (long snout/narrow face), revealed a significant logarithm-of-

68 rs: they follow along walls, and "dab" their snouts on the ground at frequencies related to the whisk

69 ealing of tongue ulcers in mice subjected to snout-only irradiation.

70 When whiskers on the snout or the sensory nerves innervating them are damaged

71 Our results show that the curvature of the snout plays a critical role in determining the impact fo

72 sox9 essential functions, including the jaw/snout region, otic vesicle, eye, and brain.

73 -side deviation of their facial skeleton and snout regions; 4 x 2 ANOVA and post hoc t-tests revealed

74 ws down soon thereafter, and the matching of snout scaling between mid-sized and larger individuals i

75 The long-snouted seahorse (Hippocampus guttulatus) is one of two

76 es, except for companion dogs having extreme snout shape.

77 In contrast to these results, grafts of snout skin yielded many melanomas, each originating from

78 d at the representation of the vibrissae and snout, so that the orientation of S2 formed an upright r

79 s not a transient juvenile condition of deep-snouted species, but a characteristic of a major tyranno

80 lution pinpointed reductions in interior mid-snout structures and occipital bones in both the models

81 On the snout, sustained robust replication of 17tBTK(-) in the

82 ly in response to tactile stimulation of the snout, this property was not related to activity associa

83 f an applicator mount for a conventional PBS snout to allow for ocular treatments are given.

84 tetrapods, most under 1 meter in length from snout to tail, radiated to dominate postextinction ecosy

85 growth rate and the strength of selection on snout to vent length.

86 we describe a remarkable new species of long-snouted tyrannosaurid from the Maastrichtian of southeas

87 utyrannosauria and recover the massive, deep-snouted Tyrannosaurini and the smaller, gracile, shallow

88 olateral defects including narrow, elongated snouts, underdeveloped lower jaw and a high incidence of

89 ength of laterality index (ABSLI) scores for snout use at 4 weeks of age were positively correlated w

90 than side-preferent for both lying side and snout use at 6 weeks of age.

91 corded in fifty pigs across five measures: a snout use task, step-up task, detour task, tail curling

92 Directional laterality index (LI) scores for snout use were positively correlated with those of the s

93 Snout use, step-up and detour side preferences were obse

94 ot strength, of their lateral biases for the snout use, step-up and detour tasks.

95 ntonasal sutures, and (2) a reduction in the snout vasculature.

96 posed animals had significantly shorter SVL [snout-vent length (mm)] with significantly increased bod

97 ed in the 1,000 uS/cm treatments had shorter snout-vent length (SVLs) (mean = 25.44 mm) than those re

98 d via larval fish tests, indicating that the snout-vent length and pericardial area warrant considera

99 rs and American toads and was dependent upon snout-vent length in western toads, American toads, and

100 g whether select developmental abnormalities-snout-vent length, eye size, and pericardial area-are li

101 characteristics of sexual maturity including snout-vent length, total length, sex, tympanum diameter,

102 e the environment whisking with their motile snout vibrissae.

103 arkedly reduced virus titers in the skin and snout, whereas parenteral treatment did not, suggesting

104 deed, Asph-knockout mice had a foreshortened snout, which corresponds to the facial abnormalities in

105 cited by electrical stimulation of the swine snout, which is somatotopically represented in the rostr

106 d from the sensory receptors surrounding the snout whiskers and transmitted centrally to the brainste

107 F2 progeny of 2 mouse strains, DBA/2J (short snout/wide face) and C57BL/6J (long snout/narrow face),

108 These include an elongate snout with an array of conical teeth, a dorsoventrally f

109 f Cartorhynchus with which it shares a short snout with rostrally extended nasals.

110 they protract their whiskers in front of the snout without large movements.