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Relevant bibliographies by topics / Chick spinal cord development

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Academic literature on the topic 'Chick spinal cord development'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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Journal articles on the topic "Chick spinal cord development"

1

Ono, K., R. Bansal, J. Payne, U. Rutishauser, and R. H. Miller. "Early development and dispersal of oligodendrocyte precursors in the embryonic chick spinal cord." Development 121, no. 6 (1995): 1743–54. http://dx.doi.org/10.1242/dev.121.6.1743.

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Oligodendrocytes, the myelinating cells of the vertebrate CNS, originally develop from cells of the neuroepithelium. Recent studies suggest that spinal cord oligodendrocyte precursors are initially localized in the region of the ventral ventricular zone and subsequently disperse throughout the spinal cord. The characteristics of these early oligodendrocyte precursors and their subsequent migration has been difficult to assay directly in the rodent spinal cord due to a lack of appropriate reagents. In the developing chick spinal cord, we show that oligodendrocyte precursors can be specifically

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2

Sholomenko, G. N., and M. J. O'Donovan. "Development and characterization of pathways descending to the spinal cord in the embryonic chick." Journal of Neurophysiology 73, no. 3 (1995): 1223–33. http://dx.doi.org/10.1152/jn.1995.73.3.1223.

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1. We used an isolated preparation of the embryonic chick brain stem and spinal cord to examine the origin, trajectory, and effects of descending supraspinal pathways on lumbosacral motor activity. The in vitro preparation remained viable for < or 24 h and was sufficiently stable for electrophysiological, pharmacological, and neuroanatomic examination. In this preparation, as in the isolated spinal cord, spontaneous episodes of both forelimb and hindlimb motor activity occur in the absence of phasic afferent input. Motor activity can also be evoked by brain stem electrical stimulation or mo

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3

Alrefaei, Abdulmajeed Fahad, Andrea E. Münsterberg, and Grant N. Wheeler. "Expression analysis of chick Frizzled receptors during spinal cord development." Gene Expression Patterns 39 (March 2021): 119167. http://dx.doi.org/10.1016/j.gep.2021.119167.

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4

Tanaka, H., M. Kinutani, A. Agata, Y. Takashima, and K. Obata. "Pathfinding during spinal tract formation in the chick-quail chimera analysed by species-specific monoclonal antibodies." Development 110, no. 2 (1990): 565–71. http://dx.doi.org/10.1242/dev.110.2.565.

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In order to analyse the spinal tract formation at early stages of development in avian embryos, chick-quail spinal cord chimeras were prepared and species-specific monoclonal antibodies (MAb) were developed. MAbs CN, QN and CQN uniquely stained chick, quail, and both chick and quail nervous tissues, respectively. All three antibodies appeared to bind to the same membrane molecule, but to different epitopes. Cord reversal revealed the features of axonal growth of both cord interneurons and dorsal root ganglion cells. Quail cord interneurons grew along an originally ventral marginal layer in the

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Plateroti, M., A. L. Vignoli, S. Biagioni, A. M. M. di Stasi, T. C. Petrucci, and G. Augusti-Tocco. "Synapsin I expression in spinal cord neurons during chick embryo development." Journal of Neuroscience Research 39, no. 5 (1994): 535–44. http://dx.doi.org/10.1002/jnr.490390505.

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6

VIGNOLI, A., M. PLATEROTI, S. BIAGIONI, and G. TOCCO. "Synapsin I distribution in the development of chick spinal cord neurons." Cell Biology International Reports 14 (September 1990): 153. http://dx.doi.org/10.1016/0309-1651(90)90711-7.

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7

Hao, Hailing, and David I. Shreiber. "Axon Kinematics Change During Growth and Development." Journal of Biomechanical Engineering 129, no. 4 (2007): 511–22. http://dx.doi.org/10.1115/1.2746372.

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The microkinematic response of axons to mechanical stretch was examined in the developing chick embryo spinal cord during a period of rapid growth and myelination. Spinal cords were isolated at different days of embryonic (E) development post-fertilization (E12, E14, E16, and E18) and stretched 0%, 5%, 10%, 15%, and 20%, respectively. During this period, the spinal cord grew ∼55% in length, and white matter tracts were myelinated significantly. The spinal cords were fixed with paraformaldehyde at the stretched length, sectioned, stained immunohistochemically for neurofilament proteins, and ima

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8

Holley, John A., and Jerry Silver. "Growth pattern of pioneering chick spinal cord axons." Developmental Biology 123, no. 2 (1987): 375–88. http://dx.doi.org/10.1016/0012-1606(87)90396-4.

