ライフサイエンスコーパス: gland

1 rain; blood; thyroid, adrenal, and pituitary glands).

2 or expression of marker genes of the thyroid gland.

3 e disease that primarily affects the thyroid gland.

4 ons in other organs, like breast and thyroid gland.

5 uring endoreplication in Drosophila salivary gland.

6 rome in the absence of DVH for the lachrymal gland.

7 that is expressed from the female accessory gland.

8 sence of the subcommissural organ and pineal gland.

9 ects on progenitor cell pools in the mammary gland.

10 tive stress and inflammation in the lacrimal gland.

11 ma and fibrous capsule of the virgin mammary gland.

12 multiple functions in the developing mammary gland.

13 identify proton sensors in the rat pituitary gland.

14 ch the requirements of the lactating mammary gland.

15 urgical removal of the offending parathyroid glands.

16 , vasculature, hair follicles, and sebaceous glands.

17 nnervation in other tissues such as salivary glands.

18 x (ECM) remodeling in the partially resected glands.

19 ) and phosphorylated ERK1/2) in the prostate glands.

20 ganization and functionality of the salivary glands.

21 r follicles that are equipped with sebaceous glands.

22 gs, spleen, bone marrow, thyroid and adrenal glands.

23 findings with those in five normal lacrimal glands.

24 ong with those associated with the accessory glands.

25 immature esophagus that contains respiratory glands.

26 te and adaptive immune responses in salivary glands.

27 onomic nervous system and endo- and exocrine glands.

28 s necessary to localize all hyperfunctioning glands.

29 proliferative, premalignant Hi-Myc prostatic glands.

30 ily in the mesenchyme of developing salivary glands.

31 dibular glands (0.1479 mSv), and the parotid glands (0.1137 mSv/MBq).

32 kidneys (0.1722 mSv/MBq), the submandibular glands (0.1479 mSv), and the parotid glands (0.1137 mSv/

33 a and paraganglioma than for healthy adrenal glands (11.9 +/- 2.0 vs. 9.9 +/- 1.5 vs. 3.7 +/- 0.2, re

34 SUV(max) and SUV(mean) being in the thyroid gland (30.3 +/- 2.2 and 22.5 +/- 1.6, respectively), pan

35 tids (24% +/- 14%, P = 0.001), submandibular glands (35% +/- 11%, P < 0.001), and kidneys (23% +/- 26

36 decreases were also observed in the lacrimal glands (49% +/- 13%, P < 0.001), liver (15% +/- 6%, P <

37 elease of melatonin at night from the pineal gland activates melatonin receptors in the suprachiasmat

38 (SGs) of Drosophila larvae, we overrode the glands adaptability to growth signals and induced hypert

39 ests cellular plasticity within the salivary gland and a possibility for therapeutic intervention tha

40 l, P. zopfii GT-II replicated in the mammary gland and caused severe inflammation with infiltration o

41 When compared with the normal lacrimal gland and complex choristoma, all isolated epibulbar lac

42 estigate an enlarged dacryoadenotic lacrimal gland and normal lacrimal glands for the presence of gob

43 -specific promoters of the pancreas, mammary gland and other secretory tissues, as well as an interfe

44 nd gene fusion detection methods in lacrimal gland and primary orbital and ocular adnexal soft tissue

45 ice redirects SmgGDS splicing in the mammary gland and slows tumorigenesis in this aggressive model o

46 in 22 (AeOBP22) within the mosquito salivary gland and that siRNA mediated knockdown of AeOBP22 led t

47 ions throughout the CNS, including the optic gland and the peduncle, optic, dorso-lateral, basal, sub

48 nsduce progenitor cells of the adult mammary gland and use that as a platform to functionally screen

49 ted with extracts from the coat or kernel of glanded and glandless cottonseed.

50 thesized that Siglec-8 ligands in submucosal glands and ducts are normally transported to the airway

51 ccumulation of PSMA radiotracers in salivary glands and kidneys.

52 ethal postnatal inflammation of the salivary glands and mediastinum.

