ライフサイエンスコーパス: evagination

1 that rod discs are formed by plasma membrane evagination.

2 ina, resulting in further laterally directed evagination.

3 Laminin1 severely compromises optic vesicle evagination.

4 lar non-neural ectoderm during optic vesicle evagination.

5 n proliferation is required for initial bulb evagination.

6 e, approximately coincident with the time of evagination.

7 arly in the first mitotic cycle, well before evagination.

8 the inductive effect of decapitation on bud evagination.

9 onal increase in the size of plasma membrane evaginations.

10 revealed that new discs are plasma membrane evaginations.

11 choroid plexus is maintained through initial evagination and appearance in all ventricles.

12 h disk morphogenesis occurs through membrane evagination and extends other recent studies assigning P

13 roepithelium of the ventral forebrain by the evagination and formation of the optic vesicle.

14 monitoring effects on the onset of first bud evagination and the time necessary to reach the 50% budd

15 leg decreased as the tissue extended during evagination and we observed cell rearrangement to be com

16 The early evaginations are associated with premature mesenchymal c

17 These evaginations are recognized by I-BAR proteins, which tri

18 rbs tooth formation, producing a large domed evagination at early stages and supernumerary teeth late

19 rin/rds coincided with the overgrowth of the evaginations at the base of the OS.

20 EM particle averaging showed that the evagination base was surrounded by an 8-fold rotationall

21 Extension of a new basal evagination (BE) applies radial (lateral) traction to me

22 rhodopsin and peripherin/rds to the membrane evaginations believed to be disk membrane precursors.

23 erization burst subsequently re-flattens the evagination, completing the mechanochemical feedback loo

24 Given the physical dimensions of the evaginations, coupled with likely instability of the mem

25 errant PCP signaling, misdirected epithelial evaginations, defective crypt formation, and blastocyst

26 chambers (crypts) that originate within the evaginations directed from the primary lumen toward the

27 each disc is initiated by a ciliary membrane evagination driven by an unknown molecular mechanism rep

28 membranes (INM and ONM, respectively) within evaginations/extensions of the perinuclear space.

29 asma membrane followed by fusion of adjacent evaginations have been proposed.

30 he PM in a way that generates local membrane evaginations in the 100 nm scale.

31 Evagination involves a dramatic change in morphology and

32 Our observations show that disc evagination involves multiple cellular behaviors, as is

33 network in the ciliary stalk, where membrane evagination is initiated, or the actin core of the calyc

34 tors use the evolutionary conserved membrane evagination mechanism to build their discs.

35 odel, in contrast to the previously proposed evagination model, suggests that the vesicular delivery

36 We propose that invagination versus evagination morphogenesis is regulated by the relative t

37 In common with Ikkalpha mutants, Irf6 mutant evagination occurs in a NF-kappaB-independent manner and

38 f the connecting cilium, we propose that the evagination occurs via a process akin to blebbing and is

39 We have reexamined the evagination of both the leg and wing discs and find that

40 The evagination of Drosophila imaginal discs is a classic sy

41 ry factor (Irf) family, Irf6 also results in evagination of incisor epithelium.

42 mbrane discs in photoreceptor cells requires evagination of its ciliary plasma membrane by an unknown

43 Specifically, wal affects evagination of the Malpighian tubule buds, fas and thr a

44 nt cell proliferation, a complete failure of evagination of the neuroectoderm in the ventral dienceph

45 ed from the infundibulum, which is formed by evagination of the neuroectoderm in the ventral dienceph

46 ent of retinal precursors is responsible for evagination of the optic primordia.

47 specification of the anterior neural plate, evagination of the optic vesicles from the ventral foreb

48 the eyes and telencephalon and in defective evagination of the optic vesicles.

49 racellular rhodopsin-bearing vesicles or the evagination of the plasma membrane followed by fusion of

50 This factor appears to stimulate the initial evagination of the ureteric bud from the Wolffian duct,

51 Development initiates with evagination of two ventral buds of foregut endoderm into

52 Mammalian lung develops as an evagination of ventral gut endoderm into the underlying

53 ls of the conducting airways caused atypical evaginations of small capillary-like vessels into large

54 Intermediates were dome-shaped evaginations of the inner nuclear membrane (INM), that g

55 since Ikkalpha mutant mice show protrusions (evaginations) of incisor tooth, whisker and hair follicl

56 During later evagination, optic vesicle cells shorten, drawing their

57 Optic vesicle evagination persists for longer than expected; cells mov

58 ma membrane, subsequently forming successive evaginations that "zipper" up proximally, but at their l

59 ) signaling orchestrates directed epithelial evaginations to form crypts for implantation in mice.

60 by fusion of the leading edges of successive evaginations to form discrete discs.

61 gels retained a rounded shape with membrane evaginations visible on their surface.

62 s injured or removed, the onset of first bud evagination was delayed and/or the time until the 50% bu

63 When PF tissue was doubled, precocious bud evagination was induced, regardless of graft location.

64 t discs are formed as serial plasma membrane evaginations, whereas a recent alternative postulates th

65 New discs are formed as serial membrane evaginations, which eventually enclose through a complex