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1 del of aqueous-deficient dry eye produced by lacrimal ablation, topical administration of 0.1 nmol CF
2 basal tear protein secretion in cultured rat lacrimal acinar cells and proliferation of subconfluent
3 y were (1) to develop a procedure to culture lacrimal acinar cells from monkey and (2) to determine t
10 (IP(3)Rs), and ryanodine receptors (RyRs) in lacrimal acinar cells, however, little is known regardin
12 Sox9 is required for the development of the lacrimal and harderian glands and contributes to the for
15 Lubricin messenger RNA is also present in lacrimal and meibomian glands, as well as in a number of
16 lopment of new strategies to maintain normal lacrimal and salivary gland function in patients with SS
19 me is a chronic autoimmune disease affecting lacrimal and salivary glands that often is accompanied b
20 The autoantigen Klk1b22, isolated from the lacrimal and salivary glands, readily induced Sjogren's
26 patients (group 2) who had an absence of the lacrimal artery or deviated from the treatment protocol
28 that optimal surgical management of chronic lacrimal canaliculitis allows for both accurate microbio
29 st documented case of A. aphrophilus chronic lacrimal canaliculitis illustrates that optimal surgical
30 ral chronic epiphora associated with chronic lacrimal canaliculitis resistant to prolonged topical an
31 The "wedge sign" frequency is assessed in lacrimal carcinoma, lacrimal lymphoma, or dacryoadenitis
34 ting a hereditary component in patients with lacrimal disorders is helpful in determining the underly
36 mpletion of chemotherapy, patients underwent lacrimal drainage evaluation by computed tomographic dac
37 Tear film impairment (aqueous and lipid) and lacrimal drainage obstruction should be considered in su
40 blish a nomenclature for each segment of the lacrimal duct system and provide evidence that ducts pla
43 er blood flow changes around the ipsilateral lacrimal duct, superior salivatory nucleus stimulation e
46 unction (11% prevalence) was associated with lacrimal dysfunction (P = 0.010) and xerostomia with xer
47 ent (erythema and sclerosis, skin symptoms), lacrimal dysfunction (Schirmer's tear test, xerophthalmi
49 eaction when cocultured with purified rabbit lacrimal epithelial cells, induce a Sjogren's-like autoi
51 ear volume and tear composition (osmolarity, lacrimal factors, inflammatory mediators, growth and dif
52 al role of the proteins in the regulation of lacrimal fluid secretion under physiological and disease
54 n produce a significant deterioration of the lacrimal function unit in female SS dry eye patients.
57 athology of DED involves inflammation of the lacrimal functional unit (LFU), comprising the cornea, c
66 us, and evaluate its effects on the inflamed lacrimal gland (LG) of non-obese diabetic mouse (NOD), a
68 ia receptor-mediated transcytosis across the lacrimal gland (LG), which produces the bulk of human te
70 the eyelids (n = 53 [82%]), followed by the lacrimal gland (n = 5), conjunctiva (n = 4), and eyebrow
82 (typically the lateral) and, less often, the lacrimal gland and is often mild when it arises during o
83 but not Pax6(PE/PE) mice, developed stunted lacrimal gland and lens hypoplasia which was significant
85 regulator (aire)-deficient mice, we assessed lacrimal gland and ocular surface immunopathology by qua
91 vated by adenosine triphosphate (ATP) in rat lacrimal gland and to determine their role in protein se
92 X(7) purinergic receptors are present in rat lacrimal gland and when stimulated increase [Ca(2+)](i),
93 pproach, however, we have identified a novel lacrimal gland autoantigen, odorant binding protein 1a,
