Adrian ED, Matthews R (1927) The action of light on the eye. Part I. The discharge of impulses in the optic nerve and its relation to the electric changes in the retina. J Physiol 63:378–414
PubMed
CAS
Google Scholar
Armington JC, Johnson EP, Riggs LA (1952) The scotopic a-wave in the electrical response of the human retina. J Physiol 118:289–298
PubMed
CAS
Google Scholar
Basar E, Rosen B, Basar-Eroglu C, Greitschus F (1987) The associations between 40 Hz-EEG and the middle latency response of the auditory evoked potential. Int J Neurosci 33:103–117
PubMed
CAS
Google Scholar
Bayer AU, Mittag T, Cook P, Brodie SE, Podos SM, Maag K-P (2000) Comparisons of the amplitude size and the reproducibility of three different electrodes to record the corneal flash electroretinogram in rodents. Doc Ophthalmol 98:233–246
Article
Google Scholar
Beaulieu C, Dumont M, Lachapelle P (2005) Photostasis modifies cone and rod responses in rats. ARVO abstracts, Rockville, MD, USA
Benoit J, Lachapelle P (1990) Temporal relationship between ERG components and geniculate unit activity in rabbit. Vision Res 30:797–806
PubMed
Article
CAS
Google Scholar
Bernhard CG (1942) Temporal sequence of component potentials in the frog’s retina and the electrotonic potential in the optic nerve. Acta Physiol Scand 3:301–309
Google Scholar
Brandt ME (1997) Visual and auditory evoked phase resetting of the alpha EEG. Int J Psychophysiol 26:285–298
PubMed
Article
CAS
Google Scholar
Brankack J, Klingberg F (1985) Intensity-dependent changes of visually evoked potential components in the superior colliculus of freely moving rats. Biomed Biochim Acta 44:737–742
PubMed
CAS
Google Scholar
Brown KT, Murakami M (1964) A new receptor potential of the monkey retina with no detectable latency. Nature 201:626–628
PubMed
Article
CAS
Google Scholar
Cicerone CM (1976) Cones survive rods in the light-damaged eye of the albino rat. Science 194:1183–1185
PubMed
Article
CAS
Google Scholar
Copenhagen DR, Ashmore JF, Schnapf JK (1983) Kinetics of synaptic transmission from photoreceptors to horizontal and bipolar cells in turtle retina. Vision Res 23:363–369
PubMed
Article
CAS
Google Scholar
Dodt E, Echte K (1961) Dark and light adaptation in pigmented and white rat as measured by electroretinogram threshold. J Neurophysiol 24:427–445
PubMed
CAS
Google Scholar
Donner K (1989) Visual latency and brightness: an interpretation based on the responses of rods and ganglion cells in the frog retina. Vis Neurosci 3:39–51
PubMed
CAS
Google Scholar
Donner K, Koskelainen A, Djupsund K, Hemilä S (1995) Changes in retinal time scale under background light: observations on rods and ganglion cells in the frog retina. Vision Res 35:2255–2266
PubMed
Article
CAS
Google Scholar
Dowling JE (1967) Visual adaptation: its mechanism. Science 157(788):584–585
PubMed
CAS
Google Scholar
Falk G (1991) Retinal physiology. In: Heckenlively JR, Arden GB (eds) Principles and practice of clinical electrophysiology of vision. CV Mosby, St Louis, pp 69–84
Google Scholar
Freeman B, Singer W (1983) Direct and indirect visual inputs to superficial layers of cat superior colliculus: a current source-density analysis of electrically evoked potentials. J Neurophysiol 49:1075–1091
PubMed
CAS
Google Scholar
Galambos R, Szabó-Salfay O, Barabás P, Pálhalmi J, Szilágyi N, Juhász G (2000) Temporal distribution of the ganglion cell volleys in the normal rat optic nerve. Proc Natl Acad Sci USA 97:13454–13459
PubMed
Article
CAS
Google Scholar
Goto Y, Tobimatsu S, Shigematsu J, Akazawa K, Kato M (1999) Properties of rat cone-mediated electroretinograms during light adaptation. Curr Eye Res 19:248–253
PubMed
Article
CAS
Google Scholar
Granit R (1941) Isolation of colour-sensitive elements in a mammalian retina. Acta Physiol Scand 2:93–109
Google Scholar
Granit R (1947) Sensory mechanisms of the retina. Oxford University Press, New York
Google Scholar
Granit R, Helme T (1939) Changes in retinal excitability due to polarization and some observations on the relation between the processes in retina and nerve. J Neurophysiol 2:556–565
Google Scholar
Granit R, Therman PO (1935) Excitation and inhibition in the retina and in the optic nerve. J Physiol 88:359–381
Google Scholar
Green DG (1971) Light adaptation in the rat retina: evidence for two receptor mechanisms. Science 174:598–600
PubMed
Article
CAS
Google Scholar
Green DG (1973) Scotopic and photopic components of the rat electroretinogram. J Physiol 228:781–797
PubMed
CAS
Google Scholar
Green DG, Herreros de Tejada P, Glover MJ (1994) Electrophysiological estimates of visual sensitivity in albino and pigmented mice. Vis Neurosci 11:919–925
PubMed
CAS
Google Scholar
Gurevich L, Slaughter MM (1993) Comparison of the waveforms of the ON bipolar neuron and the b-wave of the electroretinogram. Vision Res 33:2431–2435
PubMed
Article
CAS
Google Scholar
Gönder A, Basar E (1978) Evoked frequency stabilization in the electrical activity of the cat brain. Biol Cybern 31:193–204
PubMed
Article
