ライフサイエンスコーパス: lacrimal gland

1 mediated assembly to form a depot inside the lacrimal gland.

2 e formation of secretory acinar lobes in the lacrimal gland.

3 on were determined at the ocular surface and lacrimal gland.

4 nic inflammation in the underlying stroma or lacrimal gland.

5 ptors P2X(1-4) and P2X(6) are present in the lacrimal gland.

6 olycystin-2L2) were expressed in adult mouse lacrimal gland.

7 that P2X(7)receptors were functional in the lacrimal gland.

8 een oxidative stress and inflammation in the lacrimal gland.

9 ion of interleukin (IL)-1 into the exorbital lacrimal gland.

10 es (Hs2st, Hs6st1, and Hs6st2) in developing lacrimal gland.

11 esenchymal transition (EMT) in repair of the lacrimal gland.

12 thelium, but not in the CN epithelium or the lacrimal gland.

13 in AL2 mRNA was detected only in male rabbit lacrimal gland.

14 2, BL, CL, and CL2 were detected only in the lacrimal gland.

15 veral lipophilins were expressed only in the lacrimal gland.

16 f Tregs and CD4(+) IFN-gamma(+) cells in the lacrimal gland.

17 gher uptake in kidneys, urinary bladder, and lacrimal gland.

18 of unipotent KRT5(+) epithelial cells in the lacrimal gland.

19 uclear cell infiltration in the salivary and lacrimal glands.

20 mpare the findings with those in five normal lacrimal glands.

21 utoimmune disease affecting the salivary and lacrimal glands.

22 from IL-1-injected, but not saline-injected, lacrimal glands.

23 autoimmune diseases of ovary, prostate, and lacrimal glands.

24 surface epithelia and on fluid secretion by lacrimal glands.

25 so known as lipophilins, are found in rabbit lacrimal glands.

26 njunctiva, cornea, and tears produced by the lacrimal glands.

27 lymphocyte infiltrations in the extraorbital lacrimal glands.

28 e exocrine glands including the salivary and lacrimal glands.

29 ning cells in both dacryoadenotic and normal lacrimal glands.

30 4 h but did not reduce uptake in kidneys and lacrimal glands.

31 alpha1, collagen type IIIalpha1 and NF-kB in lacrimal glands.

32 ltration of inflammatory/immune cells in the lacrimal glands.

33 y excessive inflammation and fibrosis in the lacrimal glands.

34 immune disease mainly affecting salivary and lacrimal glands.

35 The lacrimal gland (28%), conjunctiva (28%), and orbit (28%)

36 nificant decreases were also observed in the lacrimal glands (49% +/- 13%, P < 0.001), liver (15% +/-

37 g from the orbit (19), conjunctivae (18) and lacrimal gland (6).

38 Lacrimal gland abscess or dacryoadenitis was the present

39 Fourteen patients with primary lacrimal gland ACC were included.

40 Lacrimal gland ACCs are frequently positive for the MYB-

41 Our findings show that lacrimal gland ACCs are genetically and clinically simil

42 The results show that lacrimal gland acinar cells are lost through programmed

43 Dysfunction of lacrimal gland acinar cells can ultimately result in ocu

44 hexosaminidase secretion from primary rabbit lacrimal gland acinar cells.

45 Rat lacrimal gland acini were incubated with H89, an inhibit

46 Rat lacrimal gland acini were isolated by collagenase digest

47 Lacrimal gland acini were isolated by collagenase digest

48 signaling components of this pathway in rat lacrimal gland acini.

49 Idiopathic inflammatory tumor of the lacrimal gland, also called idiopathic dacryoadenitis, g

50 When compared with the normal lacrimal gland and complex choristoma, all isolated epib

51 t (LFU), comprising the cornea, conjunctiva, lacrimal gland and interconnecting innervation.

52 (typically the lateral) and, less often, the lacrimal gland and is often mild when it arises during o

53 but not Pax6(PE/PE) mice, developed stunted lacrimal gland and lens hypoplasia which was significant

54 Lacrt has prosecretory activity in the lacrimal gland and mitogenic activity at the corneal epi

55 as to investigate an enlarged dacryoadenotic lacrimal gland and normal lacrimal glands for the presen

56 regulator (aire)-deficient mice, we assessed lacrimal gland and ocular surface immunopathology by qua

57 Lymphocytic infiltration of the lacrimal gland and ocular surface in autoimmune diseases

58 TLR2 and 5 were upregulated in lacrimal gland and overall, there was a corresponding ch

59 an essential transcription factor for lens, lacrimal gland and pancreas development.

