ライフサイエンスコーパス: retinae

1 localization in photoreceptors of Rs1h(-/Y) retinae.

2 protein of similar size in bovine and murine retinae.

3 ung (4-year-old) and old (80-year-old) human retinae.

4 interneuron in the rod pathway of mammalian retinae.

5 ension of axons from temporal regions of the retinae.

6 ictly equivalent projection sites of the two retinae.

7 ed by the cone mechanism in mixed (rod/cone) retinae.

8 at occupy corresponding positions on the two retinae.

9 e due to donor cells integrating within host retinae.

10 h corresponding points in the left and right retinae.

11 ed to retinal degeneration in Brg1-deficient retinae.

12 nocturnal, with small eyes and rod-dominated retinae.

13 significantly downregulated in myopic mouse retinae.

14 There was 1 case of extramacular sclopetaria retinae.

15 umatic maculopathy and extramacular commotio retinae.

16 nd differentiation defects in Id2a-deficient retinae.

17 nt with human and animal studies of commotio retinae.

18 oblastomas as compared to three normal human retinae.

19 higher in retinoblastoma than in human fetal retinae.

20 h proteins in mouse, rat, rabbit, and monkey retinae.

21 iation defects associated with pRb-deficient retinae.

22 ynaptic elements in wild-type and Lamb2-null retinae.

23 For extramacular commotio retinae, 117 patients were identified, of whom 58 had ad

24 For macular commotio retinae, 53 patients were identified, of whom 34 had ade

25 When the method is applied to mouse retinae a significant increase in the DOPAC/DA ratio is

26 and capillaries in brain slices and isolated retinae, allowing investigators to probe the role of cap

27 vivo in developing pigmented and albino rat retinae along with other parameters of cell division to

28 ed in retinoblastoma relative to human fetal retinae and a subset of samples had somatic mutations th

29 bino mammals have specific deficits in their retinae and in the pattern of decussation at their optic

30 specifically eliminated microglia in murine retinae and optic nerves with high efficiency.

31 unoassay measurements of BDNF protein in the retinae and SC of normal and BDNF-treated hamsters demon

32 Among its oscillators are the pineal gland, retinae, and a hypothalamic structure assumed to be homo

33 inflammatory ICAM-1 is increased in diabetic retinae, and it is implicated in pathogenesis of retinop

34 , which transmits light information from the retinae, and the geniculohypothalamic tract (GHT) from t

35 Their retinae are crisply layered following the typical verteb

36 on requires that inputs arising from the two retinae are integrated and precisely organized within ce

37 uropean starling, Sturnus vulgaris, even the retinae are morphologically asymmetrical in terms of pho

38 s of photoreceptor cells found in vertebrate retinae are organized in specific patterns, which are im

39 Despite their diversity, vertebrate retinae are specialized to maximize either photon catch

40 half of the ganglion cells in whole-mounted retinae bound antibodies against both isoforms.

41 n purified from rod outer segments of bovine retinae by immunoaffinity chromatography in octyl glucos

42 s (r-iPSCs) and scored their ability to make retinae by using a standardized quantitative protocol ca

43 The coordinates in reconstructed retinae can be transformed to visuotopic coordinates.

44 However, mosaic retinae composed of wild-type and flo cells show that de

45 We propose a model in which light-exposed retinae contain a mixed population of phosphorylated and

46 ion and differentiation, with Id2a-deficient retinae containing an abundance of proliferative retinob

47 an vision is that it occurs through "duplex" retinae containing both rod and cone photoreceptors, the

48 c mice and transplanted into adult recipient retinae; CrxGFP is a marker of cone and rod photorecepto

49 nous dopamine release from isolated goldfish retinae cultured in continuous darkness for 56 h clearly

50 In contrast, dendrites in untreated retinae degenerated slowly after the axonal trauma and n

51 Retinae derived from f-iPSCs had fewer amacrine cells an

52 In the complementary experiment, retinae derived from NeuroD-null mice demonstrated a two

53 The original and the duplicate neural retinae differentiate and laminate with mirror-image pol

54 nt project to different locations on the two retinae, differing principally in their horizontal coord

55 Whereas explants from nasal retinae extended fibers across their natural target popu

56 population, fibers from temporal regions of retinae failed to invade areas of growing posterior tect

57 Using whole retinae from adult mice, we performed immunohistochemist

58 xperiments, these parameters are compared in retinae from animals with different targeted deletions o

59 1-dependent fluorescence was detected in rat retinae from birth, albeit at low levels.

