Relevant bibliographies by topics / Neuronal cells

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Neuronal cells'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Neuronal cells"

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Robinson, Richard. "NEURONAL PROGENITOR CELLS." Neurology Today 5, no. 2 (February 2005): 70. http://dx.doi.org/10.1097/00132985-200502000-00024.

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Robinson, Richard. "NEURONAL STEM CELLS." Neurology Today 6, no. 14 (July 2006): 15–16. http://dx.doi.org/10.1097/00132985-200607180-00007.

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Gerszon, J., and A. Rodacka. "Determination of trans-resveratrol action on two different types of neuronal cells, neuroblastoma and hippocampal cells." Czech Journal of Food Sciences 34, No. 2 (June 3, 2016): 118–26. http://dx.doi.org/10.17221/401/2015-cjfs.

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Gorman, Adrienne M., Sten Orrenius, and Sandra Ceccatelli. "Apoptosis in neuronal cells." NeuroReport 9, no. 10 (July 1998): R49—R55. http://dx.doi.org/10.1097/00001756-199807130-00001.

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Doms, Robert W. "Intracellular A-beta in neuronal and non-neuronal cells." Neurobiology of Aging 21 (May 2000): 70. http://dx.doi.org/10.1016/s0197-4580(00)82535-x.

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Zemková, H., F. Vyskočil, J. Kůšek, and J. Vaněček. "Neuronal GABAA receptor in non-neuronal anterior pituitary cells." Journal of Physiology-Paris 88, no. 6 (January 1994): 393. http://dx.doi.org/10.1016/0928-4257(94)90059-0.

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Thorn, Peter, Robert Zorec, Jens Rettig, and Damien J. Keating. "Exocytosis in non-neuronal cells." Journal of Neurochemistry 137, no. 6 (May 2, 2016): 849–59. http://dx.doi.org/10.1111/jnc.13602.

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Cogliati, Tiziana. "Stem Cells and neuronal repair." Annals of Neurosciences 16, no. 4 (October 1, 2009): 143–45. http://dx.doi.org/10.5214/ans.0972-7531.0916401.

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Freeman, Marc R. "Glial (and Neuronal) Cells Missing." Neuron 48, no. 2 (October 2005): 163–65. http://dx.doi.org/10.1016/j.neuron.2005.10.002.

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Kukucka, Jessica, Tessa Wyllie, Justin Read, Lauren Mahoney, and Cenk Suphioglu. "Human neuronal cells: epigenetic aspects." BioMolecular Concepts 4, no. 4 (August 1, 2013): 319–33. http://dx.doi.org/10.1515/bmc-2012-0053.

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AbstractHistone acetyltransferases (HATs) and histone deacetylases (HDACs) promote histone posttranslational modifications, which lead to an epigenetic alteration in gene expression. Aberrant regulation of HATs and HDACs in neuronal cells results in pathological consequences such as neurodegeneration. Alzheimer’s disease is the most common neurodegenerative disease of the brain, which has devastating effects on patients and loved ones. The use of pan-HDAC inhibitors has shown great therapeutic promise in ameliorating neurodegenerative ailments. Recent evidence has emerged suggesting that certain deacetylases mediate neurotoxicity, whereas others provide neuroprotection. Therefore, the inhibition of certain isoforms to alleviate neurodegenerative manifestations has now become the focus of studies. In this review, we aimed to discuss and summarize some of the most recent and promising findings of HAT and HDAC functions in neurodegenerative diseases.
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Dissertations / Theses on the topic "Neuronal cells"

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Stanke, Jennifer J. "Beyond Neuronal Replacement: Embryonic Retinal Cells Protect Mature Retinal Neurons." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1250820277.

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Wang, Li. "CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS." Case Western Reserve University School of Graduate Studies / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=case1184254319.

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Anderson, Alexandra Antoinette. "The morphoregulatory function of acetylcholinesterase in neuronal and non-neuronal cells." Thesis, Imperial College London, 2007. http://hdl.handle.net/10044/1/7169.

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Doszyn, Olga. "Sex differences in neuronal differentiation of human stem cells." Thesis, Uppsala universitet, Institutionen för biologisk grundutbildning, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-384661.

