ライフサイエンスコーパス: ossicle

1 r of the inner ear) or columella (middle ear ossicle).

2 um, which affects the normal mobility of the ossicle.

3 umber of hematopoietic cells isolated within ossicles.

4 , the shape and spatial configuration of the ossicles.

5 nic differentiation of ectopically implanted ossicles.

6 in the evolution of the mammalian middle ear ossicles.

7 ok for bone erosion and the integrity of the ossicles.

8 ition of the proximal jawbones to middle ear ossicles.

9 of acoustical response of sheep's middle-ear ossicles.

10 marrow cells were directly injected into the ossicles after lethal irradiation, the PTH-treated group

11 implanted with MSCs showed increased ectopic ossicle and bone formation when recipients received low

12 In rare cases surgical excision of the ossicle and/or free cartilaginous material may give good

13 beled preparations and includes the Weberian ossicles and fluid spaces.

14 Endogenous HSCs homed to tissue-engineered ossicles and individually sorted HSCs from ossicles were

15 ntify shape and functional properties of the ossicles and the tympanic cavity and make comparisons wi

16 e hampered by the small sample of Neandertal ossicles and the unavailability of methods combining ana

17 -2 adenovirus, seeded on collagen scaffolds (ossicles), and implanted subcutaneously in the flank reg

18 eover, EBM stimulated formation of new bone, ossicles, and marrow spaces, similar to active DBM.

19 The humanized ossicles are formed by in situ differentiation of BM-der

20 The middle ear ossicles are only rarely preserved in fossil hominins.

21 d in a reduced osteoinduction score, reduced ossicle area, and reduced new bone formation.

22 ctions restrain the motion of the middle ear ossicles, attenuating the transmission of low-frequency

23 rmore, human CD34(+) cells transplanted into ossicle-bearing mice engrafted and maintained human HSCs

24 yrinthectomy or disruption of the middle ear ossicles, caused a reduction in Glyt2, but not Glyt1 mRN

25 Compared with BM ossicles, CB ossicles showed a predominance of red marro

26 bones homologous to the mammalian middle ear ossicles compose the proximal jaw bones that form the ja

27 x1 following the transition to the mammalian ossicle configuration is not due to a change in expressi

28 Marrow cavities of the ossicles contained phenotypically defined hematopoietic

29 All ossicles demonstrated chemical composition characteristi

30 hanges contributing to the detachment of ear ossicles during mammalian evolution.

31 hanism bridging the dentary and the detached ossicles during mammalian evolution.

32 The ossicles formed by the BMP-7-transduced HOKC were smalle

33 Subcutaneously implanted ossicles formed heterotopic bone.

34 anthropus robustus as well as additional ear ossicles from Australopithecus africanus.

35 Ossicles from mice with burn injuries developed signific

36 The analysis of arm ossicles in Ophiocoma showed that in light-sensitive spe

37 n nude mice gave rise to perfect heterotopic ossicles in vivo with ultrastructure of dentin, enamel,

38 Marrow cavities from CB and BM ossicles included donor-derived CD146-expressing osteopr

39 that the width, but not the length, of this ossicle is decreased in the mutant mice.

40 pment of the neural crest-derived middle ear ossicles is defective.

41 ements to the cranium of mammals as auditory ossicles is one of the central topics in evolutionary bi

42 The diminutive middle ear ossicles (malleus, incus, stapes) housed in the tympanic

43 bsequently be transplanted directly into the ossicle marrow space or by intravenous injection.

44 m reconstitution assay, HSC frequency in the ossicle marrow was 3 times greater in PTH groups than in

45 ne marrow and support the future use of this ossicle model in elucidating the composition and regulat

46 d striking morphological differences between ossicles of AMHs and Neandertals.

47 Ossicles of both Neandertals and AMHs appear derived com

48 The few known ossicles of Neandertals are distinctly different from th

49 The air-filled cavity and ossicles of the mammalian middle ear conduct sound to th

50 burn injury enhanced vascularization of the ossicles (P < 0.05).

51 frequencies as native bones, and marrow from ossicles reconstituted multilineage long-term hematopoie

52 Motion of the stapes (the stirrup ossicle) sets the cochlear fluid in motion, which in tur

53 Compared with BM ossicles, CB ossicles showed a predominance of red marrow over yellow

54 haped eardrum can transfer more force to the ossicles than a flat eardrum, especially at high frequen

55 apparatus is composed of three endochondrial ossicles (the stapes, incus and malleus) and two membran

56 The ossicles, therefore, allow for accelerated and superior

57 analysis of the largest sample of Neandertal ossicles to date, including many previously unknown spec

58 hearing impairment, otitis media, fusions of ossicles to the middle ear wall, and deformed stapes.

59 h act as structural components to anchor the ossicles to the skull.

60 These remarkable fully mineralized ossicles underscore the importance of epithelial-mesench

61 er simulation of the ear canal, eardrum, and ossicles was developed.

62 d ossicles and individually sorted HSCs from ossicles were able to reconstitute lethally irradiated m

63 el as a system to study the stem cell niche, ossicles were established with or without anabolic parat

64 CB ossicles were regularly observed upon transplantation.

65 ondral ossification can engineer a scaled-up ossicle with features of a "bone organ," including physi

66 ete workflow for the generation of humanized ossicles with an accessible BM microenvironment that fai

67 ntation model bearing subcutaneous humanized ossicles with an accessible BM microenvironment, formed

68 vailability of methods combining analyses of ossicles with surrounding structures.

69 This humanized ossicle xenotransplantation approach provides a system f