Results for 'V1-ATPase'

116 found
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  1.  22
    Tender love and disassembly: How a TLDc domain protein breaks the V‐ATPase.Stephan Wilkens, Md Murad Khan, Kassidy Knight & Rebecca A. Oot - 2023 - Bioessays 45 (7):2200251.
    Vacuolar ATPases (V‐ATPases, V1Vo‐ATPases) are rotary motor proton pumps that acidify intracellular compartments, and, when localized to the plasma membrane, the extracellular space. V‐ATPase is regulated by a unique process referred to as reversible disassembly, wherein V1‐ATPase disengages from Vo proton channel in response to diverse environmental signals. Whereas the disassembly step of this process is ATP dependent, the (re)assembly step is not, but requires the action of a heterotrimeric chaperone referred to as the RAVE complex. Recently, an (...)
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  2.  3
    Nikon 1 J1/V1 for Dummies.Julie Adair King - 2012 - For Dummies.
    Master Nikon's first mirrorless camera with this full-color guide The Nikon 1 is a revolutionary new pocket-size camera line that packs the power of a digital SLR into a smaller body. This easy-to-follow guide covers both the J1 and V1 models, showing you all the modes and capabilities of each and how to use them. Illustrated with full-color images to show what you can achieve, it explores all the controls, different lenses, auto and video shooting modes, and how you can (...)
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  3.  15
    Ongoing Slow Fluctuations in V1 Impact on Visual Perception.Afra M. Wohlschläger, Sarah Glim, Junming Shao, Johanna Draheim, Lina Köhler, Susana Lourenço, Valentin Riedl & Christian Sorg - 2016 - Frontiers in Human Neuroscience 10:1-13.
    The human brain’s ongoing activity is characterized by intrinsic networks of coherent fluctuations, measured for example with correlated functional magnetic resonance imaging signals. So far, however, the brain processes underlying this ongoing blood oxygenation level dependent (BOLD) signal orchestration and their direct relevance for human behavior are not sufficiently understood. In this study, we address the question of whether and how ongoing BOLD activity within intrinsic occipital networks impacts on conscious visual perception. To this end, backwardly masked targets were presented (...)
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  4.  14
    The vacuolar proton‐ATPase of eukaryotic cells.Nathan Nelson - 1987 - Bioessays 7 (6):251-254.
    A novel class of proton‐ATPase has been identified in the vacuolar system of eukaryotic cells. The properties of these enzymes and their relation to other proton‐ATPases is discussed.
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  5.  97
    Striate cortex (v1) activity Gates awareness of motion.Juha Silvanto, Alan Cowey, Nilli Lavie & Vincent Walsh - 2005 - Nature Neuroscience 8 (2):143-144.
    A key question in understanding visual awareness is whether any single cortical area is indispensable. In a transcranial magnetic stimulation experiment, we show that observers' awareness of activity in extrastriate area VS depends on the amount of activity in striate cortex (Vl). From the timing and pattern of effects, we infer that back-projections from extrastriate cortex influence information content in Vl, but it is Vl that determines whether that information reaches awareness.
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  6.  40
    A 200‐amino acid ATPase module in search of a basic function.Fabrice Confalonieri & Michel Duguet - 1995 - Bioessays 17 (7):639-650.
    A fast growing family of ATPases has recently been highlighted. It was named the AAA family, for ATPases Associated to a variety of cellular Activities. The key feature of the family is a highly conserved module of 230 amino acids present in one or two copies in each protein. Despite extensive sequence conservation, the members of the family fulfil a large diversity of cellular functions: cell cycle regulation, gene expression in yeast and HIV, vesicle‐mediated transport, peroxisome assembly, 26S protease function (...)
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  7. Neurogeometry of v1 and Kanizsa contours.Jean Petitot - 2003 - Axiomathes 13 (3):347-363.
    We present a neuro-geometrical model for generating the shape of Kanizsa's modal subjective contours which is based on the functional architecture of the primary areas of the visual cortex. We focus on V1 and its pinwheel structure and model it as a discrete approximation of a continuous fibration π: R × P → P with base space the space of the retina R and fiber the projective line P of the orientations of the plane. The horizontal cortico-cortical connections of V1 (...)
