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1 the understanding of crowding effects in the eye lens.
2 out the growth of a key optical element, the eye lens.
3  the most abundant chaperone proteins in the eye lens.
4 the refractive properties of the transparent eye lens.
5 g the predominant proteins of the vertebrate eye lens.
6 ial role in the development of a transparent eye lens.
7 nd the most abundant membrane protein in the eye lens.
8  reduction of total cholesterol level in the eye lens.
9 lins comprise the protein-rich tissue of the eye lens.
10  involved in cholesterol biosynthesis in the eye lens.
11  most abundant membrane protein of the human eye lens.
12 for the optical properties of the vertebrate eye lens.
13 es a basis for understanding its role in the eye lens.
14 he aggregation of crystallin proteins in the eye lens.
15 cally altering the optical properties of the eye lens.
16 d crystallin proteins extracted from a sheep eye lens.
17 1.98 x 10(-9)), a major protein component of eye lens.
18 f UV-damaged human gammaD-crystallins in the eye lens.
19 0, the most abundant membrane protein of the eye lens.
20 n component in the nucleus of the vertebrate eye lens.
21 is a highly stable structural protein of the eye lens.
22  abundant structural component of vertebrate eye lens.
23 gammaD-crystallin (gammaD), a protein in the eye lens.
24  (2D IR) spectra on tissue slices of porcine eye lenses.
25 ure group when compared to the control, with eye lens abnormalities being the most prominent of all a
26                                              Eye lens alpha-crystallin is a member of the small heat
27  simulations, and analysis show that aqueous eye lens alpha-crystallin solutions exhibit a glass tran
28 d dynamics of dilute and concentrated bovine eye lens alpha-crystallin solutions, using small-angle X
29 ll Hsps (sHsps) and the structurally related eye lens alpha-crystallins are ubiquitous stress protein
30                                        Whole eye lens and alpha-crystallin gels and solutions were in
31        Crystallins are major proteins of the eye lens and essential for lens transparency.
32 n establishing the optical properties of the eye lens and in maintaining its transparency.
33  We suggest routine dosimetry measurement of eye lens and proper protection for patients with benign
34  analogy with the diverse crystallins of the eye lens and with the putative enzyme-crystallins (aldeh
35  form complex organs such as brain vesicles, eyes, lens and olfactory placodes.
36 tes, they act to maintain the clarity of the eye lens, and in humans, sHsp mutations are linked to my
37 of erythrocytes), central fibre cells of the eye lens, and keratinocytes.
38 t been confirmed as a function of the intact eye lens, and no mechanism for lens phagocytosis has bee
39 amniote lateral line system), as well as the eye lenses, and most cranial sensory neurons.
40              beta gamma-Crystallins from the eye lens are proteins consisting of two domains joined b
41               betagamma-crystallins from the eye lens are proteins consisting of two similar domains
42 n proteins, the dominant constituents of the eye lens, are prototypes of long-lived proteins.
43  Here, we used fiber cells of the vertebrate eye lens as a model system to determine how the membrane
44 gation presents finite element models of the eye lens based on data from human lenses aged 16 and 35
45 erized by the clouding of the normally clear eye lens brought about by deposition of crystallin prote
46            Tryptophan can be oxidized in the eye lens by both enzymatic and non-enzymatic mechanisms.
47 hous aggregation of gamma-crystallins in the eye lens causes cataract, a widespread disease of aging.
48 ntiation of muscle, lung, liver, thymus, and eye lens cells during mouse embryo development.
49        Defective cholesterol biosynthesis in eye lens cells is often associated with cataracts; howev
50                        The correspondence of eye lens core Delta(14)C with a regional reference serie
51  bomb radiocarbon chronometer which utilized eye lens cores instead of more traditional otolith cores
52  of alphaVbeta5-mediated phagocytosis by the eye lens could result in accumulation of toxic cell debr
53                                          The eye lens Crystallin proteins are subject to UV irradiati
54 elopment and regulates the expression of the eye lens crystallins.
55   Finally, Hspb1 knockdown in Xenopus causes eye/lens defects.
56 nd how they contribute to distinct stages of eye lens development.
57 is in 7 eyes, afferent pupillary defect in 6 eyes, lens dislocation or subluxation in 5 eyes, and cyc
58 ozygous for HIV-1 protease expression in the eye lens, display degradation of some lens crystallins a
59 ts role as a structural protein in the human eye lens essential for its optical transparency.
60 long-lived, unusually stable proteins of the eye lens exhibiting duplicated, double Greek key domains
61 ns of AQP0 isolated and purified from bovine eye lens, existing as multiple forms due to the differen
62 , the most prevalent membrane protein in the eye lens, from the early days when AQP0 was a protein of
63 bohydrate intake may be optimized to prolong eye lens function.
64                                 In the human eye lens, gammaS-crystallin (gammaS-WT) forms a densely
65 l procedure time, and radiation exposures to eye lens, hands, and legs were recorded.
66 he contralateral breast, ipsilateral eye and eye lens, heart, ipsilateral lung, and thymus.
67  distance between the bismuth shield and the eye lens helped reduce CT number errors, but the increas
68 pecific crystallin, a major component of the eye lens in elephant shrews (Macroscelidea).
69 ade it possible to investigate growth of the eye lens in the zebrafish.
