Retinofugal projections in the mouse
暂无分享,去创建一个
[1] H. Pemberton. Recent investigations on the structure and relations of the optic thalami , 1891 .
[2] G B Arden,et al. The Visual System , 2021, AMA Guides to the Evaluation of Permanent Impairment, 6th Edition, 2021.
[3] F. Scalia,et al. Topographic organization of the projections of the retina to the pretectal region in the rat , 1979, The Journal of comparative neurology.
[4] G. E. Pickard,et al. Direct retinal projections to the hypothalamus, piriform cortex, and accessory optic nuclei in the golden hamster as demonstrated by a sensitive anterograde horseradish peroxidase technique , 1981, The Journal of comparative neurology.
[5] S. Newman,et al. Olfactory bulbectomy prevents the gonadal regression associated with short photoperiod in male golden hamsters , 1984, Brain Research.
[6] R. Mooney,et al. Anatomical and functional organization of pathway from superior colliculus to lateral posterior nucleus in hamster. , 1984, Journal of neurophysiology.
[7] J. K. Harting,et al. Connectional organization of the superior colliculus , 1984, Trends in Neurosciences.
[8] L. Swanson. The Rat Brain in Stereotaxic Coordinates, George Paxinos, Charles Watson (Eds.). Academic Press, San Diego, CA (1982), vii + 153, $35.00, ISBN: 0 125 47620 5 , 1984 .
[9] G. E. Pickard. Bifurcating axons of retinal ganglion cells terminate in the hypothalamic suppachiasmatic nucleus and the intergeniculate leaflet of the thalamus , 1985, Neuroscience Letters.
[10] F. Macrides,et al. Reproductive effects of olfactory bulbectomy in the Syrian hamster. , 1986, Biology of reproduction.
[11] R. F. Johnson,et al. Loss of entrainment and anatomical plasticity after lesions of the hamster retinohypothalamic tract , 1988, Brain Research.
[12] J. Simpson,et al. The accessory optic system of rabbit. I. Basic visual response properties. , 1988, Journal of neurophysiology.
[13] J I Simpson,et al. The Accessory Optic System Analyzer of Self‐Motion a , 1988, Annals of the New York Academy of Sciences.
[14] A. Cowey,et al. Development and retraction of a crossed retinal projection to the inferior colliculus in neonatal pigmented rats , 1990, Neuroscience.
[15] J. Mikkelsen. Visualization of efferent retinal projections by immunohistochemical identification of cholera toxin subunit B , 1992, Brain Research Bulletin.
[16] Henning Scheich,et al. Functional Organization of Auditory Cortex in the Mongolian Gerbil (Meriones unguiculatus). I. Electrophysiological Mapping of Frequency Representation and Distinction of Fields , 1993, The European journal of neuroscience.
[17] E. Nevo,et al. Visual system of a naturally microphthalmic mammal: The blind mole rat, Spalax ehrenbergi , 1993, The Journal of comparative neurology.
[18] H. Collewijn,et al. Three-dimensional organization of optokinetic responses in the rabbit. , 1993, Journal of neurophysiology.
[19] M. Herbin,et al. Neuroanatomical pathways linking vision and olfaction in mammals , 1994, Psychoneuroendocrinology.
[20] L. P. Morin. The circadian visual system , 1994, Brain Research Reviews.
[21] H. Urbanski,et al. Lesions in the bed nucleus of the stria terminalis, but not in the lateral septum, inhibit short-photoperiod-induced testicular regression in Syrian hamsters , 1995, Brain Research.
[22] S. Sugita,et al. Retinal projections to the subcortical nuclei in the Japanese field vole (Microtus montebelli). , 1995, Experimental animals.
[23] R. Guillery,et al. Functional organization of thalamocortical relays. , 1996, Journal of neurophysiology.
[24] George Paxinos,et al. The Mouse Brain in Stereotaxic Coordinates , 2001 .
[25] Michael Davis,et al. Double Dissociation between the Involvement of the Bed Nucleus of the Stria Terminalis and the Central Nucleus of the Amygdala in Startle Increases Produced by Conditioned versus Unconditioned Fear , 1997, The Journal of Neuroscience.
[26] L. P. Morin,et al. Neuropeptide Y and enkephalin immunoreactivity in retinorecipient nuclei of the hamster pretectum and thalamus , 1997, Visual Neuroscience.
