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Journal articles on the topic 'Neural development'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 May 2024

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1

Katz, Lawrence C., Monica Driscoll, Kathy Zimmermann, and Torsten N. Wiesel. "Neural development." Brain Research Reviews 17, no. 2 (May 1992): 171–81. http://dx.doi.org/10.1016/0165-0173(92)90013-c.

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2

Lillien, Laura. "Neural development: Instructions for neural diversity." Current Biology 7, no. 3 (March 1997): R168—R171. http://dx.doi.org/10.1016/s0960-9822(97)70080-0.

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3

Dang, Lan, and Vincent Tropepe. "Neural induction and neural stem cell development." Regenerative Medicine 1, no. 5 (September 2006): 635–52. http://dx.doi.org/10.2217/17460751.1.5.635.

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4

Clinton, Julian. "POPLOG-Neural ? a neural network development toolkit." Expert Systems 7, no. 3 (August 1990): 174. http://dx.doi.org/10.1111/j.1468-0394.1990.tb00226.x.

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5

Yashchenko, V. O. "Neural-like growing networks in the development of general intelligence. Neural-like element (P. I)." Mathematical machines and systems 4 (2022): 15–36. http://dx.doi.org/10.34121/1028-9763-2022-4-15-36.

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The article discusses a new approach to the creation of artificial neurons and neural networks as the means of developing artificial intelligence similar to natural. The article consists of two parts. In the first one, the system of artificial intelligence formation is considered in comparison with the system of natural intelligence formation. Based on the consideration and analysis of the structure and functions of a biological neuron, it was concluded that memory is stored in brain neurons at the molecular level. Information perceived by a person from the moment of his birth and throughout his life is stored in the endoplasmic reticulum of the neuron. There are about 100 billion neurons in the human brain, and each neuron contains millions of ribosomes that synthesize a mediator consisting of about 10,000 molecules. If we assume that one mole-cule corresponds to one unit of information, then human memory is unlimited. In the nerve cell, there is a synthesis of biologically active substances necessary for the analysis and memorizing information. The “factory” for the production of proteins is the endoplasmic reticulum which accumulates millions of ribosomes. One ribosome synthesizes protein at a rate of 15–20 amino acids per second. Considering that the functional structure of ribosomes is similar to the Turing machine, we can conclude that the neuron is an analog multimachine complex – an ultra-fast molecular multimachine supercomputer with an unusually simple analog programming device. An artificial neuron proposed by J. McCulloch and W. Pitts is considered a highly simplified mathematical model of a biological neuron. A maximally approximate analogue of a biological neuron, a neural-like element, is proposed. A description of the neural-like element is given. The process of perception and memorizing information in a neuron-like element is shown in comparison with a similar process in a nerve cell of the brain.

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6

Doe, Chris Q., and Joshua R. Sanes. "Development: Neural development at the Millennium." Current Opinion in Neurobiology 10, no. 1 (February 2000): 31–37. http://dx.doi.org/10.1016/s0959-4388(99)00065-3.

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7

Jessen, Kristjan R., and Rhona Mirsky. "Neural Development: Fate diverted." Current Biology 4, no. 9 (September 1994): 824–27. http://dx.doi.org/10.1016/s0960-9822(00)00183-4.

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8

MEDNICK, SARNOFF A., and J. MEGGIN HOLLISTER. "Neural Development and Schizophrenia." Journal of Nervous and Mental Disease 184, no. 9 (September 1996): 575. http://dx.doi.org/10.1097/00005053-199609000-00011.

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9

Price, Jack. "Neural Development: Brain stems." Current Biology 5, no. 3 (March 1995): 232–34. http://dx.doi.org/10.1016/s0960-9822(95)00046-7.

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10

Fineberg, Sarah K., Kenneth S. Kosik, and Beverly L. Davidson. "MicroRNAs Potentiate Neural Development." Neuron 64, no. 3 (November 2009): 303–9. http://dx.doi.org/10.1016/j.neuron.2009.10.020.

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11

Brockes, Jeremy. "Principles of Neural Development." Trends in Neurosciences 8 (January 1985): 369. http://dx.doi.org/10.1016/0166-2236(85)90126-2.

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12

Lance-Jones, Cynthia. "Essentials of neural development." Trends in Neurosciences 14, no. 10 (October 1991): 475. http://dx.doi.org/10.1016/0166-2236(91)90051-u.

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13

Coleman, James R. "Principles of neural development." Brain Research Bulletin 16, no. 2 (February 1986): 305. http://dx.doi.org/10.1016/0361-9230(86)90047-x.

