Electrical and Metabolic Manifestations of Receptor and Higher-Order Neuron Activity in Vertebrate Retina

Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording.

Werblin, F. S., & Dowling, J. E. (1969) · Journal of Neurophysiology · doi:10.1152/jn.1969.32.3.339 · Cited by 1,384 · see citing works

Handbook of Sensory Physiology

Newell, F. W. (1973) · American Journal of Ophthalmology · doi:10.1016/0002-9394(73)90115-3 · Cited by 986 · see citing works

Dark Current and Photocurrent in Retinal Rods

Hagins, W. A., Penn, R. D., & Yoshikami, S. (1970) · Biophysical Journal · doi:10.1016/s0006-3495(70)86308-1 · Cited by 562 · see citing works

The electroretinogram: Its components and their origins

Brown, K. T. (1968) · Vision Research · doi:10.1016/0042-6989(68)90041-2 · Cited by 558 · see citing works

Electrical responses of single cones in the retina of the turtle

Baylor, D. A., & Fuortes, M. G. F. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009049 · Cited by 546 · see citing works

Sensory Mechanisms of the Retina

Matthews, B. H. C. (1949) · Nature · doi:10.1038/163423a0 · Cited by 504 · see citing works

Electrophysiological Study of the Mechanisms Subserving Color Coding in the Fish RetinaPreprint

Tomita, T. (1965) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1965.030.01.054 · Cited by 335 · see citing works

THE VISUAL SYSTEM: NEUROPHYSIOLOGY AND PSYCHOPHYSICS

Brindley, G. S. (1962) · Quarterly Journal of Experimental Physiology and Cognate Medical Sciences · doi:10.1113/expphysiol.1962.sp001627 · Cited by 286 · see citing works

Sensory Mechanisms of the Retina

Lebensohn, J. E. (1947) · American Journal of Ophthalmology · doi:10.1016/0002-9394(47)90405-4 · Cited by 219 · see citing works

Clinical Electroretinography

Carr, R. E. (1966) · JAMA · doi:10.1001/jama.1966.03110140105029 · Cited by 184 · see citing works

Einführung in die Physiologie des Menschen

Rein, H. (1938) · Springer eBooks · doi:10.1007/978-3-662-36784-1 · Cited by 152 · see citing works

EFFECTS OF SOME COMMON CATIONS ON ELECTRORETINOGRAM OF THE TOAD

Furukawa, T., & Hanawa, I. (1955) · The Japanese Journal of Physiology · doi:10.2170/jjphysiol.5.289 · Cited by 124 · see citing works

Retinal Metabolism in Dark and Light

Sickel, W. (1972) · Handbook of sensory physiology · doi:10.1007/978-3-642-65340-7_19 · Cited by 121 · see citing works

The rod response in the frog as studied by intracellular recording

Toyoda, J., Hashimoto, H., Anno, H., & Tomita, T. (1970) · Vision Research · doi:10.1016/0042-6989(70)90026-x · Cited by 93 · see citing works

The Visual System: Neurophysiology and Psychophysics

Enroth‐Cugell, C. (1962) · American Journal of Ophthalmology · doi:10.1016/0002-9394(62)92206-7 · Cited by 90 · see citing works

Respiratory and Electrical Responses to Light Stimulation in the Retina of the Frog

Sickel, W. (1965) · Science · doi:10.1126/science.148.3670.648 · Cited by 71 · see citing works

An electrical model of the vertebrate photoreceptor cell

Bortoff, A., & Norton, A. L. (1967) · Vision Research · doi:10.1016/0042-6989(67)90089-2 · Cited by 53 · see citing works

Delayed off-responses recorded from the isolated frog retina

Crescitelli, F., & Sickel, E. (1968) · Vision Research · doi:10.1016/0042-6989(68)90131-4 · Cited by 46 · see citing works

Delayed decay of the late receptor potential of monkey cones as a function of stimulus intensity

Brown, K. T., & Murakami, M. (1967) · Vision Research · doi:10.1016/0042-6989(67)90082-x · Cited by 26 · see citing works

Delayed responses of ganglion cells in the frog retina: The influence of stimulus parameters upon the length of the delay time

