[PDF] Top 20 Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina
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Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina
... investigated the ontogeny of light-driven responses in mouse retinal ganglion cells ...recorded from hundreds to thousands of RGCs ... Voir le document complet
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Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina
... investigated the ontogeny of light-driven responses in mouse retinal ganglion cells ...recorded from hundreds to thousands of RGCs ... Voir le document complet
15
Neural circuits in the mouse retina support color vision in the upper visual field
... difference in center and surround chro- matic preference in Off BCs may be due to a stronger contribu- tion of HCs compared to ACs in generating the Off BCs’ inhibitory ...feature ... Voir le document complet
15
Red‐shifted channelrhodopsin stimulation restores light responses in blind mice, macaque retina, and human retina
... strategy of expressing ReaChR in RGCs could be a therapeutic option for blind patients with severe retinal degeneration who display highly disorganized bipolar cell layers (Jacobson et al, 2013; ... Voir le document complet
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The effect of retinal GABA Depletion by Allylglycine on mouse retinal ganglion cell responses to light
... project of the Future and Emerging Technologies (FET) programme and from Newcastle University, Faculty of Medical ...course of GABA (green) expression at the onset of ... Voir le document complet
2
Rods contribute to the light-induced phase shift of the retinal clock in mammals
... melanopsin-containing ganglion cells (ipRGCs) all drive light entrainment of the master circadian pacemaker of the suprachias- matic nucleus, recent studies have proposed ... Voir le document complet
21
Activation of Neuropeptide Y Receptors Modulates Retinal Ganglion Cell Physiology and Exerts Neuroprotective Actions In Vitro
... and the Y 1 receptor localizes to rat hori- zontal cells (D’Angelo et ...2002). In another experimental paradigm, ex vivo rat retinal preparations were exposed to NMDA in order to ... Voir le document complet
22
Zac1 functions through TGFbetaII to negatively regulate cell number in the developing retina.
... as the final signal to halt amacrine cell genesis (Figure ...exist in diverse biological systems, including the counting factor in Dictyostelium, which dictates group size [2], Drosophila ... Voir le document complet
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Neuroprotection and regeneration of adult lesioned retinal ganglion cells by the modulation of fibroblast growth factor-2 and receptor tyrosine phosphatase-sigma
... Thirteen days afier nerve injury, RGC axons were anterogradely Iabeled by 10 injection of CTf3 and, 24 hrs later (2 weeks post-rnicrocrush lesion), animais were sacrificed and the optic [r] ... Voir le document complet
404
Characterisation of liver pathogenesis, human immune responses and drug testing in a humanised mouse model of HCV infection
... renders the direct-acting antiviral drugs ineffective even in the presence of IFN ...50 In the quest to achieve an effective IFN-free regimen, extensive research is now focused ... Voir le document complet
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Hyperactivation of retina by light in mice leads to photoreceptor cell death mediated by VEGF and retinal pigment epithelium permeability
... to mouse retinas was carried out as described by Wenzel et ...weeks in cyclic light at or below 80 ...lux of diffuse white-fluorescent light (TLD36 W/965 tubes, Philips, Hamburg, ... Voir le document complet
12
A biophysical model explains the spontaneous bursting behavior in the developing retina
... observed in many vertebrate species - chicks 1 , ferrets 2 , mice 3 , turtles 4 , macaques 5 ...bursts of activity propagating in the developing retina and playing a fundamental ... Voir le document complet
24
Dimensionality Reduction in spatio-temporal MaxEnt models and analysis of Retinal Ganglion Cell Spiking Activity in experiments
... for retina data obtained in a diurnal rodent (Octodon degus, having 30% of cones photoreceptors) and a 252-MEA ...types of stimuli were used: spatio-temporal uniform light, white noise ... Voir le document complet
2
Regulation of ERK signalling pathway in the developing mouse blastocyst
... for the deposit and dissemination of sci- entific research documents, whether they are pub- lished or ...not. The documents may come from teaching and research institutions in France ... Voir le document complet
29
Mitochondrial Protection by Exogenous Otx2 in Mouse Retinal Neurons
... However, the first hypothesis was not applicable to T2 OFF-cone bipolar cells, which did not differ in P13 Otx2 +/+ and Otx2 +/GFP mouse retinas but later degenerated more rapidly than ... Voir le document complet
15
Expression of the Fgf6 gene is restricted to developing skeletal muscle in the mouse embryo
... RESULTS In situ analysis of the fetal expression of FGF6 In order to localize Fgf6 expression during embryogenesis, sections of prefixed mouse embryos at various ... Voir le document complet
11
The LEI/L-DNase II pathway is activated in light-induced retinal degeneration in rats.
... results of these experiments are shown in figure 2. The acid DNase activity increases with the time of ...days of illumination, DNA degradation is observed after 150 minutes ... Voir le document complet
15
Separation of the retinal and central contribution to changes in visual performance after light exposure
... Effect of light on the eye It is well known that the mammalian visual system undergoes a complex diurnal transition between processes optimized for high (photopic) and low (scotopic) ... Voir le document complet
52
Cochlear hair cell regeneration from neonatal mouse supporting cells
... Here, using in vitro lineage tracing with the supporting cell markers Sox2 and Lgr5, we show that Lgr5-positive inner pillar and 3 rd Deiter's cells in gentamicin-damaged o[r] ... Voir le document complet
91
Developing electrical properties of postnatal mouse lumbar motoneurons
... 20% of motoneurons with a delayed onset firing pattern. In another set of motoneurons, a maximal proportion of 27% of such delayed firing was reached at an age between P6 and P8 (not ... Voir le document complet
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