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

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