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Sexual dimorphism has been long noted in human neurobiology, apparent most notably in sex-biased distribution of multiple neurological disorders or diseases, from autism spectrum disorder to Parkinson's disease. With the advances in molecular biology, genetics and epigenetics have come into focus as key players in sexually dimorphic neural development; and yet, many studies in the field of neuroscience overlook the importance of sex for the human brain. For this project, human embryonic and neural stem cells were chosen for three main reasons. Firstly, they provide an easily obtainable, scalable and physiologically native model for the early stages of development. Secondly, neural stem cells populations are retained within the adult human brain, and are implicated to play a role in cognition and mental illness, and as such are of interest in themselves. Thirdly, stem cell lines are widely used in research, including clinical trials of transplantation treatments, and for this reason should be meticulously examined and characterized. Here, the morphology, behaviour, and expression of selected genes in four stem cell lines, two of female and two of male origin, was examined in side-by-side comparisons prior to and during neuronal differentiation using a variety of methods including light microscopy, time-lapse two-photon microscopy, quantitative real-time PCR and immunocytochemistry. The obtained results have shown previously uncharacterised differences between those cell lines, such as a higher rate of proliferation but a slower rate of neuronal differentiation in male cell cultures compared to female cells cultivated in the same conditions, and a sex-biased expression of several markers of neuronal maturation at late stages of differentiation, as well as diverse patterns of expression of X- and Y-linked genes involved in stem cell proliferation and neural development.
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Gaughwin, Philip Michael. "Neuronal potential of oligodendrocyte precursor cells." Thesis, University of Cambridge, 2005. https://www.repository.cam.ac.uk/handle/1810/251963.

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Heitz, Stéphane Bailly Yannick Kapfhammer Josef P. Poulain Bernard. "Neuronal death mechanisms in cerebellar Purkinje cells." Strasbourg : Université Louis Pasteur, 2008. http://eprints-scd-ulp.u-strasbg.fr:8080/1012/01/HEITZ_Stephane_2008.pdf.

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Thèse de doctorat : Neurosciences : Strasbourg 1 : 2008. Thèse de doctorat : Neurosciences : Universität Basel, Switzerland : 2008.
Thèse soutenue en co-tutelle. Titre provenant de l'écran-titre. Bibliogr. 37 p.
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Mark, Melanie Danelle. "The mechanisms underlying EGF-stimulated neuronal differentiation in PC12 cells /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/6261.

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Perruisseau-Carrier, Claire. "Neuronal commitment of Umbilical Cord Mesenchymal Stem Cells for brain regenerative medicine." Thesis, Lyon 1, 2013. http://www.theses.fr/2013LYO10192.

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De nos jours, aucune prévention ou aucun remède efficace n'existe pour guérir les maladies du cerveau humain. Les cellules souches représentent un grand espoir pour la réparation et la régénération des tissus neuraux endommagés. L'objectif de cette thèse est d'évaluer la capacité des cellules souches du cordon ombilical humain (hUC MSCs) à se différencier en neurones, pour une thérapie cellulaire appliquée au cerveau. Nous avons isolé, multiplié et caractérisé les hUC MSCs naïves à l'échelle des gènes et des protéines. Ensuite, les e_ets sur l'expansion des hUC MSCs et leur différenciation neuronale de différents paramètres ont été évalués par qPCR et marquages immunologiques principalement: milieux et matrices de culture, oxygénation, culture en 3D, ainsi que divers facteurs et molécules tels que les microARNs. Les résultats montrent que les hUC MSCs prolifèrent mieux sans sérum et en conditions de normoxie du cerveau (1-5 % O2). Les hUC MSCs naïves semblent préparées à devenir des neurones à l'échelle des gènes et des protéines, mais pas suffisamment pour supporter leur complète différenciation. L'introduction de microARNs requiert des améliorations pour réguler efficacement les voies de signalisation des hUC MSCs. Au cours de cette étude, nous avons identifé les paramètres favorisant l'expansion des hUC MSCs dans des conditions compatibles avec la clinique. Cependant, une question reste ouverte: les hUC MSCs sont-elles capables de vraie transdifferentiation en neurones fonctionnels malgré les controverses? Des recherches supplémentaires sont nécessaires, mais cette étude constitue une première étape vers l'utilisation des hUC MSCs en médecine régénératrice du cerveau
Nowadays, no effective prevention or cure of human brain diseases is available. Stem cells hold great promise for the repair and regeneration of damaged neural tissues. This thesis aims to evaluate the potency of human umbilical cord mesenchymal stem cells (hUC MSCs) to be committed to the neuronal lineage, for brain cell-based therapy. To achieve this goal, naive hUC MSCs were isolated, expanded, and characterized at the gene and protein level, while particularly focusing on the neuronal lineage and clinical-grade culture conditions. Then, several parameters were investigated for hUC MSCs proliferation and neuronal commitment, including media, coatings, 3D culture, hypoxia, chemicals and molecules. Growth curves drawings, qPCRs, and immunostainings were used among other methods for identifying the best conditions for hUC MSCs expansion, differentiation, culture in 3D, and microRNAs delivery. The results indicate that hUC MSCs better proliferate in serum-free media and brain's normoxia condition (1-5 % O2). Naive hUC MSCs appear primed for neuronal fate at gene and protein level, but not su_ciently to support their neuronal di_erentiation. microRNAs delivery requires further improvement to efficiently promote neuronal signaling pathways in hUC MSCs. Along this study we identified the best parameters for hUC MSCs expansion in clinical-grade conditions. However, a question still remains: are hUC MSCs capable of full transdifferentiation towards functional neurons despite all controversies? Additional work is needed, but this study is a first step towards answering this question, bringing more clues to make transplantation of hUC MSCs for brain regenerative medicine closer
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Vogt, Angela Katrin. "Synaptic connectivity in micropatterned networks of neuronal cells." [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968908543.

