ライフサイエンスコーパス: parotid gland

1 of the lesions showed lower uptake than the parotid glands).

2 t of SLPI isolated previously from the human parotid gland.

3 iated lymphoid tissue (MALT) lymphoma in the parotid gland.

4 astic hypertrophy and hyperplasia of the rat parotid gland.

5 ess mucous acinar genes not intrinsic to the parotid gland.

6 d found later in development surrounding the parotid gland.

7 ed in the superficial-deep lobe of the right parotid gland.

8 2 females, presented painless masses in the parotid gland.

9 retion and regulatory volume decrease in the parotid gland.

10 rted DNase I mRNA transcript cloned from rat parotid gland.

11 the various epithelial cell types within the parotid gland.

12 in the submandibular glands, but not in the parotid glands.

13 submandibular glands and rat sublingual and parotid glands.

14 ease characterized by the enlargement of the parotid glands.

15 ormalities in the parenchyma relative to the parotid glands.

16 istent uptake in the salivary, lacrimal, and parotid glands.

17 therapy (IMRT) can reduce irradiation of the parotid glands.

18 om the native pancreas and submandibular and parotid glands.

19 the in vivo functions of these exchangers in parotid glands.

20 revealed that AC5/6 and AC3 are expressed in parotid glands.

21 ncluding human gingiva and submandibular and parotid glands.

22 e submandibular glands (0.1479 mSv), and the parotid glands (0.1137 mSv/MBq).

23 ecules demonstrated a comparable dose to the parotid glands (0.5 Gy/GBq, P = 0.27).

24 cycle ranged from 0.19 to 0.4 Gy/GBq for the parotid gland, 0.14 to 0.28 Gy/GBq for the submandibular

25 d epidermal cyst (1), Warthin's tumor of the parotid gland (1), surgical wound inflammation (2), leio

26 11.2 vs. 11.9), small bowel (16.2 vs. 17.1), parotid gland (19.2 vs. 19.6), lacrimal gland (8.9 vs. 1

27 ubjects for several organ systems, including parotid gland (50% vs. 3%), tongue (53% vs. 10%), and lu

28 ypes of embryonic mouse salivary glands: the parotid gland (a serous gland) and the submandibular gla

29 dings included gross enlargement of the left parotid gland, a focal lesion in the right parotid gland

30 nd amylase secretion (16-93%) from, isolated parotid gland acinar cells.

31 in submandibular and minor AdCCs compared to parotid gland AdCCs, and NRF2 pathway expression is asso

32 IL14alphaTG mice, but they lacked the later parotid gland and lung injury.

33 ixty neutral sugars were identified from the parotid gland and many of these were additionally found

34 One or both parotid glands and at least two-thirds of the tongue wer

35 erian, lacrimal, mandibular, sublingual, and parotid glands and from liver, kidney, pancreas, testis

36 ons, BPIFA2 is expressed specifically in the parotid glands and is abundant in salivary secretions.

37 s, and lymphocytic infiltrates in the lungs, parotid glands and kidneys.

38 y in secretory endpieces isolated from sheep parotid glands and loaded with the pH-sensitive fluoropr

39 or bilateral nonsuppurative swelling of the parotid glands and neurological complications that can r

40 This hormone has been purified from porcine parotid glands and partially sequenced in our previous s

41 associated with high viral loads in infected parotid glands and that late viral protein expression is

42 an, lacrimal, submandibular, sublingual, and parotid glands and the liver.

43 35 +/- 0.78 and 0.80 +/- 0.41 Gy/GBq for the parotid gland, and 0.67 +/- 0.62 and 0.30 +/- 0.27 Gy/GB

44 iver, 2.35 0.78 and 0.80 0.41 Gy/GBq for the parotid gland, and 0.67 0.62 and 0.30 0.27 Gy/GBq for th

45 t parotid gland, a focal lesion in the right parotid gland, and cervical lymphadenopathy.

46 while DNase I is expressed in the pancreas, parotid gland, and kidney.

47 ritical structures were the spinal cord, the parotid glands, and the mandible.

48 Uptake in bone marrow, parotid glands, and tonsils was slightly but statistical

49 Parotid glands appeared to exert a positive effect on de

50 hly fucosylated glycans that co-exist in the parotid gland are not fully known.

51 IgG and IgA repertoire within pSS patients' parotid glands are distinct from those in non-pSS contro

52 Parotid glands are one of the most common sites for sali

53 data for the largely understudied embryonic parotid gland as compared with the submandibular gland,

54 dynamic contrast-enhanced MR imaging of the parotid gland at 1.5 T.

55 The mean (SD) excretory function of the parotid gland at 12 months, measured by scintigraphy, im

56 inductive site of the mucosal immune system (parotid gland) become polyclonal in piglets reared germf

57 r players and pathways that are relevant for parotid gland biology.

58 very of novel molecular players important in parotid gland biology.

59 d focus of follicular lymphoma in the second parotid gland biopsy.

60 mRNA expression was detected in the gingiva, parotid gland, buccal mucosa, and tongue.

