ライフサイエンスコーパス: ciliary muscle

1 e intraocular pressure via relaxation of the ciliary muscle.

2 annular electrode operating as an artificial ciliary muscle.

3 through receptor-mediated mechanisms in the ciliary muscle.

4 as observed in the ciliary processes and the ciliary muscle.

5 djacent sclera and could be traced up to the ciliary muscle.

6 n that TIGR protein also is expressed in the ciliary muscle.

7 the isolated human outflow system devoid of ciliary muscle.

8 decreases the amount of TIGR protein in the ciliary muscle.

9 alter the amount of TIGR protein within the ciliary muscle.

10 rved in ciliary muscle fibers throughout the ciliary muscle.

11 ular anterior segments, which lack an intact ciliary muscle.

12 outflow tissues in the absence of an intact ciliary muscle.

13 ial preparations of isolated human or monkey ciliary muscles.

14 sting the shape of its lens with the help of ciliary muscles.

15 as decreased and structurally altered in the ciliary muscle (46 +/- 5.6%) and trabecular meshwork (37

16 olvement occurred in the ciliary body and/or ciliary muscle (7 eyes [58%]), iris (6 eyes [50%]), and

17 ermine the cellular distribution of MMP-1 in ciliary muscle, additional sections were double-immunost

18 Moderate labeling was detected in the ciliary muscle and in the blood vessels of the ciliary b

19 and the functional relationship between the ciliary muscle and lens during aging are unclear.

20 ceptors do not mediate the relaxation of the ciliary muscle and reduction of intraocular pressure in

21 Ciliary muscle and sphincter isolated from cows, cats, d

22 poral relationship between thickening of the ciliary muscle and the onset of myopia.

23 sses through extracellular spaces within the ciliary muscle and then through the suprachoroidal space

24 ured human eyes, or on contraction of bovine ciliary muscle and trabecular meshwork strips.

25 Contraction of fresh bovine ciliary muscle and trabecular meshwork was measured isom

26 r inflow and outflow and in contractility of ciliary muscle and trabecular meshwork.

27 ptors solubilized from human iris sphincter, ciliary muscle, and ciliary processes.

28 ected in the anterior corneal stroma, in the ciliary muscle, beneath the anterior border of the iris,

29 y (OD) along two line segments overlying the ciliary muscle, by using a high-resolution imaging densi

30 expression in preconfluent and postconfluent ciliary muscle cell cultures by immunocytochemistry.

31 hypothesis that increased MMP production by ciliary muscle cells has a role in increasing uveosclera

32 ior segment tissues as well as expression in ciliary muscle cells in vitro.

33 undertaken to determine whether treatment of ciliary muscle cells with the prostaglandin (PG) analogu

34 In the cultured ciliary muscle cells, calponin stained straight cable-li

35 landin FP receptor were downregulated in the ciliary muscle cells.

36 at ciliary muscle MMP-1 was primarily inside ciliary muscle cells.

37 es in extracellular matrix (ECM) adjacent to ciliary muscle cells.

38 n cell membranes isolated from rhesus monkey ciliary muscle, ciliary processes, trabecular meshwork,

39 WDR36 gene expression in lens, iris, sclera, ciliary muscles, ciliary body, trabecular meshwork, reti

40 meshwork (TM) cells and nontransformed human ciliary muscle (CM) cells were used.

41 Ciliary muscle contractile activity remains active in al

42 Age-related changes in lens elasticity and ciliary muscle contractility can affect how ocular param

43 on HCSM may be relevant to the regulation of ciliary muscle contraction and aqueous humor outflow.

44 g to the findings, authors suggest that both ciliary muscle contraction and ciliary body edema may pl

45 The per diopter ciliary muscle contraction is age independent, even as t

46 ing aqueous outflow, probably by stimulating ciliary muscle contraction.

47 The ciliary muscle controls the shape of the lens through th

48 Human TM and three other ocular cells (ciliary muscle, corneoscleral fibroblast, and lamina cri

49 se changes in uveoscleral outflow across the ciliary muscle could cause elevation of intraocular pres

50 Parallel assessments of RNA from ciliary muscle cultures exposed to latanoprost acid for

51 and William Wallace had all zeroed in on the ciliary muscle, describing its anatomy in varying detail

52 A decrease in the unaccommodated ciliary muscle diameter, along with the previously noted

53 ngs quantify the movements of the zonule and ciliary muscle during accommodation, and identify their

54 ation and support the view that reduction of ciliary muscle ECM may contribute to increased uveoscler

55 data support the possibility that changes in ciliary muscle ECM may contribute to increased uveoscler

56 This fluorescence in the ciliary muscle extended from the posterior edge of the c

57 lymphocytes and macrophages dispersed among ciliary muscle fibers and in the iris.

