ライフサイエンスコーパス: albino

1 ow mice after UVB or UVA irradiation than in albino.

2 storic axolotl pigment phenotypes: white and albino.

3 eration as they age than C57BL/6J-c(2J) (B6) albinos.

4 he existing competence of visual function in albinos.

5 from pigmented rats are lower than that from albinos.

6 Tyr alleles to progeny in test crosses with albinos.

7 l morphogenesis and differentiation, whereas albino (a/a) mutants lack melanin.

8 SS) into the subretinal space of 4-5-day-old albino Abca4 null mutant and Abca4 wild-type mice.

9 ll-trans-retinal dimer-PE) also decreases in albino Abca4(-/-) mice reared in cyclic light compared w

10 In albino Abca4(-/-) mice receiving a diet supplemented wit

11 es lens, 488 nm excitation) were acquired in albino Abca4(-/-), Abca4(+/-), and Abca4(+/+) mice (ages

12 identified polymorphisms shared between the albino allele (tyr (a) ) and tyr alleles in a Minnesota

13 independent carcinogenesis, we introduced an albino allele, which ablates all pigment production on t

14 Wild albino and blue bilberry fruit were analyzed to compare

15 The albino and five non-albino robust capuchin monkeys were

16 riking among the overrepresented genes, with albino and pigment dispersion-prone irides both exhibiti

17 aused marked reductions in norepinephrine in albino and pigmented 15-day-old mice.

18 emistry of cryopreserved sections of eyes of albino and pigmented mice exposed to diverse levels of l

19 uring retinal ganglion cell (RGC) genesis in albino and pigmented mice from embryonic day 11 (E11) to

20 g the nasotemporal axis differ in retinas of albino and pigmented mice, both absolutely, with the tem

21 n specification, we compared the features of albino and pigmented mouse RPE cells during the period o

22 e retinal temperature increase during TTT in albino and pigmented rabbit eyes.

23 eshold power settings for visible lesions in albino and pigmented rabbits were 950 and 90 mW, respect

24 GABA-immunoreactivity in the retina of both albino and pigmented rats appeared to be unaffected by i

25 FAF images from albino and pigmented rats showed that without compensati

26 arboxylase (GAD(67)) in the visual system of albino and pigmented rats.

27 At E12.5 and E15.5, although albino and pigmented RPE cells express RPE markers Otx2

28 eous expression of tyrosinase and melanin in albino and pigmented TH wild-type mice.

29 r cells were observed in the retinas of both albino and pigmented transgenic mice.

30 Studies further extended to in vivo Swiss albino and SCID mice models also revalidated the anti-ca

31 nsiveness in two transgenic mouse lines, one albino and the other pigmented, that lack tyrosine hydro

32 gotes resulted in the generation of numerous albinos and also mice with a graded range of albino mosa

33 -ATPase mutant zebrafish were oculocutaneous albinos and presented with defects in the formation and/

34 sequencing revealed that the majority of the albinos and the mosaics had more than two new mutant all

35 ocularly into one eye of Sprague-Dawley (SD, albino) and Brown Norway (BN, pigmented) rats.

36 he temporal aspect of the retina expanded in albino, and relative to the position of the optic nerve

37 irect absorption of UVB by DNA is central in albino animal models, but melanin-pigmented models have

38 We crossed the abcr(-/-) mutation onto an albino background.

39 ated by standard zygote injection also on an albino background.

40 adermal injection of this oligonucleotide to albino BALB/c mouse skin resulted in dark pigmentation o

41 Albino berries were significantly smaller, accumulated l

42 yanins were identified in both forms, but in albino bilberries, individual anthocyanins were only det

43 e solids content and pH value were higher in albino bilberry and their surface was lighter and charac

44 or degeneration was observed in 11-month-old albino, but not pigmented, abca4(-/-) mice on both diets

45 Mesd is defined by overlapping albino (c) deletions on chromosome 7.

46 Albino C57 female mice were intratracheally inoculated w

47 lified in wound healing and cornea models in albino C57 mice compared with black C57 mice.

48 ng and extensively backcrossed mice onto the albino C57BL/6 genetic background to address variability

49 odate injection (40 mg/kg) into wild-type or albino C57Bl/6 mice.