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  8.  40
    Double dissociation of v1 and V5/MT activity in visual awareness.Juha Silvanto, Nilli Lavie & Vincent Walsh - 2005 - Cerebral Cortex 15 (11):1736-1741.
  9.  6
    Central Works of Philosophy V1: Ancient and Medieval.John Shand - 2004 - Routledge.
    This collection of essays showcases the most important and influential philosophical works of the ancient and medieval period, roughly from 600 BC to AD 1600. Each chapter takes a particular work of philosophy and discusses its proponent, its content and central arguments. These are: Plato's Republic; Aristotle' Nichomachean Ethics; Lucretius' On the Nature of the Universe; Sextus Emperiicus' Outlines of Pyrrhonism; Plotinus' The Enneads; Augustine's City of God; Anselm's Proslogion; Aquinas' Summa Theologia; Duns Scotus' Ordinatio; William of Ockham's Summa Logicae.
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  10.  16
    A regulatory switch involving a Clp atpase.Beth A. Lazazzera & Alan D. Grossman - 1997 - Bioessays 19 (6):455-458.
    Clp ATPase chaperone proteins are found in procaryotes and eucaryotes. Recently, ClpC of Bacillus subtilis was found to be part of a regulatory switch(1). ClpC, in combination with the MecA and ComS proteins, regulates the activity of a transcription factor, ComK, which is necessary for the development of genetic competence (the ability to bind and take up exogenous DNA). The complex of ClpC:MecA:ComK renders ComK inactive. Interaction between ComS and the ternary complex releases active ComK. This regulatory switch controls (...)
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  11. Sāṅkhyasaptativr̥ttiḥ: (V1) =.Esther Abraham Solomon (ed.) - 1973 - Ahmedabad: Gujarat University.
     
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  12.  54
    Unconscious inference and conscious representation: Why primary visual cortex (v1) is directly involved in visual awareness.Zhicheng Lin - 2008 - Behavioral and Brain Sciences 31 (2):209-210.
    The extent to which visual processing can proceed in the visual hierarchy without awareness determines the magnitude of perceptual delay. Increasing data demonstrate that primary visual cortex (V1) is involved in consciousness, constraining the magnitude of visual delay. This makes it possible that visual delay is actually within the optimal lengths to allow sufficient computation; thus it might be unnecessary to compensate for visual delay.
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  13.  36
    Regulation of the Ca 2+ pump atpase by cAMP‐dependent phosphorylation of phospholamban.Michihiko Tada & Masaaki Kadoma - 1989 - Bioessays 10 (5):157-163.
    Ca2+ transients in myocardial cells are modulated by cyclic AMP‐dependent phosphorylation of a protein in the sarcoplasmic reticulum. This protein, termed phospholamban, serves to regulate the Ca2+ pump ATPase of this membrane, thus altering the mode of Ca2+ transients and the myocardial contractile response. Elucidating the structure of phospholamban and its intimate interaction with the Ca2+ pump ATPase should provide the basis for understanding, at the molecular level, how the cAMP system contributes to excitation‐contraction coupling in muscle cells.
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  14.  67
    Neural mechanisms of spatial selective attention in areas v1, v2, and v4 of macaque visual cortex.Stephen Luck, Leonardo Chelazzi, Steven Hillyard & Robert Desimone - 1997 - Journal of Neurophysiology 77 (1):24-42.
  15.  58
    The role of primary visual cortex (v1) in visual awareness.Victor A. F. Lamme, H. Landman Super, P. R. R. Roelfsema & H. Spekreijse - 2000 - Vision Research 40 (10):1507-21.
  16.  25
    New insights into structure‐function relationships between archeal ATP synthase (A 1 A 0 ) and vacuolar type ATPase (V 1 V 0 ). [REVIEW]Gerhard Grüber & Vladimir Marshansky - 2008 - Bioessays 30 (11-12):1096-1109.
    Adenosine triphosphate, ATP, is the energy currency of living cells. While ATP synthases of archae and ATP synthases of pro‐ and eukaryotic organisms operate as energy producers by synthesizing ATP, the eukaryotic V‐ATPase hydrolyzes ATP and thus functions as energy transducer. These enzymes share features like the hydrophilic catalytic‐ and the membrane‐embedded ion‐translocating sector, allowing them to operate as nano‐motors and to transform the transmembrane electrochemical ion gradient into ATP or vice versa. Since archaea are rooted close to the (...)