Pickering, S. G., & Varjú, D. (1969) · Vision Research · doi:10.1016/0042-6989(69)90094-7 · Cited by 25 · see citing works

Delayed electrical responses from the isolated frog retina

Sickel, W., & Crescitelli, F. (1967) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00363818 · Cited by 22 · see citing works

Einführung in die Physiologie des Menschen

Schneider, M. (1971) · Springer eBooks · doi:10.1007/978-3-662-06868-7 · Cited by 18 · see citing works

UNTERSUCHUNGEN AN DER UMSTRÖMTEN FROSCHNETZHAUT ZUR ANALYSE DES ERG'S

Baumann, C., Dettmar, P., Hanitzsch, R., & Sickel, W. (1962) · Acta Ophthalmologica · doi:10.1111/j.1755-3768.1962.tb00317.x · Cited by 12 · see citing works

Thee-wave and inhibition in the developing retina of the frog

Crescitelli, F. (1970) · Vision Research · doi:10.1016/0042-6989(70)90025-8 · Cited by 12 · see citing works

A possible behavioral correlate of delayed retinal discharge in anurans

Ingle, D. (1971) · Vision Research · doi:10.1016/0042-6989(71)90233-1 · Cited by 10 · see citing works

La réponse électro-rétinographique aux stimulations couplées chez les sujets normaux

François, J., & Rouck, A. D. (2010) · Ophthalmologica · doi:10.1159/000303864 · Cited by 4 · see citing works

[Analysis of the distribution of potentials and currents inside of the retina curing light stimulation. II. Passive distribution of potentials and currents in the retina as in a volume conductor].

Al, B. (1960) · PubMed · Cited by 4 · see citing works

Regressive Evolution in the Mexican Cave Tetra, Astyanax mexicanus

Protas, M. E., Conrad, M. D., Gross, J. B., Tabin, C. J., & Borowsky, R. L. (2007) · Current Biology · doi:10.1016/j.cub.2007.01.051 · Cited by 263 · see citing works

Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD)

Ramkumar, H. L., Zhang, J., & Chan, C.-C. (2010) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2010.02.002 · Cited by 163 · see citing works

Oxidative Stress in Myopia

Bosch‐Morell, F., Mérida, S., & Návea, A. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/750637 · Cited by 150 · see citing works

Hypoxia-Induced Oxidative Stress in Ischemic Retinopathy

Li, S.-Y., Fu, Z., & Lo, A. (2012) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2012/426769 · Cited by 136 · see citing works

Cellular and subcellular expression of monocarboxylate transporters in the pigment epithelium and retina of the rat

Bergersen, L. H., Jóhannsson, E., Veruki, M. L., Nagelhus, E. A., Halestrap, A. P., Sejersted, O. M., & Ottersen, O. P. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00427-8 · Cited by 118 · see citing works

Phototransduction Influences Metabolic Flux and Nucleotide Metabolism in Mouse Retina

Du, J., Rountree, A. M., Cleghorn, W. M., Contreras, L., Lindsay, K. J., Sadı́lek, M., Gu, H., Djukovic, D., Raftery, D., Satrústegui, J., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.698985 · Cited by 97 · see citing works

Nutritional and Lifestyle Interventions for Age‐Related Macular Degeneration: A Review

Carneiro, Â. M., & Andrade, J. P. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/6469138 · Cited by 86 · see citing works

Oxygen consumption and ATP changes of the vertebrate photoreceptor

Kimble, E. A., Svoboda, R. A., & Ostroy, S. E. (1980) · Experimental Eye Research · doi:10.1016/s0014-4835(80)80037-6 · Cited by 66 · see citing works

Pathogenesis and Prevention of Worsening Axial Elongation in Pathological Myopia

Pugazhendhi, S., Ambati, B. K., & Hunter, A. A. (2020) · Clinical ophthalmology · doi:10.2147/opth.s241435 · Cited by 61 · see citing works

Sustained Elevation of Intracellular cGMP Causes Oxidative Stress Triggering Calpain-Mediated Apoptosis in Photoreceptor Degeneration