53 Permanent damage to the salivary glands and resulting hyposalivation and xerostomia have

54 gene CathB3, was upregulated in the salivary glands and saliva of aphids from a non-tobacco-adapted (

55 wCV in the salivary glands and spleen was 8.9% and 10.7% SUV(mean), respecti

56 l as representative normal tissues (salivary glands and spleen), were segmented separately by 2 reade

57 ypoplastic/ectopic kidneys, aplastic adrenal glands and spleen, as well as atretic trachea and palate

58 In mammalian salivary glands and teeth, we show that initial invagination occu

59 and it can be later observed in the salivary glands and the midgut.

60 and contribute to hair follicles, sebaceous glands and/or epidermis renewal.

61 opoiesis (which notably included the adrenal gland), and integration with mouse developmental atlases

62 , these data suggest that the liver, adrenal gland, and lymphatic organs are important sites of EBOV

63 tion of SMAD1/5/8 in the mouse submandibular glands, and led to a recovery of SG function and a decre

64 nding of tissue injury in the liver, adrenal glands, and lymphoid tissues remains limited.

65 Tissue-resident macrophages in the mammary gland are found in close association with epithelial str

66 e show that parasites lacking the esophageal gland are unable to lyse ingested immune cells within th

67 idguts and sporozoite prevalence in salivary glands are nevertheless commonly used to confirm success

68 ing why aberrant hair follicles or sebaceous glands are sometimes observed in non-skin tissues (e.g.

69 pithelia, including the mammary and prostate glands, are composed of basal cells (BCs) and luminal ce

70 the shrimp's excretory organ, "the antennal gland," are major candidate entry portals [M.

71 g zona glomerulosa (zG) cells of the adrenal gland arrange in distinct multi-cellular rosettes that p

72 omplexity, we propose to rename the antennal gland as the "nephrocomplex." By an intrabladder inocula

73 sted the significance of throat and salivary glands as major sites of virus replication and transmiss

74 smas entered into type III cells of salivary glands at 21-28 daas.

75 ) chief cells (ZCs) in the mammalian gastric gland base are believed to arise from descending mucous

76 resident adult epithelial stem cells at the gland base in the mouse pyloric stomach(1), but the iden

77 apidly penetrate into submandibular salivary glands, be efficiently taken up by striated and excretor

78 rimary Sjogren's syndrome (pSS) the exocrine glands become infiltrated with lymphocytes instigating s

79 ating bone marrow, skin, muscle, and mammary gland biology is emerging, but the role of adipocyte-der

80 iptome profiling data sets of minor salivary gland biopsies from controls and Sjogren's syndrome pati

81 to ductal development in the virgin mammary gland, but less is known regarding the effects of macrop

82 l, have a morphologically normal uterus with glands, but lack FOXA2-dependent GE-expressed genes, suc

83 in 2 compartments, cartilage and submucosal glands, but they were surprisingly absent from the epith

84 ithelial branching in the developing mammary gland by regulating macrophage dynamics.

85 of the most aggressive subtypes of salivary gland cancers.

86 g severe damage to the salivary and lacrimal glands causing dry eyes and dry mouth.

87 me in addition to pre- and post-infective J2 gland cell transcriptome using Next Generation Sequencin

88 Salivary gland cells responsive to Hedgehog/Gli signaling compris

89 We show that in MCF-7 mammary gland cells, AGO1 associates with transcriptional enhanc

90 and accumulated on the surfaces of salivary gland cells.

91 n and to highlight key distinctions of venom gland cellular and physiological function.

92 uction of storage proteins and key accessory gland components, a feature that impacts adult reproduct

93 hypophysis (ADH)] of the pituitary, a master gland controlling growth, metabolism, and reproduction.

94 ted in a lab scale from glandless and common glanded cottonseed meal, respectively, and one soluble p

95 protein samples (Gd-P) in a pilot scale from glanded cottonseed meal.

96 Cylindrical silk gland (CY) spigots distinguish a large clade of modern s

97 An enlarged lacrimal gland (dacryoadenosis) without obvious histopathologic a

98 rine factors and their receptors in salivary glands decreased following irradiation but were restored

99 over, 8 of 10 scenarios predicated on a soft gland demonstrated increased CR-POPF incidence.

100 ed signaling pathways between normal mammary gland development and breast cancer.

101 ors and ligands contribute to normal mammary gland development and breast tumor progression.

