ライフサイエンスコーパス: eye lens

1 cally altering the optical properties of the eye lens.

2 d crystallin proteins extracted from a sheep eye lens.

3 1.98 x 10(-9)), a major protein component of eye lens.

4 f UV-damaged human gammaD-crystallins in the eye lens.

5 0, the most abundant membrane protein of the eye lens.

6 n component in the nucleus of the vertebrate eye lens.

7 is a highly stable structural protein of the eye lens.

8 abundant structural component of vertebrate eye lens.

9 he aggregation of crystallin proteins in the eye lens.

10 gammaD-crystallin (gammaD), a protein in the eye lens.

11 the refractive properties of the transparent eye lens.

12 g the predominant proteins of the vertebrate eye lens.

13 ial role in the development of a transparent eye lens.

14 (2D IR) spectra on tissue slices of porcine eye lenses.

15 ure group when compared to the control, with eye lens abnormalities being the most prominent of all a

16 Eye lens alpha-crystallin is a member of the small heat

17 simulations, and analysis show that aqueous eye lens alpha-crystallin solutions exhibit a glass tran

18 d dynamics of dilute and concentrated bovine eye lens alpha-crystallin solutions, using small-angle X

19 ll Hsps (sHsps) and the structurally related eye lens alpha-crystallins are ubiquitous stress protein

20 Whole eye lens and alpha-crystallin gels and solutions were in

21 Crystallins are major proteins of the eye lens and essential for lens transparency.

22 n establishing the optical properties of the eye lens and in maintaining its transparency.

23 We suggest routine dosimetry measurement of eye lens and proper protection for patients with benign

24 analogy with the diverse crystallins of the eye lens and with the putative enzyme-crystallins (aldeh

25 form complex organs such as brain vesicles, eyes, lens and olfactory placodes.

26 tes, they act to maintain the clarity of the eye lens, and in humans, sHsp mutations are linked to my

27 of erythrocytes), central fibre cells of the eye lens, and keratinocytes.

28 t been confirmed as a function of the intact eye lens, and no mechanism for lens phagocytosis has bee

29 amniote lateral line system), as well as the eye lenses, and most cranial sensory neurons.

30 beta gamma-Crystallins from the eye lens are proteins consisting of two domains joined b

31 betagamma-crystallins from the eye lens are proteins consisting of two similar domains

32 Here, we used fiber cells of the vertebrate eye lens as a model system to determine how the membrane

33 gation presents finite element models of the eye lens based on data from human lenses aged 16 and 35

34 erized by the clouding of the normally clear eye lens brought about by deposition of crystallin prote

35 Tryptophan can be oxidized in the eye lens by both enzymatic and non-enzymatic mechanisms.

36 hous aggregation of gamma-crystallins in the eye lens causes cataract, a widespread disease of aging.

37 ntiation of muscle, lung, liver, thymus, and eye lens cells during mouse embryo development.

38 of alphaVbeta5-mediated phagocytosis by the eye lens could result in accumulation of toxic cell debr

39 The eye lens Crystallin proteins are subject to UV irradiati

40 elopment and regulates the expression of the eye lens crystallins.

41 ozygous for HIV-1 protease expression in the eye lens, display degradation of some lens crystallins a

42 long-lived, unusually stable proteins of the eye lens exhibiting duplicated, double Greek key domains

43 bohydrate intake may be optimized to prolong eye lens function.

44 In the human eye lens, gammaS-crystallin (gammaS-WT) forms a densely

45 l procedure time, and radiation exposures to eye lens, hands, and legs were recorded.

46 he contralateral breast, ipsilateral eye and eye lens, heart, ipsilateral lung, and thymus.

47 distance between the bismuth shield and the eye lens helped reduce CT number errors, but the increas

48 pecific crystallin, a major component of the eye lens in elephant shrews (Macroscelidea).

