ライフサイエンスコーパス: submandibular

1 y glands (parotids, 0.031 +/- 0.011 mSv/MBq; submandibular, 0.061 +/- 0.031 mSv/MBq).

2 of 50 and 8 of 50 otic, 14 of 47 and 4 of 47 submandibular, 18 of 58 and 10 of 58 superior cervical,

3 2+)](i) were nearly abolished in P2X(7)(-/-) submandibular acinar and duct cells.

4 a2+ release channels in pancreatic acini and submandibular acinar and duct cells.

5 The current study tested whether submandibular acinar cell function also relies on these

6 e activity appears to be directly related to submandibular acinar cell loss in NOD-scid mice involvin

7 were also observed in freshly dispersed rat submandibular acinar cells but not in three immortalized

8 The membrane potential of submandibular acinar cells from wild-type mice remained

9 We found that the K(+) currents in submandibular acinar cells have the biophysical and phar

10 cusing on the membrane potential in isolated submandibular acinar cells revealed mechanistic details

11 ed that NOD-scid mice develop severe loss of submandibular acinar cells with concomitant appearance o

12 t ion channels in individual mouse and human submandibular acinar cells.

13 mphatic transport and drainage of Gd-DOTA to submandibular and deep cervical lymph nodes was demonstr

14 p progressive histopathologic lesions of the submandibular and lachrymal glands similar to NOD mice,

15 vere chronic periductal inflammation in both submandibular and lacrimal glands in contrast to the muc

16 nto several stages: 1) initial injury to the submandibular and lacrimal glands via an environmental i

17 The similar neonatal submandibular and parotid gland expression patterns obse

18 ry hypofunction is correlated with decreased submandibular and parotid gland sizes.

19 Saliva from the submandibular and parotid glands contained higher concen

20 Results: Mean absorbed dose to kidneys, submandibular and parotid glands, liver, spleen, and bon

21 d HEK cells and from the native pancreas and submandibular and parotid glands.

22 mucosal tissues, including human gingiva and submandibular and parotid glands.

23 alyses of 14,441 cells from embryonic day 12 submandibular and parotid salivary glands to characteriz

24 , liver, and gut cells, and the pancreas and submandibular and pituitary glands.

25 higher uptake of (18)F-PSMA-1007 in muscle, submandibular and sublingual gland, spleen, pancreas, li

26 cin secreted by mucous acinar cells in human submandibular and sublingual glands.

27 ack of differentiated mucous acinar cells in submandibular and sublingual glands.

28 Similar results were obtained with submandibular and sublingual secretions.

29 virus-specific IgG2a was restricted to NALT, submandibular, and mesenteric lymph nodes.

30 e cranial ciliary, pterygopalatine, lingual, submandibular, and otic ganglia--arise from glial cells

31 to compare the susceptibilities of lacrimal, submandibular, and parotid cells to viral invasion.

32 sts of 3 major pairs of glands: the parotid, submandibular, and sublingual glands.

33 progressively expanding lingual, sublingual, submandibular, and submental hematomas have the tendency

34 into the rat glioma cell line C6B4, the rat submandibular cell line RSMT-A5, and the rat pancreatic

35 operties of the conductances in lacrimal and submandibular cells were similar, e.g. halide selectivit

36 was significantly underexpressed in AdCC of submandibular compared to parotid and sublingual glands

37 lar TNUR, 2-45 min; parotid DF, 20%-99%; and submandibular DF, 27%-98%.

38 rotid artery (eICA) stenoses, detectable via submandibular Doppler sonography and cervical magnetic r

39 s are co-expressed in the apical membrane of submandibular duct cells, consistent with the significan

40 Exogenous FGFs added to submandibular epithelial rudiments cultured without mese

41 chronic dermatitis with extensive facial and submandibular erosions.