Sharma, A. K., & Rohrer, B. (2007) · Current Eye Research · doi:10.1080/02713680601161238 · Cited by 61 · see citing works

Genetics of age-related macular degeneration

Ting, A., Lee, T. K. M., & MacDonald, I. M. (2009) · Current Opinion in Ophthalmology · doi:10.1097/icu.0b013e32832f8016 · Cited by 56 · see citing works

The isolated perfused bovine retina—A sensitive tool for pharmacological research on retinal function

Lüke, M., Weiergräber, M., Brand, C., Siapich, S. A., Banat, M., Hescheler, J., Lüke, C., & Schneider, T. (2005) · Brain Research Protocols · doi:10.1016/j.brainresprot.2005.09.001 · Cited by 49 · see citing works

Polymorphisms of the DNA Repair Genes XPD and XRCC1 and the Risk of Age-Related Macular Degeneration

Görgün, E., Güven, M., Ünal, M., Batar, B., Güven, G. S., Yenerel, N. M., Tatlıpınar, S., Seven, M., & Yüksel, A. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4842 · Cited by 38 · see citing works

Immediate Effect in the Retina and Choroid after 650 nm Low-Level Red Light Therapy in Children

Yang, W., Lin, F., Li, M., Wei, R., Zhou, J., & Zhou, X. (2022) · Ophthalmic Research · doi:10.1159/000527787 · Cited by 34 · see citing works

Nutraceutical Supplementation Ameliorates Visual Function, Retinal Degeneration, and Redox Status in rd10 Mice

Olivares‐González, L., Velasco, S., Campillo, I., Salom, D., García, E. G., Soriano, J. M., & Rodrigo, R. (2021) · Antioxidants · doi:10.3390/antiox10071033 · Cited by 30 · see citing works

Adherence to the Mediterranean-Style Eating Pattern and Macular Degeneration: A Systematic Review of Observational Studies

Gastaldello, A., Giampieri, F., Quiles, J. L., Navarro‐Hortal, M. D., Obregón, S. A., Villena, E. G., Pifarré, K. T., Giuseppe, R. D., Grosso, G., Cianciosi, D., et al. (2022) · Nutrients · doi:10.3390/nu14102028 · Cited by 28 · see citing works

Understanding cataract development in axial myopia: The contribution of oxidative stress and related pathways

Świerczyńska, M., Tronina, A., & Smędowski, A. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103495 · Cited by 18 · see citing works

Off-responses in the human D.C. registered electroretinogram

SKOOG, K., Welinder, E., & Nilsson, S. (1977) · Vision Research · doi:10.1016/0042-6989(77)90032-3 · Cited by 17 · see citing works

Two separate Ni 2+ ‐sensitive voltage‐gated Ca 2+ channels modulate transretinal signalling in the isolated murine retina

Alnawaiseh, M., Albanna, W., Chen, C., Campbell, K. P., Hescheler, J., Lüke, M., & Schneider, T. (2011) · Acta Ophthalmologica · doi:10.1111/j.1755-3768.2011.02167.x · Cited by 14 · see citing works

Characteristics of rod driven off-responses in cat ganglion cells

Olsen, B., Schneider, T., & Zrenner, E. (1986) · Vision Research · doi:10.1016/0042-6989(86)90142-2 · Cited by 14 · see citing works

Testing the effects of the dye Acid violet-17 on retinal function for an intraocular application in vitreo-retinal surgery

Tura, A., Alt, A., Haritoglou, C., Meyer, C. H., Schneider, T., Grisanti, S., Lüke, J., & Lüke, M. (2014) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-014-2761-9 · Cited by 12 · see citing works

Relation of the e-wave to ganglion cell activity and rod responses in the frog

Newman, E. A., & Lettvin, J. Y. (1978) · Vision Research · doi:10.1016/0042-6989(78)90102-5 · Cited by 12 · see citing works

Longer lasting electroretinographic recordings from the isolated and superfused murine retina

Albanna, W., Banat, M., Albanna, N., Alnawaiseh, M., Siapich, S. A., Igelmund, P., Weiergräber, M., Lüke, M., & Schneider, T. (2009) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-009-1119-1 · Cited by 10 · see citing works