94 to investigate the pathogenic mechanisms in lacrimal gland autoimmunity and associated ocular surfac
95 es were reviewed and microscopic sections of lacrimal gland biopsy samples were critically re-evaluat
97 on, we demonstrate that Shp2 is required for lacrimal gland budding, lens cell proliferation, surviva
99 ) and P2X(6)receptors were identified in the lacrimal gland by RT-PCR, Western blot, and immunofluore
100 ession in sarcoidosis involving the orbit or lacrimal gland can be distinguished from gene expression
103 aging for 116 patients was reviewed: 39 with lacrimal gland carcinoma, 37 with lymphoma, and 40 with
105 mposed of rabbit conjunctival epithelium and lacrimal gland cell spheroids, and recapitulates the aqu
107 ioma (n = 4; 10%), melanocytoma (n = 3; 8%), lacrimal gland choristoma (n = 2; 5%), gliosis (n = 1; 3
109 genetic rescue experiments in which the Ugdh lacrimal gland defect is ameliorated by constitutive Ras
110 tive FGF receptor only partially rescued the lacrimal gland defects in Sox9 heterozygotes, suggesting
112 Therefore, Fgf10-Fgfr2b signaling during lacrimal gland development is sensitive to the content o
114 ogether, our data reveal crucial features of lacrimal gland development that have broad implications
115 nly for modulating Ras signaling in lens and lacrimal gland development, but also for RTK signaling i
116 st;Hs6st double mutants completely abolished lacrimal gland development, suggesting that both 2-O and
122 infective debris (1 case) from the affected lacrimal gland ductule--typically the most inferolateral
124 disease, (2) salivary gland dysfunction and lacrimal gland dysfunction, and (3) limited mouth-openin
127 the co-receptors for Fgf10 signaling in the lacrimal gland epithelium, but their function in the Fgf
132 fibroblasts were elevated in cGVHD-affected lacrimal gland fibroblasts and (2) that they could be re
133 absence of recent upper respiratory illness, lacrimal gland focus, multiple orbital abscesses, and la
138 molecular signalling processes that control lacrimal gland function will give insight into correctiv
139 The Hs6st mutants exhibited significant lacrimal gland hypoplasia and a strong genetic interacti
141 te complex on the cell surface and prevented lacrimal gland induction by Fgf10 in explant cultures.
142 ts demonstrate that mesenchymal GAG controls lacrimal gland induction by restricting the diffusion of
143 se occurs in the setting of conjunctival and lacrimal gland inflammation, potentially mediated by the
145 R(-/-)) had the same submandibular gland and lacrimal gland injury as did the IL14alphaTG mice, but t
147 It was recently reported that repair of the lacrimal gland involved the mobilization of mesenchymal
149 inical and imaging features of patients with lacrimal gland involvement secondary to GPA and to compa
150 nd to have orbital inflammatory disease with lacrimal gland involvement, of whom 7 had a final diagno
152 Ongoing studies demonstrate that the murine lacrimal gland is capable of repair after experimentally
153 Previously, it was reported that the murine lacrimal gland is capable of repair after experimentally
155 , and secretion from the acinar cells of the lacrimal gland is regulated by both cholinergic and adre
156 egenerative potential in a rabbit model with lacrimal gland main excretory duct ligation-induced inju
157 erwent debulking surgery of the inflammatory lacrimal gland mass for diagnostic and therapeutic reaso
158 ot attenuate lymphocytic infiltration of the lacrimal gland or eye, it significantly reduced ocular s
159 A total of 36 tumors from 32 patients with lacrimal gland PA or Ca-ex-PA were included in the study
161 oma and generally indicates life-threatening lacrimal gland pathology that requires urgent biopsy.