42 ed the expression of muscle-related genes in submandibular fibroblasts that began to mimic parotid fi

43 hout any signs of distress and had bilateral submandibular firm nonpulsatile tender masses, each esti

44 termine variations in stimulated parotid and submandibular flow rates over 6 hours and to define sali

45 of neuronal cells within the parasympathetic submandibular ganglion (PSG) express the catecholaminerg

46 e mouse superior cervical ganglion (SCG) and submandibular ganglion (SMG) to examine the assembly of

47 pre- and postganglionic neurons in the mouse submandibular ganglion in vivo, focusing on the mechanis

48 maged nerve terminals in the parasympathetic submandibular ganglion.

49 Silencing Cav1 in human submandibular gland (HSG) cells decreased plasma membran

50 The culture of human submandibular gland (HSG) cells on laminin-1 induces aci

51 contribute to [Ca(2+)](i) increases in human submandibular gland (HSG) cells.

52 H+ exchanger (NHE) isoforms expressed in the submandibular gland (SMG) acinar and duct cells and thei

53 l-]i and the Cl- current in the rat salivary submandibular gland (SMG) acinar and duct cells was used

54 ned miRNAs expressed in the mouse developing submandibular gland (SMG) and found that miR-200c accumu

55 y studies have been done to understand mouse submandibular gland (SMG) branching morphogenesis, littl

56 a critical role for heparanase during mouse submandibular gland (SMG) branching morphogenesis.

57 Parasympathetic innervation is critical for submandibular gland (SMG) development and regeneration.

58 -inducible Cre recombinase Ela-CreERT in the submandibular gland (SMG) ductal cells, was established

59 Here, our results show that in primary mouse submandibular gland (SMG) epithelial cells, P2X7R activa

60 The mouse submandibular gland (SMG) epithelium undergoes extensive

61 f the vector to the parotid gland (PTG), the submandibular gland (SMG) or to the liver via the tail v

62 epth analysis of male and female adult human submandibular gland (SMG) samples by bulk RNA sequencing

63 y the latter two develop inflammation in the submandibular gland (SMG), a critical target of Sjogren'

64 ery (BA), middle cerebral artery (MCA)], the submandibular gland (SMG), and pineal gland was quantifi

65 king the regenerative response of the murine submandibular gland (SMG), following innate immune-media

66 infiltration and caspase-3 activation in the submandibular gland (SMG), production of antinuclear and

67 being found only in the acinar cells of the submandibular gland (SMG).

68 nants of duct specification in the embryonic submandibular gland (SMG).

69 nd the Cl- current were measured in isolated submandibular gland acinar and duct cells to characteriz

70 int of the Ca(2+)-activated Cl(-) current in submandibular gland acinar cells from Best2-deficient mi

71 In contrast, submandibular gland acinar cells from Tmem16A(-/-) mice

72 ected HEK293 cells and from the pancreas and submandibular gland also coimmunoprecipitated EBP50.

73 tive, non-vasomotor sympathetic axons in the submandibular gland and at the base of piloerector hairs

74 1 IFNR (IL14alphaTG.IFNR(-/-)) had the same submandibular gland and lacrimal gland injury as did the

75 lized in the plasma membrane region of human submandibular gland and Madin-Darby canine kidney cells.

76 sly and exogenously expressed TRPC1 in human submandibular gland and Madin-Darby canine kidney cells.

77 glands, specifically in acinar cells of the submandibular gland and palatine minor glands, as well a

78 termined by recording salivary flow from the submandibular gland and temperature changes on the tongu

79 SMGC is expressed in the submandibular gland at high levels through postnatal day

80 cover that decreasing MT-MMP activity during submandibular gland branching morphogenesis decreases pr

81 required for branching morphogenesis of the submandibular gland but not the lung.

82 g ClC-3, and ClC-3 protein, was found in rat submandibular gland by RT-PCR and Western analysis.

83 , htrp3, and Trp1 were detected in the human submandibular gland cell line (HSG).

84 ty fractions of Triton X-100-extracted human submandibular gland cell membranes.