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Weill, Cheryl L. "Characterization of androgen receptors in embryonic chick spinal cord." Developmental Brain Research 24, no. 1-2 (1986): 127–32. http://dx.doi.org/10.1016/0165-3806(86)90180-x.

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10

Oppenheim, Ronald W., Amiram Shneiderman, Iwao Shimizu, and Hiroyuki Yaginuma. "Onset and development of intersegmental projections in the chick embryo spinal cord." Journal of Comparative Neurology 275, no. 2 (1988): 159–80. http://dx.doi.org/10.1002/cne.902750202.

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Dissertations / Theses on the topic "Chick spinal cord development"

1

Lim, Tit Meng. "Segmentation in the nervous system of the chick embryo." Thesis, University of Cambridge, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329053.

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2

Schaeffer, Julia. "The molecular regulation of spinal nerve outgrowth." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/271632.

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During amniote embryogenesis, the segmented pattern characteristic of the vertebral column appears early during development through the sequential formation of multipotent structures called somites. Somites differentiate subsequently into dermomyotome (giving rise later to skin and skeletal muscles) and sclerotome (giving rise to vertebral bone structures and cartilage). In addition, sclerotomes subdivide following their rostro-caudal intrasegmental boundary into an axon growth-permissive region (anterior half) and an axon growth-repulsive region (posterior half). This binary system instructs

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3

Hanson, Martin Gartz Jr. "THE EMBRYONIC NEURAL CIRCUIT: MECHANISM AND INFLUENCE OF SPONTANEOUS RHYTHMIC ACTIVITY IN EARLY SPINAL CORD DEVELOPMENT." Case Western Reserve University School of Graduate Studies / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=case1085515804.

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4

Anderson, Emma S. "The Type IV Oligodendrocyte : experimental studies on chicken white matter /." Linköping : Univ, 2002. http://www.bibl.liu.se/liupubl/disp/disp2002/med720s.pdf.

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5

Ethell, Douglas Wayne. "Analysis of developing chick Gallus domesticus spinal cord proteins using two dimensional gel electrophoresis." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29834.

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Several recent experiments on developing chick spinal cord have established a time window when the developing spinal cord changes from a permissive to a restrictive environment for regeneration. This time window occurs during embryonic days 13-14 (E13-E14) of chick development. Recent experiments in adult rat, have found two proteins that actively inhibit axonal regeneration. This study has sought possible inhibitory proteins, in chicks, correlating to this temporal change. Proteins continuously present after this change (E14-E20) but not before (E11) were identified. Two-dimensional gel elect

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Lim, Siew-Na. "Development of novel therapeutic strategies in spinal cord injury using rodent models of spinal cord compression injury." Thesis, Queen Mary, University of London, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538663.

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Glasgow, Stacey Marie. "The role of PTF1A in spinal cord development." Access to abstract only; dissertation is embargoed until after 5/15/2007, 2006. http://www4.utsouthwestern.edu/library/ETD/etdDetails.cfm?etdID=155.

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Gibson, Claire. "Interactions between afferent pathways in spinal cord development." Thesis, University of Newcastle Upon Tyne, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311132.

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Chilton, John K. "The role of receptor protein tyrosine phosphatases in axon guidance." Thesis, University of Oxford, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365814.

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Rottkamp, Catherine Anne-Marie. "The Role of Hox Cofactors in Vertebrate Spinal Cord Development." Case Western Reserve University School of Graduate Studies / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=case1194575822.

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Books on the topic "Chick spinal cord development"

1

E, Goldberger Michael, Gorio Alfredo, and Murray Marion, eds. Development and plasticity of the mammalian spinal cord. Liviana Press, 1986.

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2

Oudega, Martin, Egbert A. J. F. Lakke, Enrico Marani, and Raph T. W. M. Thomeer. Development of the Rat Spinal Cord: Immuno- and Enzyme Histochemical Approaches. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78474-3.

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3

1925-, Altman Joseph, ed. Atlas of human central nervous system development. CRC Press, 2002.

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4

The projections to the spinal cord of the rat during development: A time-table of descent. Springer, 1997.

