Parallel processing in the mammalian retina
By H. Wässle. Nature Reviews Neuroscience, 2004
1,192 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/bf9644f1658adea61f2a72e10b25c052655fb678
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In Cellular and Molecular Neuroscience
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In Molecular Biology
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Citations in the corpus
- Approach sensitivity in the retina processed by a multifunctional neural circuit (2009, background): “In this scenario, the AII amacrine cell fulfills a function very different from the one it is well known for—namely, amplifying rod signals by conveying them to ON and OFF cone pathway”
- Retinomorphic Event-Based Vision Sensors: Bioinspired Cameras With Spiking Output (2014, background): “Biologists have reported between 20 and up to 50 different types of cells in biological retinas [14], [23].”
- Cellular Basis for Contrast Gain Control over the Receptive Field Center of Mammalian Retinal Ganglion Cells (2007, background): “With 30 distinct types, amacrine cells are the predominant inhibitory interneuron and could therefore drive gain control through synaptic inhibition (Vaney, 1990; MacNeil and Masland, 1998; Wassle, 2004).”
- The Radical-Pair Mechanism of Magnetoreception. (2016, background): “Functional neuroanatomy data alone cannot identify which cell types within the eyes contain the primary magnetic sensory molecules because all information leaving the eyes is transmitted through the retinal ganglion cells to the rest of the brain (36, 199), and the retinal ganglion cells (and a few ”
- New World Monkeys and Color (2007, background): “Why that should be so has been the subject of much comment ( Boycott and Wassle 1999; Kremers et al. 1999; Mollon 1995).”
- Do We Know What the Early Visual System Does? (2005, background): “Understanding the retinal output The retina contains a complex network of cells, divided into an estimated 60 – 80 cell types: 3– 4 photoreceptors, 40 –50 interneurons, and 15–20 ganglion cells, whose spike trains transmit visual information to the rest of the brain (Masland, 2001; Sterling and Demb”
- Functional mechanisms shaping lateral geniculate responses to artificial and natural stimuli. (2008, methodology): “X cells, which correspond to 50% of retinal ganglion cells in the cat (Masland, 2001; Rodieck et al., 1993; Wassle, 2004).”
- Information processing in the primate retina: circuitry and coding. (2007, background): “Cumulatively, amacrine cells appear to provide the greatest number of synapses to at least some types of RGCs (Bordt et al. 2006, Ghosh & Grunert 1999, Marshak et al. 2002) and express a stunning diversity of neurotransmitters (see Kolb 1997, Masland 2001, Wassle 2004).”
- Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration. (2006, neutral): “In the retina, photoreceptor cells convert light signals to electrical signals that are then relayed through second- and third-order retinal neurons to higher visual centers in the brain (Baylor, 1996; Wässle, 2004).”
- Article The Color-Vision Circuit in the Medulla of Drosophila (2008, neutral): “In the mammalian retina, horizontal and amacrine cells are interneurons that have a critical role in modulating retinal output [2].”
- Revealing neuronal function through microelectrode array recordings (2015, neutral): “Responses of RGCs can be recorded using different types of light stimulations (Segev et al., 2004; Wässle, 2004; Jones et al., 2011).”