85 tro stimulation with a muscarinic agonist of submandibular gland cells isolated from mice treated wit

86 Stimulation of human submandibular gland cells with carbachol, inositol trisp

87 In human submandibular gland cells, carbachol (CCh) induced flick

88 ivary gland cells as well as dispersed mouse submandibular gland cells.

89 th or adhesion of B16-F10 melanoma and human submandibular gland cells.

90 regulating Ca2+ signaling in pancreatic and submandibular gland cells.

91 Six patients had submandibular gland disease: three with primary neoplasm

92 renergic receptors) in pancreatic acinar and submandibular gland duct cells, respectively, evoke a Ca

93 and membrane current were measured in human submandibular gland ductal (HSG) cells to determine the

94 PC3 was detected in the apical region of rat submandibular gland ducts, whereas TRPC6 was present in

95 The most common manifestations were submandibular gland enlargement, macroglossia, and carpa

96 AdCCs of the submandibular gland exhibit unique differences in progno

97 deficient adenoviruses, lymphocytes from the submandibular gland express T-bet, GATA3, and RAR-relate

98 show that calcineurin is required for normal submandibular gland function and secretion of digestive

99 the question of a role for 5-HT in mammalian submandibular gland function was re-addressed, using iso

100 The mouse submandibular gland has been used as a model for major s

101 Submandibular gland lysates were examined by Western blo

102 ations of this stem cell population into the submandibular gland of irradiated mice successfully rest

103 tic ductal cells were injected into the left submandibular gland of the same hamsters.

104 Expression of TAg in the submandibular gland of transgenic mice from the time of

105 ional significance of FGFR1 was confirmed by submandibular gland organ culture.

106 measurements from time-lapse images of mouse submandibular gland organ explants to construct a tempor

107 chain reaction studies in cells of mammalian submandibular gland origin using consensus sequence prim

108 noculation with tcMCMV, lymphocytes from the submandibular gland preferentially express the transcrip

109 or agonists induced salivation in an ex vivo submandibular gland preparation.

110 ped large ductal-type adenocarcinomas in the submandibular gland region, where islets were transplant

111 tion of Hedgehog signaling within the murine submandibular gland rescued radiation-induced salivary g

112 ike the induced pancreatic tumors, all three submandibular gland tumors that were examined had the mu

113 bulated solid mass was detected in the right submandibular gland with similar sonographic findings.

114 previously demonstrated, immunization of the submandibular gland with tissue culture-derived murine c

115 or full-length hTrp1alpha in the HSG (human submandibular gland) cell line.

116 transcripts also are found in the pancreas, submandibular gland, and adult spleen.

117 ively influences gene expression in the male submandibular gland, and that many of the sex difference

118 f androgen control of gene expression in the submandibular gland, and to explore the degree to which

119 s observed in cultured cells in vitro and in submandibular gland, cortex, and caudate nucleus for as

120 embryonic parotid gland as compared with the submandibular gland, focusing on the mesenchymal cell po

121 ion of adenylyl cyclase and, at least in rat submandibular gland, involved in modifying the volume an

122 ncreased by LPS-induced periodontitis in the submandibular gland, returned to control values after HU

123 ce lacked comparable defects in the lung and submandibular gland, suggesting that MT1-MMP acts via me

124 Of the different cells isolated from the submandibular gland, this specific population, Lin-CD24+

125 odel of severe glandular injury in the mouse submandibular gland, we show that de novo formation of a

126 ean dose, 0.26 Gy/GBq, was seen in the right submandibular gland, whereas the lowest mean dose, 0.029

127 eptor regulates fluid secretion in the mouse submandibular gland.

128 nd correlated with acute inflammation in the submandibular gland.

129 ndrogens have profound effects on the murine submandibular gland.

130 tubule) cells of the neonatal rat and mouse submandibular gland.

131 anted, but none developed tumors in the left submandibular gland.

