ライフサイエンスコーパス: Ussing chamber

1 overcome permeability defect (quantified in Ussing chambers).

2 ical resistance in rat jejunum mounted in an Ussing chamber.

3 olayers; channel function was measured in an Ussing chamber.

4 cells, and their function was studied in an Ussing chamber.

5 BM/choroid (BM/Ch) was mounted in a modified Ussing chamber.

6 ears; range 39-84) was mounted in a modified Ussing chamber.

7 orded across Calu-3 monolayers mounted in an Ussing chamber.

8 choroid explants was evaluated in a modified Ussing chamber.

9 p technique and transepithelial secretion by Ussing chamber.

10 human neuroretina were mounted in a modified Ussing chamber.

11 e triphosphate (ATP) assay, or mounted in an Ussing chamber.

12 leum, jejunum, and colon was evaluated in an Ussing chamber.

13 s of differing age and mounted in a modified Ussing chamber.

14 human fetal eyes were mounted in a modified Ussing chamber.

15 it conjunctiva was evaluated in the modified Ussing chamber.

16 mice and increases short circuit current in Ussing chambers.

17 toskeletal damage, or enterotoxic effects in Ussing chambers.

18 rt-circuited preparations of distal colon in Ussing chambers.

19 nd Il10(-/-) mice with or without colitis in Ussing chambers.

20 to luminal nucleotide additions measured in Ussing chambers.

21 mal duodenal mucosa was examined in vitro in Ussing chambers.

22 (MTEs) were apically infected and assayed in Ussing chambers.

23 ng ion fluxes across epithelial membranes in Ussing chambers.

24 xin was evaluated in rabbit ileum mounted in Ussing chambers.

25 subjected to 1 h of ischemia was mounted in Ussing chambers.

26 in rat intestine and adenocarcinoma cells in Ussing chambers.

27 ected ileum on barrier function ex vivo with Ussing chambers.

28 Da)] in duodenal biopsy specimens mounted in Ussing chambers.

29 solateral potassium transport was studied in Ussing chambers.

30 trical conductance when assessed in modified Ussing chambers.

31 O(3)(-) secretion was measured by pH stat in Ussing chambers.

32 r function and electrogenic ion transport in Ussing chambers.

33 ts across intestinal segments as measured in Ussing chambers.

34 ained for immunohistochemistry or mounted in Ussing chambers.

35 -injured porcine ileal mucosa was mounted in Ussing chambers.

36 of small bowel from the mice were mounted in Ussing chambers.

37 ripped of seromuscular layers and mounted in Ussing chambers.

38 on, infected with Salmonella, and mounted in Ussing chambers.

39 hort circuit current ( triangle up I(sc)) in Ussing chambers.

40 d and ion transport changes were measured in Ussing chambers.

41 vated short circuit currents when mounted in Ussing chambers.

42 difference in rat jejunal tissue mounted in Ussing chambers.

43 Tissues were mounted in modified Ussing chambers.

44 l side of ileal mucosal membranes mounted in Ussing chambers after 10(9) Escherichia coli C-25 had be

45 Ussing chamber analysis of jejunum revealed that Na+/H+

46 otential difference analyses and in vitro by Ussing chamber analysis.

47 lation have been investigated using both the Ussing chamber and a superfusion apparatus.

48 gically removed sclera clamped in a modified Ussing chamber and connected to a water column set at in

49 nasal epithelia cultures using experimental (Ussing Chamber and microelectrode) data reported in the

50 rmeable support to confluence, mounted in an Ussing chamber and permeabilized apically with amphoteri

51 as used for in vitro functional studies with Ussing chamber and pH stat techniques.

52 By Ussing chamber and radiotracer flux studies, claudin-8 e

53 current from rat jejunal tissue mounted in a Ussing chamber and rounding of intestinal epithelial cel

54 mined using ciliary body sections mounted in Ussing chambers and a perfused eye preparation.

55 Rabbit intestine was mounted in Ussing chambers and exposed to increasing concentrations

56 om C57BL/6 (wild-type) and Cftr(-/-) mice in Ussing chambers and measured transcellular secretion of

57 paracellular permeability were monitored in Ussing chambers and micro-snapwells.

58 anges, we mounted bladder tissue in modified Ussing chambers and subjected the tissue to mechanical s

59 tion was assessed in vitro with 51Cr-EDTA in Ussing chambers and was expressed as the permeability co

60 fluence on a porous substrate, mounted in an Ussing chamber, and the apical plasma membrane permeabil

61 gnificance, NRC monolayers were mounted in a Ussing chamber, and the short-circuit current ( I sc ) w

62 Segments of jejunum were mounted in Ussing chambers, and short circuit current responses to

63 Using patch clamp and Ussing chamber approaches, this study reveals that BK ch

64 allenge, we used a capillary to construct an Ussing chamber (area <1 mm(2)) to measure electrolyte tr

65 tested for their biological activity in the Ussing chamber assay and their ability to bind to the ta

66 In Ussing chambers, basolaterally applied AVP reduced colon

67 In Ussing chambers, BFT had two effects.

68 in rabbit colonic mucosal sheets mounted in Ussing chambers by 91%.