Energy in Vertebrate Photoreceptor Function

Sickel, W. (1973) · Springer eBooks · doi:10.1007/978-3-642-85769-0_22 · Cited by 10 · see citing works

Metabolomic profiling of ocular tissues in rabbit myopia: Uncovering differential metabolites and pathways

Liang, C., Li, F., Gu, C., Xie, L. F., Wen, Y., Wang, X., Shi, R., Linghu, S., & Liu, T. (2024) · Experimental Eye Research · doi:10.1016/j.exer.2024.109796 · Cited by 9 · see citing works

Electroretinographic Assessment of Inner Retinal Signaling in the Isolated and Superfused Murine Retina

Albanna, W., Lüke, J. N., Sjapic, V., Kotliar, K. E., Hescheler, J., Clusmann, H., Sjapic, S., Alpdogan, S., Schneider, T., Schubert, G. A., et al. (2017) · Current Eye Research · doi:10.1080/02713683.2017.1339807 · Cited by 9 · see citing works

Early Retinal Findings Following Cooling in Neonatal Encephalopathy

Şahin, Ö., Cansever, M., Sırakaya, E., Robertson, N. J., & Akın, M. A. (2018) · Neuropediatrics · doi:10.1055/s-0038-1669425 · Cited by 8 · see citing works

The Retinal Biocompatibility of Dyes in the ex vivo Model of the Isolated Superfused Vertebrate Retina

Lüke, M., Grisanti, S., & Lüke, J. (2013) · Ophthalmologica · doi:10.1159/000353867 · Cited by 6 · see citing works

Addressing retinal hypoxia: pathophysiology, therapeutic innovations, and future prospects

Gnanasambandam, B., Prince, J., Limaye, S. R., Moran, E., Lee, B., Huynh, J., Irudayaraj, J., & Tsipursky, M. S. (2024) · Therapeutic Advances in Ophthalmology · doi:10.1177/25158414241280187 · Cited by 6 · see citing works

Lipid Peroxidation in Subretinal Fluid: Some Light on the Prognosis Factors

Bosch‐Morell, F., García-Gen, E., Mérida, S., Penadés, M., Desco, C., & Návea, A. (2021) · Biomolecules · doi:10.3390/biom11040514 · Cited by 6 · see citing works

The dihydropyridine isradipine inhibits the murine but not the bovine a‐wave response of the electroretinogram

Banat, M., Lüke, M., Siapich, S. A., Hescheler, J., Weiergräber, M., & Schneider, T. (2008) · Acta Ophthalmologica · doi:10.1111/j.1600-0420.2007.01126.x · Cited by 6 · see citing works

Identification of fast spurts of pyridine nucleotide oxidation evoked by light stimulation in the isolated perfused vertebrate retina

Walter, P., & Sickel, W. (1994) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/bf00194483 · Cited by 6 · see citing works

Comparison of Different Cell Culture Media in the Model of the Isolated and Superfused Bovine Retina: Investigating the Limits of More Physiological Perfusion Solutions

Hurst, J., Vitkute, M., Hofmann, K., Müller, S., Löscher, M., Bartz‐Schmidt, K. U., Spitzer, M. S., Schnichels, S., & Januschowski, K. (2017) · Current Eye Research · doi:10.1080/02713683.2017.1387668 · Cited by 5 · see citing works

Age-related macular degeneration (AMD): Current concepts in pathogenesis and prospects for treatment

Shin, O. R., & Kim, Y. H. (2013) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-012-0374-0 · Cited by 5 · see citing works

Evaluation of choroidal thickness, retinal vascular caliber, and nerve fiber layer thickness in idiopathic interstitial pneumonia.