132 ression for all 10 known active genes is the submandibular gland.

133 rotid gland, paralleling our findings in the submandibular gland.

134 CB1 receptors on neurons that innervate the submandibular gland.

135 at is essential for saliva production by the submandibular gland.

136 mSv/MBq), the kidneys (0.1722 mSv/MBq), the submandibular glands (0.1479 mSv), and the parotid gland

137 on in the parotids (24% +/- 14%, P = 0.001), submandibular glands (35% +/- 11%, P < 0.001), and kidne

138 ration in the parotids (24% 14%, P = 0.001), submandibular glands (35% 11%, P < 0.001), and kidneys (

139 15 and 5-lipoxygenase) is expressed in mouse submandibular glands (mSMG), using qPCR and Western blot

140 generation in a wound-healing model of mouse submandibular glands (mSMGs).

141 93), spinal cord (PRP, 64%; mean SUV, 2.12), submandibular glands (PRP, 53%; mean SUV, 2.11), parotid

142 ain/neck muscles, and sialorrhea/parotid and submandibular glands (reporting odds ratios 0.79-0.27).

143 ctive of this study was to determine whether submandibular glands (SMG) from ALX/FPR2(-/-) mice displ

144 involved in SPM biosynthesis were altered in submandibular glands (SMG) from NOD/ShiLtJ female mice a

145 sequently, this DC subset became resident in submandibular glands (SMGs) and nasal passages (NPs) in

146 Using ex vivo cultured embryonic mouse submandibular glands (SMGs) as models to study branching

147 cumulation of PSMA-targeting radioligands in submandibular glands (SMGs) can be explained with PSMA e

148 issues such as the nasal passages (NPs), the submandibular glands (SMGs), and nasopharyngeal-associat

149 Salivary glands, such as submandibular glands (SMGs), are composed of branched ep

150 equired for branching morphogenesis of mouse submandibular glands (SMGs).

151 ated the function of laminin alpha5 in mouse submandibular glands (SMGs).

152 e acinar cells in developing rat parotid and submandibular glands and are also products of the sublin

153 s re-addressed, using isolated, perfused rat submandibular glands and dispersed-cell aggregates from

154 ved in cells isolated from mouse and opossum submandibular glands and rat sublingual and parotid glan

155 ein occurred in the nasal lamina propria and submandibular glands and the frequencies of CD11c+CD8+ d

156 When AdhAQP1 was administered to rat submandibular glands by retrograde ductal instillation,

157 , we report that ex vivo branching of intact submandibular glands decreases when either FGFR2 express

158 Immunohistochemical stainings of submandibular glands from C57BL/6.NOD-Aec1Aec2 mice and

159 Submandibular glands from NOD-scid mice exhibited the gr

160 alivation was suppressed by more than 70% in submandibular glands from P2X(7)-null mice.

161 cells as well as lymphocytic infiltrates in submandibular glands from patients with pSS demonstrated

162 F, and administration of beta-NGF from mouse submandibular glands induced ovulation in llamas.

163 t adenoviral-mediated gene transfer to mouse submandibular glands is possible by intraductal cannulat

164 Branching morphogenesis of mouse submandibular glands is regulated by multiple growth fac

165 respectively), AdhAQP1 administration to rat submandibular glands led to a two- to threefold increase

166 an hamsters were transplanted into the right submandibular glands of 50 female hamsters that were or

167 of immunoglobulin A (IgA) was studied in the submandibular glands of anaesthetized rats by stimulatin

168 on was upregulated upon radiation therapy in submandibular glands of both mice and humans.

