ライフサイエンスコーパス: sodium iodide

1 complex formed between sulfonyl chloride and sodium iodide.

2 nistration of approximately 28 MBq of (124)I-sodium iodide.

3 tient administration of larger activities of sodium iodide 131I than previously permitted.

4 MYMD-1 (185 mg/l) or water supplemented with sodium iodide (500 mg/l) that contained (16 mice) or did

5 y coupling with AZT and O-demethylation with sodium iodide, afforded 3'-azido-3'-deoxy-5'-O-[[(1-octa

6 By in situ 1) oxidation of sodium iodide and 2) sequestration of the transiently ge

7 characteristics, and only 2 (thallium-doped sodium iodide and bismuth germanate) have found widespre

8 ith increasing glycosaminoglycan content for sodium iodide and Gd-DTPA only, diffusivity significantl

9 h significant decreases in diffusivities for sodium iodide and Gd-DTPA, with similar (but not signifi

10 ted by the presence of 10 mg/L soap, 15 mg/L sodium iodide, and 6000 mg/L sodium thiosulfate.

11 substituted by silver acetate, sodium azide, sodium iodide, and silver nitrate.

12 the corresponding sugar aldehydes through a sodium iodide-catalyzed Henry reaction with bromonitrome

13 h sodium bromide or sodium chloride, but not sodium iodide, competitively oxidized some haloalcohols

14 ction of tertiary amides by a sodium hydride/sodium iodide composite, in situ treatment of the result

15 ion conducted a model-independent test using sodium iodide crystal detectors, the same target materia

16 The camera uses a 10 x 10 cm thallium-doped sodium iodide crystal, a 2 x 2 array of 53 x 53 mm photo

17 OET clearance was monitored for 1 hr using a sodium iodide detector in 22 isolated, buffer-perfused r

18 Mechanistic explanations for the large sodium iodide effect as well as possible mechanistic pat

19 generation of hydroiodic acid from catalytic sodium iodide, employing phosphorus acid as the stoichio

20 nerated from bis(trifluoromethyl)mercury and sodium iodide] gave fused-ring 2,2-difluorocyclopropane

21 nctional CCR6, as detected by the binding of sodium iodide I 125-labeled liver and activation-regulat

22 Exposure of the as-isolated AcN2OR to sodium iodide led to reduction of the electron-donating

23 S) analysis in positive detection mode using sodium iodide (NaI) as an additive.

24 during DNA isolation is eliminated using the sodium iodide (NaI) isolation method and that the level

25 By simple combination of water and sodium iodide (NaI) with chlorotrimethylsilane (TMSCl),

26 rcent of IFN-gamma(-/-) NOD.H-2h4 mice given sodium iodide (NaI)-supplemented water develop a slow on

27 iment, consisting of 106 kg of tallium-doped sodium iodide [NaI(Tl)] target material, is aimed to tes

28 Four hours after being given (123)I-sodium iodide orally, each patient received (99m)Tc-sest

29 um iodide SPECT/CT, (99m)Tc-sestamibi/(123)I-sodium iodide planar subtraction imaging, and (99m)Tc-se

30 ernal environment, as seen by an increase in sodium iodide quenching.

31 on, fluorescence-quenching experiments using sodium iodide revealed a small reduction in the extent o

32 ed diffusivities as the smallest one tested, sodium iodide, showed higher diffusivity than sodium dia

33 single-wavelength anomalous dispersion using sodium-iodide-soaked crystals and diffraction data colle

34 n diffusion of three common contrast agents: sodium iodide, sodium diatrizoate, and gadolinium diethy

35 Mixing copper(II) perchlorate and sodium iodide solutions results in copper(I) species and

36 aphy, consisting of (99m)Tc-sestamibi/(123)I-sodium iodide SPECT/CT, (99m)Tc-sestamibi/(123)I-sodium

37 We incorporated the human sodium iodide symporter (hNIS) and the human somatostati

38 differentiation, including the loss of human sodium iodide symporter (hNIS) expression, radioactive i