70 oned primarily in the eyes (specifically the eye lens, iris, and retinal pigmented epithelium), diges
71                                          The eye lens is an encapsulated avascular organ whose functi
72                Here, we demonstrate that the eye lens is capable of phagocytizing extracellular lens
73                                    The human eye lens is composed of fiber cells packed with crystall
74                  The spheroidal shape of the eye lens is crucial for precise light focusing onto the
75                                          The eye lens is dependent upon a network of gap junction-med
76                                          The eye lens is packed with soluble crystallin proteins, pro
77  finding that lipoxygenase expression in the eye lens is restricted to the region at which organelle
78 or intrinsic protein (MIP) of the vertebrate eye lens is the first identified member of a sequence-re
79      Age-related cataract, an opacity of the eye lens, is the leading cause of visual impairment in t
80 relate of opacity or light scattering in the eye lens, is usually caused by the presence of high-mole
81 ed DNA damage in the epithelial cells of the eye lens (LECs) has been proposed as a possible contribu
82 diation doses for the left hand, right hand, eye lens, left leg, and right leg were 0.28, 0.28, 0.03,
83 he core function of gammaS-crystallin in the eye lens may be precisely its capacity to preserve a rob
84       Preferential accumulation of Se in the eye lens may suggest a direct cause-and-effect relations
85                        Radiocarbon dating of eye lens nuclei from 28 female Greenland sharks (81 to 5
86                 The gamma-crystallins of the eye lens nucleus are among the longest-lived proteins in
87 stallin, a monomeric protein abundant in the eye lens nucleus, must remain stably folded for an indiv
88 that maps to mouse Chromosome 1 close to the eye lens obsolescence mutation (Cryge(Cat2-Elo)), a memb
89 quired a role as a structural protein in the eye lens of elephant shrews, members of an ancient order
90 termine that the speciation of Se within the eye lens of the intact larva was a selenomethionine-like
91 allin genes that are expressed highly in the eye lens of this jellyfish.
92 (crystallins) of the transparent, refractive eye lens of vertebrates are a surprisingly diverse group
93 three-dimensional gradient index profiles in eye lenses of zebrafish from late larval to adult stages
94 0 (AQP0), the major intrinsic protein of the eye lens, plays a vital role in maintaining lens clarity
95 erization of aqueous solutions of the bovine eye lens protein beta(H) crystallin from dilute conditio
96 n (HgammaD-Crys) is a two-domain, beta-sheet eye lens protein found in the lens nucleus.
97                               The structural eye lens protein gammaD-crystallin is a major component
98 interactions in the natively monomeric human eye lens protein gammad-crystallin, whose aggregation le
99                                     The fish eye lens protein gammaM7-crystallin (gammaM7) is found i
100 in (gammaS) is an important human and bovine eye lens protein involved in maintaining the transparenc
101                Human gammaD-crystallin is an eye lens protein that aggregates into amyloid fibrils un
102 D-crystallin (HgammaD-Crys) is a very stable eye lens protein that must remain soluble and folded thr
103  temperature and pressure on the LLPS of the eye-lens protein gamma-crystallin using UV/vis and IR ab
104                     Here, we investigate the eye-lens protein gammaB-crystallin in the ribosomal exit
105 nvestigate the aggregation propensity of the eye-lens protein gammaS-crystallin.
106           Human betaB1-crystallin is a major eye-lens protein that undergoes in vivo truncation at th
107 ene encoding gamma-B crystallin, a mammalian eye-lens protein, modulate the rates of translation and
108 an interesting evolutionary link between the eye lens proteins and the ancestral intermediate filamen
109                                              Eye lens proteins arose separately and make up a diverse
110  loss through the large-scale aggregation of eye lens proteins as a result of ageing or congenital mu
111 by high-molecular-weight aggregates of human eye lens proteins that scatter light, causing lens opaci
112  (non-Trp) fluorescence of porcine and human eye lens proteins was identified by Mass Spectrometry (M
113        J3-crystallin, one of the three major eye-lens proteins of the cubomedusan jellyfish (Tripedal
114                                              Eye lens radiation dose may be higher with a flat-panel
115                                              Eye lens radiation dose was significantly higher for pro
116 igh refractive index and transparency of the eye lens require uniformly shaped and precisely aligned
117 er factors damage crystallin proteins in the eye lens, resulting in cataracts that scatter light and
118 ted in multiple diverse cell types including eye lens, retina, HEK-293, and HELA cells.
119                                     Here the eye lens serves as a model for the cleavage and modifica
120                                Lengsin is an eye lens-specific member of the glutamine synthetase (GS
121 e major protein components of the vertebrate eye lens that maintain lens transparency, are exposed to
122 o classes of channel-forming proteins in the eye lens, the water channel aquaporin-0 (AQP-0) and the
123         Although larger in the decentralized eyes, lens thickness appeared unchanged in either eye fo
124 olipids and proteins from both intact bovine eye lens tissue and tissue ablated by ultrashort laser p
125 eral tens of micrometers from the surface of eye lens tissue while leaving the underlying tissue rela
126                                        Human eye lens transparency requires life long stability and s
127 n to the delicate balance of forces ensuring eye lens transparency.
128 sing distance between the bismuth shield and eye lens was also investigated.
129           The sole crystallin of the scallop eye lens was found to be homologous to Omega-crystallin,
130              This is well illustrated in the eye lens where epithelial cells elongate extensively dur
131 human sHSPs, including in muscle, brain, and eye lens where it is constitutively present at high leve
132 ens protein found in the outer region of the eye lens, where the refractive index is low.
133  are present at millimolar concentrations in eye lens, where they are responsible for maintaining len
134 ase 2 (ALR2) and accumulation of sorbitol in eye lens which could have contributed to diabetic catara
135                          The proteins of the eye lens, which do not turn over throughout life, underg
136 d SOD activity on in vitro incubation of the eye lens with 55mM glucose.
137 les measured along the optical axis of human eye lenses with age-related nuclear cataract showed incr
138 ntially accumulated to highest levels in the eye lens, with lower levels in the retina, yolk and othe
139 ct assembly directly from a section of sheep eye lens without sample pre-treatment.

 
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