
Raymon M. Glantz - US grants
Affiliations: | Rice University, Houston, TX |
Area:
CrayfishWebsite:
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The funding information displayed below comes from the NIH Research Portfolio Online Reporting Tools and the NSF Award Database.The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
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High-probability grants
According to our matching algorithm, Raymon M. Glantz is the likely recipient of the following grants.Years | Recipients | Code | Title / Keywords | Matching score |
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1972 — 1977 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Coding of Visual Information by the Crayfish Nervous System @ William Marsh Rice University |
0.915 |
1977 — 1978 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Undergraduate Research Participation @ William Marsh Rice University |
0.915 |
1977 — 1979 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Ensemble Coding of Visual Information in Command Interneurons @ William Marsh Rice University |
0.915 |
1979 — 1983 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Distributed Processing of Sensory Information @ William Marsh Rice University |
0.915 |
1983 — 1985 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Integration in Identifiable Dendrites @ William Marsh Rice University |
0.915 |
1984 — 1987 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Functional Organization of Crayfish Lamina Ganglionaris @ William Marsh Rice University |
0.915 |
1987 — 1991 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Ensemble Coding in the Crayfish Lamina Ganglion @ William Marsh Rice University The means by which information from sensory receptors is encoded is an important general problem in neurobiology. This project is a study of a specific example of this problem, the coding of visual information in a relatively simple neuronal network, the crayfish lamina ganglion. The ganglia of the crayfish optical system are arranged in columnar fashion. Their neurons are distributed in an ordered manner such that they form a map of the retina. Each point in visual space is encoded by five ganglion neurons which form a single column. These neurons have graded responses to light. Thus, each column can encode intensity, local contrast, orientation of polarized light, and wavelength (color) at a small region of the visual field. The Principal Investigator has characterized the morphology and connections of many of the ganglion cells in this neural network, and has also determined the chemical messengers by which some of them communicate. In this project he hopes to determine how the neural circuits already identified compute the values of various aspects of the stimulus, including polarization angle and velocity of movement, and how visual behavior is influenced by their activity. The methods he is using include electrical recording from neurons that can be identified microscopically from dye injected into them at the time of recording, and using immunocytochemical and pharmacological procedures to identify their chemical messengers (neurotransmitters). |
0.915 |
1991 — 1995 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Synaptic Mechanisms of Directionally Selective Movement Detection @ William Marsh Rice University A remarkable property of many visual systems is the capacity to abstract the direction, velocity and position of a moving target. Detection occurs over a wide range of velocities, stimulus configurations and lighting conditions. Although the neuronal apparatus of visual motion detection has been studied intensively for over 30 years, the mechanism is still unknown. A major impediment to our current understanding is an absence of both measurements and realistic theoretical constructs regarding the synaptic processes by which a network of visual interneurons can compute the direction and velocity of a moving target. In this respect, arthropods, particularly large crustaceans like crayfish, provide a favorable model for a combined experimental and theoretical approach to the problem. Our studies indicate that a mechanism can be resolved into interactions among four classes of identified neurons. |
0.915 |
1995 — 1998 | Rudolph, Frederick [⬀] Glantz, Raymon |
N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Mechanisms of Directionally Selective Motion Detection @ William Marsh Rice University IBN-9507878 Raymon Glantz A broad spectrum of brain activities, from object recognition to postural adjustments, require that neurons and neural circuits make computations. In recent years, neurobiologists have made impressive progress in two related areas: one concerns the biophysical and molecular mechanisms of synapses and the second concerns the mathematical and logical operations which formally describe what whole systems of nerve cells do. In the study of how the visual system works, algorithms successfully model visual tracking and fixation, binocular vision, and motion detection. Future progress in understanding more about the visual system depends upon integrating the biophysical and algorithmic approaches. This will require detailed information about the structure and dynamic properties of neurons involved in particular computations. Many visual systems can compute the direction and velocity of moving targets. Recent studies indicate that directional motion detection is achieved through synaptic operations embedded in the structure of the neuron's receptive field. The same directional mechanisms were independently found in visual neurons in higher vertebrates and in the crayfish. The mechanisms depends upon spatial and temporal asymmetries of the excitation and inhibition within the receptive field. This project focuses on experimental and theoretical studies of the synaptic mechanisms which support directional motion detection. Physiological measurements will quantify the characteristics of the synapses which form the directional mechanism. The simulations will determine if the measured properties of the synapses are sufficient to support the directional mechanism. |
0.915 |