169 y of a replication-deficient adenovirus-5 in submandibular glands of C57BL/6 mice through retrograde

170 Temporal expression of IL-17 and IL-23 in submandibular glands of C57BL/6.NOD-Aec1Aec2 mice correl

171 d enriched the number of functional acini in submandibular glands of irradiated animals and enhanced

172 The exocrine pancreas, liver, and submandibular glands of the rat were used to express and

173 rt a RCC case with metastasis to parotid and submandibular glands that has the same sonographic and s

174 pine-stimulated in vivo fluid secretion from submandibular glands was essentially normal in double-nu

175 diffuse lymphocytic infiltration was seen in submandibular glands, a major target of pSS, by age 6 wk

176 of primary salivary tissue, both parotid and submandibular glands, and differentiating hS/PCs, we con

177 ences in ABPs secreted by mouse lacrimal and submandibular glands, and in ABPs secreted by male and f

178 ed phosphorylation of SMAD1/5/8 in the mouse submandibular glands, and led to a recovery of SG functi

179 ed ipsilateral/contralateral parotid glands, submandibular glands, and oral cavity surrogates for eac

180 for each organ at risk (kidney, parotid and submandibular glands, bone marrow, liver, and lacrimal g

181 This activity appeared in the submandibular glands, but not in the parotid glands.

182 caspase-3, lack of leukocyte infiltration of submandibular glands, reduced synthesis of disease-assoc

183 DNA levels were lower in the spleen than in submandibular glands, the number of individual viral gen

184 al saliva obtained from both the parotid and submandibular glands, with highest levels of activity pr

185 on of the cannulated main excretory ducts of submandibular glands.

186 roxylase (TH) in developing murine and human submandibular glands.

187 OC, of acinar and ductal cells in intact rat submandibular glands.

188 AdCCs of parotid gland compared to minor and submandibular glands.

189 crease in NOS and BH4 biosynthetic enzyme in submandibular glands.

190 zed a stem cell population from adult murine submandibular glands.

191 egions of interest on lacrimal, parotid, and submandibular glands; left ventricle; liver; spleen; kid

192 receptors were found in cell lines from the submandibular (HSG) and parotid (HSY) salivary glands.

193 and was removed under general anesthesia via submandibular incision.

194 These results demonstrate that the submandibular LN is the primary site for early clonal ex

195 e day 3 accumulation of KJ1-26+ cells in the submandibular LN was inhibited if the eye was removed wi

196 cells accumulated primarily in the draining, submandibular lymph node (LN) within 3 days.

197 25(+)FOXP3(+) cells and CD4/CD8 ratio in the submandibular lymph node (p < 0.05).

198 ng OVA peptide in vivo was only found in the submandibular lymph node and not in other lymph nodes, s

199 rP(Sc), was first detected in the tongue and submandibular lymph node at 1 to 2 weeks following inocu

200 While 10% to 30% of mesenteric and submandibular lymph node CD4(+) cells became robust T-re

201 anced STAT6 and decreased STAT4 induction in submandibular lymph node cells.

202 ll clonal expansion was only observed in the submandibular lymph node following conjunctival applicat

203 Subconjunctival and submandibular lymph node macrophages in mice given local

204 0(+) macrophage infiltration of gingival and submandibular lymph node tissues and significantly (p <

205 ease in F4/80(+) macrophages in gingival and submandibular lymph node tissues.

206 he a.c. OT-I T cells increased 9-fold in the submandibular lymph nodes and 3-fold in the spleen follo

207 phenotype (M2) of macrophages isolated from submandibular lymph nodes as observed by flow cytometry.

208 Nasal mucosa-associated lymphoid tissue and submandibular lymph nodes initially accumulated PrP(d) a

209 ad bronchial tree-associated lymph nodes and submandibular lymph nodes that were 5-10 times larger th

210 including teeth and surrounding tissues, and submandibular lymph nodes were obtained for histomorphom

211 The animals were sacrificed, the submandibular lymph nodes were removed for FACS analysis

212 ity in the spleens, superficial cervical and submandibular lymph nodes, and inoculated eyes peaked at

213 in the spleen, the superficial cervical and submandibular lymph nodes, and the inoculated eye by lys

214 ans, including hypertrophy of the spleen and submandibular lymph nodes, glomerulonephritis, and periv

215 antigen was detected in the lung, hilar and submandibular lymph nodes, spleen, and colon.