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5

Joshi, Mital. Development and characterization of a graded, in vivo, compressive, murine model of spinal cord injury. National Library of Canada, 2000.

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6

Lakke, E. A. J. F. The Projections to the Spinal Cord of the Rat During Development: A Timetable of Descent. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60601-4.

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7

Bayer, Shirley A. Atlas of human central nervous system development: The human brain during the late first trimester. CRC Press, 2006.

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8

McLaughlin, Hooley Michael Graham. Morphological patterning and stability in the regenerating spinal cord of the chick embryo. 1985.

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9

1956-, Oudega Martin, ed. Development of the rat spinal cord: Immuno- and enzyme histochemical approaches. Springer-Verlag, 1993.

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10

Normal and Pathologic Development of the Human Brain and Spinal Cord. John Libbey Eurotext Limited, 1999.

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Book chapters on the topic "Chick spinal cord development"

1

Santos, Edalmarys, and Chad A. Noggle. "Spinal Cord." In Encyclopedia of Child Behavior and Development. Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-79061-9_2769.

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2

Tabak, Joel, Peter Wenner, and Michael J. O’Donovan. "Rhythm Generation in Embryonic Chick Spinal Cord." In Encyclopedia of Computational Neuroscience. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7320-6_45-2.

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Tabak, Joel, Peter Wenner, and Michael J. O’Donovan. "Rhythm Generation in Embryonic Chick Spinal Cord." In Encyclopedia of Computational Neuroscience. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-7320-6_45-3.

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Tabak, Joel, Peter Wenner, and Michael J. O’Donovan. "Rhythm Generation in Embryonic Chick Spinal Cord." In Encyclopedia of Computational Neuroscience. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4614-6675-8_45.

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5

Daly, Brian P., and Heather F. Russell. "Spinal Cord Injury." In Encyclopedia of Child Behavior and Development. Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-79061-9_2770.

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6

Heimer, Lennart. "Development of the Nervous System." In The Human Brain and Spinal Cord. Springer New York, 1995. http://dx.doi.org/10.1007/978-1-4612-2478-5_2.

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7

Baas, Peter W. "Elaboration of the Axonal Microtubule Array During Development and Regeneration." In Neurobiology of Spinal Cord Injury. Humana Press, 2000. http://dx.doi.org/10.1007/978-1-59259-200-5_7.

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8

Wyndaele, Jean Jacques, and Apichana Kovindha. "Different Types of Intravesical Pressure Development." In Urodynamic Testing After Spinal Cord Injury. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-54900-2_16.

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9

Blight, A. R. "Axonal Regeneration in the Context of Spinal Cord Trauma." In Neural Development and Regeneration. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73148-8_38.

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Goldberg, William J., and Jerald J. Bernstein. "Grafted Fetal Astrocytes Migrate from Host Thoracic Spinal Cord to Lumbar Cord and Medulla." In Neural Development and Regeneration. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73148-8_44.

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Conference papers on the topic "Chick spinal cord development"

1

Elias, Ragi A. I., Jason Maikos, and David I. Shreiber. "Mechanical Properties of the Chick Embryo Spinal Cord." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176773.

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Determining the mechanical properties of the spinal cord are useful to identify its response to sub-injurious loading experienced during normal motion, to evaluate the biomechanics of spinal cord injury (SCI) [1], and to understand the role of the changing mechanical environment in growth and development. While an array of studies have focused on the mechanical properties of adult spinal cords, those properties may not be the same as pediatric spinal cords, which undergoes significant changes during development. Additionally, during embryonic and fetal development, axon growth and neural precu

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2

Shreiber, David I., Hailing Hao, and Ragi A. I. Elias. "The Effects of Glia on the Tensile Properties of the Spinal Cord." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-190184.

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Glia, the primary non-neuronal cells of the central nervous system, were initially believed to bind or glue neurons together and/or provide a supporting scaffold [1, 2]. It is now recognized that these cells provide specialized and essential biological and regulatory functions. Still, their contributions to the overall mechanical properties would also strongly influence the tissue’s tolerance to loading conditions experienced during trauma and potentially regulate of function and growth in neurons and glia [3, 4]. White matter represents an intriguing tissue to appreciate the role of glia in t

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3

Sundararaghavan, Harini G., Gary A. Monteiro, and David I. Shreiber. "Microfluidic Generation of Adhesion Gradients Through 3D Collagen Gels: Implications for Neural Tissue Engineering." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192987.

