ライフサイエンスコーパス: corneal endothelial cell

1 differentiation of the neural crest derived corneal endothelial cell.

2 ike coupling mechanisms play roles in CCE in corneal endothelial cells.

3 taken to investigate the mechanism of CCE in corneal endothelial cells.

4 AQP1 does not contribute to PCO(2) in corneal endothelial cells.

5 hesion molecule, N-cadherin, is expressed by corneal endothelial cells.

6 soforms expressed in primary cultures of rat corneal endothelial cells.

7 ial and possibly other cellular functions in corneal endothelial cells.

8 these cells often fail to differentiate into corneal endothelial cells.

9 a, -eta, -gamma, and -theta were detected in corneal endothelial cells.

10 n important role in Fas ligand expression in corneal endothelial cells.

11 us humor did not promote apoptosis of murine corneal endothelial cells.

12 aqueous humor suppress S-phase entry of rat corneal endothelial cells.

13 n aqueous humor on DNA synthesis in cultured corneal endothelial cells.

14 n corneal epithelial cells, keratocytes, and corneal endothelial cells.

15 tein which inhibits the NK-mediated lysis of corneal endothelial cells.

16 ittle ALDH3 is present in the keratocytes or corneal endothelial cells.

17 y conjunctiva, corneal epithelial cells, and corneal endothelial cells.

18 rbol esters on the function and structure of corneal endothelial cells.

19 port the adhesion and proliferation of human corneal endothelial cells.

20 in or a matrix elaborated by cultured bovine corneal endothelial cells.

21 cell proliferation and cell shape changes in corneal endothelial cells.

22 ized FN and to cultured monolayers of bovine corneal endothelial cells.

23 only a potent mitogen, it is a modulator for corneal endothelial cells.

24 glandin E2 synthesis is increased in injured corneal endothelial cells.

25 ranscriptional control of type I collagen in corneal endothelial cells.

26 a highly effective, novel carrier for human corneal endothelial cells.

27 r integrity in monolayers of cultured bovine corneal endothelial cells.

28 P) was used to transduce cryopreserved human corneal endothelial cells.

29 oxic to cryopreserved human primary cultured corneal endothelial cells.

30 t is undetectable on stromal fibroblasts and corneal endothelial cells.

31 g-term viability of the neural crest derived corneal endothelial cells.

32 sease involving metaplasia and overgrowth of corneal endothelial cells.

33 lts in replication in nonproliferating human corneal endothelial cells.

34 /gld mice did not induce apoptosis of BALB/c corneal endothelial cells.

35 Human corneal endothelial cells and Descemet's membrane (HCEC-

36 alpha 2(I) collagen RNA obtained from normal corneal endothelial cells and from modulated corneal end

37 ed for overexpression of E2F2 in transfected corneal endothelial cells and permitted calculation of t

38 ggest that type I collagen is synthesized in corneal endothelial cells and that such undesired expres

39 Two forms of cyclooxygenase are present in corneal endothelial cells, and pharmacologic studies ind

40 Limbal basal cells and corneal endothelial cells appear to be inhibited in the

41 Corneal endothelial cells are arranged as a monolayer on

42 It is possible that in situ human and rabbit corneal endothelial cells are arrested at different poin

43 Since corneal endothelial cells are crucial for maintaining co

44 Human corneal endothelial cells are derived from neural crest

45 The corneal endothelial cells are enlarged and reduced in nu

46 Adult human corneal endothelial cells are G1-arrested, even in respo

47 In neonatal rat, corneal endothelial cells are still entering the cell cy

48 Cryopreserved, primary, cultured human corneal endothelial cells are viable and retain their ab

49 not induce acute significant cytotoxicity in corneal endothelial cells at concentrations up to 100 mi

50 lated onto the matrices elaborated by bovine corneal endothelial cells attached to the culture dish a

51 ssion levels in confluent cultures of bovine corneal endothelial cells (BCECs) affects membrane PCO(2

52 ence of Ca(2+) stores in lysosomes of bovine corneal endothelial cells (BCECs) and examines their int

53 inhibition of CA activity in cultured bovine corneal endothelial cells (BCECs) by dorzolamide, a topi

54 LC4A11 expression in cultured primary bovine corneal endothelial cells (BCECs) was determined by semi

55 xperiments were performed in cultured bovine corneal endothelial cells (BCECs).