102 rine-specific deletion of Arid1a compromises gland development and diminishes Foxa2 and Lif expressio

103 ls that TET2 plays a pivotal role in mammary gland development and luminal lineage commitment.

104 dipose stroma, and are important for mammary gland development and tissue homeostasis.

105 was tested in two studies related to mammary gland development and tumorigenesis.

106 wn mechanism controlling the rate of mammary gland development during puberty and highlights potentia

107 ew, we outline the various stages of mammary gland development in the mouse, with a particular focus

108 ocesses, including those involved in mammary gland development.

109 guingly, schistosomes lacking the esophageal gland die after transplantation into naive mice, but sur

110 ), or both the extraorbital and intraorbital glands (double LGE) was performed in male and female C57

111 the unique biology of the postpartum mammary gland drives tumor progression.

112 helial cells of the oral mucosa and salivary gland ducts via ACE2 receptors.

113 xamine schistosomes that lack the esophageal gland due to knockdown of a forkhead-box transcription f

114 ng a hyperactive STAT5 mutant in the mammary gland during postlactational remodeling.

115 sociation between dyslipidemia and meibomian gland dysfunction (MGD).

116 lar gland rescued radiation-induced salivary gland dysfunction.

117 s (MSCs) injected into contralateral mammary gland, evidenced by the lack of tumor growth at MSC-inje

118 Salivary glands exert exocrine secretory function to provide sali

119 Lacrimal glands exhibited much higher levels of both ions compare

120 Following infection, both liver and adrenal glands exhibited significant and early downregulation of

121 Fourth, the exocrine scent glands express vvl and are regulated by Hox genes.

122 rgin measurements, meibum quality, meibomian gland expressability, ocular surface disease index (OSDI

123 predicted protein-coding genes, 12,346 venom-gland-expressed genes constitute the 'venom-ome' and thi

124 we compared the chemical profiles of femoral gland exudate from adults caught on Wolf Volcano.

125 used on two years in particular when femoral gland exudate was collected from adults during the repro

126 For normal tissues, parotid gland factors were 6.7, 9.4, 13.3, and 19.3 Gy per MBq/m

127 senting an energy reserve) and the digestive gland (fast turnover rate organ, reflecting recent consu

128 These models exhibit reduced endometrial glands, features of posteriorization and implantation fa

129 ely accumulate in the submandibular salivary gland, followed by being excreted in its excretory duct.

130 oadenotic lacrimal gland and normal lacrimal glands for the presence of goblet cells (mucocytes).

131 cal states over a lifetime and is lined by a gland-forming epithelium(1,2).

132 Normal endometrial glands frequently carry 'driver' mutations in cancer gen

133 oid hormone secretion, releasing the thyroid gland from pituitary control.

134 transcriptome from whole larvae and salivary glands from nymphs, males and females feeding on genetic

135 y and fully engorged females; (iii) salivary glands from partially engorged females; (iv) fat body fr

136 ent, causing posteriorization and diminished gland function during pregnancy that contribute to impla

137 have proved successful in rescuing salivary gland function in a number of animal models that reflect

138 efects in dental enamel production and sweat gland function.

139 could prevent chronic stimulation of thyroid gland function.

140 n of the Foxa2 gene required for endometrial gland function.

141 ncy establishment through the maintenance of gland function.

142 Surface Staining, Schirmer I test, Meibomian gland functionality in 757 patients (1514 eyes) with dry

143 The presence of lacrimal gland goblet cells may have physiologic implications for

144 es disorders involving a hyperactive thyroid gland (Graves disease, toxic multinodular goiter, toxic

145 y, the synthesis of androgens by the adrenal gland has been considered of little physiologic importan

146 ls, yet molecular underpinnings of the lymph gland hemocytes have been less investigated.

147 ween embryonically derived- and larval lymph gland hemocytes.

148 on with stemness, contributes to the mammary gland homeostasis, evolution of early neoplastic lesions

149 In isopods, the Insulin-like Androgenic Gland hormone (IAG) induces male differentiation: Wolbac

150 Melatonin is an important pineal gland hormone that has been shown to protect against Abe

151 In the pituitary gland, hormones are stored in a functional amyloid state

152 objective was to test whether goat's mammary gland immune response to E. coli lipopolysaccharide (LPS

153 ormal lacrimal gland tissue and the lacrimal gland in a complex choristoma.