60 hanism, and gene fusion detection methods in lacrimal gland and primary orbital and ocular adnexal so

61 whether these cells can be isolated from the lacrimal gland and propagated in vitro.

62 ESP22 is secreted from the lacrimal gland and released into tears of 2- to 3-week-o

63 gle injection of interleukin-1alpha into the lacrimal gland and that this effect was reversible.

64 y localized gp340 to the acinar cells of the lacrimal gland and the deeper layers of the conjunctival

65 vated by adenosine triphosphate (ATP) in rat lacrimal gland and to determine their role in protein se

66 X(7) purinergic receptors are present in rat lacrimal gland and when stimulated increase [Ca(2+)](i),

67 Tissue from 3 normal lacrimal glands and 1 complex choristoma were included f

68 lands of Wolfring is similar to that of main lacrimal glands and are consistent with secretion electr

69 Absorbed radiation doses to the salivary and lacrimal glands and bone marrow were low.

70 ive correlation between the ADC value of the lacrimal glands and CAS (r = 0.73, p = 0.001).

71 oimmune disease starting in the salivary and lacrimal glands and continuing to involve the lungs and

72 sialin, a known nitrate transporter, in the lacrimal glands and other eye components, and also xanth

73 sing the frequency of CD45(+)CD4(+) cells in lacrimal glands and significantly increasing conjunctiva

74 ation of primarily CD4(+) T cells within the lacrimal glands and with increased expression of IL-4.

75 re equally noted to involve the conjunctiva, lacrimal gland, and orbit.

76 cells in the inflammatory infiltrates of the lacrimal gland, and the presence of anti-Sjogren's syndr

77 tissue PMN population in the corneal limbus, lacrimal glands, and cervical lymph nodes of healthy mal

78 low, occurred mainly around the salivary and lacrimal glands, and could easily be corrected.

79 MECs can be isolated from rat lacrimal glands, and they express P2X(7), P2Y(1), P2Y(11

80 ch as marked lymphocytic infiltration of the lacrimal glands, antinuclear antibodies in the serum, an

81 The accessory lacrimal glands are assumed to contribute to the product

82 The results of our study indicate that lacrimal glands are capable of tissue repair after duct

83 ounds localize to the parotid, salivary, and lacrimal glands as well as to the kidney, leading to dos

84 idosis (7 in adipose tissue; 5 affecting the lacrimal gland) as well as comparable tissue from 6 heal

85 inflammatory CD4(+) T cells detected in the lacrimal gland, as well as those in the periphery of old

86 to mononuclear infiltration of salivary and lacrimal glands, as well as to expansion of bronchial ly

87 increased apoptosis and deterioration in the lacrimal gland, associated dysfunction, and development

88 pproach, however, we have identified a novel lacrimal gland autoantigen, odorant binding protein 1a,

89 to investigate the pathogenic mechanisms in lacrimal gland autoimmunity and associated ocular surfac

90 expression profiles of C57BL/6.NOD-Aec1Aec2 lacrimal glands before, or concomitant with, the first a

91 es were reviewed and microscopic sections of lacrimal gland biopsy samples were critically re-evaluat

92 , downstream of FGF signaling, in regulating lacrimal gland branching and differentiation.

93 In the lacrimal gland, branching morphogenesis depends on the i

94 ran sulfates by Ndst genes at the tip of the lacrimal gland bud.

95 Consistent with this, Fgf10-induced ectopic lacrimal gland budding in explant cultures is dependent

96 , and epithelial deletion of Fgfr2 abolishes lacrimal gland budding, its specific modification of hep

97 on, we demonstrate that Shp2 is required for lacrimal gland budding, lens cell proliferation, surviva

98 st1, Fgfr2 or Shp2 disrupts ERK signaling in lacrimal gland budding.

99 g robustly rescue the lens proliferation and lacrimal-gland-budding defects in the Shp2 mutants.

