ライフサイエンスコーパス: basal surface

1 a lower bound on the elastic modulus of the basal surface.

2 embling interdigitated foot processes at the basal surface.

3 or two distinct egress zones per cell at the basal surface.

4 a concomitant increase in actomyosin on the basal surface.

5 , where it restricts protein delivery to the basal surface.

6 nner by promoting dendritic retention on the basal surface.

7 otal internal reflection fluorescence on the basal surface.

8 urface directly displaced podosomes near the basal surface.

9 adial glia/progenitor fibers toward the pial/basal surface.

10 two distinct steps, acute and obtuse, on the basal surface.

11 esulting in rearrangement of contacts on the basal surface.

12 arized MTs along the migratory axis at their basal surfaces.

13 dge surfaces of kaolinite rather than to the basal surfaces.

14 the middle surface bisecting the apical and basal surfaces.

15 ce of the epithelium must be softer than the basal surface, a result which we confirmed experimentall

16 ly with the expression of an integrin on the basal surface all blastomeres.

17 p of the colony and rod cells dominating the basal surface and edges.

18 ne RGCs retards process outgrowth toward the basal surface and impairs apical polarity and adherens j

19 ribution of the SDF-1 alpha receptor, to the basal surface and leading edge of the cell.

20 d epithelium, nuclei synthesize DNA near the basal surface and move apically to divide.

21 but the cell nuclei are not polarized to the basal surface and no lumen formation occurs, indicating

22 in a Triton-X-100-insoluble structure at the basal surface and that the staining of this structure is

23 This positions them near the basal surface and the basal-most region of the lateral d

24 s and their mitotic spindles parallel to the basal surface and undergo symmetric cell divisions in wh

25 face between the Co and Mo atoms on the MoS2 basal surface and we ascribe the higher activity to the

26 l that considers two binding sites: external basal surfaces and edge sites.

27 calcium-binding protein that is found on the basal surfaces and in the extracellular matrix of cells

28 rovilli, an increase in actin bundles at the basal surface, and a reduction in cell height without an

29 The electroactivity is dominated by the basal surface, and studies that have used AQDS as a mark

30 The basal surfaces are flat and well-formed on one side and

31 These basal surfaces are shown to leach, hydrate, and expand t

32 currence of atherosclerosis localized in the basal surface arteries.

33 to show that the CFTR+ cell line (S9) had a basal surface ATP concentration that could be detected w

34 ls, which retain contact with the apical and basal surfaces but where basolateral proteins (LGL) beco

35 atively that the electroactivity of the HOPG basal surface can be significantly lowered by the adsorp

36 needed to catalyze many reactions, with the basal surface considered to be inert.

37 ribbon (rib) gene disrupt this coupling: the basal surface continues to extend towards its normal tar

38 egrin and non-muscle myosin-II to coordinate basal surface contraction and cell growth along the apic

39 Remarkably, inhibiting basal surface contraction-both in silico and through gen

40 ong the apical-basal axis of the tissue, and basal surface contraction.

41 ced availability of mutant Bnl on the source basal surface decreases ASP cytoneme numbers, leading to

42 eous oscillations in the contraction of cell basal surfaces develop in a subset of follicle cells.

43 ations compromised NHE3 activity by reducing basal surface expression and/or loss of basal transport

44 ectrin by small interference RNA reduces the basal surface expression of alphahTRPC4 and prevents the

45 ecreased constitutive shedding and increased basal surface expression of c-Kit, with diminished apopt

46 In flow cytometry experiments, the basal surface expression of L-selectin and CD11b was mod

47 E cells, together with a concomitant loss of basal surface expression of monocarboxylate transporter

48 The overall basal surface, facing the developing lens, is increasing

49 sfer localized stress from the apical to the basal surface globally, resulting in rearrangement of co

50 ing from hydroxyl functional groups, whereas basal surfaces have a permanent negative charge arising

51 T84d) to DN32.D3 cells was greater along the basal surface in comparison with the apical surface.

52 t the leading edge and are restricted to the basal surface in migrating cells.

53 alpha6beta4 integrin is localized on the basal surface in structures referred to as type II hemid

54 re the nucleus oscillates from the apical to basal surfaces in proliferative neuroepithelia.

55 th aqueous humor is hexagonal, whereas their basal surface is irregular.

56 involvement of Tf in Fe transport across the basal surface, laser scanning confocal microscopy with 3

57 m cells biotinylated at either the apical or basal surface localized membrane 25- and 27-kDa heat sho

58 achol inside a patch pipette attached to the basal surface of an acinar unit.

59 of actin filaments is coordinated across the basal surface of cells encircling the oocyte.

60 l basal geometry remodeling by anchoring the basal surface of cells to the extracellular matrix at sp

61 are large protein complexes organized at the basal surface of cells, which physically connect the ext

62 moting localized Laminin accumulation at the basal surface of cells.

63 ement complex C5b-9 assembles rapidly on the basal surface of cultured primary porcine RPE cells but

64 The protein remains at high levels on the basal surface of ectoderm cells but is temporarily reduc

65 s the turnover of type IV collagen along the basal surface of endocardial cells.

66 sory neurons can be positioned either at the basal surface of epidermal cells, or enclosed within epi

67 sal plane pyrolytic graphite (BPPG), and the basal surface of highly oriented pyrolytic graphite (HOP

68 ntially uniform and high activity across the basal surface of HOPG.