39 carcinoembryonic antigen (CEA) or the human sodium iodide symporter (hNIS) for oncolytic potential i

40 ionuclide accumulation mediated by the human sodium iodide symporter (hNIS) gene in conjunction with

41 ntification of cardiac gene expression after sodium iodide symporter (hNIS) gene transfer in cardiac

42 ic vaccinia virus, GLV-1h153, carrying human sodium iodide symporter (hNIS), in combination with radi

43 virus (VSV)-murine interferon beta (IFNbeta)-sodium iodide symporter (NIS) (VSV-mIFNbeta-NIS) oncolyt

44 second strategy involves transduction of the sodium iodide symporter (NIS) and free radionuclide ther

45 cells with retroviral vectors containing the sodium iodide symporter (NIS) and thyroperoxidase (TPO)

46 aft breast cancer model expressing the human sodium iodide symporter (NIS) as a reporter.

47 The application of sodium iodide symporter (NIS) as a theranostic gene allo

48 In the current study, we used the sodium iodide symporter (NIS) as a theranostic gene to i

49 cancer cells to express functionally active sodium iodide symporter (NIS) by targeted NIS gene trans

50 ast cancer cells stably expressing the human sodium iodide symporter (NIS) fused to a red fluorescent

51 n the matrix protein and expresses the human sodium iodide symporter (NIS) gene.

52 The sodium iodide symporter (NIS) is required for iodide upt

53 The sodium iodide symporter (NIS) is widely used as a report

54 The sodium iodide symporter (NIS) mediates iodide uptake int

55 its binding factor PBF repress expression of sodium iodide symporter (NIS) messenger RNA (mRNA), and

56 In this study, sodium iodide symporter (NIS) transgene imaging was eval

57 cancer cells to express functionally active sodium iodide symporter (NIS) would enable those cells t

58 din-Darby canine kidney cells expressing the sodium iodide symporter (NIS), pendrin, or NIS and pendr

59 ne levels by up-regulating expression of the sodium iodide symporter (NIS), thyroid peroxidase (TPO),

60 T tracer with excellent properties for human sodium iodide symporter (NIS)-based imaging in patients

61 is one of the most promising candidates for sodium iodide symporter (NIS)-mediated gene therapy.

62 f therapeutic genes, such as the theranostic sodium iodide symporter (NIS).

63 receptor expressing cells also expressed the sodium iodide symporter and thyroglobulin genes.

64 Sodium iodide symporter expression in patient tumors aft

65 MV engineered to express the sodium iodide symporter gene (MV-NIS) facilitates locali

66 profound inhibition of the expression of the sodium iodide symporter gene.

67 ted with a vaccinia virus carrying the human sodium iodide symporter GLV-1h153.

68 isease, based on decreased expression of the sodium iodide symporter SLC5A5 (NIS), diminished membran

69 A levels for thyroglobulin, thyroperoxidase, sodium iodide symporter, and deiodinase type 2, and deio

70 tinib, which modulates the expression of the sodium iodide symporter, and hence iodine uptake, in the

71 2, sodium hydrogen exchanger 3, aquaporin 7, sodium iodide symporter, and hydrogen potassium adenosin

72 Pax-8, thereby suppressing expression of the sodium iodide symporter, thyroid peroxidase, TG, and thy

73 thyroid-specific target genes thyroglobulin, sodium iodide symporter, thyroperoxidase, and thyroid-st

74 Anion transport by the human sodium-iodide symporter (hNIS) is an established target

75 man norepinephrine transporter (hNET), human sodium-iodide symporter (hNIS), a human deoxycytidine ki

76 and polymerase chain reaction for gal-3 and sodium-iodide symporter (NIS) expression.

77 We examined the sodium-iodide symporter (NIS), which promotes in vivo ce

78 h uptake into thyroid tissue mediated by the sodium-iodide symporter (NIS).

