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1 pe voltage-gated Ca(2+) channels (Cav1.4) in retinal photoreceptor cells.
2 n nuclear receptor expressed specifically by retinal photoreceptor cells.
3 r responsible for the capture of a photon in retinal photoreceptor cells.
4 ransduction in olfactory sensory neurons and retinal photoreceptor cells.
5 te and continuously supply 11-cis-retinal to retinal photoreceptor cells.
6 rtant during phototransduction in vertebrate retinal photoreceptor cells.
7 laevis its mRNA is specifically expressed in retinal photoreceptor cells.
8 -sensitive regulator of phototransduction in retinal photoreceptor cells.
9 MD) leads to dysfunction and degeneration of retinal photoreceptor cells.
10 ion and proper development of hair cells and retinal photoreceptor cells.
11  to adaptation to background illumination in retinal photoreceptor cells.
12 ndition characterized by progressive loss of retinal photoreceptor cells.
13                  Melatonin is synthesized in retinal photoreceptor cells and acts as a neuromodulator
14 ns-retinal triggers phototransduction in the retinal photoreceptor cells and causes ultimately the se
15 gene promoter are hypomethylated in DNA from retinal photoreceptor cells and pineal gland compared to
16 sorders characterized by degeneration of the retinal photoreceptor cells and progressive loss of visi
17  of Hmgb1 at the protein level occurs in rat retinal photoreceptor cells and to a lesser extent in bi
18         Melatonin receptors are expressed in retinal photoreceptor cells, and this study was undertak
19                                              Retinal photoreceptor cells are particularly vulnerable
20 th transgenic mice that expressed betagal in retinal photoreceptor cells (arrbetagal mice).
21 sion of beta-galactosidase (beta gal) on the retinal photoreceptor cell arrestin promoter, in conjunc
22 showed that both GCAP genes are expressed in retinal photoreceptor cells, but GCAP2 was nearly undete
23  vertebrates is triggered when light strikes retinal photoreceptor cells causing photoisomerization o
24                        Circadian shedding of retinal photoreceptor cell discs with subsequent phagocy
25 oA are used as alternative Nmt substrates in retinal photoreceptor cells, even though they do not exh
26           In vivo, AANAT activity in chicken retinal photoreceptor cells exhibits a circadian rhythm
27 c factors (NTFs) are effective in protecting retinal photoreceptor cells from the damaging effects of
28                                        Mouse retinal photoreceptor cell generation and morphogenesis
29                    Several proteins found in retinal photoreceptor cells (guanylate cyclase activatin
30  maintain the blood-retinal barrier, sustain retinal photoreceptor cell health and function, and may
31 ses selective irreversible apoptotic loss of retinal photoreceptor cells in vivo.
32 ngly, an eye with restored cornea, iris, and retinal photoreceptor cells is formed when a surface fis
33               Retinal pigment epithelial and retinal photoreceptor cell lines were treated with TP de
34 esis and cohesion of stereocilia bundles and retinal photoreceptor cell maintenance or function.
35 ramide metabolism plays an important role in retinal photoreceptor cell survival and apoptosis.
36 era) visual system contains three classes of retinal photoreceptor cells that are maximally sensitive
37 is a canonical G protein-mediated cascade of retinal photoreceptor cells that transforms photons into
38 ythmically expressed in the cytoplasm of the retinal photoreceptor cells, the only other described ve
39       Notably, expression is not observed in retinal photoreceptor cells, the opsin-containing cells
40  links photoactivation of visual pigments in retinal photoreceptor cells to a change in their membran
41                   LEDGF enhanced survival of retinal photoreceptor cells under serum starvation and h
42 ects of LEDGF on survival of embryonic chick retinal photoreceptor cells under serum starvation and h
43 hed transgenic mice expressing human E2F1 in retinal photoreceptor cells under the regulation of the
44 pression pattern of LEDGF in embryonic chick retinal photoreceptor cells was investigated with protei
45 vels were both high in the inner segments of retinal photoreceptor cells where energy-demanding activ
46 urnin is rhythmically transcribed in Xenopus retinal photoreceptor cells, which contain endogenous ci

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