69 l adhesion-like clusters of integrins on the basal surface of imaginal disc epithelia and junctional

70 elial cell biology, nutrient delivery to the basal surface of intestinal epithelial cell membranes ma

71 displayed reduced O-glycosylation along the basal surface of larval wing imaginal discs, which was r

72 s ligand VCAM-1, of polarized T cells at the basal surface of lymphatic but not blood vessel endothel

73 beta 4 integrin subunits are present at the basal surface of many epithelial cells and serve as rece

74 Human Ferroportin1 is found at the basal surface of placental syncytiotrophoblasts, suggest

75 alpha II b beta 3 receptors at the basal surface of platelets engage fibrinogen in a ringli

76 ocalizes with focal adhesion proteins at the basal surface of polarized cells.

77 serve as a recruitment signal for PMN to the basal surface of polarized epithelia.

78 ase variants were able to transcytose to the basal surface of rat and human BMEC in a manner dependen

79 lization of these receptors to the apical or basal surface of RPE cells was determined with immunocyt

80 5, unlike CCR5 and CXCR4, is abundant at the basal surface of small intestinal epithelium.

81 racellular matrix, the T cell adheres to the basal surface of the bronchial epithelial cell using alp

82 all-trans retinol (ROL) was delivered to the basal surface of the cultured RPE by serum retinol-bindi

83 getal (high) to animal (low) gradient on the basal surface of the ectoderm.

84 bumin was segregated from transferrin at the basal surface of the epithelial cells and did not coloca

85 rane stained positively for laminin, and the basal surface of the epithelial cells stained positively

86 a 2, and alpha 3 integrins, whereas only the basal surface of the epithelial cells, where they are in

87 tegrins to coordinate actin filaments at the basal surface of the follicular epithelium.

88 that alphaSMA-expressing cells appear at the basal surface of the future epithelial cleft prior to bi

89 The basal surface of the hepatocytes is separated from adjac

90 endothelial cells migrate along the maturing basal surface of the hepatocytes.

91 nique interaction of apotransferrin with the basal surface of the intestinal epithelium.

92 the in situ gland localized mainly near the basal surface of the mammary alveolar cells.

93 lls intercalate by first wedging between the basal surface of the outer epithelium but only insert ap

94 accumulates at discrete locations across the basal surface of the retina.

95 , known as drusen, that accumulate along the basal surface of the retinal pigmented epithelium.

96 demonstrated that CD46 was polarized to the basal surface of the RPE along with beta1 integrin, show

97 iently extend two long protrusions along the basal surface of the spinal cord before axon initiation.

98 es of wing and squamous cells but not at the basal surface of these cells or on basal cells.

99 is distributed in a punctate pattern at the basal surface of ureteric bud epithelia.

100 analysis indicated that cells move along the basal surface of vessels by adhering to the basement mem

101 Basally secreted Cochlin diffuses along the basal surface of vestibular epithelia, while apically se

102 ucted by sequentially seeding the apical and basal surfaces of acellular dermis with cultured human k

103 ermitted the visualization of the apical and basal surfaces of an acinus.

104 unctions, thereby effecting its release from basal surfaces of an infected epithelium to the apical o

105 AR proteins localize to either the apical or basal surfaces of cells prior to blastocoel formation; w

106 mobility in adsorbed water films on external basal surfaces of clay is similar to that in the near-su

107 It is expressed at lateral and basal surfaces of epithelia during kidney and lung devel

108 isappear, numerous filopodia extend from the basal surfaces of epithelial cells, the space between th

109 uids on both the hydrophilic and hydrophobic basal surfaces of kaolinite, a common clay mineral.

110 ochastic nuclear movement between apical and basal surfaces of neuroepithelia during interkinetic nuc

111 FN pillars, long filopodia protrude from the basal surfaces of somite epithelial cells.

112 nts demonstrated that MCO1 is located on the basal surfaces of the digestive system and Malpighian tu

113 i of progenitors move between the apical and basal surfaces of the neuroepithelium in phase with thei

114 tory) system, the cell bodies and apical and basal surfaces of the tracheal epithelium normally move

115 ed that ICAM-1 was present on the apical and basal surfaces of umbilical vein endothelium in vitro an

116 of negative electrostatic potential from the basal surface onto the edge surface.

117 through genetic manipulations targeting the basal surface receptor integrin and non-muscle myosin-II

118 ct with the extracellular matrix defines the basal surface, setting in motion E-cadherin-mediated cel

119 After 10 min, basal surface sites were implicated due to slow Co oxida

120 demonstrates definitively that the pristine basal surface supports fast ET, and that ET is not confi

121 membrane (BM) extracellular matrix at their basal surfaces that plays essential roles in adhesion an

122 Since single cells can mechanosense stiff basal surfaces through soft hydrogels of <10 mum thickne

123 investigated by imaging the response of the basal surface to localized force application over the ap

124 r in transmission of the FGF signal from the basal surface to the rest of the cell or in the apical c

125 asurements at different locations across the basal surface, unambiguously revealing it to be highly e

126 cular surface of polarized cells, apical and basal surfaces were infected with wild-type virus or a g

127 Truncated Bnl sorts asymmetrically to the basal surface, where it is received by cytonemes that ex

128 isplayed a pH-independent negative charge on basal surfaces whereas the positive charge on edges incr

129 t and ceased as laminin 111 localized to the basal surface, whereas dissemination of carcinoma cells

130 ere more sensitive when CPE-treated on their basal surface, whereas Vero cells were more sensitive wh

131 Misshapen decreases integrin levels at the basal surface, which may facilitate detachment of each c

132 reactivity ratio of biotite edge surfaces to basal surfaces, while acetate does not impact this relat