154 expression analyses of the rattlesnake venom gland in comparison with several non-venom tissues to ch

155 ne session or group 2 (n = 28) with RFA of 2 glands in a first session and other 2 glands in a second

156 localization of hyperfunctioning parathyroid glands in a larger series of PHPT patients.

157 A of 2 glands in a first session and other 2 glands in a second session.

158 to either group 1 (n = 28) with RFA of all 4 glands in one session or group 2 (n = 28) with RFA of 2

159 Neuronal and muscle cells of the 2 glands in particular showed different markers and locali

160 head-thorax section (containing the salivary glands) in 26.7-30.0% of nymphs and 37-45% of adults.

161 nts over a period of 56 d and found that the gland increased slightly in size.

162 ractions and that A. marginale tick salivary gland infection is dose dependent.

163 However, salivary gland infection rates decreased as the percentage of par

164 me-infected blood that cause higher salivary gland infections and potentially increase parasite trans

165 tolerogenic mechanisms and reduced salivary gland inflammation.

166 t al that studied the regulation of lacrimal gland innervation by sympathetic and parasympathetic com

167 orozoite gliding motility, mosquito salivary gland invasion and mouse infection.

168 calcitonin, a hormone product of the thyroid gland involved in bone metabolism(3), is also produced b

169 The mammary gland is a highly vascularized tissue capable of expansi

170 The adrenal gland is a source of sex steroid precursors, and its act

171 The mammary gland is a unique tissue and the defining feature of the

172 e barcodes, we found that each mouse mammary gland is generated from a defined number of ~120 early p

173 gical removal of hyperfunctional parathyroid gland is the definitive treatment for primary hyperparat

174 Irreversible hypofunction of salivary glands is a common side effect of radiotherapy for head

175 s the physiology and regulation of the venom gland itself, remain virtually unstudied.

176 istered MSG significantly decreased salivary gland, kidney, and other normal-organ PSMA radiotracer u

177 rest on lacrimal, parotid, and submandibular glands; left ventricle; liver; spleen; kidneys; bowel; u

178 the data on this unusual epibulbar lacrimal gland lesion remain sparse.

179 ochemically this isolated epibulbar lacrimal gland lesion.

180 that a subset of isolated epibulbar lacrimal gland lesions differs morphologically and immunohistoche

181 suggesting that isolated epibulbar lacrimal gland lesions may have originated from precursor cellula

182 choristoma, all isolated epibulbar lacrimal gland lesions were composed predominantly of variably di

183 toimmune dacryoadenitis and altered lacrimal gland (LG) secretion are features of Sjogren's syndrome

184 Multiple organs, including the lacrimal glands (LGs), are negatively affected by cGVHD and lose

185 nificant damage to the liver and the adrenal glands, little is known about the molecular signatures o

186 er than 40 mL, and was lower in the anterior gland location (P = .04 and .01, respectively).

187 echanisms driving acidification of the venom gland lumen during venom production and storage.

188 g organs, including the salivary and mammary glands, lung, and kidney, arise as epithelial buds that

189 The subtype distribution of lacrimal gland lymphoma resembles that of the ocular adnexa.

190 Conversely, depletion of salivary gland macrophages by clodronate liposomes compromised th

191 partial sialoadenectomy, we performed whole-gland measurements over a period of 56 d and found that

192 We conclude that lacrimal gland MEC function is altered by inflammation because th

193 Salivary gland MEC patient-derived xenografts were used to examin

194 helial disruption and lower eyelid meibomian gland (MG) dropout, adjusted for age and sex (odds ratio

195 roper glucose supply often threatens mammary gland (MG) health.

196 ype of the ventral prostate (VP) and mammary gland (MG) in ERbeta(crispr-/-) mice was similar to, but

197 yslipidemia and its treatment with meibomian gland (MG) morphologic changes by standardized meibograp

198 ipid secretion that is produced by Meibomian glands (MG) in a process termed meibogenesis-plays a cri

199 Lipids secreted by the meibomian glands (MGs) of the eyelids are essential to the protect

200 In a three-dimensional (3D) model of mammary gland morphogenesis, sEV treatment induced hallmarks of

201 Recently, sequencing of salivary-gland mRNA libraries revealed increasingly complex and c

202 Patients with advanced salivary gland mucoepidermoid carcinoma (MEC) are treated with su

203 ight be beneficial to patients with salivary gland mucoepidermoid carcinoma.