[27] M. Harrington. The Ventral Lateral Geniculate Nucleus and the Intergeniculate Leaflet: Interrelated Structures in the Visual and Circadian Systems , 1997, Neuroscience & Biobehavioral Reviews.
[28] G. Schneider,et al. Target-specific morphology of retinal axon arbors in the adult hamster , 1998, Visual Neuroscience.
[29] A. Silverman,et al. Evidence for estrogen receptor in cell nuclei and axon terminals within the lateral habenula of the rat: Regulation during pregnancy , 1998, The Journal of comparative neurology.
[30] R. W. Rodieck. The First Steps in Seeing , 1998 .
[31] W. P. Hayes,et al. Melanopsin: An opsin in melanophores, brain, and eye. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[32] S. Nakagawa,et al. The retinal projections to the ventral and dorsal divisions of the medial terminal nucleus and mesencephalic reticular formation in the Japanese monkey (Macaca fuscata): a reinvestigation with cholera toxin B subunit as an anterograde tracer , 1998, Brain Research.
[33] L. P. Morin,et al. Interconnections among nuclei of the subcortical visual shell: The intergeniculate leaflet is a major constituent of the hamster subcortical visual system , 1998, The Journal of comparative neurology.
[34] L. P. Morin,et al. Forebrain connections of the hamster intergeniculate leaflet: Comparison with those of ventral lateral geniculate nucleus and retina , 1999, Visual Neuroscience.
[35] H. Scheich,et al. Functional organization of auditory cortex in the Mongolian gerbil (Meriones unguiculatus). IV. Connections with anatomically characterized subcortical structures , 2000, The European journal of neuroscience.
[36] L. P. Morin,et al. Neuromodulator content of hamster intergeniculate leaflet neurons and their projection to the suprachiasmatic nucleus or visual midbrain , 2001, The Journal of comparative neurology.
[37] C. Leamey,et al. Evidence for a visual subsector within the zona incerta , 2001, Visual Neuroscience.
[38] Satchidananda Panda,et al. Melanopsin (Opn4) Requirement for Normal Light-Induced Circadian Phase Shifting , 2002, Science.
[39] D. Berson,et al. Phototransduction by Retinal Ganglion Cells That Set the Circadian Clock , 2002, Science.
[40] K. Yau,et al. Melanopsin-Containing Retinal Ganglion Cells: Architecture, Projections, and Intrinsic Photosensitivity , 2002, Science.
[41] D. Boire,et al. Retinal projections in the cat: A cholera toxin B subunit study , 2003, Visual Neuroscience.
[42] H. Rodman,et al. Pattern of retinal projections in the California ground squirrel (Spermophilus beecheyi): Anterograde tracing study using cholera toxin , 2003, The Journal of comparative neurology.
[43] Andrew D Huberman,et al. Crossed and uncrossed retinal projections to the hamster circadian system , 2003, The Journal of comparative neurology.
[44] M. Biel,et al. Melanopsin and rod–cone photoreceptive systems account for all major accessory visual functions in mice , 2003, Nature.
[45] F. Davis,et al. Disruption of masking by hypothalamic lesions in Syrian hamsters , 2004, Journal of Comparative Physiology A.
[46] L. P. Morin,et al. Intergeniculate leaflet and ventral lateral geniculate nucleus afferent connections: An anatomical substrate for functional input from the vestibulo‐visuomotor system , 2004, The Journal of comparative neurology.
[47] J. Pokorny,et al. Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN , 2005, Nature.
[48] B. Rusak,et al. Circadian firing-rate rhythms and light responses of rat habenular nucleus neurons in vivo and in vitro , 2005, Neuroscience.
[49] L. P. Morin,et al. Descending projections of the hamster intergeniculate leaflet: Relationship to the sleep/arousal and visuomotor systems , 2005, The Journal of comparative neurology.
[50] L. P. Morin,et al. The circadian visual system, 2005 , 2006, Brain Research Reviews.
[51] F. Lui,et al. The accessory optic system: basic organization with an update on connectivity, neurochemistry, and function. , 2006, Progress in brain research.
[52] P. May. The mammalian superior colliculus: laminar structure and connections. , 2006, Progress in brain research.