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14

Davis, Brian M. "Essentials of neural development." Journal of the Neurological Sciences 106, no. 2 (December 1991): 234. http://dx.doi.org/10.1016/0022-510x(91)90266-a.

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15

Welshhans, Kristy, and Leah Kershner. "RACK1 regulates neural development." Neural Regeneration Research 12, no. 7 (2017): 1036. http://dx.doi.org/10.4103/1673-5374.211175.

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16

Nurcombe, Victor. "Laminin in neural development." Pharmacology & Therapeutics 56, no. 2 (January 1992): 247–64. http://dx.doi.org/10.1016/0163-7258(92)90019-v.

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17

Abuwarda, Hamid, and Medha M. Pathak. "Mechanobiology of neural development." Current Opinion in Cell Biology 66 (October 2020): 104–11. http://dx.doi.org/10.1016/j.ceb.2020.05.012.

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18

Yashchenko, V. O. "Neural-like growing networks in the development of general intelligence. Neural-like growing networks (P. II)." Mathematical machines and systems 1 (2023): 3–29. http://dx.doi.org/10.34121/1028-9763-2023-1-3-29.

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This article is devoted to the development of general artificial intelligence (AGI) based on a new type of neural networks – “neural-like growing networks”. It consists of two parts. The first one was published in N4, 2022, and describes an artificial neural-like element (artificial neuron) in terms of its functionality, which is as close as possible to a biological neuron. An artificial neural-like element is the main element in building neural-like growing networks. The second part deals with the structures and functions of artificial and natural neural networks. The paper proposes a new approach for creating neural-like growing networks as a means of developing AGI that is as close as possible to the natural intelligence of a person. The intelligence of man and living organisms is formed by their nervous system. According to I.P. Pavlov's definition, the main mechanism of higher nervous activity is the reflex activity of the nervous system. In the nerve cell, the main storage of unconditioned reflexes is the deoxyribonucleic acid (DNA) molecule. The article describes ribosomal protein synthesis that contributes to the implementation of unconditioned reflexes and the formation of conditioned reflexes as the basis for learning biological objects. The first part of the work shows that the structure and functions of ribosomes almost completely coincide with the structure and functions of the Turing machine. Turing invented this machine to prove the fundamental (theoretical) possibility of constructing arbitrarily complex algorithms from extremely simple operations, and the operations themselves are performed automatically. Here arises a stunning analogy, nature created DNA and the ribosome to build complex algorithms for creating biological objects and their communication with each other and with the external environment, and the ribosomal protein synthesis is carried out by many ribosomes at the same time. It was concluded that the nerve cells of the brain are analog multi-machine complexes – ultra-fast molecular supercomputers with an unusually simple analog programming device.

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19

Martinek, Sebastian, and Ulrike Gaul. "Neural development: How cadherins zipper up neural circuits." Current Biology 7, no. 11 (November 1997): R712—R715. http://dx.doi.org/10.1016/s0960-9822(06)00363-0.

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20

Placzek, Marysia, and Andrew Furley. "Neural development: Patterning cascades in the neural tube." Current Biology 6, no. 5 (May 1996): 526–29. http://dx.doi.org/10.1016/s0960-9822(02)00533-x.

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21

Sun, Meiqi, Hongli You, Xiaoxuan Hu, Yujia Luo, Zixuan Zhang, Yiqun Song, Jing An, and Haixia Lu. "Microglia–Astrocyte Interaction in Neural Development and Neural Pathogenesis." Cells 12, no. 15 (July 27, 2023): 1942. http://dx.doi.org/10.3390/cells12151942.

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The interaction between microglia and astrocytes exhibits a relatively balanced state in order to maintain homeostasis in the healthy central nervous system (CNS). Disease stimuli alter microglia–astrocyte interaction patterns and elicit cell-type-specific responses, resulting in their contribution to various pathological processes. Here, we review the similarities and differences in the activation modes between microglia and astrocytes in various scenarios, encompassing different stages of neural development and a wide range of neural disorders. The aim is to provide a comprehensive understanding of their roles in neural development and regeneration and guiding new strategies for restoring CNS homeostasis.

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22

Feliciano, DavidM, and AidanM Sokolov. "Slc7a5 regulation of neural development." Neural Regeneration Research 16, no. 10 (2021): 1994. http://dx.doi.org/10.4103/1673-5374.308086.

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23

Tang, Bor Luen. "REST regulation of neural development." Cell Adhesion & Migration 3, no. 2 (April 2009): 141–42. http://dx.doi.org/10.4161/cam.3.2.8278.

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24

Punovuori, Karolina, Mattias Malaguti, and Sally Lowell. "Cadherins in early neural development." Cellular and Molecular Life Sciences 78, no. 9 (April 1, 2021): 4435–50. http://dx.doi.org/10.1007/s00018-021-03815-9.