216 e-covered superficial cervical lymphatics to submandibular lymph nodes.

217 8(+) T cells first appeared in the draining (submandibular) lymph node on day 5 and were detectable i

218 gued tonsillitis with moss, pharyngitis, and submandibular lymphadenitis with tenderness.

219 eful landmark in determining the origin of a submandibular mass.

220 Thirteen patients with 14 palpable submandibular masses, surgical and histologic confirmati

221 22-kilodalton protein was isolated from the submandibular (mental) gland of the male terrestrial sal

222 s indicated that the direct contact of mouse submandibular (mSMG) cell clusters and hHF-MSCs was not

223 These results indicate that a decrease in submandibular NO-BH4 protein expression may provide insi

224 andibular PP, 4%-31%; parotid NUR, 2.2-16.0; submandibular NUR, 1.4-16.2; parotid TNUR, 8-45 min; sub

225 causing intense burning rectal, ocular, and submandibular pain and flushing.

226 In contrast, GFRalpha1-deficient submandibular parasympathetic neurons retain normal resp

227 xpression of SLPI transcripts was evident in submandibular, parotid, and minor salivary glands from b

228 g ranges were observed: parotid PP, 22%-49%; submandibular PP, 4%-31%; parotid NUR, 2.2-16.0; submand

229 mbryonic cells are tagged by AID(cre) in the submandibular region, where conditional deletion of the

230 In addition, the introduction of the mouse submandibular renin (mRen-2d) transgene into Sprague-Daw

231 The submandibular saliva proteases were shown to be sensitiv

232 Human submandibular saliva reduces human immunodeficiency viru

233 dentify the salivary protein(s) responsible, submandibular saliva was fractionated by anion- exchange

234 In the present study, we have analyzed submandibular saliva, collected without contaminating ce

235 and stimulated glandular (i.e., parotid and submandibular) saliva flow rate and composition alterati

236 orted to affect electrolyte transport by the submandibular salivary gland (adrenaline, carbachol, iso

237 Cleft formation is the initial step in submandibular salivary gland (SMG) branching morphogenes

238 lished the epigenomic landscape of the mouse submandibular salivary gland (SMG) by performing chromat

239 d H(+) and HCO3- transport mechanisms in the submandibular salivary gland (SMG) ducts of wild type, N

240 e-dependent regulatory role during embryonic submandibular salivary gland (SMG) morphogenesis.

241 artial sialoadenectomy, in the female murine submandibular salivary gland (SMG) to establish a model

242 The submandibular salivary gland (SMG), a major site of pers

243 ductal (mSG-DUC1) cell line, from the murine submandibular salivary gland (SMG), which recapitulate d

244 ly, SERCA2b was found in the luminal pole of submandibular salivary gland acinar and duct cells.

245 pared the properties of native CaCC in mouse submandibular salivary gland acinar cells to the Ca(2+)-

246 were observed in both rat lacrimal gland and submandibular salivary gland acinar cells.

247 Cleft formation during submandibular salivary gland branching morphogenesis is

248 ifferentiation in early developing embryonic submandibular salivary gland buds.

249 e in mobilizing Ca2+ from internal stores of submandibular salivary gland but not pancreatic acinar c

250 ession of ryanodine receptor was detected in submandibular salivary gland cells but not pancreatic ac

251 ClC-3 was examined in rat lacrimal gland and submandibular salivary gland cells using RT-PCR and West

252 n profiles at five different stages of mouse submandibular salivary gland development provide insight

253 During murine submandibular salivary gland development, the vasculatur

254 owth factor (FGF) signaling is essential for submandibular salivary gland development.