56 ymal transition and preserve the function of corneal endothelial cells both during ex vivo culture an

57 sage (<4) stromal cells and to low levels in corneal endothelial cells but not in corneal epithelial

58 ness of cryopreserved human primary cultured corneal endothelial cells by characterizing their morpho

59 that WNT10B promotes proliferation in human corneal endothelial cells by simultaneously utilizing bo

60 Regardless of donor age, corneal endothelial cells can enter and complete the cel

61 Cultured bovine corneal endothelial cells (CBCECs) were grown to conflue

62 water channel protein(s) in cultured bovine corneal endothelial cells (CBCECs).

63 In vivo corneal endothelial cell (CEC) counts and morphology wer

64 e current study, we performed in vivo rabbit corneal endothelial cell (CEC) injury via CEC scraping,

65 ated cells with pseudopodia is observed when corneal endothelial cells (CECs) are simultaneously trea

66 Corneal endothelial cells (CECs) are terminally differen

67 mation (EMT), in which the contact-inhibited corneal endothelial cells (CECs) become multilayers of s

68 However, Wnt5a signaling in corneal endothelial cells (CECs) has not been well chara

69 othelial corneal dystrophy (FECD) and normal corneal endothelial cells (CECs) to oxidative stress, an

70 Corneal endothelial cells (CECs) treated with FGF-2 from

71 elial mesenchymal transformation observed in corneal endothelial cells (CECs).

72 FGF-2 is a potent mitogen of rabbit corneal endothelial cells (CECs).

73 ollagen was posttranslationally regulated in corneal endothelial cells (CECs).

74 which is a morphogen and a potent mitogen of corneal endothelial cells (CECs).

75 iferative capacity (premature senescence) of corneal endothelial cells (CECs).

76 othelial corneal dystrophy (FECD) and normal corneal endothelial cells (CECs).

77 cilia that subsequently disassemble in adult corneal endothelial cells (CECs).

78 EDTA released corneal endothelial cell-cell contacts in a dose- and ti

79 Here, isolated primary human corneal endothelial cells (CEnCs) propagated using a dua

80 owed by ciliary body, lens epithelial cells, corneal endothelial cells, conjunctiva, retina, and corn

81 Human corneal endothelial cells could be reliably scored for t

82 heral anterior synechiae, visual acuity, and corneal endothelial cell count (CECC).

83 0.05; 95% CI, -0.01 to 0.12; P = 0.10), and corneal endothelial cell count (WMD, 73.39; 95% CI, -6.2

84 ly received PIOL implantation and have a low corneal endothelial cell count.

85 rm safety, particularly in eyes with reduced corneal endothelial cell counts from prior intraocular s

86 The corneal thickness, corneal endothelial cell counts, specular microscopy par

87 enhanced the proliferative response of human corneal endothelial cell cultures to endothelial cell gr

88 l to modulate alloimmunity and/or to prevent corneal endothelial cell death.

89 talloproteinase activity in confluent bovine corneal endothelial cells decreased the level of endothe

90 n the subjects who underwent trabeculectomy, corneal endothelial cell density (ECD) significantly dec

91 In this study we compare corneal endothelial cell density and morphometry measure

92 Measurement of corneal endothelial cell density is important both for c

93 Corneal endothelial cell density, endothelial cell viabi

94 Human corneal endothelial cell-Descemet's membrane (HCEC-DM) c

95 grafts did not recover clarity in vivo, and corneal endothelial cells did not proliferate in organ c

96 Type I collagen synthesis in corneal endothelial cells does not correlate with steady

97 ly of bicarbonate transporters, give rise to corneal endothelial cell dystrophies.