50 Five immunocompetent C57BL/6-cBrd/cBrd/Cr (albino C57BL/6) mice were injected with GL261-luc2 cells

51 esting a suppression of abnormal activity in albino cat cortex, which could underlie the existing com

52 Previous research on tyrosinase-negative albino cats has shown that (1) approximately 95% of all

53 have been studied extensively in Siamese and albino cats.

54 niculate nucleus (LGNd) and visual cortex in albino cats.

55 arthropod lineages, ii) is retained in most albino cave species, and iii) has been lost several time

56 njury in most species tested, including even albino cave-adapted species.

57 ins induces transient ocular hypertension in albino CD-1 mice.

58 However, we also found that albino cells can express the tdy1 phenotype and overaccu

59 We used congenic mice of black, yellow, and albino coat colors to investigate the induction of DNA l

60 ng the wild-type alleles created a sector of albino, cr4 mutant tissue in an otherwise normal leaf.

61 The proximal albino deletions identify several functional regions on

62 -specific segregation is not complete in the albino dLGN and, upon perturbing postnatal retinal activ

63 ing and activity-dependent refinement in the albino dLGN arise from RGC misspecification together wit

64 2 and CLPR4 showed delayed embryogenesis and albino embryos, with seedling development blocked in the

65 limited to the inner retinal layers, but in albino eyes 5D4+ cells were found in the outer retinal l

66 dhesion experiments performed with 3T3-Swiss albino fibroblasts showed substantially reduced cell adh

67 We have confirmed that zebrafish albino fish are mutant in slc45a2; wild-type slc45a2 mRN

68 idual sugars and organic acids; however, the albino form had 33% higher content of total sugars and 9

69 wild-type embryos resulted in one completely albino founder carrying two different Tyr mutations.

70 In the wild-type frogs and in the albinos, ganglion cells giving rise to the crossed proje

71 punkt, blurred, fade out, weiss, sandy, and albino genes.

72 We used WAG/Rij rats (Wistar albino Glaxo rats of Rijswijk), an established animal mo

73 ormation were observed between pigmented and albino groups.

74 model for understanding RGC decussation, as albinos have a reduced ipsilateral projection and altere

75 ntation studies between pigmented donors and albino hosts showed that neurons are induced both in don

76 2- to 4-month-old C57BL/6 and 7.5-month-old albino hrhoG/hrhoG mice after application of A or P sing

77 acuity data were collected for a group of 25 albino individuals that included the following: 18 oculo

78 o determine whether RPE abnormalities in the albino influence these aspects of retinal development.

79 685 transcripts differentially expressed in albino irides, 403 in pigment dispersion-prone irides, a

80 lthough the initiation of RGC genesis in the albino is unchanged.

81 ungs of two strains of mice (CBA/J and Swiss Albino) later in infection was also associated with cyto

82 Null ppr2 mutants have albino leaves and lack plastid rRNA and translation prod

83 y1gun4 to be semi-albino plants, and hy1gun5 albino lethal, in a high-light-sensitive manner.

84 e find that, as in albino visual cortex, the albino LGNd contains (1) normal cells with RFs in the vi

85 Thus, the albino LGNd is arranged into hemiretinal and not ocular

86 Additionally, we show that in the albino light damage model cell death was not associated

87 0-II and tic20-I tic20-V double mutants were albino, like the corresponding tic20-I parent.

88 We mapped the albino locus to tyrosinase (tyr) and identified polymorp

89 ally, into the lateral ventricles of Fischer albino male rats (1 nmol/2 microl/side).

90 d IOP and anterior segment anomalies between albino mammals and hypopigmented fish are important.

91 Because albino mammals have increased IOP and are prone to anter

92 Albino mammals lacking melanin in the embryonic retinal

93 In albino mammals, lack of pigment in the retinal pigment e

94 ivo hairless MC1R model containing Mc1r(-/-) albino, MC1R(+)Mc1r(-/-) albino, Mc1r(-/-) pigmented, an

95 ontaining Mc1r(-/-) albino, MC1R(+)Mc1r(-/-) albino, Mc1r(-/-) pigmented, and MC1R(+)Mc1r(-/-) pigmen

96 greater oxidative DNA and lipid damage than albino-Mc1r(e/e) mouse skin.

97 d when infections were performed with mutant albino (Mel(-)) C. neoformans strains.