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During development, neurites are directed by gradients of attractive and repulsive soluble (chemotactic) cues and substrate-bound adhesive (haptotactic) cues. Many of these cues have been extensively researched in vitro, and incorporated into strategies for nerve and spinal cord regeneration, primarily to improve the regenerative environment. To enhance and direct growth, we have developed a system to create 1D gradients of adhesion through a 3D collagen gel using microfluidics. We test our system using collagen grafted with bioactive peptide sequences, IKVAV and YIGSR, from laminin — an extra

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Sundararaghavan, Harini G., Gary A. Monteiro, and David I. Shreiber. "Guided Axon Growth by Gradients of Adhesion in Collagen Gels." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-69124.

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During development, neurites are directed by gradients of attractive and repulsive soluble (chemotactic) cues and substrate-bound adhesive (haptotactic) cues. Many of these cues have been extensively researched in vitro, and incorporated into strategies for nerve and spinal cord regeneration, primarily to improve the regenerative environment. To enhance and direct growth, we have developed a system to create 1D gradients of adhesion through a 3D collagen gel using microfluidics. We test our system using collagen grafted with bioactive peptide sequences, IKVAV and YIGSR, from laminin — an extra

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Bourget, Duane, Jeffrey Herron, Ben Isaacson, and Melanie Goodman Keiser. "Research Development Kit Enabling Expanded Spinal Cord Stimulation Research." In 2019 9th International IEEE/EMBS Conference on Neural Engineering (NER). IEEE, 2019. http://dx.doi.org/10.1109/ner.2019.8716966.

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Strausser, Katherine A., Timothy A. Swift, Adam B. Zoss, H. Kazerooni, and Bradford C. Bennett. "Mobile Exoskeleton for Spinal Cord Injury: Development and Testing." In ASME 2011 Dynamic Systems and Control Conference and Bath/ASME Symposium on Fluid Power and Motion Control. ASMEDC, 2011. http://dx.doi.org/10.1115/dscc2011-6042.

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For those who have lost the ability to walk due to paralysis or other injuries, eLEGS, a mobile robotic exoskeleton, offers the chance to walk again. The device is a mobile exoskeleton with actuated sagittal plane hip and knee joints which supports the user and moves their legs through a natural gait. The device uses a multi-leveled controller that consists of a state machine to determine the user’s intended motion, a trajectory generator to establish desired joint behavior, and a low level controller to calculate individual joint controller output. The system can be controlled by a physical t

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Nozaki, Takahiro, Toshiyuki Murakami, Tomoyuki Shimono, Kouhei Ohnishi, and Roberto Oboe. "Development of meal assistance device for patients with spinal cord injury." In 2016 IEEE 14th International Workshop on Advanced Motion Control (AMC). IEEE, 2016. http://dx.doi.org/10.1109/amc.2016.7496381.

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Ihsan, Izzat Aqmar, Razali Tomari, Wan Nurshazwani Wan Zakaria, and Nurmiza Othman. "Alternative input medium development for wheelchair user with severe spinal cord injury." In ADVANCES IN ELECTRICAL AND ELECTRONIC ENGINEERING: FROM THEORY TO APPLICATIONS: Proceedings of the International Conference on Electrical and Electronic Engineering (IC3E 2017). Author(s), 2017. http://dx.doi.org/10.1063/1.5002050.

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Busch, David R., Feng Gao, Chia Chieh Goh, Wei Lin, Arjun G. Yodh, and Thomas F. Floyd. "Development of a Continuous, Axially-Resolved, Optical Monitor of Spinal Cord Blood Flow." In Frontiers in Optics. OSA, 2018. http://dx.doi.org/10.1364/fio.2018.jtu2a.141.

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Kimura, Hiroki, Eiichi Genda, Keiichi Nakamura, Hirotaka Tanaka, and Haruhisa Kawasaki. "Development of upper-limb motion-assist device for high cervical spinal cord injury." In 2014 53rd Annual Conference of the Society of Instrument and Control Engineers of Japan (SICE). IEEE, 2014. http://dx.doi.org/10.1109/sice.2014.6935207.

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Reports on the topic "Chick spinal cord development"

1

Edgerton, V. R. Electrode Array Development for Recovery of Stepping Following Spinal Cord Injury. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada562459.

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Edgerton, V. R. Electrode Array Development for Recovery of Stepping Following Spinal Cord Injury. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada587581.

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