79 y antagonists increase the expression of the sodium-iodide symporter and uptake of iodine.

80 HR expression was required for expression of sodium-iodide symporter but was not required for thyrogl

81 this observation was the lack of detectable sodium-iodide symporter expression in TSHR-KO thyroid gl

82 BLI and sodium-iodide symporter imaging may be useful for in viv

83 nal obtained by firefly luciferase and human sodium-iodide symporter labeling of cardiosphere-derived

84 ansmembrane receptor Smoothened, and 13-pass Sodium-iodide symporter to extracellular vesicles (EVs)

85 9m)technetium pertechnetate (mediated by the sodium-iodide symporter), (99m)technetium sestamibi (car

86 as attributed to decreased expression of the sodium-iodide symporter.

87 virus type I thymidine kinase and the human sodium-iodide symporter.

88 yroid-stimulating hormone in stimulating the sodium-iodide symporter.

89 novel PET radioligand for imaging the human sodium/iodide symporter (hNIS).

90 t tissue and some breast cancers express the sodium/iodide symporter (NIS) and concentrate iodide.

91 The sodium/iodide symporter (NIS) concentrates iodide in the

92 The sodium/iodide symporter (NIS) has been identified as an

93 Perchlorate, thiocyanate, and nitrate are sodium/iodide symporter (NIS) inhibitors that block iodi

94 The sodium/iodide symporter (NIS) is the essential plasma me

95 The sodium/iodide symporter (NIS) is under investigation as

96 The sodium/iodide symporter (NIS) mediates active I(-) trans

97 The sodium/iodide symporter (NIS) mediates active iodide (I(

98 sitron emission tomography imaging using the sodium/iodide symporter (NIS) reporter gene revealed sta

99 The sodium/iodide symporter (NIS) stimulates iodide uptake i

100 ds to the 3'-untranslated region of PAX8 and sodium/iodide symporter (NIS), leading to impaired prote

101 wn that RET/PTC1 decreases expression of the sodium/iodide symporter (NIS), the molecule that mediate

102 se model of hypothyroidism: mice lacking the sodium/iodide symporter (NIS), the plasma membrane prote

103 in the thyroid and breast is mediated by the sodium/iodide symporter (NIS).

104 functional role in tumor progression of the sodium/iodide symporter (NIS; aka SLC5A5), which is upre

105 The rat sodium/iodide symporter gene (rNIS) was cloned into a re

106 Here we show that a specialized form of the sodium/iodide symporter in the mammary gland mediates ac

107 hese results indicate that the mammary gland sodium/iodide symporter may be an essential breast cance

108 The sodium/iodide symporter mediates active iodide transport

109 pression of TTF1 increased thyroglobulin and sodium/iodide symporter mRNA levels, cell migration, and

110 mputed tomography imaging of the hNIS (human sodium/iodide symporter) to noninvasively quantify adeno

111 sed expression of thyroglobulin (Tg) and the sodium/iodide symporter).

112 the hormonal regulation of the mammary gland sodium/iodide symporter, we demonstrate by scintigraphy

113 egulated expression of thyroglobulin and the sodium/iodide symporter.

114 The addition of sodium iodide to catalysts 2a-4a (to form 2b-4b in situ)

115 /6 mice) of various ages were measured using sodium iodide to prevent oxidative damage to DNA during

116 Addition of 1 equiv of sodium iodide to the reaction improved the chemoselectiv

117 ogenic anion that competitively inhibits the sodium iodide transporter and has been detected in forag

118 ng hormone receptor, thyroid peroxidase, and sodium iodide transporter.

119 luorine 18 fluorodeoxyglucose and iodine 131 sodium iodide were generated.

120 1 h plus an additional separation step using sodium iodide which can be used to reduce mineral residu

121 ormation of the CF2I group is based on using sodium iodide, with the sodium serving as a scavenger of

122 of one methyl group from the triesters with sodium iodide yielded monosodium salts, whereas treatmen