1998 — 2002 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Synaptic Mechanisms of Directional Selectivity @ William Marsh Rice University A fundamental property of most visual systems is directional sensitivity, in which objects moving one direction are quickly discriminated from objects moving in an opposite direction. The cellular mechanisms for this property are largely unknown. This collaborative research project brings together the skills of a physiologist and an ultrastructural anatomist in a multidisciplinary approach involving electrophysiology, biochemistry, computational neuroscience and electron microscopy. Using the well-studied visual system of crayfish as a model, this project tests a novel hypothesis that excitatory and inhibitory effects of two different neurotransmitter compounds can be integrated by the same excitable membrane channel. The technical difficulties give the project a high level of risk, but the potentially very high impact of the results, along with the experience and skills of the PIs, make taking the risk worthwhile. Results will be important beyond simply invertebrate vision, to understanding a fundamental property of visual systems, and to clarifying a cellular mechanism of integration important to all neuroscience as well as to cell physiology. |
0.915 |
2000 — 2002 | Glantz, Raymon M | R01Activity Code Description: To support a discrete, specified, circumscribed project to be performed by the named investigator(s) in an area representing his or her specific interest and competencies. |
Only Neurons Read Neural Codes @ Rice University Nervous systems represent external events by trains of impulses in sensory interneurons, but the exact mapping between stimuli and response features is generally unknown. The central thesis of this proposal is that any mapping between stimuli and response functions is generally unknown. The central thesis of this proposal is that any biologically useful neural information code must represent external signals and be decoded (i.e. read) by other neurons or effectors. Elucidating the neural code requires mapping the relationship between the stimulus and the neural response and between that neural response and post-synaptic (or effector) action which results in measurable behavior. Practical problems in deciphering a neural code are mitigated by studying relatively simple systems with known connectivity and simple behaviors. The neuronal pathway subserving the crayfish dorsal light reflex is one such system, consisting of an afferent ensemble of 14 identified sustaining fibers which monosynaptically excite a set of identified optomotor neurons. We propose a four part study of the coding-decoding issues raised above. i) Behavioral Studies- to determine the steady-state and dynamic stimulus parameters that result in movement ii) An analysis of the sustaining fiber encoder mechanism to quantify the information transfer in the light to sustaining fiber EPSP and from the EPSP to spike trains (i.e. the encoder mechanism). Using new information-theoretical data analysis techniques can quantify the efficacy of neural information processing as represented by analog signals (EPSPs), and by impulse trains of single neurons or neural populations. Pulse trains elicited with extrinsic current injection will provide an independent characterization of the encoder mechanism. iii) Analysis of the sustaining fiber to motoneuron functional connections to determine how sustaining fiber impulse train features control motoneuron excitability. The decoding features of the synapse will be examined with information-theoretic analysis of simultaneously recorded sustaining fiber and motoneuron impulse trains, by conditional cross- correlations and by subjecting the synapse to artificial pulse trains generated by current injections into the sustaining fibers. iv) Analysis of the relation between motoneuron response and behavior. This simple system will thus be examined from an information-theoretic perspective, using both empirical and modeling techniques. The goal is to both decipher the code and elucidate how the code is formed. The problem of neural coding has important implications for the design of prosthetic devices and the linkage between such devices and the nervous system. |
1 |
2006 — 2007 | Glantz, Raymon | N/AActivity Code Description: No activity code was retrieved: click on the grant title for more information |
Sger: Polarized Light Images and Visual Field Segmentation @ William Marsh Rice University The object of this proposal is to test the hypothesis that polarization vision (like color vision) has the capacity to segment the visual field based upon spatial and/or temporal variations in e-vector orientation. As such polarization contrast can provide a complete basis for form and motion vision. For maximum utility such a system should be available over all of an organism's visual field, it should operate across the entire visible spectrum, it should be independent of specific electric-vector (e-vector) angles and it should operate with a modest degree (_50 %) of polarization. Behavioral and neurophysiological studies of crayfish optomotor reflexes are proposed to examine the limits of polarization vision for the detection of self-motion. In the proposed study, moving images will be formed by polarized light and segmented only by variations in e-vector angles. The stimuli will be produced by software driving a modified LCD projection panel. Eyestalk movements are measured with an inductive transducer. Visual interneurons and the motoneurons of the optomotor pathway will be studied with conventional intracellular and extracellular recording procedures while the neurons respond to the identical stimuli used in the behavioral studies. The behavioral studies will reveal the limitations of polarized light as a source of perceptual contrast and the extent to which the system is confined by intrinsic filters, e.g. a bias toward certain evector angles. Specific measurements include the dependence or independence on absolute e-vector angles, the sensitivity to differences in e-vector angles (at segmentation boundaries), and the dependence of the system upon the degree of polarization. The neurophysiological studies will determine the strategies employed by the neural pathway to extract the relevant information. The working hypothesis is that the stimulus e-vector angles are detected by selective photoreceptors, and the signals related to the spatial e-vector distribution are refined by documented polarization-opponent interneurons in the second optic neuropile (medulla externa). |
0.915 |