100 P2X(7) receptors were present in the lacrimal gland by RT-PCR and Western blot analysis.

101 ) and P2X(6)receptors were identified in the lacrimal gland by RT-PCR, Western blot, and immunofluore

102 st that nitrate ions are concentrated in the lacrimal glands by sialin and can be secreted into eye c

103 ession in sarcoidosis involving the orbit or lacrimal gland can be distinguished from gene expression

104 Lacrimal gland carcinoma can form a triangle of tissue b

105 It is significantly more common in lacrimal gland carcinoma compared with dacryoadenitis an

106 aging for 116 patients was reviewed: 39 with lacrimal gland carcinoma, 37 with lymphoma, and 40 with

107 The "wedge sign" is most common in lacrimal gland carcinoma, but can occur in patients with

108 nstigating severe damage to the salivary and lacrimal glands causing dry eyes and dry mouth.

109 mposed of rabbit conjunctival epithelium and lacrimal gland cell spheroids, and recapitulates the aqu

110 In lacrimal gland cells, the activation of M3AChRs stimulat

111 Mice were killed at various times, and lacrimal gland cellularity was analyzed by flow cytometr

112 ioma (n = 4; 10%), melanocytoma (n = 3; 8%), lacrimal gland choristoma (n = 2; 5%), gliosis (n = 1; 3

113 eased infiltration of mononuclear cells into lacrimal glands compared with 4-1BB intact lpr mice.

114 Murine lacrimal glands contain mesenchymal stem cells that seem

115 The lacrimal gland contains stem/progenitor cells capable of

116 auxiliary eye structures such as the eyelid, lacrimal gland, cornea and conjunctiva.

117 Human fibroblasts were isolated from the lacrimal gland, cornea, and Tenon's capsule and treated

118 l, T-cell infiltration into the salivary and lacrimal glands could be successfully visualized.

119 An enlarged lacrimal gland (dacryoadenosis) without obvious histopat

120 genetic rescue experiments in which the Ugdh lacrimal gland defect is ameliorated by constitutive Ras

121 tive FGF receptor only partially rescued the lacrimal gland defects in Sox9 heterozygotes, suggesting

122 To address if lacrimal gland development and FGF signaling depends on

123 Therefore, Fgf10-Fgfr2b signaling during lacrimal gland development is sensitive to the content o

124 Here, we show that lacrimal gland development requires specific modificatio

125 We further show that lacrimal gland development requires the mesenchymal expr

126 ogether, our data reveal crucial features of lacrimal gland development that have broad implications

127 nly for modulating Ras signaling in lens and lacrimal gland development, but also for RTK signaling i

128 st;Hs6st double mutants completely abolished lacrimal gland development, suggesting that both 2-O and

129 ellular matrix components during early stage lacrimal gland development.

130 e main downstream target of Shp2 in lens and lacrimal gland development.

131 nd epithelial lineage dynamics that underlie lacrimal gland development.

132 hy in NOD/LtJ mice an in-depth evaluation of lacrimal gland disease in the NOD/LtJ mouse has remained

133 The cause of bilateral lacrimal gland disease most commonly was inflammatory, f

134 Klf5CN lacrimal glands displayed increased vasculature and larg

135 provides an excellent approach for studying lacrimal gland duct cells about which relatively little

136 Lacrimal gland ductal cysts (dacryops) are uncommon, occ

137 infective debris (1 case) from the affected lacrimal gland ductule--typically the most inferolateral

138 Infective lacrimal gland ductulitis, commonly from Actinomyces inf

139 disease manifested primarily by salivary and lacrimal gland dysfunction resulting in dry mouth/dry ey

140 disease, (2) salivary gland dysfunction and lacrimal gland dysfunction, and (3) limited mouth-openin

141 in ATD and Sjogren syndrome, conditions with lacrimal gland dysfunction.

142 gland involvement, orbital pseudotumor, and lacrimal gland enlargement.

143 ecific requirement of Ndst1 and Ndst2 in the lacrimal gland epithelial, but not mesenchymal, cells, a

144 the co-receptors for Fgf10 signaling in the lacrimal gland epithelium, but their function in the Fgf

145 or budding morphogenesis in the presumptive lacrimal gland epithelium.

146 Lacrimal gland excision (LGE) induced dry eye produces m

147 c scopolamine, or by performing extraorbital lacrimal gland excision.

148 Lacrimal glands exhibited much higher levels of both ion

149 otype but led to significant improvements in lacrimal gland exocrinopathy and tear secretion.

150 Cultured MSCs isolated from injured lacrimal glands expressed Snai1 and vimentin alongside n

151 multifactorial chronic disorder in which the lacrimal glands fail to produce enough tears to maintain

152 portance of heparan sulfate 6-O sulfation in lacrimal gland FGF signaling.