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  17. A TMS study of the ventral projections from v1 with implications for the finding of neural correlates of consciousness.Morten Overgaard, Jorgen Feldbaek Nielsen & Anders Fuglsang-Frederiksen - 2004 - Brain and Cognition 54 (1):58-64.
     
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  18. Accuracy of identification of grating contrast by human observers: Bayesian models of V1 contrast processing show correspondence between discrimination and identification performance.Mazviita Chirimuuta & David Tolhurst - unknown
     
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  19. Does a Bayesian model of V1 contrast coding offer a neurophysiological account of human contrast discrimination?Mazviita Chirimuuta & David Tolhurst - unknown
     
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  20. Brain activity along the apparent motion path-recurrent feedback of area hMT/V5 to V1.L. Muckli, A. Kohler, M. Wibral & W. Singer - 1996 - In Enrique Villanueva (ed.), Perception. Ridgeview Pub. Co. pp. 22-22.
  21. Disruption of visual evoked potentials following a v1 lesion: Implications for blindsight.Anling Rao, Anna C. Nobre & Alan Cowey - 2001 - In Beatrice de Gelder, Edward H. F. De Haan & Charles A. Heywood (eds.), Out of Mind: Varieties of Unconscious Processes. New York: Oxford University Press. pp. 69-86.
     
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  22.  11
    Animal plasma membrane energization by proton-motive V-ATPases.Helmut Wieczorek, Dennis Brown, Sergio Grinstein, Jordi Ehrenfeld & William R. Harvey - 1999 - Bioessays 21 (8):637-648.
  23. Meditation on Natural Luminosity 9 v1.Rudolph Bauer - 2011 - Transmission 1.
    This paper focuses on meditation as natural luminousity.
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  24. The Visible and the Invisible 16 v1.Rudolph Bauer - 2011 - Transmission 1.
    This paper describes the non dual relationship between the visible and the invisible.
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  25.  38
    Retinotopic patterns of background connectivity between V1 and fronto-parietal cortex are modulated by task demands.Joseph C. Griffis, Abdurahman S. Elkhetali, Wesley K. Burge, Richard H. Chen & Kristina M. Visscher - 2015 - Frontiers in Human Neuroscience 9.
  26. Origin of suppressive signals in the receptive-field surround of V1 neurons in macaque.B. S. Webb, N. T. Dhruv, J. W. Peirce, S. G. Solomon & P. Lennie - 1996 - In Enrique Villanueva (ed.), Perception. Ridgeview Pub. Co. pp. 46-46.
     
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  27.  57
    On the logics related to A. Arruda’s system V1.V. M. Popov - 1999 - Logic and Logical Philosophy 7:87.
  28. Long-distance feedback projections to area v1: Implications for multisensory integration, spatial awareness, and visual consciousness.Simon Clavagnier, Arnaud Falchier & Henry Kennedy - 2004 - Cognitive, Affective and Behavioral Neuroscience. Special Issue 4 (2):117-126.
  29.  54
    Parallel processing of face and house stimuli by V1 and specialized visual areas: a magnetoencephalographic (MEG) study.Yoshihito Shigihara & Semir Zeki - 2014 - Frontiers in Human Neuroscience 8.
  30.  20
    Emotion And Attention Interactively Regulate The Flow Of Information In V1 As Early As 75 ms After Stimulus Onset.Rossi Valentina & Pourtois Gilles - 2015 - Frontiers in Human Neuroscience 9.
  31. ffytche, DH (2002). Neural codes forconsciousvision. Trends inCognitiveScience, 6, 493–495. ffytche, DH, Guy, CN, & Zeki, S.(1995). The parallel visual motion inputs into areas V1 and V5 of human cerebral cortex. Brain, 118, 1375–1394. ffytche, DH, Howard, RJ, Brammer, MJ, David, A., Woodruff, P., & Williams, S.(1998). The anatomy of conscious vision: an fMRI study of visual halluci. [REVIEW]J. A. Nunn & L. J. Gregory - 2005 - In Robertson, C. L. & N. Sagiv (eds.), Synesthesia: Perspectives From Cognitive Neuroscience. Oxford University Press. pp. 57--144.