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AbstractDuring early neural development, changes in signalling inform the expression of transcription factors that in turn instruct changes in cell identity. At the same time, switches in adhesion molecule expression result in cellular rearrangements that define the morphology of the emerging neural tube. It is becoming increasingly clear that these two processes influence each other; adhesion molecules do not simply operate downstream of or in parallel with changes in cell identity but rather actively feed into cell fate decisions. Why are differentiation and adhesion so tightly linked? It is now over 60 years since Conrad Waddington noted the remarkable "Constancy of the Wild Type” (Waddington in Nature 183: 1654–1655, 1959) yet we still do not fully understand the mechanisms that make development so reproducible. Conversely, we do not understand why directed differentiation of cells in a dish is sometimes unpredictable and difficult to control. It has long been suggested that cells make decisions as 'local cooperatives' rather than as individuals (Gurdon in Nature 336: 772–774, 1988; Lander in Cell 144: 955–969, 2011). Given that the cadherin family of adhesion molecules can simultaneously influence morphogenesis and signalling, it is tempting to speculate that they may help coordinate cell fate decisions between neighbouring cells in the embryo to ensure fidelity of patterning, and that the uncoupling of these processes in a culture dish might underlie some of the problems with controlling cell fate decisions ex-vivo. Here we review the expression and function of cadherins during early neural development and discuss how and why they might modulate signalling and differentiation as neural tissues are formed.

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25

Fam, Anzhelika, and Sergey Chihachev. "NEURAL NETWORK DEVELOPMENT IN SCILAB." Modern Technologies and Scientific and Technological Progress 2022, no. 1 (May 16, 2022): 147–48. http://dx.doi.org/10.36629/2686-9896-2022-1-147-148.

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26

Lumsden, Andrew, Bill Harris, Joshua R. Sanes, and Rachel Wong. "Neural Development – one year on." Neural Development 3, no. 1 (2008): 1. http://dx.doi.org/10.1186/1749-8104-3-1.

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27

Flores, Eduardo Garcia. "DEVELOPMENT OF HUMAN NEURAL TRANSPLANTATION." Neurosurgery 30, no. 4 (April 1, 1992): 651. http://dx.doi.org/10.1097/00006123-199204000-00034.

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28

Madrazo, Ignacio, and Rebecca E. Franco-Bourland. "DEVELOPMENT OF HUMAN NEURAL TRANSPLANTATION." Neurosurgery 30, no. 4 (April 1, 1992): 651–52. http://dx.doi.org/10.1097/00006123-199204000-00035.

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29

Levivier, Marc, and Serge Przedborski. "DEVELOPMENT OF HUMAN NEURAL TRANSPLANTATION." Neurosurgery 30, no. 5 (May 1, 1992): 811–12. http://dx.doi.org/10.1097/00006123-199205000-00063.

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30

RICHARDSON, MICHAEL K., and DOROTHY C. BENNETT. "Symposium on Neural Crest Development." Journal of Anatomy 191, no. 4 (November 1997): 481. http://dx.doi.org/10.1046/j.1469-7580.1997.19140481.x.

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31

Hur, Eun-Mi, and Feng-Quan Zhou. "GSK3 signalling in neural development." Nature Reviews Neuroscience 11, no. 8 (August 2010): 539–51. http://dx.doi.org/10.1038/nrn2870.

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32

Nelson, Charles A. "Neural Plasticity and Human Development." Current Directions in Psychological Science 8, no. 2 (April 1999): 42–45. http://dx.doi.org/10.1111/1467-8721.00010.

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33

Mitchell, Donald E. "Neural Development: A New Series." Contemporary Psychology: A Journal of Reviews 32, no. 2 (February 1987): 153–54. http://dx.doi.org/10.1037/026777.

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34

Borges, Lawrence F. "Historical Development of Neural Transplantation." Stereotactic and Functional Neurosurgery 51, no. 6 (1988): 265–77. http://dx.doi.org/10.1159/000099972.

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35

van Ooyen, A. "Activity-dependent neural network development." Network: Computation in Neural Systems 5, no. 3 (January 1994): 401–23. http://dx.doi.org/10.1088/0954-898x_5_3_006.

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36

Haldin, Caroline E., and Carole LaBonne. "Trap230 and neural crest development." Developmental Biology 319, no. 2 (July 2008): 570–71. http://dx.doi.org/10.1016/j.ydbio.2008.05.366.

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37

Raff, M. "Neural Development: Mysterious No More?" Science 274, no. 5290 (November 15, 1996): 1063–0. http://dx.doi.org/10.1126/science.274.5290.1063.

