ライフサイエンスコーパス: pharyngeal pouch

1 es, and disorganized patterning of the third pharyngeal pouch.

2 um that forms from the endoderm of the third pharyngeal pouch.

3 botympanic recess, a derivative of the first pharyngeal pouch.

4 ds originate from the endoderm of the caudal pharyngeal pouches.

5 des while Bmp7 and PRDC are expressed in the pharyngeal pouches.

6 r to be secondary to failed outgrowth of the pharyngeal pouches.

7 etic mechanisms that direct formation of the pharyngeal pouches.

8 e separated by endodermal outpocketings, the pharyngeal pouches.

9 egrity of patterning in the otic placode and pharyngeal pouches.

10 ompensatory function of Nkx2.5 in the mutant pharyngeal pouches.

11 tory epithelium, mid-hindbrain junction, and pharyngeal pouches.

12 s fail to generate a late-forming portion of pharyngeal pouch 1 (termed late-p1) and skeletal element

13 e thymus and parathyroids develop from third pharyngeal pouch (3rd pp) endoderm.

14 a shared endodermal primordium in the third pharyngeal pouch (3rd pp).

15 alling molecules are expressed correctly and pharyngeal pouch and epibranchial placode formation are

16 FGF8 during development of pharyngeal arch, pharyngeal pouch and neural crest-derived tissues.

17 In Shh-/- mutants, the pharyngeal pouches and arches formed by E9.5 and marker

18 ed in the epithelium of branchial clefts and pharyngeal pouches and during branching morphogenesis in

19 living embryos, we show that contact between pharyngeal pouches and the surface ectoderm coincides wi

20 e earliest reported spleen marker and in the pharyngeal pouches and their derivatives including the t

21 thymus and parathyroid are derived from 3rd pharyngeal pouches and their development is initiated vi

22 ed delayed or absent formation of the caudal pharyngeal pouches, and disorganized patterning of the t

23 Shh signalling in patterning the vertebrate pharyngeal pouches, and show that Hh signalling may be i

24 The pharyngeal pouches are a segmental series of epithelial

25 The pharyngeal pouches are first evident as localised sites

26 otopic transplantation of CNC cells into the pharyngeal pouch area or both in combination failed to p

27 hes, we segregate pharyngeal arch artery and pharyngeal pouch defects in RA receptor mutants, and sho

28 were no obvious abnormalities in the caudal pharyngeal pouch derivatives (the thymus, parathyroid gl

29 shown that the Hoxa3 null mutant lacks third pharyngeal pouch derivatives, the thymus and parathyroid

30 re, Hoxa3 was required for survival of third pharyngeal pouch-derived organs, but expression in eithe

31 e cell type-specific roles of Hoxa3 in third pharyngeal pouch development, we analyzed tissue-specifi

32 Here, we examined their roles in pharyngeal pouch development.

33 lar markers revealed a serious disruption of pharyngeal pouch endoderm (ppe) morphogenesis and reduce

34 foo is expressed in pharyngeal pouch endoderm and is required for pouch expr

35 ere, in chick, we show that cells within the pharyngeal pouch endoderm have an abundance of apically

36 ltimobranchial body epithelium emerging from pharyngeal pouch endoderm in early organogenesis, differ

37 l common primordia that develop from the 3rd pharyngeal pouch endoderm in mouse embryos at about E11,

38 erlying ectoderm, core paraxial mesoderm and pharyngeal pouch endoderm of the mandibular arch as well

39 perfamily, is among the prominent markers of pharyngeal pouch endoderm, but to date no role has been

40 arathyroid glands are derived from the third pharyngeal pouch endoderm.

41 , expression of shh in endoderm of the first pharyngeal pouch fails to extend as far laterally as in

42 Using time-lapse microscopy, we show that pharyngeal pouches form by the directed lateral migratio

43 provide us with vital insights into how the pharyngeal pouches form their normal morphology.

44 vertebrate head, endodermal branches, called pharyngeal pouches, form through the transient stratific

45 ling: an early phase during which FGFs drive pharyngeal pouch formation, and a later phase when they

46 type is likely to be secondary to defects in pharyngeal pouch formation.

47 This suggests that the process of pharyngeal pouch morphogenesis involves the constraining

48 development in jawed vertebrates, including pharyngeal pouch morphogenesis, patterning of the oral s

49 They also give insight into the formation of pharyngeal pouches, of which little is known in vertebra

50 To determine the role of Tbx1 in the first pharyngeal pouch (PPI) in forming outer and middle ears,

51 The thymus originates from bilateral third pharyngeal pouch primordia containing endodermal progeni

52 In contrast, Pax1 expression in all pharyngeal pouches requires both Eya1 and Six1 function.

53 the 4th and 6th arch arteries and to the 4th pharyngeal pouch, respectively, suggesting that differen

54 of defective RA signaling occur secondary to pharyngeal pouch segmentation defects, although this mod

55 pharyngeal development: the formation of the pharyngeal pouches that segment the pharyngeal region by

56 Nkx2.6 is expressed in the caudal pharyngeal pouches, the caudal heart progenitors, the si

57 in lateral endoderm of the second and third pharyngeal pouches, the posterior portion of the aortic

58 which direct Eya1 expression to the somites, pharyngeal pouches, the preplacodal ectoderm (the common

59 The pharyngeal pouches, which form by budding of the foregut