98 Corneal endothelial cells express IRK1 (Kir2.1) inwardly

99 All corneal and limbal epithelial and corneal endothelial cells express protein kinases, p33cd

100 That limbal basal and corneal endothelial cells express receptors for TGF-beta

101 ct intraocular tumors, 5) CD4(+) T cells and corneal endothelial cells express TRAIL and induce apopt

102 Limbal basal cells and corneal endothelial cells expressed mRNA and protein for

103 Both CD4(+) T cells and corneal endothelial cells expressed TRAIL and induced ap

104 reatments for reversible blindness caused by corneal endothelial cell failure involve replacing the f

105 Corneal endothelial cells from both mice and humans disp

106 These results indicate that corneal endothelial cells from both the central and peri

107 Corneal endothelial cells from FECD patients harbor a po

108 late a significant proliferative response in corneal endothelial cells from old individuals.

109 stance (rho) was measured in cultured bovine corneal endothelial cells grown on permeable substrates

110 The use of substratum elaborated by bovine corneal endothelial cells has proved useful in the prepa

111 ction, no definitive effects of TNF alpha on corneal endothelial cells have been reported.

112 Human corneal endothelial cells have long telomeres throughout

113 es of SiNPs (50, 100, and 150 nm) in a human corneal endothelial cell (HCEC) line, B4G12.

114 Human corneal endothelial cell (HCEC) proliferation is control

115 ative DNA damage increases with age in human corneal endothelial cells (HCECs) and contributes to the

116 Human corneal endothelial cells (HCECs) are considered to be n

117 Human corneal endothelial cells (HCECs) have limited prolifera

118 lation, preservation, and expansion of human corneal endothelial cells (HCECs).

119 Human corneal endothelial cells (HCEnCs) are responsible for m

120 Human corneal endothelial cells (HCEnCs) are terminally differ

121 and COL4A3 mRNA expression in primary human corneal endothelial cells (HCEnCs) was assayed in both P

122 corneal fibroblasts, and immortalized human corneal endothelial cells (HCEnCs), and in vivo intralam

123 In media for human corneal endothelial cells, immature cells differentiated

124 ase (MAPK) signaling pathway was examined in corneal endothelial cells in 1 patient.

125 microscopy showed moderate to severe loss of corneal endothelial cells in all patients.

126 Accelerated loss of corneal endothelial cells in Fuchs' dystrophy is multifa

127 Corneal endothelial cells in humans do not replicate to

128 specific DTH and induced apoptosis of BALB/c corneal endothelial cells in vitro.

129 roteins in donor corneas suggests that human corneal endothelial cells in vivo have not exited the ce

130 the relative proliferative status of rabbit corneal endothelial cells in vivo.

131 in G(0)-phase synchronized subconfluent rat corneal endothelial cells incubated for 24 hours in 10%

132 ption factor E2F2 in nonproliferating rabbit corneal endothelial cells induces cell cycle progression

133 emove corneal epithelial cells, conjunctiva, corneal endothelial cells, iris, ciliary body, lens epit

134 we show that gene transfer to nonreplicating corneal endothelial cells is feasible using recombinant

135 PK signaling pathway was demonstrated in the corneal endothelial cells isolated from the NF-1 eyes.

136 humor suppress S-phase entry in cultured rat corneal endothelial cells, it is not known whether TGF-b

137 nd binding of RAC1 and beta-catenin in human corneal endothelial cells, leading to the activation of

138 n the eye, we employed an immortalized mouse corneal endothelial cell line (C3H3) that constitutively

139 A human corneal endothelial cell line and primary human corneal

140 studies, immortalized normal and FECD human corneal endothelial cell lines (HCECi and FECDi, respect

141 t surgery is known to lead to some degree of corneal endothelial cell loss (ECL).

142 ent studies have demonstrated a reduction in corneal endothelial cell loss after phacoemulsification

143 operative and perioperative risk factors for corneal endothelial cell loss during cataract surgery, a

144 re and describes in detail how the degree of corneal endothelial cell loss is influenced by specific

145 Corneal endothelial cell loss remains a well known, unde

146 erative and postoperative complications, and corneal endothelial cell loss were assessed at 6 months

147 Although clinical outcomes and corneal endothelial cell loss were similar in both group

148 rative MMC was not associated with long-term corneal endothelial cell loss.

149 to elucidate the factors that predispose to corneal endothelial cell loss.