153 fibroblasts were elevated in cGVHD-affected lacrimal gland fibroblasts and (2) that they could be re

154 absence of recent upper respiratory illness, lacrimal gland focus, multiple orbital abscesses, and la

155 2283 genes) were significantly lower in the lacrimal gland for patients with sarcoidosis.

156 ged dacryoadenotic lacrimal gland and normal lacrimal glands for the presence of goblet cells (mucocy

157 l types and lineage relationships that drive lacrimal gland formation are unclear.

158 other orbital inflammatory conditions in the lacrimal gland fossa.

159 We show that the lacrimal gland from its earliest developmental stages is

160 Exorbital lacrimal glands from male Sprague-Dawley rats were divid

161 Exorbital lacrimal glands from male Sprague-Dawley rats were divid

162 deficient in 4-1BB were generated, and their lacrimal gland function was studied.

163 molecular signalling processes that control lacrimal gland function will give insight into correctiv

164 Lacrimal glands function to produce an aqueous layer, or

165 The presence of lacrimal gland goblet cells may have physiologic implica

166 The Hs6st mutants exhibited significant lacrimal gland hypoplasia and a strong genetic interacti

167 ly from normal lacrimal gland tissue and the lacrimal gland in a complex choristoma.

168 IL-1beta activated ERK in the lacrimal gland in vitro and in vivo, and this effect was

169 cant difference (p = 0.03) in the ADC of the lacrimal glands in patients with active (n = 24) and ina

170 The mean ADC of lacrimal glands in thyroid eye disease (1.73 x 10(-3) mm

171 te complex on the cell surface and prevented lacrimal gland induction by Fgf10 in explant cultures.

172 ts demonstrate that mesenchymal GAG controls lacrimal gland induction by restricting the diffusion of

173 Lacrimal gland inflammation was induced by injection of

174 se occurs in the setting of conjunctival and lacrimal gland inflammation, potentially mediated by the

175 FN-gamma and substantial IL-4 at the site of lacrimal gland inflammation.

176 IL-1beta injection into the lacrimal gland inhibited aqueous tear production by 52%

177 Injection of LPS into the lacrimal gland inhibited neurally and adrenergic agonist

178 was to determine the mechanisms involved in lacrimal gland injury and repair.

179 R(-/-)) had the same submandibular gland and lacrimal gland injury as did the IL14alphaTG mice, but t

180 Lacrimal gland injury was induced by injection of interl

181 by Jin et al that studied the regulation of lacrimal gland innervation by sympathetic and parasympat

182 It was recently reported that repair of the lacrimal gland involved the mobilization of mesenchymal

183 Lacrimal gland involvement in granulomatosis with polyan

184 inical and imaging features of patients with lacrimal gland involvement secondary to GPA and to compa

185 nd to have orbital inflammatory disease with lacrimal gland involvement, of whom 7 had a final diagno

186 The tear-producing lacrimal gland is a tubular organ that protects and lubr

187 Ongoing studies demonstrate that the murine lacrimal gland is capable of repair after experimentally

188 Previously, it was reported that the murine lacrimal gland is capable of repair after experimentally

189 The lacrimal gland is primarily responsible for the aqueous

190 , and secretion from the acinar cells of the lacrimal gland is regulated by both cholinergic and adre

191 A normal cytologic feature of the lacrimal gland is the presence of acinar goblet cells th

192 The ADC of the lacrimal glands is a non-invasive imaging parameter that

193 disease affecting primarily the salivary and lacrimal glands leading to xerostomia (dry mouth) and xe

194 sociates, the data on this unusual epibulbar lacrimal gland lesion remain sparse.

195 mmunohistochemically this isolated epibulbar lacrimal gland lesion.

196 confirms that a subset of isolated epibulbar lacrimal gland lesions differs morphologically and immun

197 to overt, suggesting that isolated epibulbar lacrimal gland lesions may have originated from precurso

198 Deletion of 4-1BB in lpr mice accelerates lacrimal gland lesions through increased CD4(+) T-cell i

199 d complex choristoma, all isolated epibulbar lacrimal gland lesions were composed predominantly of va

200 Four patients with isolated epibulbar lacrimal gland lesions, 2 male and 2 female, with a medi

201 searched for all cases of isolated epibulbar lacrimal gland lesions.