172 ants (e.g., urinary pheromones, extraorbital lacrimal gland secretions, major histocompatibility comp
173 ut ((-/-)) mice have impaired ocular surface-lacrimal gland signaling, rendering them susceptible to
175 The results provide further insights into lacrimal gland stem/progenitor cell physiology and their
177 iple pustules/abscesses in the region of the lacrimal gland that were expressing purulent fluid into
180 fforts, the molecular and cellular events in lacrimal gland tissues initiating inflammatory responses
181 und that EMT is induced during repair of the lacrimal gland to generate MSCs to initiate repair, and
185 e were noted to have significantly increased lacrimal gland weight, with enlarged, carbohydrate-rich,
190 idosis (7 in adipose tissue; 5 affecting the lacrimal gland) as well as comparable tissue from 6 heal
193 cells in the inflammatory infiltrates of the lacrimal gland, and the presence of anti-Sjogren's syndr
194 inflammatory CD4(+) T cells detected in the lacrimal gland, as well as those in the periphery of old
195 increased apoptosis and deterioration in the lacrimal gland, associated dysfunction, and development
197 Human fibroblasts were isolated from the lacrimal gland, cornea, and Tenon's capsule and treated
198 eyelid, conjunctiva, choroid, ciliary body, lacrimal gland, or orbit (OA-uveal lymphoma) were includ
199 Lacritin protein is highly expressed in the lacrimal gland, secreted into tear fluid, and detected o
200 Secretory function also increased in the lacrimal gland, suggesting this local therapy could trea
201 rkers between the developing mouse and human lacrimal gland, supporting the use of mice to understand
202 voked macrophage infiltration to the eye and lacrimal gland, where they played a functional role in d
219 g robustly rescue the lens proliferation and lacrimal-gland-budding defects in the Shp2 mutants.
220 me-related immunopathological changes in the lacrimal glands (LGs) of CD25KO mice, we examined LGs of
223 lands of Wolfring is similar to that of main lacrimal glands and are consistent with secretion electr
224 oimmune disease starting in the salivary and lacrimal glands and continuing to involve the lungs and
227 ounds localize to the parotid, salivary, and lacrimal glands as well as to the kidney, leading to dos
228 expression profiles of C57BL/6.NOD-Aec1Aec2 lacrimal glands before, or concomitant with, the first a
233 multifactorial chronic disorder in which the lacrimal glands fail to produce enough tears to maintain
237 gene expression profiles were generated for lacrimal glands of C57BL/6.NOD-Aec1Aec2 mice 4 to 20 wee
240 ioration of the autonomic innervation of the lacrimal glands rather than an impaired corneal innervat
244 cterize the role of Orai1 in the function of lacrimal glands using a mouse model in which the gene fo
245 : 1) initial injury to the submandibular and lacrimal glands via an environmental insult and LTalpha;
247 ted acinar epithelial monolayers from rabbit lacrimal glands were exposed to varying concentrations o
250 tissue PMN population in the corneal limbus, lacrimal glands, and cervical lymph nodes of healthy mal
253 to mononuclear infiltration of salivary and lacrimal glands, as well as to expansion of bronchial ly
254 usly, in single lacrimal cells isolated from lacrimal glands, we demonstrated that muscarinic recepto
266 conjunctival epithelium, eyelids and ocular [lacrimal, harderian (HG), and meibomian (MG)] glands and
268 Exclusion criteria included evidence of lacrimal hypersecretion, eyelid malposition, and punctal
271 of orbital GPA, especially in patients with lacrimal involvement as the initial presentation, can be
273 y affects exocrine glands--mainly labial and lacrimal--leading to complaints of dry mouth and eyes.
275 pendages: skin, teeth, and nails--as well as lacrimal, mammary, salivary, sebaceous and sweat glands.
277 cluded that the modified preserved nasal and lacrimal mucosal flap technique in EES-DCR for treating
279 e we describe a modified preserved nasal and lacrimal mucosal flap technique in endonasal endoscopic
280 (OCT) and to identify characteristics of the lacrimal punctum in patients who benefit from punctoplas
282 mine the application of imaging the stenotic lacrimal punctum with infrared photographs and optical c
283 tion of exocrine glands, mainly salivary and lacrimal, resulting in oral and ocular dryness, although
284 n to receive either percutaneous drainage of lacrimal sac abscess followed by EN-DCR after the acute
287 le participants had acute dacryocystitis and lacrimal sac abscess presenting within 2 weeks of onset,
288 Primary EN-DCR in acute dacryocystitis with lacrimal sac abscess results in faster resolution compar
289 obstruction to include DCR revisions, acute lacrimal sac abscesses, nasolacrimal duct obstructions i
295 al applications, and an increasing number of lacrimal surgeons have focused on laser-assisted approac
299 reports of inherited disorders affecting the lacrimal system that have not been elucidated molecularl
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