     
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  32.  26
    Releasing the cohesin ring: A rigid scaffold model for opening the DNA exit gate by Pds5 and Wapl.Zhuqing Ouyang & Hongtao Yu - 2017 - Bioessays 39 (4):1600207.
    The ring‐shaped ATPase machine, cohesin, regulates sister chromatid cohesion, transcription, and DNA repair by topologically entrapping DNA. Here, we propose a rigid scaffold model to explain how the cohesin regulators Pds5 and Wapl release cohesin from chromosomes. Recent studies have established the Smc3‐Scc1 interface as the DNA exit gate of cohesin, revealed a requirement for ATP hydrolysis in ring opening, suggested regulation of the cohesin ATPase activity by DNA and Smc3 acetylation, and provided insights into how Pds5 and (...)
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  33.  38
    Contrasting Approaches to a Biological Problem: Paul Boyer, Peter Mitchell and the Mechanism of the ATP Synthase, 1961–1985. [REVIEW]John N. Prebble - 2013 - Journal of the History of Biology 46 (4):699-737.
    Attempts to solve the puzzling problem of oxidative phosphorylation led to four very different hypotheses each of which suggested a different view of the ATP synthase, the phosphorylating enzyme. During the 1960s and 1970s evidence began to accumulate which rendered Peter Mitchell’s chemiosmotic hypothesis, the novel part of which was the proton translocating ATP synthase (ATPase), a plausible explanation. The conformational hypothesis of Paul Boyer implied an enzyme where ATP synthesis was driven by the energy of conformational changes in (...)
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  34. A Linked Aggregate Code for Processing Faces (Revised Version).Michael J. Lyons & Kazunori Morikawa - 2000 - Pragmatics and Cognition 8 (1):63-81.
    A model of face representation, inspired by the biology of the visual system, is compared to experimental data on the perception of facial similarity. The face representation model uses aggregate primary visual cortex (V1) cell responses topographically linked to a grid covering the face, allowing comparison of shape and texture at corresponding points in two facial images. When a set of relatively similar faces was used as stimuli, this Linked Aggregate Code (LAC) predicted human performance in similarity judgment experiments. When (...)
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  35.  13
    The Strengths of Some Violations of Covering.Heike Mildenberger - 2001 - Mathematical Logic Quarterly 47 (3):291-298.
    We consider two models V1, V2 of ZFC such that V1 ⊆ V2, the cofinality functions of V1 and of V2 coincide, V1 and V2 have that same hereditarily countable sets, and there is some uncountable set in V2 that is not covered by any set in V1 of the same cardinality. We show that under these assumptions there is an inner model of V2 with a measurable cardinal κ of Mitchell order κ++. This technical result allows us to show (...)
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  36.  12
    Structural basis of the conformational and functional regulation of human SERCA2b, the ubiquitous endoplasmic reticulum calcium pump.Yuxia Zhang & Kenji Inaba - 2022 - Bioessays 44 (7):2200052.
    Sarco/endoplasmic reticulum Ca2+ ATPase 2b (SERCA2b), a member of the SERCA family, is expressed ubiquitously and transports Ca2+ into the sarco/endoplasmic reticulum using the energy provided by ATP binding and hydrolysis. The crystal structure of SERCA2b in its Ca2+‐ and ATP‐bound (E1∙2Ca2+‐ATP) state and cryo‐electron microscopy (cryo‐EM) structures of the protein in its E1∙2Ca2+‐ATP and Ca2+‐unbound phosphorylated (E2P) states have provided essential insights into how the overall conformation and ATPase activity of SERCA2b is regulated by the transmembrane helix (...)
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  37. Visual experience and blindsight: A methodological review.Morten Overgaard - 2011 - Experimental Brain Research 209:473-479.
    Blindsight is classically defined as residual visual capacity, e.g., to detect and identify visual stimuli, in the total absence of perceptual awareness following lesions to V1. However, whereas most experiments have investigated what blindsight patients can and cannot do, the literature contains several, often contradictory, remarks about remaining visual experience. This review examines closer these remarks as well as experiments that directly approach the nature of possibly spared visual experiences in blindsight.