61 ter mRNA increased dramatically in Nhe1(-/-) parotid glands but not in those of Nhe2(-/-) or Nhe3(-/-

62 Stimulation of amylase secretion from parotid glands by beta-adrenergic agonists is mediated b

63 Mumps viral antigen was detected in parotid glands by immunohistochemistry (IHC).

64 volumes for head and neck tumors as well as parotid glands can be well-defined on cross-sectional CT

65 uterine leiomyosarcoma, and 1 had oncocytic parotid gland carcinoma and continued receiving treatmen

66 at the stimulation of amylase secretion from parotid gland cells by NaF may be mediated by an increas

67 timulate amylase secretion from isolated rat parotid gland cells.

68 y against bands of 140-190 and 120 kd in the parotid gland, colon, and stomach, sites where the secre

69 rall survival, was overexpressed in AdCCs of parotid gland compared to minor and submandibular glands

70 Saliva from the submandibular and parotid glands contained higher concentrations of adreno

71 The parotid gland contributes a variety of secretory protein

72 ls were assessed in 77 ACC and 11 unaffected parotid gland control samples by immunohistochemistry an

73 that ACh-evoked HCO3- secretion in the sheep parotid gland differs from that in many other salivary g

74 In the present work we used the parotid gland duct which expressed Slc26a4 and Slc26a6 a

75 Patients with parotid gland enlargement accompanied by sicca symptoms

76 They all had parotid gland enlargement and lymphocytic interstitial p

77 gnosis of DILS was established in those with parotid gland enlargement by minor salivary gland biopsy

78 ere found in secondary end points except for parotid gland excretory function, as assessed by scintig

79 that Ca++ and calmodulin may play a role in parotid gland exocytosis by modulating the interaction b

80 The fluid-secreting acinar cells of the parotid gland express both IK and BK channels, raising q

81 ssory protein, LRRC26, which is expressed in parotid glands: expressed parSlo + LRRC26 channels were

82 The similar neonatal submandibular and parotid gland expression patterns observed for these gen

83 For normal tissues, parotid gland factors were 6.7, 9.4, 13.3, and 19.3 Gy p

84 For normal tissues, parotid gland factors were 6.7, 9.4, 13.3, and 19.3 Gy p

85 The stimulated parotid gland fluid secretion rate was normal, but the s

86 Systems biology analyses of the parotid glands from patients with primary SS and those w

87 p53 is similar in primary parotid cells and parotid glands from PKCdelta(+/+) and PKCdelta(-/-) mice

88 on is suppressed in vivo in gamma-irradiated parotid glands from PKCdelta(-/-) mice.

89 st that with the use of 3-DTP, contralateral parotid gland function can be partially preserved for at

90 l solute movement led us to hypothesize that parotid gland function(s) may have a role in regulating

91 cute time points (30 min to 2 h), irradiated parotid glands had significantly decreased levels of the

92 A parotid gland hormone that stimulates intradentinal flui

93 ed in the inhibition of beta-agonist-induced parotid gland hypertrophy and hyperplasia.

94 A transfer to a single previously irradiated parotid gland in 11 subjects using an open label, single

95 and to probe its specific roles, we studied parotid glands in mice with the K(Ca)1.1 gene ablated.

96 salivary gland dysfunction to contralateral parotid glands in patients with head and neck cancers.

97 Nevertheless, due to the size of the parotid gland, increased elastographic resolution is req

98 of the lesions showed higher uptake than the parotid glands) intermediate (neither low nor high), and

99 Acetylcholine-evoked secretion from the parotid gland is substantially potentiated by cAMP-raisi

100 esting secretion of salivary proteins by the parotid gland is sustained in situ between periods of ea

101 The parotid gland is the mostly affected site among major sa

102 In perfused rat parotid glands, isoproterenol induced staining of both a

103 f the salivary glands, adrenal gland, colon, parotid gland, kidney, thyroid gland, thymus, or uterus

104 Based on these observations, the parotid gland kinase may be related to other Golgi-local

105 The absorbed doses to kidneys, parotid glands, lacrimal glands, and red marrow were 23,

106 absorbed dose to kidneys, submandibular and parotid glands, liver, spleen, and bone marrow was 0.39,

107 the production of type 1 IFN; injury to the parotid glands, lungs, and kidneys is seen; 3) progressi

108 The follicular lymphoma of the parotid gland lymph node and the follicular lymphoma of

109 We propose that follicular lymphoma in the parotid gland lymph node may have resulted from coloniza

110 ulness in the quantitative assessment of the parotid glands, making it difficult to differentiate bet

111 y and accurately differentiate epitopes from parotid gland N-glycans and milk oligosaccharides based

112 mong healthy organs were in the lacrimal and parotid glands-not, however, resulting in any significan

113 rotection analyses indicated the presence in parotid gland of mRNA homologous to ClC-2.

