ライフサイエンスコーパス: submandibular gland

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

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

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

4 eptor regulates fluid secretion in the mouse submandibular gland.

5 nd correlated with acute inflammation in the submandibular gland.

6 ndrogens have profound effects on the murine submandibular gland.

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

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

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

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

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

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

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

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

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

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

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

18 1 IFNR (IL14alphaTG.IFNR(-/-)) had the same submandibular gland and lacrimal gland injury as did the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 Submandibular glands from NOD-scid mice exhibited the gr

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Submandibular gland lysates were examined by Western blo

69 15 and 5-lipoxygenase) is expressed in mouse submandibular glands (mSMG), using qPCR and Western blot

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 The mouse submandibular gland (SMG) epithelium undergoes extensive

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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