ライフサイエンスコーパス: cranium

1 l morphology and evolutionary changes in the cranium.

2 e Holocene based on the overall shape of the cranium.

3 y that some CM attacks originate outside the cranium.

4 caused his death are the two to the inferior cranium.

5 greater functionality to fit into a smaller cranium.

6 l openings in nematodes, ants, and the mouse cranium.

7 tract or for neoplasms of the inner ear and cranium.

8 ation of a balloon catheter placed under the cranium.

9 s in a finite model of a Macaca fascicularis cranium.

10 1 expression and dermal cell identity in the cranium.

11 during morphogenesis of membrane bone of the cranium.

12 ess, heavy-bodied and had a much more robust cranium.

13 tly ventral to the disc on the dorsum of the cranium.

14 d in a 11 x 14 cm2 scalp defect with exposed cranium.

15 rain via a hollow screw inserted through the cranium.

16 nounced, with large portions of the face and cranium affected, including the mandible and frontal and

17 amera-type eyes, paired nasal sacs, possible cranium and arcualia, W-shaped myomeres, and a post-anal

18 n is a partial skeleton with nearly complete cranium and associated lower jaws with in situ dentition

19 tissues contribute to the development of the cranium and associated sensory organs, which were crucia

20 rain injury mechanical forces applied to the cranium and brain cause irreversible primary neuronal an

21 Congenital abnormalities of the cranium and face present complex diagnostic and therapeu

22 and pelvic fins, and has fused bones in the cranium and jaw.

23 ertebrate anatomical innovations such as the cranium and jaws.

24 Three of the injuries-two to the inferior cranium and one to the pelvis-could have been fatal.

25 of approximately 95% is possible if both the cranium and os coxae are present and intact, but this is

26 ollar, but they failed to form the posterior cranium and other bones derived from endochondral ossifi

27 Additional morphological data from the cranium and postcranium of certain poorly understood Pal

28 an adults differ in skeletal features of the cranium and postcranium, and it is clear that many of th

29 cal evidence provided by the rest of the LB1 cranium and postcranium, and no study thus far has addre

30 near-complete human skeleton with an intact cranium and preserved DNA found with extinct fauna in a

31 frequently involves the anterior base of the cranium and results in encasement of the optic-nerve can

32 n, 12 radionuclides that localize within the cranium and spinal skeleton and 12 radionuclides that se

33 in which unequivocal specializations in its cranium and teeth for high-fibre herbivory are well pres

34 he mandible may not evolve as rapidly as the cranium and the mandible is not reliable for identifying

35 For both the cranium and the postcranium, changes in diet or activity

36 s well as for neoplasms of the inner ear and cranium, and b) there is consistency and value in RI stu

37 Total vertical has a continuous cranium, and inter-twin axial facial rotation <40 degree

38 -functional basis for the derived chimaeroid cranium, and shed new light on the chondrichthyan respon

39 pecies of Homo erectus A recently discovered cranium (Aroeira 3) from the Gruta da Aroeira (Almonda k

40 The combination of traits in the Aroeira 3 cranium augments the previously documented diversity in

41 he Atapuerca (SH) fossils and the Swanscombe cranium belong to the Neandertal clade, whereas the Arag

42 nasion-glabella region of the Taung partial cranium (but not along the frontal crest), this characte

43 chain of bones attached to the mandible and cranium, but in adult mammals the chain is detached from

44 involves curvature and axial torsion of the cranium, but no telescoping.