114 ultiple compensatory changes in the exocrine parotid gland of Nhe1(-/-) mice that together attenuate

115 The skin and parotid glands of certain toads accumulate a variety of

116 Similar results were observed in the parotid glands of mice pretreated with imatinib prior to

117 n vitro functioning of acinar cells from the parotid glands of mice with targeted disruption of Na(+)

118 Indeed, the parotid glands of Nhe1(-/-) mice expressed higher levels

119 sis is suppressed by greater than 60% in the parotid glands of PKCdelta(-/-) mice.

120 ping the Ig-producing cell repertoire in the parotid glands of primary Sjogren's syndrome (pSS) patie

121 culate that B cell hyperproliferation within parotid glands of pSS patients may result from Ag-indepe

122 ts in a robust induction of apoptosis in the parotid glands of wild type mice, whereas apoptosis is s

123 There was no significant difference in parotid gland or splenic SUV(max) or lesion-to-parotid g

124 Involvement of the parotid gland (OR, 0.39; 95% CI, 0.18-0.85) and segment

125 ptors are expressed in axons innervating the parotid gland, paralleling our findings in the submandib

126 ice packs on (177)Lu-PSMA-617 uptake by the parotid glands (PGs).

127 andibular glands (PRP, 53%; mean SUV, 2.11), parotid glands (PRP, 51%; mean SUV, 1.90), and vocal cor

128 mice following delivery of the vector to the parotid gland (PTG), the submandibular gland (SMG) or to

129 rotid gland or splenic SUV(max) or lesion-to-parotid gland ratios between the 2 tracers although ther

130 Treated parotid glands received an average dose of 5745 cGy, whi

131 Parotid glands received higher doses (1.3 mGy/MBq) than

132 ound (US) with painful swelling in the right parotid gland region.

133 The adjoining parotid gland releases saliva in response to olfactory o

134 hDF-EpiSC-loaded native de-cellularized rat parotid gland scaffolds into the renal capsule of nude m

135 correlated with decreased submandibular and parotid gland sizes.

136 epresent important players that could impart parotid gland-specific biological properties.

137 our detailed analysis has revealed a unique parotid gland-specific gene signature that may represent

138 us, ESE-2, but not ESE-1, transactivates the parotid gland-specific PSP promoter and the prostate-spe

139 -tissue metastases) as well as normal liver, parotid gland, spleen, and mediastinal blood-pool SUV(ma

140 Results: Tracer uptake by the parotid gland, submandibular gland, and spleen was moder

141 metrically defined ipsilateral/contralateral parotid glands, submandibular glands, and oral cavity su

142 Parotid gland swelling appeared to be the sine qua non o

143 ound uptake than (68)Ga-HBED-PSMA-11 (in the parotid glands, the mean SUVmax for (68)Ga-THP-PSMA was

144 that IGF-1 promotes DNA repair in irradiated parotid glands through the maintenance and activation of

145 l transcripts correlated with viral loads in parotid gland tissue and saliva.

146 systems biology approach was used to analyze parotid gland tissue samples obtained from patients with

147 Furthermore, the ability of the parotid gland to conserve NaCl was abolished in NKCC1-de

148 We propose that CB1 receptors act at the parotid gland to inhibit stimulated salivation but also

149 on (amylase-positive area) within irradiated parotid glands to levels similar to untreated controls.

150 were obtained using Hermes software for the parotid gland, tongue, thyroid, lung, gastric wall, panc

151 vation of p53 is required and sufficient for parotid gland transformation in the presence of activate

152 In contrast to the dramatic effect of p53 in parotid gland transformation, p53 loss has little effect

153 thyroid carcinoma, basal cell carcinoma, and parotid gland tumor, and 68.5% +/- 6.4% for those with n

154 The etiology of Warthin's tumor, a benign parotid gland tumor, is unknown.

155 [SIR] 52.3), non-Hodgkin lymphoma (SIR 8.3), parotid gland tumors (SIR 33.4), thyroid cancer (SIR 13.

156 mice heterozygous for a p53 deletion develop parotid gland tumors and loose their wild type p53 allel

157 accompanied by the down regulation of p21 in parotid gland tumors but not breast tumors.

158 the risk of meningioma, acoustic neuroma, or parotid gland tumors in relation to mobile phone use.

159 The parotid gland tumors were aneuploid and demonstrated inc

160 th the risks of brain, acoustic neuroma, and parotid gland tumors.

161 AdhAQP1 vector delivery to a single parotid gland was safe and transfer of the hAQP1 cDNA in

162 t Raf-1 protein kinase activity in the mouse parotid glands was induced by chronic isoproterenol admi

163 IK channels, activated fluid secretion from parotid glands was normal.

164 core (SUV(mean) ratio of whole-body tumor to parotid glands) was semiautomatically calculated on base

165 better elucidate the molecular nature of the parotid gland, we have performed RNA sequencing to gener

166 Homogenates and subfractions from macaque parotid glands were able to phosphorylate synthetic pept

167 ng demonstrated that the acinar cells of the parotid glands were the primary location for both the pa

168 ells among AdCC of minor, submandibular, and parotid glands while plasma cells were enriched in norma

169 Sparing the parotid glands with IMRT significantly reduces the incid