98 Intracellular localization was monitored in albino melanocytes carrying the native mutation, as well

99 The albino mice (22-30 g) and albino rats (100-155 g) of bot

100 Pigmented mice and albino mice (n = 6 eyes) were used to isolate the photot

101 0 days induced damages in the liver of Swiss albino mice as evidenced by histopathology, disturbances

102 of QW-296 loaded nanoparticles into C57/BL6 albino mice bearing lung metastatic melanoma at the dose

103 The 5 mg kg(-1) dose of compound 30 rescued albino mice by 80% from capsaicin-induced paw licking an

104 in peripheral dopamine between pigmented and albino mice disappeared with advancing age following cha

105 BALB/cByJ (C) albino mice have significantly more retinal degeneration

106 The retinoid profiles in albino mice indicated higher retinal illuminance than in

107 LIOH in albino mice may be useful as a mouse model to examine me

108 The subretinal space of eyes of albino mice raised from birth in complete darkness conta

109 diretinal adducts in cyclic light-reared and albino mice reflect photodegradative loss of bisretinoid

110 Deletion of Fmod in albino mice resulted in a marked reduction in the amount

111 g a peroxidase-labeled secondary antibody in albino mice revealed heavy labeling of the RPE in the in

112 at melanocytes from light-skinned humans and albino mice secrete high levels of fibromodulin (FMOD),

113 Investigations of Swiss Albino mice through capsaicin induced paw lickings and d

114 f metastatic melanoma to the lung in C57/BL6 albino mice to determine in vivo efficacy of P-SMART and

115 s eye-specific retinogeniculate targeting in albino mice using the C57BL/6 Tyr(c-2J/c-2J) strain, in

116 Wild type Swiss albino mice were fed i-Extract, and hippocampal cells fr

117 Iris samples from albino mice with a Tyr mutation, pigment dispersion-pron

118 al form in normal Sprague Dawley rats, Swiss Albino mice, and the PSMA-expressing LNCaP subcutaneous

119 ehyde was higher; this included black versus albino mice, dark-adapted versus light-adapted mice, and

120 In albino mice, fewer RGCs from the ventrotemporal (VT) ret

121 sociated with the retinal neuroepithelium in albino mice, is consistent with other results showing th

122 nt mice and were higher in pigmented than in albino mice, regardless of the presence or absence of TH

123 ogether with comparisons of pigmented versus albino mice, revealed a relationship between intraocular

124 xpectedly, A2E levels were not higher in the albino mice.

125 f ipsilateral innervation was smaller, as in albino mice.

126 e fragments are grafted into tyrosinase null albino mice.

127 oglia migration into the subretinal space in albino mice.

128 inst MES and scPTZ induced seizures in Swiss Albino mice.

129 han E. coli DH5alpha possessing BLP in Swiss albino mice.

130 We discovered that albino Micos cavefish harbor two copies of a loss-of-fun

131 In the albino, mitotic indices were elevated, an excess of cell

132 albinos and also mice with a graded range of albino mosaicism.

133 In the albino mouse eye, MFRP is localized to the apical and ba

134 al epithelial sheets were isolated from CD-1 albino mouse eyeballs by incubating for 18 hours at 4 de

135 Thus, the light damage albino mouse model may be a good model to study compleme

136 Toward this end, we analyzed the common albino mouse mutation Tyr(C85S), the frequent human albi

137 ion of horizontal cells in the pigmented and albino mouse retina.

138 ALB/cByJ (BALB) and B6(Cg)-Tyr(c-2J)/J (B6a) albino mouse strains, RD-modifying quantitative trait lo

139 m various screenings performed in normal and albino murine melanocytes and zebrafish.

140 development1 (spd1), an Arabidopsis seedling albino mutant capable of producing normal green vegetati

141 y complementation of the mel3 mutation in an albino mutant of W. dermatitidis using a cosmid library.

142 slc45a2; wild-type slc45a2 mRNA rescued the albino mutant phenotype.

143 Chromosomal DNA from the albino mutant was subsequently used in a vector-recaptur

144 transcripts is significantly reduced in the albino mutants and inhibitor-treated seedlings.

145 editing of ndhD-2 is also completely lost in albino mutants and norflurazon-treated seedlings.

146 Albino mutants derived from random mutagenesis technique

147 ype tyrosinase in melanoma cells and certain albino mutants in untransformed melanocytes are targeted

148 seedlings (etiolated, cia5-2, ispF and ispG albino mutants, lincomycin-, and norflurazon-treated).