45 , the external cranial morphology of the LB1 cranium cannot be accommodated within a large global sam

46 root of the eighth cranial nerve within the cranium caused rapid effects on unit responses to head r

47 Here we describe an African fossil cranium constrained by 40Ar/39Ar analyses, magnetostrati

48 ed tissue (14 +/- 2%; P < 0.05) within a rat cranium critical defect compared with a non-mineralized

49 The small size of the Proteopithecus cranium demonstrates that the defining cranial character

50 Rather-as is seen elsewhere in the cranium, dentition, and postcranial skeleton-these mandi

51 rative morphometric analyses of the KNM-LH 1 cranium document the temporal and spatial complexity of

52 Alcian Blue and Alizarin Red staining of the cranium exhibited an unfused nasal capsule and palatine

53 The cranium exhibits a mosaic of primitive and derived featu

54 e risk of CNS tumours after radiation to the cranium for a paediatric cancer, compared with the risk

55 of fiber optic emitters and detectors on the cranium for volumetric imaging of brain activation.

56 d shows strong affinities to the KNM ER 1470 cranium from Kenya (Homo rudolfensis), a morphotype prev

57 Here we report on a modern human cranium from Tam Pa Ling, Laos, which was recovered from

58 ndwanatherian, a complete and well-preserved cranium from Upper Cretaceous strata in Madagascar that

59 d via rapid acceleration-deceleration of the cranium, giving rise to subtle pathological changes appr

60 The cranium has a derived modern human morphology in feature

61 erning population history, just as the human cranium has done.

62 d physiology of pain transmission within the cranium have been elucidated, and advances been made int

63 Given the fixed volume of the cranium in adulthood, it is surprising that most studies

64 This cranium is about 15% larger than size estimates based on

65 The Hofmeyr cranium is consistent with the hypothesis that UP Eurasi

66 We find that the avian cranium is highly modular, consisting of seven independe

67 When the cranium is modeled with the highest level of accuracy (h

68 The cranium is modified for an enlarged vocal sac typical of

69 This cranium is represented by most of the right half of a ca

70 ffect shape comparisons between a diminutive cranium like LB1 and the much larger crania of modern hu

71 ielded a largely complete early modern human cranium, Oase 2, scattered on the surface of a Late Plei

72 st significant specimen is the near-complete cranium of a large individual, designated LES1, with an

73 e to radiation that a single low dose to the cranium of a mature rat is sufficient to ablate hippocam

74 Here we describe the partial cranium of a new medium-sized (about 15-20 kg) fossil ca

75 The most complete and best-preserved cranium of a Paleogene anthropoid ever found, that of a

76 however, an additional, minimally distorted cranium of a young juvenile from a nearly contemporaneou

77 ew species, represented by the most complete cranium of forstercooperiines known to date, shows the e

78 osseous defects (5 mm) were prepared in the cranium of immunocompromised mice and were treated with

79 r than size estimates based on a fragmentary cranium of its contemporary and close relative Apidium p

80 sference of post-dentary jaw elements to the cranium of mammals as auditory ossicles is one of the ce

81 in transparent windows in the dorsal skin or cranium of mice.

82 toff size was reduced in tumors grown in the cranium or in regressing tumors after hormone withdrawal

83 ing to electrical stimulation of the thinned cranium overlying the middle meningeal artery (MMA).

84 MicroCT scans of a male cranium recovered in 1966 [Egyptian Geological Museum, C

85 Although the cranium represents possibly the smallest adult or near-a

86 strate that the mandible, in contrast to the cranium, significantly reflects subsistence strategy rat

87 y 2.8- to 2.6-million-year-old early hominid cranium (Stw 505) from Sterkfontein, South Africa, tenta

88 y unique dentition and only known ptolemaiid cranium, that of Ptolemaia grangeri, is described.

89 ological comparison of the adolescent Oase 2 cranium to relevant Late Pleistocene human samples docum

90 fractures as the sphenoid bone connects the cranium vault to the facial bones.

91 When only the cranium was considered, the distance was 39% +/- 4% (ran

92 both stresses and strains occurred when the cranium was modeled with a low level of non-homogeneity

93 All material property values for the cranium were randomized with a Gaussian distribution wit

94 focused ultrasound through the intact human cranium with magnetic resonance imaging (MRI) guidance.

95 makes it the most complete Oligocene primate cranium worldwide.

96 , to our knowledge, most complete fossil ape cranium yet described, recovered from the 13 million-yea