202 The lacrimal gland (LG) delivers defensive and metabolic fac

203 The lacrimal gland (LG) develops through branching morphogen

204 Bilateral lacrimal gland (LG) disease is a unique presentation tha

205 To describe the involvement of the lacrimal gland (LG) in blepharophimosis-ptosis-epicanthu

206 Lacrimal gland (LG) morphogenesis and repair are regulat

207 us, and evaluate its effects on the inflamed lacrimal gland (LG) of non-obese diabetic mouse (NOD), a

208 Autoimmune dacryoadenitis and altered lacrimal gland (LG) secretion are features of Sjogren's

209 in the parasympathetic neural stimulation of lacrimal gland (LG) secretion.

210 ia receptor-mediated transcytosis across the lacrimal gland (LG), which produces the bulk of human te

211 progenitor cells in the uninjured, adult rat lacrimal gland (LG).

212 -adrenergic receptors in the mouse exorbital lacrimal gland (LG).

213 yndrome (SS) patients tears and in tears and lacrimal glands (LG) of male non-obese diabetic (NOD) mi

214 me-related immunopathological changes in the lacrimal glands (LGs) of CD25KO mice, we examined LGs of

215 Lacrimal glands (LGs) of male NOD mice, a model of Sjogr

216 Paraffin-embedded lacrimal glands (LGs) were stained with hematoxylin and

217 Multiple organs, including the lacrimal glands (LGs), are negatively affected by cGVHD

218 xual dimorphic expression patterns of rabbit lacrimal gland lipophilins AL, AL2, BL, CL, and CL2 were

219 N) preferentially suppress AOD and Treg from lacrimal gland LN preferentially suppress dacryoadenitis

220 The subtype distribution of lacrimal gland lymphoma resembles that of the ocular adn

221 A total of 260 patients with lacrimal gland lymphoma were identified.

222 orted collection of data of subtype-specific lacrimal gland lymphoma.

223 ents of alpha-fodrin were found in tears and lacrimal gland lysates, respectively, of lpr/4-1BB(-/-)

224 egenerative potential in a rabbit model with lacrimal gland main excretory duct ligation-induced inju

225 erwent debulking surgery of the inflammatory lacrimal gland mass for diagnostic and therapeutic reaso

226 We conclude that lacrimal gland MEC function is altered by inflammation b

227 t therapy, and bioartificial devices such as lacrimal gland microdevices and keratoprostheses, or tis

228 the eyelids (n = 53 [82%]), followed by the lacrimal gland (n = 5), conjunctiva (n = 4), and eyebrow

229 hat occur in myoepithelial cells (MECs) from lacrimal glands of a mouse model of Sjogren syndrome.

230 ha, 1 microg in 2 microL) into the exorbital lacrimal glands of anesthetized female BALB/c mice.

231 gene expression profiles were generated for lacrimal glands of C57BL/6.NOD-Aec1Aec2 mice 4 to 20 wee

232 MECs were cultured from lacrimal glands of C57BL/6J [wild type (WT)] and thrombo

233 s infiltrate the corneal stroma, limbus, and lacrimal glands of diseased mice.

234 amma than IL-13 mRNA relative transcripts in lacrimal glands of MRL/lpr/IL-4(tm) mice (mean differenc

235 tial biomarkers of impending autoimmunity in lacrimal glands of SjS-prone mice.

236 ot attenuate lymphocytic infiltration of the lacrimal gland or eye, it significantly reduced ocular s

237 eyelid, conjunctiva, choroid, ciliary body, lacrimal gland, or orbit (OA-uveal lymphoma) were includ

238 A total of 36 tumors from 32 patients with lacrimal gland PA or Ca-ex-PA were included in the study

239 ed a rare case of pleomorphic adenoma of the lacrimal gland (PALG) causing hyperopic shift and CFs wi

240 tance for disease progression in a subset of lacrimal gland PAs.

241 oma and generally indicates life-threatening lacrimal gland pathology that requires urgent biopsy.

242 w of images from patients with biopsy-proven lacrimal gland pathology.

243 Carbachol increased ATP release from lacrimal gland pieces but not from acini.

244 Biophysical properties of lacrimal gland polycystin-2 channels were similar to tho

245 The lacrimal gland possesses many features that make it an e

246 nitrite levels in components of the eye and lacrimal glands, primarily in porcine samples.