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38

Senturias, Yasmin. "Neural Plasticity and Cognitive Development." Journal of Developmental & Behavioral Pediatrics 37, no. 2 (2016): 175. http://dx.doi.org/10.1097/dbp.0000000000000246.

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39

Zimmermann, Herbert. "Purinergic signaling in neural development." Seminars in Cell & Developmental Biology 22, no. 2 (April 2011): 194–204. http://dx.doi.org/10.1016/j.semcdb.2011.02.007.

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40

Tyssowski, K., Y. Kishi, and Y. Gotoh. "Chromatin regulators of neural development." Neuroscience 264 (April 2014): 4–16. http://dx.doi.org/10.1016/j.neuroscience.2013.10.008.

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41

Rowitch, David H., Q. Richard Lu, Nicoletta Kessaris, and William D. Richardson. "An ‘oligarchy’ rules neural development." Trends in Neurosciences 25, no. 8 (August 2002): 417–22. http://dx.doi.org/10.1016/s0166-2236(02)02201-4.

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42

Marusich, Michael F., and James A. Weston. "Development of the neural crest." Current Opinion in Genetics & Development 1, no. 2 (August 1991): 221–29. http://dx.doi.org/10.1016/s0959-437x(05)80074-7.

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43

Roidl, Deborah, and Christine Hacker. "Histone methylation during neural development." Cell and Tissue Research 356, no. 3 (May 13, 2014): 539–52. http://dx.doi.org/10.1007/s00441-014-1842-8.

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44

Sladek, John R. "Neural development, a risky period." Experimental Neurology 237, no. 1 (September 2012): 43–45. http://dx.doi.org/10.1016/j.expneurol.2012.05.024.

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45

Fulwiler, Carl, and Walter Gilbert. "Zebrafish embryology and neural development." Current Opinion in Cell Biology 3, no. 6 (December 1991): 988–91. http://dx.doi.org/10.1016/0955-0674(91)90118-i.

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46

Watanabe, Masahiko. "Glutamate transporters in neural development." Neuroscience Research 31 (January 1998): S38. http://dx.doi.org/10.1016/s0168-0102(98)81632-5.

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47

Madrazo, Ignacio, Rebecca Franco-Bourland, Maricarmen Aguilera, Feggy Ostrosky-Solis, Carlos Cuevas, Hugo Castrejón, Eduardo Magalloón, and Mario Madrazo. "Development of Human Neural Transplantation." Neurosurgery 29, no. 2 (August 1, 1991): 165–77. http://dx.doi.org/10.1227/00006123-199108000-00001.

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Abstract The possibility of altering the course of Parkinson's disease by brain grafting is slowly becoming a reality through the efforts of many research groups worldwide. It has been shown that this procedure, as performed in high-level medical research centers, usually produces no permanent adverse effects and can effectively ameliorate parkinsonian signs in certain patients. This progress has served to reinforce our commitment to develop neural transplantation into an effective therapy to treat such a devastating neurodegenerative disease. We have summarized the most important events that have shaped the initial phase of this research. In the course of the last 4 years, considerable knowledge has been gained in the clinical neurosciences regarding the real potential of various brain grafting procedures in treating Parkinson's disease, their shortcomings, and their usefulness in carefully selected patients. There is still no consensus regarding the various fundamental aspects of human brain grafting in Parkinson's disease. Questions concerning surgical technique, candidate selection, the optimal brain regions for implantation, the optimal tissue for implantation, and the real usefulness of brain grafting must be addressed. The importance of the quality of adrenal medulla fragments for grafting, the requirement for immunosuppressors in fetal brain grafting, and the optimal fetal age and the amount of donor tissue for effective grafting are additional areas of concern. The potential of xenografting, preserved tissues, and genetically engineered cells for human brain grafting remain unanswered. The development of human neural transplantation is the responsibility and privilege of neurosurgery.

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48

Flores, Eduardo Garcia. "DEVELOPMENT OF HUMAN NEURAL TRANSPLANTATION." Neurosurgery 30, no. 4 (April 1992): 651. http://dx.doi.org/10.1227/00006123-199204000-00034.

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49

Madrazo, Ignacio, and Rebecca E. Franco-Bourland. "DEVELOPMENT OF HUMAN NEURAL TRANSPLANTATION." Neurosurgery 30, no. 4 (April 1992): 651–52. http://dx.doi.org/10.1227/00006123-199204000-00035.

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50

Levivier, Marc, and Serge Przedborski. "DEVELOPMENT OF HUMAN NEURAL TRANSPLANTATION." Neurosurgery 30, no. 5 (May 1992): 811–12. http://dx.doi.org/10.1227/00006123-199205000-00063.

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