149 tan mutant tissue marked by a closely linked albino mutation were examined to determine the phenotype

150 any discernable effect brought about by the albino mutation, despite numerous developmental abnormal

151 The mutant cr4 allele was marked with the albino mutation, Oy-700.

152 pathway by comparing the targeting of APG1 (albino or pale green mutant 1), an example of a stop-tra

153 Introduction of the L374F polymorphism into albino or the A111T polymorphism into slc24a5 (golden) a

154 study, we report that immunization of adult Albino Oxford rats by an infection limited to the muscle

155 Arabidopsis transgenic lines showing various albino patterns caused by IspH transgene-induced gene si

156 le mutants tic56-1 and ppi2 (toc159) have an albino phenotype and are able to grow heterotrophically,

157 Tic56 mutant plants have an albino phenotype and are unable to grow without an exter

158 howed no morphological defects other than an albino phenotype and grew at the same rate as their blac

159 opsis thaliana) ispH null mutant that has an albino phenotype and have generated Arabidopsis transgen

160 in the TYR gene is responsible for the OCA1 albino phenotype in the capuchin monkey, classified as S

161 ient hairpin RNA expression, resulting in an albino phenotype in the leaves and the male and female f

162 eoplast-chloroplast transition leading to an albino phenotype in the light.

163 After a spontaneous initiation, the albino phenotype is systemically spread toward younger t

164 Homozygous tic20-I plants had an albino phenotype that correlated with abnormal chloropla

165 The BALB/c albino phenotype-associated Tyr(c) tyrosinase mutation a

166 st, homozygous tha2 mutations cause a lethal albino phenotype.

167 hraea, generating a mutant that displayed an albino phenotype.

168 similar engineered alleles recapitulated the albino phenotype.

169 components and the molecular basis for their albino phenotype.

170 The initiation of albino phenotypes rendered by IspH gene silencing can ar

171 We observed hy1gun4 to be semi-albino plants, and hy1gun5 albino lethal, in a high-ligh

172 We found that the albino plastid protein import2 (ppi2) mutant lacking Toc

173 SCRPE transport followed the trend albino rabbit > pigmented rabbit > human > porcine > bov

174 anin content of the CRPE exhibited the trend albino rabbit << pigmented rabbit < porcine approximatel

175 ek survival of porcine RPE xenografts in the albino rabbit subretinal space, but there was poor survi

176 excised sclera/sclera-choroid-RPE (SCRPE) of albino rabbit, pigmented rabbit, human, porcine, and bov

177 Fourteen New Zealand albino rabbits aged 5 weeks underwent unilateral surgica

178 Adult male albino rabbits and Long-Evans rats received iontophoreti

179 ngs required to produce threshold lesions in albino rabbits caused retinal temperature increases in p

180 Fifteen adult New Zealand White albino rabbits had ECT devices secreting CNTF at 22, 5,

181 Twenty-four albino rabbits underwent glaucoma filtration surgery in

182 Temperature increases in albino rabbits were 1.5 times higher with subretinal blo

183 Young albino rabbits were anesthetized, intubated, and exposed

184 Trabeculectomy was performed on albino rabbits' eyes.

185 ata for prednisolone at a dose of 2.61 mg in albino rabbits, and the model was validated at two other

186 ere injected into the subretinal space of 24 albino rabbits, with half the rabbits maintained on trip

187 ure increases were measured in pigmented and albino rabbits, with or without subretinal blood and cho

188 ons were higher in pigmented rabbits than in albino rabbits.

189 ilateral PRK was performed on 21 New Zealand albino rabbits.

190 bits that were five times higher than in the albino rabbits.

191 PBN protects the albino rat retina from the damaging effects of constant

192 entation in vivo in developing pigmented and albino rat retinae along with other parameters of cell d

193 The Munich Wistar albino rat shows progressive chronic nephrosis with age

194 s of 28 healthy new born Sprague Dawley male albino rat.

195 The albino mice (22-30 g) and albino rats (100-155 g) of both sexes were infected oral

196 to different tonotopic regions of the LSO of albino rats and analyzed the neurons labeled retrogradel

197 ptotic photoreceptors in living pigmented or albino rats and mice with retinal degeneration.

