ライフサイエンスコーパス: lower jaw

1 x5/6(-/-) mouse mandibular arch (prospective lower jaw).

2 ns in both jaws, and a dermal element in the lower jaw.

3 might negatively regulate Hh signals in the lower jaw.

4 pecifically, mesodermal Tbx1, in shaping the lower jaw.

5 effects on both the length and height of the lower jaw.

6 lls form the distal skeletal elements of the lower jaw.

7 on of bone development between the upper and lower jaws.

8 olar, canine, and incisor teeth in upper and lower jaws.

9 th of the retroarticular (RA) process of the lower jaw, a change predicted to increase speed of jaw r

10 of the hindlimb skeleton and absence of the lower jaw (agnathia).

11 subsequent formation of aberrant bone in the lower jaw along with proximal-distal duplications.

12 an ocean), which possesses the largest known lower jaw among Triassic sauropterygians.

13 ing narrow, elongated snouts, underdeveloped lower jaw and a high incidence of cleft palate.

14 pecifies ventral pharyngeal cartilage of the lower jaw and bapx1 specifies the jaw joint.

15 replacement in basal therian mammals and on lower jaw and basicranial morphology.

16 t the representations of the hand and of the lower jaw and neck are strongly interconnected.

17 dibular nerve, and the representation of the lower jaw and neck region, innervated by the second and

18 Overlap of the hand and of the lower jaw and neck representations and of their horizont

19 lacks connections with the hand and with the lower jaw and neck representations, but the representati

20 migratory cranial neural crest specifies the lower jaw and other ventral arch fates.

21 of sucker (suc) disrupts development of the lower jaw and other ventral cartilages in pharyngeal seg

22 Although the body scales, fin rays, lower jaw and palate are comparable to those in more pri

23 is reduced early in development the ventral lower jaw and supporting structures are reduced in size

24 Second, both the lower jaw and tongue skeleton display an organisation wh

25 ologies, having a short, broad skull, robust lower jaw, and a dentition with relatively few teeth tha

26 receptive fields of the mystacial vibrissae, lower jaw, and glaborous snout.

27 of the glaborous snout, mystacial vibrissae, lower jaw, and oral cavity (the rostrum).

28 of the first pharyngeal arch, from which the lower jaw arises.

29 ircular impressions created by the upper and lower jaws, bearing some similarity to fossil traces int

30 al axonal projections that cross the forepaw/lower jaw border as compared to projections remaining wi

31 of neurons in layer II/III near the forepaw/lower jaw border in rat somatosensory cortex, comparing

32 orepaw and lower jaw representation (forepaw/lower jaw border,(1) FP/LJ border) in SI of adult rats,

33 e for adaptive variation in the shape of the lower jaw both within and among genera of Lake Malawi ci

34 lly the mechanical coupling of the upper and lower jaw by the postorbital ligament.

35 f Ednra1 leads to fusions between upper- and lower-jaw cartilages, whereas the combined loss of Ednra

36 osed mouth, (ii) opening the mouth until the lower jaw contacted the sea surface, which created a cur

37 on and position of the teeth in the upper or lower jaw could not be determined with certainty; even t

38 tional system that affects the kinematics of lower jaw depression--the opercular four-bar linkage app

39 Lower jaw development is a complex process in which mult

40 ablishment of a 'mandibular identity' during lower jaw development requires both Ednra-dependent and

41 mandibular arch domain that is conducive for lower jaw development, including the initiation of tongu

42 in relation to the skeletal elements of the lower jaw elements.

43 onasal organ (VNO), nasal cavity, forebrain, lower jaw, eyelids and pinnae.

44 per jaw development, while Dlx5/6 confer the lower jaw fate.

45 excessive bone degradation of the upper and lower jaws followed by development of fibrous tissue mas

46 that they play partially redundant roles in lower-jaw formation and development of the jaw joint.

47 Ednra) to promote ventral skeletal fates and lower-jaw formation.

48 reviously known only from isolated teeth and lower jaw fragments recovered from the Cretaceous and Pa

49 nes--the 'Dlx code' that specifies upper and lower jaw identity in mammals and teleosts--is a primiti

50 mesenchymal survival and development of the lower jaw in the mandibular epithelium.

51 the proximal-distal patterning of the mouse lower jaw, in part through establishing a negative-feedb

52 -) results in homeotic transformation of the lower jaw into upper jaw.

53 The most proximal region of the lower jaw is derived from second arch (r4) NC.

54 The lower jaw is derived from the mandibular process of the

55 om Dlx-5; Dlx-6 double mutants, in which the lower jaw is transformed to an upper jaw.

56 lan including leaf-shaped teeth, a beak-like lower jaw, long, gracile limbs, and a quadrupedal stance

57 ten flexible along their length, whereas the lower jaw (mandible) is usually a rigid structure formed

58 Acquisition of the lower jaw (mandible) was evolutionarily important for ja

59 al hearing (such as pan-bone thinning of the lower jaws, mandibular fat pads, and isolation of the ea

60 of the splanchnic mesoderm that produces the lower jaw muscles and SHF of vertebrates.

61 details of the representations of the hand, lower jaw, neck, and face in area 3b of normal macaque m

62 presence of an ameloblastoma neoplasm in the lower jaw of a specimen referred to the derived non-hadr

63 odel of large-scale bone regeneration in the lower jaw of adult zebrafish, we show that chondrocytes

64 Defects in the lower jaw, or mandible, occur commonly either as isolate

65 rate kinematic chain as well as the quadrate-lower jaw-postorbital ligament-braincase-quadrate kinema

66 had a cleft palate and abnormalities of the lower jaw, raising the possibility that they might serve

67 The in vivo zebrafish lower jaw regeneration model reveals that NHFs enhance b

68 action on in vitro wound healing and in vivo lower jaw regeneration of zebrafish.

69 e located the border between the forepaw and lower jaw representation (forepaw/lower jaw border,(1) F

70 ons may form one basis for expansions of the lower jaw representation into that of the hand when peri

71 e located the border between the forepaw and lower jaw representation of SI in vivo, and used whole c

72 cation of the border between the forepaw and lower jaw representations in rat S1 was determined elect

73 rt segment of the border between the forepaw-lower jaw representations in rat S1 was mapped using sta

74 close to the border between the forepaw and lower jaw representations.

75 Most significantly, the lower jaw shows evidence for neurovasculature that is al

76 ned loss of Ednra1 and Ednra2 eliminates the lower jaw, similar to edn1-/- mutants.

77 observed in most of the neural crest-derived lower jaw skeleton and surrounding connective tissues.

78 The lower jaw skeleton is derived from cephalic neural crest

79 s) of the mandibular adductor muscles on the lower jaw skeleton.

80 We show that most lower jaw structures in Ednra(-/-) embryos undergo a hom

81 e defects include homeotic transformation of lower jaw structures into upper jaw-like structures, sug

82 tes skeletal development of the hindlimb and lower jaw through discrete populations of cells that giv

83 mutants exhibit a homeotic transformation of lower jaws to upper jaws.

84 Morphological changes to the lower jaw were detected at 96 hpf in response to 1 mug/L

85 and closing lever mechanisms of the cichlid lower jaw, which have traditionally been used to describ

86 with nearly complete cranium and associated lower jaws with in situ dentitions.