49 The eye lens is an encapsulated avascular organ whose functi

50 Here, we demonstrate that the eye lens is capable of phagocytizing extracellular lens

51 The human eye lens is composed of fiber cells packed with crystall

52 The eye lens is dependent upon a network of gap junction-med

53 The eye lens is packed with soluble crystallin proteins, pro

54 finding that lipoxygenase expression in the eye lens is restricted to the region at which organelle

55 or intrinsic protein (MIP) of the vertebrate eye lens is the first identified member of a sequence-re

56 Age-related cataract, an opacity of the eye lens, is the leading cause of visual impairment in t

57 diation doses for the left hand, right hand, eye lens, left leg, and right leg were 0.28, 0.28, 0.03,

58 he core function of gammaS-crystallin in the eye lens may be precisely its capacity to preserve a rob

59 Preferential accumulation of Se in the eye lens may suggest a direct cause-and-effect relations

60 Radiocarbon dating of eye lens nuclei from 28 female Greenland sharks (81 to 5

61 that maps to mouse Chromosome 1 close to the eye lens obsolescence mutation (Cryge(Cat2-Elo)), a memb

62 quired a role as a structural protein in the eye lens of elephant shrews, members of an ancient order

63 termine that the speciation of Se within the eye lens of the intact larva was a selenomethionine-like

64 allin genes that are expressed highly in the eye lens of this jellyfish.

65 (crystallins) of the transparent, refractive eye lens of vertebrates are a surprisingly diverse group

66 0 (AQP0), the major intrinsic protein of the eye lens, plays a vital role in maintaining lens clarity

67 n (HgammaD-Crys) is a two-domain, beta-sheet eye lens protein found in the lens nucleus.

68 The structural eye lens protein gammaD-crystallin is a major component

69 interactions in the natively monomeric human eye lens protein gammad-crystallin, whose aggregation le

70 in (gammaS) is an important human and bovine eye lens protein involved in maintaining the transparenc

71 Human gammaD-crystallin is an eye lens protein that aggregates into amyloid fibrils un

72 D-crystallin (HgammaD-Crys) is a very stable eye lens protein that must remain soluble and folded thr

73 nvestigate the aggregation propensity of the eye-lens protein gammaS-crystallin.

74 Human betaB1-crystallin is a major eye-lens protein that undergoes in vivo truncation at th

75 ene encoding gamma-B crystallin, a mammalian eye-lens protein, modulate the rates of translation and

76 an interesting evolutionary link between the eye lens proteins and the ancestral intermediate filamen

77 Eye lens proteins arose separately and make up a diverse

78 loss through the large-scale aggregation of eye lens proteins as a result of ageing or congenital mu

79 (non-Trp) fluorescence of porcine and human eye lens proteins was identified by Mass Spectrometry (M

80 J3-crystallin, one of the three major eye-lens proteins of the cubomedusan jellyfish (Tripedal

81 Eye lens radiation dose may be higher with a flat-panel

82 Eye lens radiation dose was significantly higher for pro

83 igh refractive index and transparency of the eye lens require uniformly shaped and precisely aligned

84 Lengsin is an eye lens-specific member of the glutamine synthetase (GS

85 e major protein components of the vertebrate eye lens that maintain lens transparency, are exposed to

86 o classes of channel-forming proteins in the eye lens, the water channel aquaporin-0 (AQP-0) and the

87 Although larger in the decentralized eyes, lens thickness appeared unchanged in either eye fo

88 olipids and proteins from both intact bovine eye lens tissue and tissue ablated by ultrashort laser p

89 eral tens of micrometers from the surface of eye lens tissue while leaving the underlying tissue rela

90 Human eye lens transparency requires life long stability and s

91 sing distance between the bismuth shield and eye lens was also investigated.

92 The sole crystallin of the scallop eye lens was found to be homologous to Omega-crystallin,

93 This is well illustrated in the eye lens where epithelial cells elongate extensively dur

94 ens protein found in the outer region of the eye lens, where the refractive index is low.

95 The proteins of the eye lens, which do not turn over throughout life, underg

96 d SOD activity on in vitro incubation of the eye lens with 55mM glucose.

97 les measured along the optical axis of human eye lenses with age-related nuclear cataract showed incr

98 ntially accumulated to highest levels in the eye lens, with lower levels in the retina, yolk and othe