150 utive expression of MHC class I molecules on corneal endothelial cells makes them potential targets f

151 luorophotometry, [protein]Ac by Lowry assay, corneal endothelial cell morphology by specular micropho

152 Ex vivo culture or regeneration of corneal endothelial cells often is subjected to gradual

153 the coculture of lens epithelial cells with corneal endothelial cells on the proliferation of rabbit

154 h either Ia- spleen cells, Ia+ spleen cells, corneal endothelial cells, or corneal epithelial cells f

155 Corneal endothelial cell origin was confirmed by morphol

156 Human corneal endothelial cells plated onto the matrices elabo

157 ally with regard to decreased keratocyte and corneal endothelial cell populations noted months to yea

158 ous studies from this laboratory showed that corneal endothelial cell proliferation ceases in neonata

159 Corneal endothelial cell proliferation under our culture

160 Corneal endothelial cell proliferation under our culture

161 ermine the role of protein kinase C (PKC) in corneal endothelial cell proliferation.

162 -epsilon activity, is important in promoting corneal endothelial cell proliferation.

163 GF-2 stimulates cell proliferation of rabbit corneal endothelial cells (rCECs) by degrading the cycli

164 .37; 95% CI, -11.88 to -0.86; P = 0.02), and corneal endothelial cell reduction (WMD, -55.43; 95% CI,

165 Descemet's membrane supports corneal endothelial cell regeneration in rabbits after e

166 ranscription factor E2F2 in nonmitotic human corneal endothelial cells results in short-term expressi

167 AC priming with Ia- NZB spleen cells or NZB corneal endothelial cells results in the permanent accep

168 Human primary cultured corneal endothelial cells retain their phenotypic proper

169 neal endothelial cell line and primary human corneal endothelial cells retained their characteristic

170 Corneal endothelial cells showed intense labeling for ra

171 arkedly increased the tolerizing activity of corneal endothelial cells, so that a single dose of chol

172 atinocyte growth factors, and coculture with corneal endothelial cells stimulated proliferation of ra

173 Evidence indicates that corneal endothelial cells synthesize mRNA for TGF-beta1

174 ing for the RIII protein was more intense in corneal endothelial cells than in limbal basal cells.

175 ive neurons and into p75(NTR)-positive human corneal endothelial cells that exhibited transendothelia

176 demonstrated that EMAP is a novel protein in corneal endothelial cells that is capable of inducing pr

177 corneal endothelial cells and from modulated corneal endothelial cells that predominantly produce typ

178 The capacity of pig corneal endothelial cells to proliferate in vivo was ass

179 Human corneal endothelial cells, transformed with human papill

180 DM) helps maintain phenotype and function of corneal endothelial cells under physiological conditions

181 we found that during ex vivo culture, bovine corneal endothelial cells underwent endothelial-mesenchy

182 antagonist, vMIP II, was introduced into the corneal endothelial cells using a non-viral vector consi

183 examined the feasibility of gene transfer to corneal endothelial cells using replication-defective re

184 hether Alamar blue could be used to evaluate corneal endothelial cell viability in vitro.

185 ton fraction of the normal and the modulated corneal endothelial cells was immunoprecipitated with PL

186 Apoptosis of BALB/c corneal endothelial cells was mediated by double negativ

187 lagen RNA structures of normal and modulated corneal endothelial cells were analyzed by S1 nuclease p

188 Bovine corneal endothelial cells were cultured to confluence.

189 Human corneal Descemet's membrane and corneal endothelial cells were digested with collagenase

190 Primary cultures of bovine corneal endothelial cells were established on membrane-p

191 Rat corneal endothelial cells were grown in explant culture

192 Corneal endothelial cells were morphologically normal; h

193 Human corneal endothelial cells were plated onto tissue cultur

194 Images of corneal endothelial cells were recorded by using specula

195 oliferation studies, primary cultures of rat corneal endothelial cells were serum-starved for 48 hour

196 Infected corneal endothelial cells were swollen and partly detach

197 We observed LOXHD1 mRNA in cultured human corneal endothelial cells, whereas antibody staining of

198 he anterior chamber of the eye is lined with corneal endothelial cells, which are terminally differen

199 Corneal endothelial cells, which line the back of the co

200 eta3 induced myofibroblast transformation of corneal endothelial cells, with formation of stress fibe

201 as found to be almost entirely restricted to corneal endothelial cells, with scattered expression in