ライフサイエンスコーパス: cataractous

1 inhibition, retain their LFC nuclei, and are cataractous.

2 were determined in young, precataractous and cataractous alphaA knockout lenses.

3 GSH levels decreased with increasing age in cataractous alphaA(-/-) lenses but not in the noncatarac

4 RNAs from 50 pooled cataractous and 25 pooled noncataractous epithelia were

5 Cataractous and aged human lenses were hydrolyzed and fr

6 and insoluble (WIS; P < 0.05) fractions from cataractous and normal lenses.

7 in gene expression were detected between the cataractous and the noncataractous epithelia.

8 WI) lens fractions from young, aged, nuclear cataractous, and brunescent cataractous lenses.

9 Cataractous canine LEC demonstrated significantly (P < 0

10 Normal and cataractous canine LECs were evaluated for expression of

11 choroidal coloboma is associated with early cataractous changes.

12 erminus, observed in the control nuclear and cataractous cortical membranes, was not observed in the

13 were immunoprecipitated from young, old, and cataractous crystallins using affinity-purified CML anti

14 s the baby boomer population moves into the "cataractous decades," the number of patients requiring c

15 omly selected single eye in bilateral cases; cataractous eye in unilateral cases) and to compare the

16 AL of the unilateral cataractous eye was significantly shorter than that of t

17 compare the biometry data of the unilateral cataractous eye with the data of the corresponding nonca

18 kening, and cataract surgery in an initially cataractous eye.

19 To report the biometry data of pediatric cataractous eyes (randomly selected single eye in bilate

20 dwork for calculating pediatric IOL power in cataractous eyes by using pediatric ocular measurements.

21 Fifty cataractous eyes scheduled for surgery between July and

22 r estrone treatment reduced the incidence of cataractous eyes to 12% or 25%, respectively.

23 Reduced signal strength in cataractous eyes was found in 65% of the 800-nm OCT imag

24 erior visualization of the posterior pole in cataractous eyes.

25 The H-chain identified in cataractous fiber cells (29 kDa) differed from the 21-kD

26 RC causes age-onset cataract in mice and the cataractous human lens has increased expression of osteo

27 Young, old, and cataractous human lens protein fractions were glycated w

28 tein was readily detected in the cortex of a cataractous human lens.

29 llin mutation was detected in an age-matched cataractous human lens.

30 Calcium is elevated in most cataractous human lenses and may contribute to cataracto

31 f a novel process occurring predominately in cataractous human lenses.

32 n of these domains in membranes of clear and cataractous human lenses.

33 se of blindness worldwide, is to extract the cataractous lens and implant an artificial intraocular l

34 ystallin is bound to the membrane of old and cataractous lens cells in vivo.

35 binding, and generation of free radicals by cataractous lens crystallins can be duplicated by ascorb

36 ly correlated (r = +0.58), suggesting that a cataractous lens does not influence the MP measurement t

37 Cell density in cataractous lens epithelia was similar to that in normal

38 owever, no method to halt the formation of a cataractous lens has been shown to be effective.

39 be part of a defense mechanism by which the cataractous lens limits iron-catalyzed oxidative damage.

40 rison of diffraction patterns indicated that cataractous lens membranes contained more pronounced and

41 The cataractous lens opacity decreases as the mice age.

42 y examine the structural organization of the cataractous lens plasma membrane versus control.

43 Enzyme-digested cataractous lens proteins displayed 3OHKYN-derived modif

44 showed consistently stronger reactions with cataractous lens proteins than those from noncataractous

45 Brunescent cataractous lens proteins were digested by enzymes, the

46 acquired in 100-mum steps across normal and cataractous lens sections.

47 d female presented with a partially absorbed cataractous lens that was dislocated into the anterior c

48 shi et al. toward the dream of replacing the cataractous lens with a flexible artificial lens, suppor

49 umulation of light-scattering centers in the cataractous lens.

50 a novel L52F alphaA-crystallin mutation in a cataractous lens.

51 of higher order associates in the aging and cataractous lens.

52 f Na,K-ATPase is markedly upregulated in the cataractous lens.

53 atched, aged (16.1 +/- 8 pmol/mg) or nuclear cataractous lenses (49.0 +/- 26 pmol/mg).

