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