247 Lacrimal gland progenitor cells isolated from ligated ti

248 Isolated lacrimal gland progenitor cells were tested and characte

249 L-1beta activates the ERK pathway to inhibit lacrimal gland protein secretion and aqueous tear produc

250 Lacrimal gland protein secretion was measured using a sp

251 t of IL-1beta on aqueous tear production and lacrimal gland protein secretion.

252 An enlarged salivary gland or lacrimal gland raises a wide differential diagnosis that

253 ioration of the autonomic innervation of the lacrimal glands rather than an impaired corneal innervat

254 Lacrimal glands regulate the production and secretion of

255 ment of one of more salivary gland(s) and/or lacrimal gland(s).

256 Lacrimal glands secrete proteins, electrolytes and water

257 Lacritin protein is highly expressed in the lacrimal gland, secreted into tear fluid, and detected o

258 LPS inhibits lacrimal gland secretion by activating caspase 1, and IL

259 tear protein, it promotes basal tearing and lacrimal gland secretion.

260 (ERK) in inflammation-induced inhibition of lacrimal gland secretion.

261 1 alleviated the inhibitory effect of LPS on lacrimal gland secretion.

262 ants (e.g., urinary pheromones, extraorbital lacrimal gland secretions, major histocompatibility comp

263 ferential display analysis, and a new rabbit lacrimal gland secretoglobin, lipophilin AL2, was identi

264 Aged C57BL/6 lacrimal glands showed significantly greater lymphocytic

265 ut ((-/-)) mice have impaired ocular surface-lacrimal gland signaling, rendering them susceptible to

266 e a critical role for Orai1-mediated SOCE in lacrimal gland signalling and function.

267 The results provide further insights into lacrimal gland stem/progenitor cell physiology and their

268 The existence of lacrimal gland stem/progenitor cells was proposed in sev

269 Secretory function also increased in the lacrimal gland, suggesting this local therapy could trea

270 rkers between the developing mouse and human lacrimal gland, supporting the use of mice to understand

271 The ligation-injured lacrimal glands temporarily decreased in weight and had

272 iple pustules/abscesses in the region of the lacrimal gland that were expressing purulent fluid into

273 ically and immunohistochemically from normal lacrimal gland tissue and the lacrimal gland in a comple

274 ryops) are uncommon, occurring anywhere that lacrimal gland tissue is present.

275 Studies were performed in adult lacrimal gland tissue of Swiss-Webster mice.

276 nctiva (hamartia) and grew into disorganized lacrimal gland tissue.

277 fforts, the molecular and cellular events in lacrimal gland tissues initiating inflammatory responses

278 und that EMT is induced during repair of the lacrimal gland to generate MSCs to initiate repair, and

279 ied the expression of MYB-NFIB in 19 non-ACC lacrimal gland tumors.

280 The cutoff ADC value of lacrimal gland used for differentiation of thyroid eye d

281 The cutoff ADC value of the lacrimal gland used to suspect active disease was 1.76 x

282 cterize the role of Orai1 in the function of lacrimal glands using a mouse model in which the gene fo

283 : 1) initial injury to the submandibular and lacrimal glands via an environmental insult and LTalpha;

284 notype, in which the exorbital branch of the lacrimal gland was absent in most cases.

285 The major lacrimal gland was involved in 13 lesions; 2 lesions aro

286 Cytokine expression of lacrimal glands was assessed by flow cytometry and RT-PC

287 usly, in single lacrimal cells isolated from lacrimal glands, we demonstrated that muscarinic recepto

288 e were noted to have significantly increased lacrimal gland weight, with enlarged, carbohydrate-rich,

289 Acinar cells from monkey lacrimal gland were cultured and characterized.

290 erified primary or secondary lymphoma of the lacrimal gland were included.

291 Acini from rat lacrimal gland were isolated by collagenase digestion.

292 Caspase 1 and ERK activities in the lacrimal gland were measured by immunohistochemistry, We

293 nt diffusion coefficient (ADC) values of the lacrimal glands were calculated and correlated with the

294 RNAs from male and female rabbit lacrimal glands were compared in a differential display

295 Acinar cells from monkey lacrimal glands were cultured with or without tumor necr

296 ted acinar epithelial monolayers from rabbit lacrimal glands were exposed to varying concentrations o

297 Two and half days after injection, the lacrimal glands were removed and used to prepare explant

298 Rat lacrimal glands were subjected to collagenase digestion,

299 Exorbital lacrimal glands were then removed and processed for meas

300 voked macrophage infiltration to the eye and lacrimal gland, where they played a functional role in d