54 A irradiation, pigmented proteins from human cataractous lenses also oxidized ASC.

55 were isolated from both normal (control) and cataractous lenses and assayed for cholesterol and phosp

56 ritin H-chain and its distribution in canine cataractous lenses compared with noncataractous lenses.

57 chain was distributed differently throughout cataractous lenses compared with noncataractous lenses.

58 soluble proteins and was higher in a pool of cataractous lenses compared with normal aged lenses, rea

59 Ferritin from cataractous lenses contained more H-chain and bound 11-f

60 In cataractous lenses from eye bank eyes, cell density in t

61 racting crystalline deposits were present in cataractous lenses from two affected family members but

62 nd increase transparency in dissected rabbit cataractous lenses in vitro and cataract severity in viv

63 e loss of protein observed in human cortical cataractous lenses in vivo.

64 ndergone cataract surgery and epithelia from cataractous lenses of eye bank eyes were compared with e

65 erritin was comparable in noncataractous and cataractous lenses of similarly aged dogs.

66 projections of z-series from aged normal and cataractous lenses suggested that some of the stained li

67 weight complex obtained from young, old, and cataractous lenses suggesting potential interactions bet

68 roximately seven times greater in brunescent cataractous lenses than in aged noncataractous lenses.

69 Cataractous lenses were grouped into four classification

70 and C-terminal cleavage in selenite-induced cataractous lenses were identified.

71 Whole human cataractous lenses were obtained from donors after extra

72 rtical and nuclear regions of aged clear and cataractous lenses were obtained.

73 blocked all patterned visual input until the cataractous lenses were removed and the affected eyes fi

74 ound, the argpyrimidine levels in brunescent cataractous lenses were significantly higher (254.0 +/-

75 e dnajb1a morphants exhibited underdeveloped cataractous lenses with persistent apoptotic nuclei.

76 CML-rich proteins (immunoprecipitated from cataractous lenses) oxidized ascorbate approximately 4 t

77 he disulfide bonded gamma S-crystallins from cataractous lenses, supports this hypothesis.

78 t directly contribute to light-scattering in cataractous lenses.

79 ly the only treatment is surgical removal of cataractous lenses.

80 g, aged, nuclear cataractous, and brunescent cataractous lenses.

81 y significant differences between normal and cataractous lenses.

82 vels with no differences between control and cataractous lenses.

83 e not continuous with LFC plasma membrane of cataractous lenses.

84 ction analyses of the sterol-poor regions of cataractous membranes indicated increased membrane rigid

85 tectable amounts of light-density domains in cataractous membranes suggest either disruption of these

86 rable for sedimenting fractions of clear and cataractous membranes.

87 We identified a dominant cataractous mouse line (L1), caused by a missense alpha8

88 A dominant cataractous mouse line was identified from chemically in

89 -S11R mutant protein, was identified in this cataractous mouse line.

90 slit lamp screening, we identified two mouse cataractous mutant lines.

91 cortical membranes, was not observed in the cataractous nuclear membranes.

92 This size range corresponds well to MLBs in cataractous nuclei (average MLB radius, 1.4 microm) and,

93 close to the observed dimensions of MLBs in cataractous nuclei.

94 of young adult mouse lenses, these areas in cataractous old mouse lenses were found to contain accum

95 tly into the underlying cortex, resulting in cataractous opacities.

96 nescent lens proteins than in either nuclear cataractous or normal lenses.

97 Both normal and cataractous oriented membranes yielded meridional diffra

98 Lens fiber swelling and related cataractous outgrowth positively correlated to the degre

99 ffractive, are highly suited for working-age cataractous patients in terms of visual outcomes, readin

100 A uptake was markedly suppressed in diabetic cataractous rat lenses, which accumulated both the F-DHA

101 expression of the MT IIA gene in age-related cataractous relative to normal human lenses, suggesting

102 displayed lower levels of expression in the cataractous samples compared with that in the noncatarac

103 These were correlated with cataractous stages visually observed by slit lamp biomic

104 ded species are precursors to the aggregated cataractous states responsible for light scattering.

105 d Cu(II) binding was 20% to 30% increased in cataractous versus old and young lenses in WS (P < 0.01)

106 rkedly elevated in WS and WIS fractions from cataractous versus old or young crystallins (20% to seve

107 Control and cataractous whole lens membranes had C/P mole ratios of