ライフサイエンスコーパス: vitreous humor

1 ular media surrounding the lens (aqueous and vitreous humor).

2 in the bloodstream, cerebrospinal fluid, and vitreous humor.

3 dia: nuclease-free water, aqueous humor, and vitreous humor.

4 drugs or drug delivery vehicles through the vitreous humor.

5 n D metabolite concentrations in aqueous and vitreous humor.

6 ed vitamin D(3) were detected in aqueous and vitreous humor.

7 apeutics are difficult to determine in human vitreous humor.

8 ites of OLM are the peripheral retina and/or vitreous humor.

9 hed the mechanical properties of the natural vitreous humor.

10 ied FGF, and sufficient for up-regulation by vitreous humor.

11 family are present in chicken and mammalian vitreous humor.

12 factor that is constitutively present in the vitreous humor.

13 ion with BMP2, but not to the same extent as vitreous humor.

14 iagnostic antibody testing of the aqueous or vitreous humor.

15 h enhanced leukocytes within the aqueous and vitreous humors.

16 0 for WM, 135 +/- 10 for CSF, 113 +/- 14 for vitreous humor, 103 +/- 36 for tumor, 68 +/- 11 for unaf

17 ctomized eyes was not different for both the vitreous humor (13,600 vs. 15,000 ng/day/mL; P = 0.73) a

18 Hmgb1 is accumulated in the vitreous humor 24 hours after IR.

19 distributions of the ion in the aqueous and vitreous humor after iontophoresis, passive delivery, an

20 nts of the CMV UL97 gene were amplified from vitreous humor, after which restriction digest screening

21 drug levels detectable after 24 hours in the vitreous humor and 4 hours in the RC.

22 recorded between an Ag-AgCl electrode in the vitreous humor and a reference electrode near the eye.

23 ts with an unclassified uveitis, aqueous and vitreous humor and cerebrospinal fluid were also analyze

24 d drug concentrations were determined in the vitreous humor and retina for 31 days (on days 2, 8, 15,

25 ucleated, and drug content quantified in the vitreous humor and retina-choroid tissue by high-perform

26 , high drug levels were observed in both the vitreous humor and the retina-choroid even on day 21 aft

27 , we measured GFAP levels in the aqueous and vitreous humors and plasma of 79 participants undergoing

28 affects the pars plana (attachment point of vitreous humor) and peripheral retina (9%-15%); posterio

29 l and throat swab samples and aqueous humor, vitreous humor, and blood samples.

30 orption spectroscopy in the retina, choroid, vitreous humor, and optic nerve after subconjunctival in

31 nd found a high fungal burden in the retina, vitreous humor, and optic nerve of TLR9-/- mice 3 weeks

32 and endothelium, iris, ciliary body, retina, vitreous humor, and optic nerve.

33 Blood, vitreous humor, and retina samples were collected at pre

34 sponse throughout the eye, including cornea, vitreous humor, and retina, suggesting a coordinated pro

35 ne depolarizing agent, was injected into the vitreous humor, and the role of matrix metalloproteinase

36 ans from liver, spleen, kidney, brain, lung, vitreous humor, and vena cava in comparison to untreated

37 IgG levels in the orbit, vitreous humor, aqueous humor, and plasma were negligibl

38 levels were measured in the choroid, retina, vitreous humor, aqueous humor, orbit, and plasma over 28

39 viding a multiparametric characterization of vitreous humor as a function of the time since death.

40 We also identify vitreous humor as an in vivo source of an FGF-like inter

41 which retinal tissue was often found in the vitreous humor as well as extraocularly.

42 inding angiogenic factors upregulated in PDR vitreous humor besides VEGF, thus inhibiting their biolo

43 dense vascularized structure located in the vitreous humor between the posterior surface of the lens

44 Bovine vitreous humor, but not FGF2, protected lens epithelial

45 e of albumin and fibrin into the aqueous and vitreous humor by 8 hours after infection.

46 Aqueous and vitreous humor cell counts and protein levels and histop

47 Aqueous humor (all cohorts), vitreous humor (cohort IV only), and blood samples (all

48 It is widely accepted that vitreous humor-derived FGFs are required for the differe

49 In contrast, vitreous humor did not reduce invasion.

50 dose of DPT-GFX sustained aqueous humor and vitreous humor drug levels during the 24-hour study, wit

51 Nanotubes persisted in the vitreous humor during the 15 days study and pazopanib le

52 of SVD include fibrillar degeneration of the vitreous humor, early-onset cataract, minute crystalline

53 DEX was detected in the retina and vitreous humor for 6 months, with peak concentrations du

54 Proteins in vitreous humor from bovine eyes were analyzed by Western

55 matter (WM), cerebrospinal fluid (CSF), and vitreous humor in 20 patients with pathologically proven

56 n (ET)-1 levels are increased in aqueous and vitreous humor in patients with glaucoma and animal mode

57 concentrations in the aqueous humor and the vitreous humor in the early dark phase showed no differe

58 d medium or medium supplemented with FGFs or vitreous humor, in the presence or absence of the FGF re

59 mber and posterior chamber (ACPC), lens, and vitreous humor increased logistically with ACPC expandin

60 e of the lens differentiation signals in the vitreous humor is a ligand for FR3, and is therefore lik

61 Injection of KA into the vitreous humor led to an up-regulation in tPA and an ind

62 7 of whom underwent aqueous humor (n = 5) or vitreous humor (n = 2) analysis and cerebrospinal fluid

63 ediate uveitis with neither snowballs in the vitreous humor nor snowbanks on the pars plana.