204 show that in cystic fibrosis, airway gland mucus gels form under conditions of high acidity a

205 or (CFTR) anion channels produced submucosal gland mucus that was abnormally acidic with an increased

206 IPMNs confined to the dorsal portion of the gland (n = 161), also demonstrated UDD to be a significa

207 s (DlEPV), a poxvirus found within the venom gland of Diachasmimorpha longicaudata wasps.

208 that secreted sphingomyelins in the mammary gland of mammals with a naturally low incidence of mamma

209 es were significantly decreased in pituitary glands of 4.1N(-/-) compared to 4.1N(+/+).

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

211 A2 (FOXA2) is expressed specifically in the glands of the uterus and a critical regulator of glandul

212 Glands of the uterus are essential for pregnancy establi

213 d/or translocation of CLas into the salivary glands of the vector.

214 Here, we establish long-term expanding venom gland organoids from several snake species.

215 F, a critical implantation factor of uterine gland origin.

216 examine messenger RNA and protein changes in glands over time.

217 case of pleomorphic adenoma of the lacrimal gland (PALG) causing hyperopic shift and CFs with the ne

218 uscle, nervous system, tegument, oesophageal gland, parenchymal/primordial gut cells, and stem cells.

219 In the pituitary gland, peptide hormones can be stored as amyloid fibrils

220 oundary of the Drosophila embryonic salivary gland placode through a negative regulation by the apica

221 mocytes have been characterized in the lymph gland: plasmatocytes, lamellocytes, and crystal cells, w

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

223 larval stage on, long before the androgenic gland primordia begin to differentiate, and exponentiall

224 l as interactions with tick gut and salivary gland proteins important for establishing infection and

225 m is a common condition in which the thyroid gland provides insufficient amounts of thyroid hormone f

226 ential means of reducing kidney and salivary gland radiation exposure using a PSMA-targeting radiotra

227 leiotropic hormone secreted by the pituitary gland, regulates immune and inflammatory responses.

228 ot nematodes revealed a subset of esophageal gland related sequences and putative effectors in common

229 secretory activity in the steady state venom gland relative to other secretory tissues and identify v

230 The adrenal gland represents a useful model to address this question

231 r 4.1N in the axis of hypothalamus-pituitary gland-reproductive system.

232 og signaling within the murine submandibular gland rescued radiation-induced salivary gland dysfuncti

233 The partial submandibular salivary gland resection model provides an opportunity to examine

234 technology, we demonstrate that the antennal gland resembles a kidney, connected to a urinary bladder

235 Quantities and activities of salivary gland resident macrophages were substantially and rapidl

236 nces paracrine interactions between salivary gland resident macrophages, epithelial progenitors, and

237 sibly due to reduced blood flow to the sweat gland resulting in a lack of tissue perfusion.

238 Examination of pituitary glands revealed that the secretory granules were signifi

239 progesterone-Receptor mRNA in bulbo-urethral gland samples, was performed: analyses were made on FFPE

240 se to respiratory insults, airway submucosal glands secrete copious mucus strands to increase mucocil

241 ow their antimicrobial, highly acidic poison gland secretion.

242 n could alter cell signaling in the salivary gland (SG) and result in the associated salivary hypofun

243 Regulatory factors controlling tick salivary glands (SGs) are direct upstream neural signaling pathwa

244 tious metacyclic cells in the fly's salivary glands (SGs) before transmission to a new host.

245 )-overexpression in the postmitotic salivary glands (SGs) of Drosophila larvae, we overrode the gland

246 vestigation of repair mechanisms in salivary glands (SGs).

247 at resolved by day 14, a small region of the gland showed an aberrant sustained fibrotic response cha

248 Aged C57BL/6 lacrimal glands showed significantly greater lymphocytic infiltra

249 le and multiple hyperfunctioning parathyroid glands, showed PET/CT to be most valuable in the group w

250 et al., 2014], suggesting that the exocrine glands, similar to the endocrine, develop from the same

251 Excision of either the extraorbital gland (single LGE), or both the extraorbital and intraor

252 se to the unique specification of submucosal gland (SMG) cells.