255 The mouse submandibular salivary gland first appears as a single m

256 asympathetic innervation of the lacrimal and submandibular salivary gland is dramatically reduced in

257 The partial submandibular salivary gland resection model provides an

258 T cells in nude mice receiving sham (submandibular salivary gland) or pituitary grafts alone

259 (GS-AgNPs) can selectively accumulate in the submandibular salivary gland, followed by being excreted

260 s controlling gene expression of the healthy submandibular salivary gland.

261 s of the small intestine and in cells of the submandibular salivary gland.

262 ration of tissue structure in the developing submandibular salivary gland.

263 urce of immature T cells in parotid (PG) and submandibular salivary glands (SMG) were studied in Fisc

264 In the present study we investigated whether submandibular salivary glands (SMGs) in F508 mice (Cftr(

265 ntly fewer focal inflammatory infiltrates in submandibular salivary glands and kidneys.

266 he role of LIMK signaling in mouse embryonic submandibular salivary glands using ex vivo organ cultur

267 re inoculated by retrograde perfusion of the submandibular salivary glands via Wharton's duct with tc

268 ithelial basal periphery in developing mouse submandibular salivary glands, and that ROCK inhibition

269 than GS-AuNPs and can rapidly penetrate into submandibular salivary glands, be efficiently taken up b

270 iltration and parenchymal cell damage in the submandibular salivary glands.

271 ical secretory tracks were also found in the submandibular salivary glands.

272 ove AAV-mediated gene transfer to the murine submandibular salivary glands.

273 ntly and focally in forming cleft regions of submandibular salivary-gland epithelia, accompanied by a

274 opoietin (hEPO) directly to individual mouse submandibular SGs.

275 Individual DLN (submandibular [SM]; superficial cervical [SC]; and inter

276 , namely parotid (PAG), sublingual (SLG) and submandibular (SMG) glands.

277 major salivary glands: the parotid (PG), the submandibular (SMG), and the sublingual glands (SLG).

278 cator space - 31 patients (82%), followed by submandibular space - 27 patients (71%).

279 ently involves masticator space, followed by submandibular space.

280 ranial parasympathetic ganglia including the submandibular, sphenopalatine and otic ganglia.

281 fferent anatomic subsites including parotid, submandibular, sublingual, and minor salivary glands dif

282 y(A)+ RNA isolated from harderian, lacrimal, submandibular, sublingual, and parotid glands and the li

283 s to blots of SDS-PAGE-separated parotid and submandibular-sublingual (SM-SL) saliva.

284 ory activity was present in whole saliva and submandibular-sublingual saliva, but it was essentially

285 35%), stimulated parotid (47%), unstimulated submandibular/sublingual (23%), and stimulated submandib

286 bmandibular/sublingual (23%), and stimulated submandibular/sublingual (39%) saliva.

287 ates for unstimulated whole and unstimulated submandibular/sublingual (SMSL) saliva as well as citrat

288 Removal of the submandibular/sublingual glands and changes in diet cons

289 sucrose diets, removal of the parotid or the submandibular/sublingual glands, and diets in powder or

290 bserved for protein secretion in parotid and submandibular/sublingual glands, and that the secretion

291 A digested submandibular/sublingual saliva sample was used for the

292 Parotid and submandibular/sublingual saliva samples and xerostomia q

293 microbial proteins in stimulated parotid and submandibular/sublingual saliva were determined.

294 encoded by MUC7), a major component of human submandibular/sublingual saliva, is a bacterial receptor

295 cin MG1 and other salivary proteins in human submandibular/sublingual secretion (HSMSL) could have a

296 Protein samples from parotid secretion, submandibular/sublingual secretion, whole saliva, and pe

297 en compared with the proteomes of parotid or submandibular/sublingual secretions.

298 cleavage of parotid secretory protein in the submandibular tissues.

299 bular NUR, 1.4-16.2; parotid TNUR, 8-45 min; submandibular TNUR, 2-45 min; parotid DF, 20%-99%; and s

300 Here we describe the under-investigated submandibular "whisker trident" on the rat's chin.