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Sridhar, Srikala. "Molecular regulation of neuronal apoptosis in PC12 cells." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq22018.pdf.

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Books on the topic "Neuronal cells"

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Amini, Shohreh, and Martyn K. White. Neuronal cell culture: Methods and protocols. New York: Humana Press, 2013.

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Kempermann, Gerd. Adult neurogenesis: Stem cells and neuronal development in the adult brain. New York, NY: Oxford University Press, 2006.

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Adult neurogenesis: Stem cells and neuronal development in the adult brain. New York: Oxford University Press, 2005.

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Ulrich, Henning. Perspectives of Stem Cells: From tools for studying mechanisms of neuronal differentiation towards therapy. Dordrecht: Springer Science+Business Media B.V., 2010.

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Carter, Sylvia M. A comparative study of Rohon-Beard cells and associated neuronal components in fish and amphibian larvae. Portsmouth: Portsmouth Polytechnic, 1991.

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Plasticity in nerve cell function. Oxford: Clarendon Press, 1998.

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Schmid, Carl J., and Jason L. Wolfe. Neuronal cell apoptosis. Hauppauge, N.Y: Nova Science Publisher's, 2011.

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Lossi, Laura, and Adalberto Merighi, eds. Neuronal Cell Death. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2152-2.

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Amini, Shohreh, and Martyn K. White, eds. Neuronal Cell Culture. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-640-5.

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Amini, Shohreh, and Martyn K. White, eds. Neuronal Cell Culture. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1437-2.

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Book chapters on the topic "Neuronal cells"

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Bellizzi, Anna, Nicholas Ahye, and Hassen S. Wollebo. "Lentiviral of Neuronal Cells." In Neuronal Cell Culture, 155–60. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1437-2_11.

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Wollebo, Hassen S., Baheru Woldemichaele, and Martyn K. White. "Lentiviral Transduction of Neuronal Cells." In Neuronal Cell Culture, 141–46. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-640-5_12.

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Horie, Nobutaka. "Neural Stem Cells/Neuronal Progenitor Cells." In Cell Therapy Against Cerebral Stroke, 27–37. Tokyo: Springer Japan, 2017. http://dx.doi.org/10.1007/978-4-431-56059-3_3.

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Marchetto, Maria C. N., Fred H. Gage, and Alysson R. Muotri. "Retrotransposition and Neuronal Diversity." In Perspectives of Stem Cells, 87–96. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-3375-8_7.

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Magavi, Sanjay S., and Jeffrey D. Macklis. "Immunocytochemical Analysis of Neuronal Differentiation." In Neural Stem Cells, 345–52. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-133-8_26.