253 in the female murine submandibular salivary gland (SMG) to establish a model for investigation of re

254 Submucosal glands (SMGs) are a prominent structure that lines human

255 t an autocrine development of the androgenic glands so that females differentiate instead: feminizati

256 compartment to the cell surface in pituitary gland somatotropes, concomitant with increasing levels o

257 Several gland-specific genes were characteristic of different rh

258 tal perspective in a mouse model of salivary gland squamous cell carcinoma.

259 of cellular plasticity in the adult salivary gland, such studies provide encouraging evidence that a

260 ulation within the mouse nulliparous mammary gland that is characterized by the expression of Lyve-1,

261 The corpus luteum is an endocrine gland that synthesizes and secretes progesterone.

262 The corpus luteum is a transient endocrine gland that synthesizes and secretes the steroid hormone,

263 pped with appendages (that is, follicles and glands), that is critical for regulating body temperatur

264 The Drosophila lymph gland, the larval hematopoietic organ comprised of prohe

265 this theory on datasets of pubertal mammary gland tips and embryonic kidney tips, as well as homeost

266 d immunohistochemically from normal lacrimal gland tissue and the lacrimal gland in a complex chorist

267 stry revealed strong PSMA staining of benign gland tissue, which impacts measured activities.

268 amartia) and grew into disorganized lacrimal gland tissue.

269 n aberrant fibrotic response within the same gland to uncover mechanisms that prevent wound healing a

270 It results in involution of the normal gland to ~90% of its original size because of the loss o

271 ic day 12 submandibular and parotid salivary glands to characterize their molecular identities during

272 toarchitecture, and the placenta and metrial gland transcriptome were observed between control and FO

273 In mammary gland tumor models, Angpt2(443) differentially affected

274 4 patients showed bilateral disease, pineal gland tumors, and a latency period of at least 1 year.

275 Endocrine cells in the pituitary gland typically display either spiking or bursting elect

276 IHC also revealed that while most of the gland underwent a wound-healing response that resolved b

277 The antennal gland, up until now morphologically underexplored, is st

278 Tumor uptake above salivary gland uptake translated into partial remission, with an

279 showed effects on the developing rat mammary gland using new quantitative and established semiquantit

280 produced a microfluidic model of submucosal glands using mucus vesicles from banana slugs.

281 diseased tissues near or distal to salivary glands using transcriptome or proteomics.

282 erved that a reduced volume in the pituitary gland was associated with the slope of neuroticism over

283 ostate, in the first 2 patients the prostate gland was incised and imaged with CLI to visualize the p

284 Using Drosophila hematopoietic organ: lymph gland, we demonstrate that Fatty Acid Oxidation (FAO) is

285 glandular injury in the mouse submandibular gland, we show that de novo formation of acini involves

286 rimary or secondary lymphoma of the lacrimal gland were included.

287 Glands were harvested at multiple time points; whole mou

288 mentary canal and type III cells of salivary glands were identified as the major sites of OY phytopla

289 Tick midgut and salivary glands were infected with A. marginale.

290 on of branching morphogenesis in the mammary gland, whereby stromal ACKR2 modulates levels of the sha

291 er and skeletal muscle, and even to salivary glands which are known to concentrate these ions.

292 se factors are actively secreted by salivary glands which suggests these factors are important in mai

293 l as epigenetic reprogramming in the mammary gland, which can affect cell fate decisions in progenito

294 evasion mechanism mediated by the esophageal gland, which is essential for schistosome survival and p

295 noparticles can be excreted through salivary glands, which often host bacteria or viruses during infe

296 . incognita were expressed in the esophageal gland with high expression during the parasitic stages o

297 scular cells in pancreas, testis and thyroid gland, with age in mice and humans.

298 in the group with multiple hyperfunctioning glands, with sensitivity of 88%, whereas conventional im

299 evelopment and maintenance of the esophageal gland, without affecting the development of other somati

300 s and restore saliva flow rate in a salivary gland wound model of C57BL/6 mice.