60 Examination of retinae from homozygous viable mutants indicated two maj

61 Retinae from mice lacking p57(Kip2) exhibited inappropri

62 Nissl staining of retinae from normal adult and 5,7-DHT-treated hamsters r

63 In birds, the pineal gland and retinae have been defined as pacemakers within this syst

64 Lineage analyses of vertebrate retinae have led to the suggestions that cell fate decis

65 Microarray analysis of zymosan-treated retinae identified several cytokines (CXCL13, endothelin

66 n undergo retinal differentiation to produce retinae in 34 d.

67 mation from either the dorsal or the ventral retinae in both median and lateral ocelli, with only thr

68 largely documented in the rodent and primate retinae in recent years.

69 Analysis of retinae in SV2B knock-out mice revealed a strong reducti

70 Patients with ONHD had thicker retinae in the inner annulus compared with patients with

71 h those of cells located in matched areas of retinae in which the density of beta ganglion cells had

72 n retinal locations of extramacular commotio retinae, in order of frequency, were inferotemporal (37%

73 estricted outgrowth pattern is observed when retinae innervate their targets in rodents.

74 the types of different neurons in mammalian retinae is now close to being completely known for a few

75 of photo-receptor activation present on our retinae; it is composed of segregated surfaces, organize

76 e use of a novel observation: isolated mouse retinae kept in standard media for routine physiologic r

77 differences between images formed on the two retinae (known as binocular disparity).

78 In the contralateral retinae, labeled RGCs were most numerous and widespread,

79 In mouse retinae lacking Sirt6, effectors of glycolytic flux were

80 in vivo retroviral infection of newborn rat retinae led to an altered photoreceptor phenotype, while

81 al lamina disruption of embryonic day 3 to 6 retinae led to the retraction of the end feet of the neu

82 ner segments in isolated intact neural mouse retinae, maintained by superfusion.

83 progenitor cells persisted in Brg1-deficient retinae, making them more susceptible to retinoblastoma.

84 Reduced VA after extramacular commotio retinae may represent occult macular injury or previousl

85 d retinal degeneration in sectioned archived retinae of 26 macaque monkeys with unilateral V1 ablatio

86 and assessed expression by mRNA analysis in retinae of 51 unselected post mortem eye specimens from

87 ERG waveforms from light-adapted retinae of all patients showed reduced amplitudes of the

88 abetes-related nitric oxide increases in the retinae of diabetic animals.

89 We recently reported an increase in Grx1 in retinae of diabetic rats and in rat retinal Muller glial

90 ncreases VEGF mRNA and protein levels in the retinae of diabetic rats.

91 was generated in chicken eggs and tested in retinae of goldfish and rat, and rat caudate putamen, by

92 depolarizing bipolar cells isolated from the retinae of goldfish.

93 glion cell recordings were obtained from the retinae of macaques (Macaca fascicularis).

94 The retinae of many bird species contain a depression with h

95 other retinal cell specific markers in adult retinae of mice.

96 istry with cell type-specific markers in the retinae of mouse, rat, rabbit, and monkey.

97 Horizontal cells are absent in retinae of Prox1-/- mice and misexpression of Prox1 in p

98 The retinae of Rpe65(-/-)Grk1(-/-) mice had negligible opsin

99 es located in the outer nuclear layer of the retinae of the 4 older patients were observed (termed ou

100 r retinal tubulation) were identified in the retinae of the GA patients.