     
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  38. The neural correlates of visual imagery: a co-ordinate-based meta-analysis.C. Winlove, F. Milton, J. Ranson, J. Fulford, M. MacKisack, Fiona Macpherson & A. Zeman - 2018 - Cortex 105 (August 2018):4-25.
    Visual imagery is a form of sensory imagination, involving subjective experiences typically described as similar to perception, but which occur in the absence of corresponding external stimuli. We used the Activation Likelihood Estimation algorithm (ALE) to identify regions consistently activated by visual imagery across 40 neuroimaging studies, the first such meta-analysis. We also employed a recently developed multi-modal parcellation of the human brain to attribute stereotactic co-ordinates to one of 180 anatomical regions, the first time this approach has been combined (...)
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  39.  33
    BioEssays 4/2010.Nick Lane, John F. Allen & William Martin - 2010 - Bioessays 32 (4).
    Despite thermodynamic, bioenergetic and phylogenetic failings, the 81‐year‐old concept of primordial soup remains central to mainstream thinking on the origin of life. But soup is homogeneous in pH and redox potential, and so has no capacity for energy coupling by chemiosmosis. Thermodynamic constraints make chemiosmosis strictly necessary for carbon and energy metabolism in all free‐living chemotrophs, and presumably the first free‐living cells too. Proton gradients form naturally at alkaline hydrothermal vents and are viewed as central to the origin of life. (...)
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  40.  72
    (1 other version)How not to find the neural correlate of consciousness.Ned Block - 1996 - In [Book Chapter] (Unpublished). pp. 1.
    There are two concepts of consciousness that are easy to confuse with one another, access-consciousness and phenomenal consciousness. However, just as the concepts of water and H2O are different concepts of the same thing, so the two concepts of consciousness may come to the same thing in the brain. The focus of this paper is on the problems that arise when these two concepts of consciousness are conflated. I will argue that John Searle’s reasoning about the function of consciousness goes (...)
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  41. fMRI measurements of color in macaque and human.Mark Augath - unknown
    We have used fMRI to measure responses to chromatic and achromatic contrast in retinotopically defined regions of macaque and human visual cortex. We make four observations. Firstly, the relative amplitudes of responses to color and luminance stimuli in macaque area V1 are similar to those previously observed in human fMRI experiments. Secondly, the dorsal and ventral subdivisions of macaque area V4 respond in a similar way to opponent (L j M)-cone chromatic contrast suggesting that they are part of a single (...)
     
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  42.  68
    Visually Driven Activation in Macaque Areas V2 and V3 without Input from the Primary Visual Cortex.Michael C. Schmid & Mark A. Augath - unknown
    Creating focal lesions in primary visual cortex (V1) provides an opportunity to study the role of extra-geniculo-striate pathways for activating extrastriate visual cortex. Previous studies have shown that more than 95% of neurons in macaque area V2 and V3 stop firing after reversibly cooling V1 [1,2,3]. However, no studies on long term recovery in areas V2, V3 following permanent V1 lesions have been reported in the macaque. Here we use macaque fMRI to study area V2, V3 activity patterns from 1 (...)
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  43.  64
    Probing unconscious visual processing with the Mccollough effect.G. Keith Humphrey & Melvyn A. Goodale - 1998 - Consciousness and Cognition 7 (3):494-519.
    The McCollough effect, an orientation-contingent color aftereffect, has been known for over 30 years and, like other aftereffects, has been taken as a means of probing the brain's operations psychophysically. In this paper, we review psychophysical, neuropsychological, and neuroimaging studies of the McCollough effect. Much of the evidence suggests that the McCollough effect depends on neural mechanisms that are located early in the cortical visual pathways, probably in V1. We also review evidence showing that the aftereffect can be induced without (...)
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  44.  11
    Truth-Value Constants in Multi-Valued Logics.Nissim Francez & Michael Kaminski - 2024 - In Thomas Piecha & Kai F. Wehmeier (eds.), Peter Schroeder-Heister on Proof-Theoretic Semantics. Springer. pp. 391-397.
    In some presentations of classical and intuitionistic logics, the objectlanguage is assumed to contain (two) truth-value constants: ⊤ (verum) and ⊥ (falsum), that are, respectively, true and false under every bivalent valuation. We are interested to define and study analogical constants ‡, 1 ≤ i ≤ n, that in an arbitrary multi-valued logic over truth-values V = {v1,..., vn} have the truth-value vi under every (multi-valued) valuation. As is well known, the absence or presence of such constants has a significant (...)