198 The data presented show that retinas from albino rats are more susceptible to ischaemia/reperfusio

199 larly, we found that callosal connections in albino rats are not patchy but instead are distributed h

200 Retinas of albino rats born and raised in bright cyclic light (300-

201 mpletely obliterated in the retinas from the albino rats but unaffected in the retinas of the pigment

202 Thus, the binocular region in V1 of albino rats includes lateral striate cortex, being there

203 Albino rats injected with either the protective antioxid

204 We therefore predicted that in albino rats input from both eyes intermix in the binocul

205 n of behavior, the authors recorded sleep in albino rats reared in continuous dark, continuous light,

206 Also, in certain areas of the retina from albino rats there was a suggestion that the calretinin-i

207 Intraocular pressure of adult male Lewis albino rats was raised to create retinal ischemia for 1

208 Albino rats were born and raised in 5- or 400-lux cyclic

209 Albino rats were born and raised in 5-lux cyclic light (

210 Thirty female Wistar albino rats were divided into three study groups as foll

211 Albino rats were dosed (subcutaneously) with AL-8309A, 8

212 Albino rats were exposed to 1 or 5 klux white fluorescen

213 Male albino rats were implanted with EEG and EMG electrodes,

214 Albino rats were injected intraperitoneally with PBN (aq

215 Sprague-Dawley albino rats were injected intravitreally with 2 microg P

216 Albino rats were intraperitoneally injected with OT-551,

217 Material/Fourteen Wistar albino rats were randomly allocated into two groups.

218 Thirty-six male Wistar albino rats were randomly divided into four groups as fo

219 ecovered to normal levels while those of the albino rats were reduced by more than 80%.

220 C57/BL6 x BALB/C mice and Albino rats were treated with 1 x 10(7) pfu of the HSV-1

221 transposase bigenic rats bred with wild-type albino rats yielded offspring with pigmentation distinct

222 In albino rats, it has been reported that lateral striate c

223 of adenosine in hippocampal slices from male albino rats.

224 ignificantly lower in pigmented rats than in albino rats.

225 Fifty-six conscious, instrumented albino rats.

226 EM sleep, a marker for pretectal function in albino rats.

227 activity against enterococci-infected Wistar albino rats.

228 he genetically matched Mc1r(e/e); Tyr(c/c) ("albino-red-haired") mice.

229 ddition to a lack of melanin in the RPE, the albino retina is characterized by abnormal patterns of c

230 The cellular organization of the albino retina is perturbed as early as E12.

231 in the early stages of neuronogenesis in the albino retina, although the initiation of RGC genesis in

232 mporal defects in neuronal production in the albino retina, which could perturb expression of genes t

233 were identical in size in the pigmented and albino retina.

234 esting residual plasticity of the developing albino retina.

235 turbations of early activity patterns in the albino retina.

236 Mosaic regularity in pigmented and albino retinas did not differ, but each differed signifi

237 r density differed between the pigmented and albino retinas.

238 Albino Rlbp(-/-) mice are protected from light damage re

239 ding to a premature stop codon (R22X) in the albino robust capuchin monkey.

240 The albino and five non-albino robust capuchin monkeys were identified as Sapaju

241 dark-adapted male control Sprague-Dawley and albino Royal College of Surgeons rats before (at develop

242 express RPE markers Otx2 and Mitf similarly, albino RPE cells are irregularly shaped and have fewer m

243 ction protein) is expressed in pigmented and albino RPE cells at E13.5 but at E15.5 albino RPE cells

244 d and albino RPE cells at E13.5 but at E15.5 albino RPE cells have fewer small connexin 43 puncta, an

245 herin appears loosely distributed within the albino RPE cells rather than tightly localized on the ce

246 Disruption of pigmentation in the albino RPE is associated with delayed neurogenesis in th

247 thaliana using spontaneously arising clonal albino sectors caused by the chloroplast mutator 1-2 mut

248 Chimeric seedlings exhibiting albino sectors shared between the cotyledons and first t

249 germination of spd1 embryos showed that the albino seedling phenotype of spd1 was dependent on the p

250 rabidopsis (Arabidopsis thaliana), result in albino seedlings and sucrose-dependent heterotrophic gro

251 A severe ZmWhy1 mutant allele conditions albino seedlings lacking plastid ribosomes; these exhibi

252 s reflecting the starvation situation of the albino seedlings.