69 etion across duodenal mucosa was measured in Ussing chambers by pH stat and (36)Cl flux methods using

70 at the existing theoretical treatment of the Ussing chamber consists of the super-imposition of two c

71 PP2A1, PP2A2) into the apical compartment of Ussing chambers containing Calu-3 monolayers.

72 Ussing chamber data indicated in vitro function consiste

73 Studies with Ussing chambers demonstrated reduced basal and/or adenos

74 00 mum) added into the apical compartment of Ussing chambers either prior or after GSNO either comple

75 GBs were mounted in Ussing chambers, electrophysiologic parameters were reco

76 by nasal potential difference in mice and by Ussing chamber electrophysiology in vitro.

77 gamma-S stimulation of monolayers mounted in Ussing chambers evoked a rapid, but transient decrease i

78 Ussing chamber experiments indicated that serosal 1 micr

79 Ussing chamber experiments revealed electrogenic glucose

80 us inhibitors and activators was examined by Ussing chamber experiments.

81 ants were grown on filters and mounted in an Ussing chamber for electrophysiological studies.

82 rabbit conjunctiva was mounted in a modified Ussing chamber for measurement of short-circuit current

83 rabbit conjunctiva was mounted in a modified Ussing chamber for the measurement of short-circuit curr

84 f bovine and human fetal RPE were mounted in Ussing chambers for measurements of cytosolic calcium le

85 der an air-liquid interface, were mounted in Ussing chambers for the measurements of chloride short c

86 The Ussing chamber method was used to study the electrophysi

87 de in the receptor chamber using an in vitro Ussing chamber model.

88 In Ussing chambered mucosa-submucosa preparations (includin

89 ed tongue epithelia were mounted in modified Ussing chambers, permitting apical stimulation of taste

90 Colon tissues were isolated and Ussing chambers, quantitative polymerase chain reaction,

91 otes) were used to determined ENaC activity (Ussing chamber recordings), ASL height (confocal microsc

92 dies of primary nasal epithelial cultures in Ussing chambers revealed that inhibition of endogenous s

93 ing, and short-circuit currents (measured in Ussing chambers) revealed 2-fold higher stretch-activate

94 ort was electrophysiologically registered in Ussing-chamber set-ups, mRNA level of selected transport

95 ties of ouabain were evaluated in a modified Ussing chamber setup, using conjunctival tissues freshly

96 In Ussing chamber studies of chloride secretion, adenine nu

97 Ussing chamber studies of rat AT2 cells indicated that a

98 either anastomosed at 4 weeks or excised for Ussing chamber studies or histology, immunohistochemistr

99 Ussing chamber studies revealed that colons infected wit

100 Ussing chamber studies showed that cAMP-dependent and ch

101 In Ussing chamber studies, 5-HT-induced I(SC) and DMBS were

102 rpose of this study is to investigate, in an Ussing chamber system, whether elemental vs. parenteral

103 normal ileal mucosal membranes tested in the Ussing chamber system.

104 from macaques infected with C. parvum by the Ussing chamber technique.

105 on consists of isotopic flux measurements in Ussing chambers, the standard apparatus for permeation s

106 misinterpreted as enhanced secretion in the Ussing chamber, this is a serious deficiency in the evid

107 vivo using canine bladder mucosa mounted in Ussing chambers to determine the inflammatory and repara

108 e and Clcn2(-/-) littermates were mounted in Ussing chambers to determine transepithelial bioelectric

109 Muscle-free colonic mucosae were mounted in Ussing chambers to measure mucosal permeability and secr

110 Segments of jejunum were mounted in Ussing chambers to measure mucosal permeability; chlorid

111 Porcine scleral tissue was placed in Ussing chambers to separate uveal and orbital compartmen

112 In Ussing chambers, trypsin and AP stimulated a short-circu

113 assessed by direct measurement of NO in the Ussing chamber using an ISO-NO meter) decreased I(sc) pa

114 TASK-3 activation was quantified by Ussing chamber voltage clamp analysis.

115 In rabbit ileum studied with the Ussing chamber-voltage clamp technique, EGF stimulation

116 confluent epithelial monolayers measured in Ussing chambers was 9-fold larger in hTE compared with C

117 nsport across the bovine ciliary body in the Ussing chambers was greater in the aqueous humor-to-bloo

118 ge across the ileal membranes mounted in the Ussing chambers was significantly increased in the ileal

119 By means of Ussing chambers, we show that AVP reduced colonic anion

120 hed healthy women (controls) were mounted in Ussing chambers; we measured numbers of fluorescently la

121 Human mucosal preparations mounted in Ussing chambers were exposed to NT.

122 esistance in human colonic mucosa mounted in Ussing chambers were reversed by 60 and 68%, respectivel

123 Ussing chambers were used to measure transepithelial (22

124 fluent monolayers of these cells, mounted in Ussing chambers, were stimulated to secrete Cl(-) by app

125 d within the intact epithelium in a modified Ussing chamber, which allowed us to flow tastants across

126 Transport studies were performed in Ussing chambers with intact and RPE-denuded specimens of

127 ches: formation of asymmetric bilayers in an Ussing chamber, with only one of two leaflets containing