Google Scholar
Hetzler BE, Burkard HK (1999) Effects of dizocilpine (MK-801) on flash-evoked potentials, body temperature, and locomotor activity of hooded rats. Pharmacol Biochem Behav 62:559–573
PubMed
Article
CAS
Google Scholar
Hood DC, Birch DG (1996) B wave of the scotopic (rod) electroretinogram as a measure of the activity of human on-bipolar cells. J Opt Soc Am A Opt Image Sci Vis 13:623–633
PubMed
CAS
Article
Google Scholar
Imai R, Sugimoto S, Ando T, Sato S (1990) A procedure for recording electroretinogram and visually evoked potential in freely moving cats. J Toxicol Sci 15:263–274
PubMed
CAS
Google Scholar
Knapp AG, Schiller PH (1984) The contribution of on-bipolar cells to the electroretinogram of rabbits and monkeys. Vision Res 24:1841–18460
PubMed
Article
CAS
Google Scholar
Lund RD (1965) Uncrossed visual pathways of hooded and albino rats. Science 149:1506–1507
Article
PubMed
Google Scholar
Molotchnikoff S, Lachapelle P, Richard D, L’Archeveque P, Lessard I (1979) Latency distribution from orthodromic stimulation at the optic nerve, in the lateral geniculate nucleus and superior colliculus of rabbits. Brain Res Bull 4:579–581
PubMed
Article
CAS
Google Scholar
Molotchnikoff S, Tremblay F (1983) Influence of the visual cortex on responses of retinal ganglion cells in the rat. J Neurosci Res 10:397–409
PubMed
Article
CAS
Google Scholar
Murayama K, Sieving PA (1992) Different rates of growth of monkey and human photopic a-, b-, and d-waves suggest two sites of ERG light adaptation. Clin Vision Sci 7:385–392
Google Scholar
Nirenberg S, Meister M (1997) The light response of retinal ganglion cells is truncated by a displaced amacrine circuit. Neuron 18:637–650
PubMed
Article
CAS
Google Scholar
Nixon PJ, Bui BV, Armitage JA, Vingrys AJ (2001) The contribution of cone responses to rat electroretinogram. Clin Experiment Ophthalmol 29:193–196
PubMed
Article
CAS
Google Scholar
Nye PW (1968) An examination of the electroretinogram of the pigeon in response to stimuli of different intensity and wavelength and following intense chromatic adaptation. Vision Res 8:679–696
PubMed
Article
CAS
Google Scholar
Paxinoss G, Watson C (1986) The rat brain in stereotaxic coordinates. Academic, New York
Google Scholar
Perlman I (1983) Relationships between the amplitudes of the b wave and the a wave as a useful index for evaluating the electroretinogram. Br J Ophthalmol 67:443–448
PubMed
CAS
Google Scholar
Pinilla I, Lund RD, Sauvé Y (2004) Contribution of rod and cone pathways to the dark-adapted electroretinogram (ERG) b-wave following retinal degeneration in RCS rats. Vision Res 44:2467–2474
PubMed
Article
CAS
Google Scholar
Porciatti V, Bagnoli P, Alesi R (1987) On and off activity in the retinal and tectal responses to focal stimulation with uniform or patterned stimuli. Clin Vision Sci 2:93–102
Google Scholar
Qiu H, Fujiwara E, Liu M, Lam BL, Hamasaki DI (2002) Evidence that a-wave latency of the electroretinogram is determined solely by photoreceptors. Jpn J Ophthalmol 46:426–432
PubMed
Article
Google Scholar
Rahn E, Basar E (1993) Enhancement of visual evoked potentials by stimulation during low prestimulus EEG stages. Int J Neurosci 72:123–136
PubMed
CAS
Article
Google Scholar
Sieving PA (1993) Photopic on- and off-pathway abnormalities in retinal dystrophies. Trans Am Ophthalmol Soc 91:701–773
PubMed
CAS
Google Scholar
Sieving PA, Murayama K, Naarendorp F (1994) Push-pull model of the primate photopic electroretinogram: a role for hyperpolarizing neurons in shaping the b-wave. Vis Neurosci 11:519–532
PubMed
CAS
Article
Google Scholar
Soucy E, Wang Y, Nirenberg S, Nathans J, Meister M (1998) A novel signaling pathway from rod photoreceptors to ganglion cells in mammalian retina. Neuron 21:481–493
PubMed
Article
CAS
Google Scholar
Sterling P (1998) Retina. In: Shepherd GM (ed) The synaptic organization of the brain. Oxford University Press, New York, pp 205–253
Google Scholar
Stockton RA, Slaughter MM (1989) B-wave of the electroretinogram. A reflection of on bipolar cell activity. J Gen Physiol 93:101–122
PubMed
Article
CAS
Google Scholar
Sumimoto I, Ide K, Iwama K, Arikuni T (1969) Conduction velocity of optic nerve fibers innervating lateral geniculate body and superior colliculus in the rat. Exp Neurol 25:378–392
Article
Google Scholar
Szabó-Salfay O, Pálhalmi J, Szatmári E, Barabás P, Szilágyi N, Juhász G (2001) The electroretinogram and visual evoked potential of freely moving rats. Brain Res Bull 56:7–14
PubMed
Article
Google Scholar
Tagawa Y (1966) On the flash impulse responses in the visual system of unanesthetized cat as related to the stimulus intensity. Acta Med Nagasaki 11:1–20
PubMed
CAS
Google Scholar
Wachtmeister L (1998) Oscillatory potentials in the retina: what do they reveal. Prog Retin Eye Res 17:485–521
PubMed
Article
CAS
Google Scholar
Weleber RG, Eisner A (1988) Retinal function and physiological studies. In: Newsome DA (ed) Retinal dystrophies and degenerations. Raven Press, New York, pp 21–69
Google Scholar