101 Expression of the TBK1 transgene in the retinae of these mice was demonstrated by real-time PCR.

102 mRNA expression was assessed in post-mortem retinae of three men with the red, green and green-red g

103 Rat retinae of various ages were stained immunohistochemical

104 tch pathway component gene expression, while retinae overexpressing id2a possess reduced expression o

105 ve found that in the adult Rb;p130-deficient retinae p107 compensation prevents ectopic proliferation

106 Id2a-deficient retinae possess elevated levels of Notch pathway compone

107 DM4 and MDM2 mRNA and protein in human fetal retinae, primary retinoblastomas, retinoblastoma cell li

108 The results suggest that in some vertebrate retinae, prolonged darkness (light-history) may regulate

109 ddle cone photoreceptors, whereas Pde6h(-/-) retinae remained PDE6H-negative.

110 the approximately 20 RGC types in mammalian retinae respond to diverse visual features and events is

111 ression is decreased by over 80%, KI/KI mice retinae retain comparable 11-cis-retinal levels with WT.

112 ble retinal injury, with central sclopetaria retinae, retinal necrosis, and surrounding commotio reti

113 Examination of transgenic IAP-null retinae revealed a failure of P84 to become associated w

114 Immunohistochemistry on murine retinae revealed an overlap of the retinoschisin-Na/K-AT

115 Analysis of mutant retinae reveals an extensive loss of photoreceptors and

116 y Western blot analysis of bleached isolated retinae showed little dephosphorylation of rhodopsin for

117 g immunoelectron microscopy of mouse and rat retinae showed that VGAT immunoreactivity was localized

118 Here we examine young and aged primate retinae stained to distinguish S from M/L-cones.

119 Eliprodil is neuroprotective of retinae subjected to either an excitotoxic or ischemic c

120 izontal cell processes in primate and rodent retinae suggested that mammalian horizontal cells releas

121 -);p130(-/-) or Rb(-/-);p107(-/-);p130(+/-), retinae suggesting that one copy of Rb or p130 was suffi

122 ors is significantly increased in Math5(-/-) retinae, suggesting a binary change in cell fate from RG

123 Finally, analysis of P4, P7, P12, and P15 retinae suggests that the apical horizontal cell process

124 SCs more efficiently produced differentiated retinae than did embryonic stem cells (ESCs) or fibrobla

125 nce of functional photoreceptors within host retinae that express an array of donor-specific proteins

126 Consequently, in photopic retinae, the application of APB disrupts the ON-channel

127 In the ipsilateral retinae, the small number of labeled cells were concentr

128 ate proliferation in the p57(Kip2)-deficient retinae to preserve the correct proportion of the major

129 d to other neurotrophins, as well as RGCs in retinae treated with BDNF but in areas not directly expo

130 In human and murine retinae, TTLL5 localized to the centrioles at the base o

131 as quantified (qAF) in subjects with healthy retinae using a standardized approach.

132 The median presenting VA retinae was 20/30; 55 patients (95%) recovered to >/= 20

133 ighest density of cells in the contralateral retinae was found in the inferior and nasal retinal quad

134 f endogenous dopamine released from in vitro retinae was greater during the subjective day than the s

135 of ON- and OFF-CBCs in Bk(-/-) and wild-type retinae was indistinguishable.

136 eature of both ipsilateral and contralateral retinae was the paucity of labeled cells found in the do

137 l gene expression analysis of Id2a-deficient retinae, we identify a number of additional intrinsic an

138 ng immunohistochemistry in macaque and human retinae, we show that NaV1.1 is concentrated in an axon

139 Two groups of retinae were compared, those recorded after 10 min dark

140 Retinae were harvested from mice ranging in age from bir

141 Macaque retinae were immunostained with monoclonal antibodies di

142 Embryonic retinae were transplanted to intracranial locations in n

143 Rabbit and human retinae were used to investigate if there are any specie

144 The retinae were whole-mounted, viewed under fluorescence, a

145 , retinal necrosis, and surrounding commotio retinae with specific photoreceptor cell death and spari

146 of alpha and beta ganglion cells from normal retinae with those of cells located in matched areas of