64 actor-alpha (TNFalpha) were evaluated in the vitreous humor obtained from patients with type 2 diabet

65 ast milk, respiratory samples, biopsies, and vitreous humor) obtained longitudinally or from differen

66 last growth factor (bFGF) accumulates in the vitreous humor of 3- and 8-week diabetic rats.

67 city, kainic acid (KA) was injected into the vitreous humor of B6.Cg-Tg(Thy1-YFP)HJrs/J mice.

68 tified and purified to near homogeneity from vitreous humor of bovine eyes.

69 stimulates non-NMDA-type receptors, into the vitreous humor of CD-1 mice and have investigated the ro

70 Here, we provide evidence in both vitreous humor of diabetic patients and in retina of a m

71 ate the inflammatory cytokine profile in the vitreous humor of diabetic patients with retinopathy und

72 Depleting vitreous humor of heparin-binding growth factors or trea

73 xpressing PRV strains were injected into the vitreous humor of one eye, and virus replication and spr

74 tes the expression of opticin as seen in the vitreous humor of ROP and could serve as a potential tar

75 ) in vivo, lactacystin was injected into the vitreous humor of the developing chicken eye.

76 ity of biological media such as blood or the vitreous humor of the eye in situ.

77 associated with the collagen network of the vitreous humor of the eye.

78 coprotein that the authors discovered in the vitreous humor of the eye.

79 ciated virus encoding GUSB directly into the vitreous humor of young adult mice.

80 ia isolates were recovered by cultivation of vitreous humor on chocolate agar and identified via conv

81 pressures that direct the movement of fluid (vitreous humor or cerebrospinal fluid) into and under th

82 ivo NIR fluorescence or ELISA in homogenized vitreous humor, reflecting the greater spatial resolutio

83 contrast, total protein concentration in the vitreous humor remained unchanged.

84 he 15 days study and pazopanib levels in the vitreous humor, retina, and choroid-RPE at the end of th

85 avage rates were developed and tested in the vitreous humor, RPE cell homogenates and intact RPE cell

86 Crucially, vitreous humor samples from PDR patients displayed highe

87 attractant protein 1 (MCP-1) was reported in vitreous humor samples of patients with RD and diabetic

88 amples, 1 of 3 aqueous humor samples, 3 of 5 vitreous humor samples, and 4 of 5 blood samples.

89 Bovine vitreous humor stimulated chicken embryo lens epithelial

90 tem, in which chicken embryo or adult bovine vitreous humor stimulates chicken embryo lens epithelial

91 hesives, and are now being investigated as a vitreous humor substitute.

92 Detection of collagenase in the vitreous humor suggested that infiltration was facilitat

93 Explants were also cultured in vitreous humor that had been depleted of heparin-binding

94 ate the intraocular environment (aqueous and vitreous humors), the capsular tissue, and the intraocul

95 Vitreous humor, the presumptive source of differentiatio

96 (TSD) via recognition and quantification of vitreous humor (VH) cystine as well as provide the porta

97 and RN6390DeltatarO were cultured in bovine vitreous humor (VH) in vitro or inoculated into the vitr

98 d settling velocity of the suspension in the vitreous humor was 3 cm/h.

99 nvitrectomized versus vitrectomized eyes for vitreous humor was 791 ng/mL (day 22) versus 731 ng/mL (

100 traocular pressure and the level of Hmgb1 in vitreous humor was analyzed 24 hours after reperfusion.

101 s 13 and 21 in groups A and B, respectively, vitreous humor was aspirated and concentrations of ampho

102 e chain reaction (PCR) testing of aqueous or vitreous humor was positive for herpes simplex virus (HS

103 /g (day 60) and 47,200 ng . d/g, and for the vitreous humor were 213 ng/mL (day 60) and 11,300 ng . d

104 Aqueous humor and vitreous humor were collected, and their protein concent

105 protein concentrations in aqueous humor and vitreous humor were determined in both eyes.

106 At the time of death, corneas or vitreous humors were cultured to determine the number of

107 size exhibited 3.5-fold lower solubility in vitreous humor, when compared with its sodium salt.

108 ity was measured in the central plane of the vitreous humor with an SLO.

109 (rPAI-1) or tPA-STOP were injected into the vitreous humor with KA, whereas a plasmin inhibitor, alp

110 itreal injection of fluorescein targeted the vitreous humor with no significant selectivity for poste