Uğurlu, E., Pekel, G., Cengiz, B., Bozkurt, K., & Altınışık, G. (2017) · Sarcoidosis vasculitis and diffuse lung diseases · doi:10.36141/svdld.v34i1.5392 · Cited by 4 · see citing works

Molecular Mechanisms in the Pathogenesis of Retinopathy of Prematurity (ROP)

Kaur, T., Patnaik, S., Kumar, S., & Kaur, I. (2022) · Springer eBooks · doi:10.1007/978-981-16-4247-0_9 · Cited by 4 · see citing works

Evaluation of short pulse laser damage to the retinal pigment epithelium layer: a key point for the assessment of devices using the nanosecond regime

Ramos, S., Reh, M., Zeck, G. M., & Heußner, N. (2018) · Biophotonics: Photonic Solutions for Better Health Care VI · doi:10.1117/12.2306893 · Cited by 4 · see citing works

Nutrition and the ageing eye

Carneiro, Â. M. (2015) · Wiley eBooks · doi:10.1002/9781118823408.ch8 · Cited by 4 · see citing works

Energy in Central Nervous (Retinal) Function

Sickel, W. (1972) · International Journal of Neuroscience · doi:10.3109/00207457209147642 · Cited by 3 · see citing works

Conceitos atuais e perspectivas na prevenção da degeneração macular relacionada à idade

Torres, R. J. D. A., Précoma, D. B., Maia, M., Kaiber, F., Prim, C. R., Luchini, A., Matos, R. S., & Farah, M. E. (2008) · Revista Brasileira de Oftalmologia · doi:10.1590/s0034-72802008000300008 · Cited by 2 · see citing works

The role of the KEAP1-NRF2 signaling pathway in form deprivation myopia guinea pigs

Gu, Z., Meng, J., Zhong, W., Lan, C., Tan, Q., Xiang, X., Zhou, H., & Liao, X. (2024) · BMC Ophthalmology · doi:10.1186/s12886-024-03754-6 · Cited by 1 · see citing works

Submicromolar copper (II) ions stimulate transretinal signaling in the isolated retina from wild type but not from Cav2.3-deficient mice

Lüke, J. N., Neumaier, F., Alpdogan, S., Hescheler, J., Schneider, T., Albanna, W., & Akhtar‐Schäfer, I. (2020) · BMC Ophthalmology · doi:10.1186/s12886-020-01451-8 · Cited by 1 · see citing works

The Biochemistry of Photoreceptor Cells

Voaden, M. J., Marshall, J., & Oraedu, A. C. I. (1981) · Documenta ophthalmologica. Proceedings series · doi:10.1007/978-94-009-8653-4_10 · Cited by 1 · see citing works

Nutritional Supplement Use and Age-Related Macular Degeneration

Lo, A., & Yeung, I. Y. L. (2012) · InTech eBooks · doi:10.5772/33893

Low concentrations of ethanol but not of dimethyl sulfoxide (DMSO) impair reciprocal retinal signal transduction

Siapich, S. A., Akhtar‐Schäfer, I., Hescheler, J., Schneider, T., & Lüke, M. (2015) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-015-3070-7

LIGHT‐INDUCED ALTERATIONS IN RETINAL PYRUVATE AND HIGH‐ENERGY PHOSPHATES,IN VIVO

Lolley, R. N. (1969) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1969.tb09899.x · Cited by 11 · see citing works

Extracellular K+ reflects light-evoked changes in retinal energy metabolism

Dmitriev, A. V., Dmitriev, A. A., & Linsenmeier, R. A. (2022) · Experimental Eye Research · doi:10.1016/j.exer.2022.109133 · Cited by 8 · see citing works

Identification of fast spurts of pyridine nucleotide oxidation evoked by light stimulation in the isolated perfused vertebrate retina

Walter, P., & Sickel, W. (1994) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/bf00194483 · Cited by 6 · see citing works

Energy Metabolism in the Vertebrate Retina

Hurley, J. B., Chertov, A. O., Lindsay, K. J., Giarmarco, M. M., Cleghorn, W. M., Du, J., & Brockerhoff, S. E. (2014) · Springer eBooks · doi:10.1007/978-4-431-54880-5_5 · Cited by 8 · see citing works

Different states of energy metabolism in the vertebrate retina can be identified by stimulus-related changesin near UV transmission

Walter, P., Alteheld, N., Huth, J., Roessler, G. F., & Vobig, M. A. (2006) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-006-0393-4