58 MT2 and CMT3), but paradoxically, the apical ciliary muscle fibers are thicker in hyperopia (CMTMAX a

59 ata indicated that in children the posterior ciliary muscle fibers are thicker in myopia (CMT2 and CM

60 IGR protein immunoreactivity was observed in ciliary muscle fibers throughout the ciliary muscle.

61 Apical ciliary muscle fibers were obtained by subtracting corre

62 the ciliary muscle to increase spaces among ciliary muscle fibers, thereby reducing hydraulic resist

63 development of new IOLs designed to harness ciliary muscle forces.

64 In the ciliary muscle, FP receptor mRNA transcript was predomin

65 rmation may be altered in glaucomatous human ciliary muscle (g-HCM) cells compared with normal (n)-HC

66 talloproteinase (MMP)-2 secretion from human ciliary muscle (HCM) cells.

67 owman and Brucke wrong about the role of the ciliary muscle in accommodation, and for different reaso

68 ry for ciliary ganglion neurons to innervate ciliary muscle in the eye.

69 meshwork, Schlemm's canal, scleral spur, and ciliary muscle indicates a structural or functional role

70 ong calponin immunoreactivity was present in ciliary muscle, iris dilator and sphincter muscles, and

71 ensity was approximately fivefold greater in ciliary muscle, iris root, and sclera than in trabecular

72 Calponin is expressed in human ciliary muscle, iris smooth muscles, blood vessel smooth

73 d distribution of calponin proteins in human ciliary muscle, iris, and other anterior segment tissues

74 trong MMP-1 immunoreactivity was observed in ciliary muscle, iris, sclera, corneal endothelium, and c

75 Sympathetic stimulation of the ciliary muscle is believed to be inhibitory, decreasing

76 in the extracellular matrix (ECM) of monkey ciliary muscle is reduced during anterior segment inflam

77 use uveoscleral outflow, which traverses the ciliary muscle, is increased by prostaglandins (PGs), th

78 -1 by 3- to 13-fold in three of five primary ciliary muscle lines.

79 Confocal microscopy showed that ciliary muscle MMP-1 was primarily inside ciliary muscle

80 During accommodation the ciliary muscle moved forward by approximately 1.0 mm, pu

81 h intracellularly and extracellularly in the ciliary muscle of the cynomolgus monkey.

82 imics the design of the crystalline lens and ciliary muscle of the human eye.

83 due to direct action of phenylephrine on the ciliary muscle or to secondary optical factors associate

84 e POAG regions compared with normal regions--ciliary muscle (P < 0.001), ciliary stroma (P < 0.001),

85 reflects a direct effect of PGs on specific ciliary muscle prostanoid receptors.

86 Human ciliary muscle proteins were analyzed by polyacrylamide

87 yperopia is associated with a thicker apical ciliary muscle region.

88 eshwork, Schlemm's canal, ciliary processes, ciliary muscle, retina, choroid, cultured RPE cells, and

89 Measurements of the ciliary muscle ring diameter (based on the inner apex),

90 Age was not related to ciliary muscle ring diameter (CMRD) or lens equatorial d

91 crease in the diameter of the unaccommodated ciliary muscle ring was highly correlated with advancing

92 scle extended from the posterior edge of the ciliary muscle's tail into the anterior choroid.

93 To assess antibody labeling of ciliary muscle structures, additional sections were doub

94 In the ciliary muscle, the functional responses to ERK1/2 activ

95 decreased (-0.105 mm/D, P < 0.001), and the ciliary muscle thickened anteriorly (+0.013 to +0.026 mm

96 e used to determine the relationship between ciliary muscle thickness in various regions of the muscl

97 r diopter of accommodation in LED, CMRD, and ciliary muscle thickness were not related to subject age

98 In linear models with ciliary muscle thicknesses and SPHEQ, SPHEQ was signific

99 tomographer was used to measure cycloplegic ciliary muscle thicknesses at 1 mm (CMT1), 2 mm (CMT2),

100 ar refractive power; this is mediated by the ciliary muscle through the zonule.

101 initiate the alteration of collagens in the ciliary muscle to increase spaces among ciliary muscle f

102 ic pathway activating the iris sphincter and ciliary muscle to mediate pupillary constriction and len

103 it may have a structural role in maintaining ciliary muscle tone.

104 wo line segments overlying the immunostained ciliary muscle using two-dimensional imaging densitometr

105 Staining intensity in the ciliary muscle was assessed by measuring optical density

106 The distribution of TIGR protein in the ciliary muscle was determined by confocal scanning laser

107 Ciliary muscle was incubated in the absence and presence

108 theory of accommodation, the anatomy of the ciliary muscle was well known.

109 cultures from normal and glaucomatous human ciliary muscle were established and characterized.

110 es extracellular matrix remodeling of ocular ciliary muscle, with a resultant increase in drainage of