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  45. Authors' reply to correspondence from Egelman.Ting-Fang Wang, Li-Tzu Chen & Andrew H.-J. Wang - 2008 - Bioessays 30 (11-12):1254-1255.
    The RecA family proteins mediate homologous recombination, a ubiquitous mechanism for repairing DNA double‐strand breaks (DSBs) and stalled replication forks. Members of this family include bacterial RecA, archaeal RadA and Rad51, and eukaryotic Rad51 and Dmc1. These proteins bind to single‐stranded DNA at a DSB site to form a presynaptic nucleoprotein filament, align this presynaptic filament with homologous sequences in another double‐stranded DNA segment, promote DNA strand exchange and then dissociate. It was generally accepted that RecA family proteins function throughout (...)
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  46.  6
    How bacteria initiate DNA replication comes into focus.Fahad Rashid & James M. Berger - 2025 - Bioessays 47 (1):2400151.
    The ability to initiate DNA replication is a critical step in the proliferation of all organisms. In bacteria, this process is mediated by an ATP‐dependent replication initiator protein, DnaA, which recognizes and melts replication origin (oriC) elements. Despite decades of biochemical and structural work, a mechanistic understanding of how DnaA recognizes and unwinds oriC has remained enigmatic. A recent study by Pelliciari et al. provides important new structural insights into how DnaA from Bacillus subtilis recognizes and processes its cognate oriC, (...)
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  47.  73
    Reichenbach's common cause principle and quantum field theory.Miklós Rédei - 1997 - Foundations of Physics 27 (10):1309-1321.
    Reichenbach's principles of a probabilistic common cause of probabilistic correlations is formulated in terms of relativistic quantum field theory, and the problem is raised whether correlations in relativistic quantum field theory between events represented by projections in local observable algebrasA(V1) andA(V2) pertaining to spacelike separated spacetime regions V1 and V2 can be explained by finding a probabilistic common cause of the correlation in Reichenbach's sense. While this problem remains open, it is shown that if all superluminal correlations predicted by the (...)
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  48. Untying the knot: imagination, perception and their neural substrates.Dan Cavedon-Taylor - 2021 - Synthese 199 (3-4):7203-7230.
    How tight is the conceptual connection between imagination and perception? A number of philosophers, from the early moderns to present-day predictive processing theorists, tie the knot as tightly as they can, claiming that states of the imagination, i.e. mental imagery, are a proper subset of perceptual experience. This paper labels such a view ‘perceptualism’ about the imagination and supplies new arguments against it. The arguments are based on high-level perceptual content and, distinctly, cognitive penetration. The paper also defuses a recent, (...)
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  49.  31
    Effective moduli from ineffective uniqueness proofs. An unwinding of de La Vallée Poussin's proof for Chebycheff approximation.Ulrich Kohlenbach - 1993 - Annals of Pure and Applied Logic 64 (1):27-94.
    Kohlenbach, U., Effective moduli from ineffective uniqueness proofs. An unwinding of de La Vallée Poussin's proof for Chebycheff approximation, Annals of Pure and Applied Logic 64 27–94.We consider uniqueness theorems in classical analysis having the form u ε U, v1, v2 ε Vu = 0 = G→v 1 = v2), where U, V are complete separable metric spaces, Vu is compact in V and G:U x V → is a constructive function.If is proved by arithmetical means from analytical assumptions x (...)
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  50. (1 other version)Problems of representation I: nature and role.Dan Ryder - 2009 - In Sarah Robins, John Symons & Paco Calvo (eds.), The Routledge Companion to Philosophy of Psychology. New York, NY: Routledge. pp. 233.
    Introduction There are some exceptions, which we shall see below, but virtually all theories in psychology and cognitive science make use of the notion of representation. Arguably, folk psychology also traffics in representations, or is at least strongly suggestive of their existence. There are many different types of things discussed in the psychological and philosophical literature that are candidates for representation-hood. First, there are the propositional attitudes – beliefs, judgments, desires, hopes etc. (see Chapters 9 and 17 of this volume). (...)
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