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 Tyr alleles to progeny in test crosses with albinos.

6 The gene products of alb1 (for "albino 1"), arp1 (for "aspergillus reddish-pink 1"), and

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 We conclude that the characteristic albino abnormalities are present in both groups of mamma

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

14 Mice that are homozygous for the albino allele at the tyrosinase locus have fewer retinal

15 yrosinase mice, which are homozygous for the albino allele on chromosome 7, X-inactivation ensures th

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

17 Wild albino and blue bilberry fruit were analyzed to compare

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43 Albino berries were significantly smaller, accumulated l

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

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

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

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

48 Albino C57 female mice were intratracheally inoculated w

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

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

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

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

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

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

55 have been studied extensively in Siamese and albino cats.

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

57 ted in the LGNd, area 17, and area 18 of six albino cats.

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

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

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

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

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

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

64 oss five strains of mouse (129 Ola, C3H, C57 albino, DBA/2, and FVB/N), in vivo.

65 The proximal albino deletions identify several functional regions on

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

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

68 2 and CLPR4 showed delayed embryogenesis and albino embryos, with seedling development blocked in the

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

70 e to image through the hypopigmented iris of albino eyes.

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

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

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

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

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

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

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

78 ormation were observed between pigmented and albino groups.

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

80 2- to 4-month-old C57BL/6 and 7.5-month-old albino hrhoG/hrhoG mice after application of A or P sing

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

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

83 685 transcripts differentially expressed in albino irides, 403 in pigment dispersion-prone irides, a

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

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

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

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

88 Transient elevated IOP was induced in albino Lewis rats through the insertion of a needle into

89 concentrations of neutralized NMDA in adult albino Lewis rats.

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

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

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

93 0-II and tic20-I tic20-V double mutants were albino, like the corresponding tic20-I parent.

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

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

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

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

98 Albino mammals lacking melanin in the embryonic retinal

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

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

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

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

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

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

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

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

107 0 days induced damages in the liver of Swiss albino mice as evidenced by histopathology, disturbances

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

109 The elimination of TH in both pigmented and albino mice described here, like pigmented TH-null mice

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 s also detected in melanocytes cultured from albino mice, but absent in cultured mouse cell lines not

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

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

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

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

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

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

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

132 e fragments are grafted into tyrosinase null albino mice.

133 oglia migration into the subretinal space in albino mice.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

151 Albino mutants derived from random mutagenesis technique

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

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

154 These studies demonstrate that the albino mutation acts indirectly upon retinal ganglion ce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 similar engineered alleles recapitulated the albino phenotype.

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

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

174 components and the molecular basis for their albino phenotype.

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

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

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

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

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

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

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

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

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

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

185 Twenty-four albino rabbits underwent glaucoma filtration surgery in

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

187 Young albino rabbits were anesthetized, intubated, and exposed

188 Trabeculectomy was performed on albino rabbits' eyes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

204 have examined the induction of REM sleep in albino rats by light-to-dark transitions, a phenomenon r

205 mfERGs were recorded from pigmented and albino rats by slowing the rate of stimulus presentation

206 Albino rats injected with either the protective antioxid

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

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

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

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

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

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

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

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

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

216 Albino rats were injected intraperitoneally with PBN (aq

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

218 Albino rats were intraperitoneally injected with OT-551,

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

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

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

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

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

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 Treatment of albino TH null mice with DOPA, a catecholamine precursor

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 nd sex-matched pigmented (Lister Hooded) and albino (Wistar) rats were used in this study.

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