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1  chromophore of an opsin pigment in a rod or cone photoreceptor cell.
2  middle to long wavelength-sensitive (M/LWS) cone photoreceptor cells.
3 e regeneration of visual pigments in rod and cone photoreceptor cells.
4 itive to loss of insm1a expression than were cone photoreceptor cells.
5 e under conditions that fully bleach rod and cone photoreceptor cells.
6 ell is essential for the survival of rod and cone photoreceptor cells.
7 characterized by the degeneration of rod and cone photoreceptor cells.
8  life because of progressive loss of rod and cone photoreceptor cells.
9 he loss of the entire corresponding class of cone photoreceptor cells.
10 and biochemical characteristics exhibited by cone photoreceptor cells.
11 contacts with axon terminals of both rod and cone photoreceptor cells.
12 , the reporters are expressed exclusively in cone photoreceptor cells.
13 ls, and could explain the ultimate demise of cone photoreceptor cells.
14 and/or transport of long-wavelength opsin in cone photoreceptor cells.
15 idylethanolamine across membranes of rod and cone photoreceptor cells.
16 rdigitate with the outer segments of rod and cone photoreceptor cells.
17  required for maturation and polarization of cone photoreceptors cells.
18                                   In rod and cone photoreceptor cells, activation of particulate guan
19      Finally, CLUL1 was localized to retinal cone photoreceptor cells and a different immunolabeling
20 Retinal is coupled to opsins in both rod and cone photoreceptor cells and is photoisomerized to all-t
21 nterneurons that receive synaptic input from cone photoreceptor cells and provide the output of the f
22 vide additional visible light to the rod and cone photoreceptor cells, and thereby improve the visual
23  Stat3 and Ascl1a proteins following rod and cone photoreceptor cell apoptosis.
24                The outer segments of rod and cone photoreceptor cells are highly specialized sensory
25           The outer segments (OS) of rod and cone photoreceptor cells are specialized sensory cilia t
26 Muller cells and maintenance of some rod and cone photoreceptor cells, as identified by vimentin, rec
27  alternative in vitro model for the study of cone photoreceptor cell biology and associated diseases.
28 laments in vitro and in vivo in both rod and cone photoreceptor cell bodies, synapses, and to a lesse
29  we demonstrated its localization in rod and cone photoreceptor cells but not in Muller cells.
30 ally detectable in outer segments of rod and cone photoreceptor cells, but is present in inner retina
31 l cell counts and separate counts of rod and cone photoreceptor cells by immunostaining were similar
32 ngated cilia of the outer segment of rod and cone photoreceptor cells can contain concentrations of v
33                                              Cone photoreceptors cells can use 11-cis-retinal from th
34 roid and retinal pigmented epithelium, early cone photoreceptor cell death, and reduced lengths of ro
35 +) dysregulation is thought to cause rod and cone photoreceptor cell death.
36 educed OS growth and progressive rod but not cone photoreceptor cell death.
37  delete Dicer1 from cone cells, we show that cone photoreceptor cells degenerate and die in the Dicer
38 he species-specific details of human rod and cone photoreceptor cell development remains limited.
39                               Mature rod and cone photoreceptor cells extend terminals to the outer p
40 a leucine zipper) is critical for rod versus cone photoreceptor cell fate choice during retinal devel
41 ranscription factor that dictates rod versus cone photoreceptor cell fate in the mammalian retina.
42 inal tumor that expresses several markers of cone photoreceptor cells has been described earlier.
43                             Although rod and cone photoreceptor cells in the vertebrate retina are an
44 structures of outer segments between rod and cone photoreceptor cells in the vertebrate retina.
45 ed unique gene expression patterns of foveal cone photoreceptor cells, including many foveal-enriched
46 te-induced cell death in 661W cells, a mouse cone photoreceptor cell line, shown to express both estr
47 An assay was developed wherein 661W cells, a cone photoreceptor cell line, were stressed with light a
48  and consequent hyperpolarization of rod and cone photoreceptor cell membranes.
49 he chromophore of visual pigments in rod and cone photoreceptor cells needed for vision.
50                          Between P4 and P11, cone photoreceptor cell nuclei were observed to be scatt
51        In addition, there was a reduction in cone photoreceptor cell number and cone b-wave amplitude
52 PE65 and raised in constant dark have higher cone photoreceptor cell number, improved cone opsin loca
53 hotoactivation of visual pigments in rod and cone photoreceptor cells of the retina.
54 oncentrations in bleached salamander rod and cone photoreceptor cell outer segments were 0.86 +/- 0.0
55 phodiesterase gene Pde6beta and lose rod and cone photoreceptor cells (PRC) within the first 6 wk of
56 ctional recording from rods and each type of cone photoreceptor cells separately.
57 e as relay interneurons that connect rod and cone photoreceptor cells to amacrine and ganglion cells.
58 t endogenous cTalpha can also translocate in cone photoreceptor cells to the same extent it does in r
59 nsequently vary for the different classes of cone photoreceptors, cells tuned to absorb bands of diff
60     To understand the importance of AIPL1 in cone photoreceptor cells, we transgenically expressed hA
61 , less is known regarding desensitization in cone photoreceptor cells, which occurs more rapidly than
62  central retina contains more densely packed cone photoreceptor cells with unique morphologies and sy