253 ed UVR exposure, the number of p53 clones in albino skin was significantly elevated when this was nul

254 53 clones were observed in pigmented than in albino skin.

255 pigmented skin relative to less-pigmented or albino skin.

256 Retinal ganglion cells (RGCs) from P35-70 albino Sprague-Dawley (normal) and P60-254 S334ter-4 (ph

257 PBN (50 mg/kg) protected albino Sprague-Dawley rat retinas when injected 0.5-12 h

258 nocular mfERGs were recorded in anesthetized albino (Sprague-Dawley) and pigmented (Long Evans) rats.

259 Administration of 1-azidoanthracene to albino stage 40-47 tadpoles was found to immobilize anim

260 idget arose spontaneously in a heterogeneous albino stock.

261 e strains: the pigmented C57BL/6 and the two albino strains Balb/c and B6(Cg)-Tyr(c-2J) /J (coisogeni

262 mouse mutation Tyr(C85S), the frequent human albino substitution TYR(T373K), and the temperature-sens

263 stically significant differences relating to albino subtype for any of the measured parameters.

264 Coronary lesions were induced in Yorkshire albino swine (n=6) with balloon angioplasty, and 4 weeks

265 ne- and two-photon) and the visual system of albino tadpoles (two-photon).

266 nce of cholinergic markers occur normally in albino TH null mice, suggesting that catecholamines act

267 contrast, fewer than one gland is active in albino TH null mice, which lack catecholamines in gland

268 are active in interdigital hind footpads of albino TH wild-type mice.

269 eral levels of dopamine were reduced only in albino TH-deficient mice and were higher in pigmented th

270 s is severely impaired in the IspH-deficient albino tissues.

271 nditions, and seedlings developed into small albino to virescent seedlings.

272 pulation of tiger salamanders from which the albino trait was introgressed.

273 us for certain chromosome 7 deletions of the albino Tyr; c locus that also include Fah die perinatall

274 maturation pathways of wild-type and mutant albino tyrosinase can already be observed for translocon

275 explored the possibility that trafficking of albino tyrosinase from the endoplasmic reticulum (ER) to

276 ence in genomic DNA of genes for both wt and albino tyrosinase, reflecting the DBA/2J (Cloudman S91)

277 alyzed the adrenal structure and function of albino tyrosine hydroxylase-null (TH-null) mice that are

278 R transgene-induced gene-silencing lines are albino, variegated, or pale green, confirming that HDR i

279 of uncrossed retinogeniculate projections in albino versus pigmented rats were paralleled by identica

280 We find that, as in albino visual cortex, the albino LGNd contains (1) norma

281 The albino visual system is highlighted as an apt comparativ

282 ity of anatomical abnormalities found in the albino visual system.

283 like A2E, the oxiranes were more abundant in albino vs. pigmented abcr(-/-) mice, and in abcr(-/-) mi

284 ehavioural response in the hooded Lister and albino Wistar rat.

285 Thirty-eight male albino Wistar rats were divided into four groups: 1) gro

286 sed to induce unilateral IOP elevation in 41 albino Wistar rats.

287 rior one third of the orbital optic nerve in albino Wistar rats.

288 HRP, are intermixed in the binocular zone of albinos, without segregating into ODCs.

289 We report a case of an albino woman in her 40s with a history of CD and pulmona

290 jections to the thalamus in adult normal and albino Xenopus frogs.

291 d measured filopodial motility in the intact albino Xenopus laevis tadpole.

292 numbers of retinal ganglion cells in living albino Xenopus laevis tadpoles to reveal the distributio

293 pse images of single optic tectal neurons in albino Xenopus tadpoles expressing dominant negative or

294 vivo time-lapse images of retinal axons from albino Xenopus tadpoles in which binocular innervation o

295 ged at daily intervals over 4 days in intact albino Xenopus tadpoles.

296 the uncrossed retinothalamic projections of albino Xenopus, even though these pathways are substanti

297 hotoreceptor apoptosis in dark-adapted adult albino zebrafish (Danio rerio).

298 The light-treated albino zebrafish displayed random cone patterns immediat

299 l flatmounts from these fish, and from adult albino zebrafish subjected to light-induced photorecepto

300 Retinas of control dark-adapted adult albino zebrafish were compared with retinas subjected to