[53] Samer Hattar,et al. Central projections of melanopsin‐expressing retinal ganglion cells in the mouse , 2006, The Journal of comparative neurology.
[54] L. P. Morin,et al. Targeted Destruction of Photosensitive Retinal Ganglion Cells with a Saporin Conjugate Alters the Effects of Light on Mouse Circadian Rhythms , 2008, PloS one.
[55] T. Badea,et al. Melanopsin cells are the principal conduits for rod–cone input to non-image-forming vision , 2008, Nature.
[56] Satchidananda Panda,et al. Inducible Ablation of Melanopsin-Expressing Retinal Ganglion Cells Reveals Their Central Role in Non-Image Forming Visual Responses , 2008, PloS one.
[57] Jeffery A Winer,et al. Connections of cat auditory cortex: I. Thalamocortical system , 2008, The Journal of comparative neurology.
[58] Charles C Lee,et al. Connections of cat auditory cortex: III. Corticocortical system , 2008, The Journal of comparative neurology.
[59] Henning Scheich,et al. Anatomical connections suitable for the direct processing of neuronal information of different modalities via the rodent primary auditory cortex , 2009, Hearing Research.
[60] C. Saper,et al. Sleep State Switching , 2010, Neuron.
[61] Clifford B. Saper,et al. A neural mechanism for exacerbation of headache by light , 2010, Nature Neuroscience.
[62] Glen T. Prusky,et al. Melanopsin-Expressing Retinal Ganglion-Cell Photoreceptors: Cellular Diversity and Role in Pattern Vision , 2010, Neuron.
[63] H. Piggins,et al. Circadian oscillators in the epithalamus , 2010, Neuroscience.
[64] R. Lucas,et al. A Distinct Contribution of Short-Wavelength-Sensitive Cones to Light-Evoked Activity in the Mouse Pretectal Olivary Nucleus , 2011, The Journal of Neuroscience.
[65] Anna Matynia,et al. Melanopsin-Positive Intrinsically Photosensitive Retinal Ganglion Cells: From Form to Function , 2011, The Journal of Neuroscience.
[66] Benjamin A Rowland,et al. Organization and plasticity in multisensory integration: early and late experience affects its governing principles. , 2011, Progress in brain research.
[67] R. Burstein,et al. Advances in understanding the mechanisms of migraine-type photophobia. , 2011, Current opinion in neurology.
[68] M. Paul,et al. A role for the habenula in the regulation of locomotor activity cycles , 2011, The European journal of neuroscience.
[69] L. P. Morin,et al. Separation of function for classical and ganglion cell photoreceptors with respect to circadian rhythm entrainment and induction of photosomnolence , 2011, Neuroscience.
[70] T. Badea,et al. Photoentrainment and pupillary light reflex are mediated by distinct populations of ipRGCs , 2011, Nature.
[71] Charles A Czeisler,et al. Melanopsin and Rod–Cone Photoreceptors Play Different Roles in Mediating Pupillary Light Responses during Exposure to Continuous Light in Humans , 2012, The Journal of Neuroscience.
[72] R. Krauzlis,et al. Superior colliculus and visual spatial attention. , 2013, Annual review of neuroscience.
[73] H. Karten,et al. Retinorecipient areas in the diurnal murine rodent Arvicanthis niloticus: A disproportionally large superior colliculus , 2013, The Journal of comparative neurology.
[74] L. P. Morin. Neuroanatomy of the extended circadian rhythm system , 2013, Experimental Neurology.
[75] R. Burstein,et al. Hypothalamic and basal ganglia projections to the posterior thalamus: Possible role in modulation of migraine headache and photophobia , 2013, Neuroscience.
[76] Onkar S Dhande,et al. Genetic Dissection of Retinal Inputs to Brainstem Nuclei Controlling Image Stabilization , 2013, The Journal of Neuroscience.
[77] L. P. Morin,et al. Brief light stimulation during the mouse nocturnal activity phase simultaneously induces a decline in core temperature and locomotor activity followed by EEG-determined sleep. , 2013, American journal of physiology. Regulatory, integrative and comparative physiology.
[78] Onkar S. Dhande,et al. Retinal ganglion cell maps in the brain: implications for visual processing , 2014, Current Opinion in Neurobiology.