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Kovalevich, Jane, Maryline Santerre, and Dianne Langford. "Considerations for the Use of Cells in Neurobiology." In Neuronal Cell Culture, 9–23. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1437-2_2.

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Azizi, S. Ausim, and Barbara Krynska. "Derivation of Neuronal Cells from Fetal Normal Human Astrocytes (NHA)." In Neuronal Cell Culture, 89–96. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-640-5_8.

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Kovalevich, Jane, and Dianne Langford. "Considerations for the Use of SH-SY5Y Neuroblastoma Cells in Neurobiology." In Neuronal Cell Culture, 9–21. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-640-5_2.

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Bonner, Joseph F., Christopher J. Haas, and Itzhak Fischer. "Preparation of Neural Stem Cells and Progenitors: Neuronal Production and Grafting Applications." In Neuronal Cell Culture, 65–88. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-640-5_7.

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Weiss, S., S. Ahmed, A. Vescovi, and B. A. Reynolds. "Neuronal Cell Specification from CNS Stem Cells." In Neural Cell Specification, 185–88. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1929-4_14.

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Conference papers on the topic "Neuronal cells"

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Previtera, Michelle L., Mason Hui, Malav Desai, Devendra Verma, Rene Schloss, and Noshir A. Langrana. "Neuronal Precursor Cell Proliferation on Elastic Substrates." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53246.

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Numerous stem cells therapies have been studied for the replacement of damaged neurons due to spinal cord injury. Our laboratory’s goal is to design an implantable platform for spinal cord neuron (SCN) proliferation and differentiation in order to replace damaged neurons in the injured spinal cord. Based on previous literature, we suspect we can promote neuronal precursor cell (NPC) proliferation and differentiation utilizing elastic matrices.
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Sasoglu, F. Mert, Devrim Kilinc, Kathleen Allen, and Bradley Layton. "Parallel Force Measurement in Cell Arrays." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-42472.

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The primary goal of this work is to establish a robust, repeatable method for growing forebrain nerve cells in a parallel manner by stretching them using a microfabricated PDMS beam array and printing arrays of neurons. The highly compliant, transparent, biocompatible PDMS micro beam array may offer a method for more rapid throughput in cell and protein mechanics force measurement experiments with sensitivities necessary for highly compliant structures such as axons. This work has two endpoints. One is to use a neural array as an experimental testbed for investigating neuronal cell growth hypotheses. The other endpoint is to build a neuronal-based, biosensor device capable of acting as a cell-based sensor. We present preliminary results for microbeams attaching to nerve cells. The attachment ratio the life-length and the axon lengths of the chick forebrain cells on microprinted spots will also be compared with an equivalent protein coated area of cells.
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Liu, Chun, Seungik Baek, and Christina Chan. "The Complementary Effect of Mechanical and Chemical Stimuli on the Neural Differentiation of Mesenchymal Stem Cells." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80131.

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Mesenchymal stem cells (MSCs), derived from bone marrow stroma, are a promising source for tissue repair and regeneration, due to their excellent abilities for proliferation and multipotent differentiation. While accumulated evidences during the past decade have shown that MSCs are able to differentiate into osteoblasts, chondrocytes, myoblasts and adipocytes, more recent research suggest their potential in neuronal differentiation [1]. Chemical stimuli, including growth factors, hormones, and other regulatory molecules, are used traditionally to direct MSC differentiation. Our group has previously shown that the intracellular second messenger, cAMP, is able to initiate early phase neuron-like morphology changes and late phase neural differentiation in MSCs [2]. Studies using chemical stimuli alone, however, have shown limited success in differentiating MSCs to mature neurons, thereby suggesting other factors are necessary for this process. In recent years, interest has grown on the impact of mechanical stimulation, such as stiffness, surface topography, and mechanical stretching, on cell fate decision [3].
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Abasi, Sara, John R. Aggas, and Anthony Guiseppi-Elie. "Permissive Electroconductive Nanocomposites for Neuronal Progenitor Cells." In 2019 9th International IEEE/EMBS Conference on Neural Engineering (NER). IEEE, 2019. http://dx.doi.org/10.1109/ner.2019.8716893.

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Testa, Ilaria. "RESOLFT Super Resolution Microscopy in Neuronal Cells." In Optics and the Brain. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/brain.2017.brw2b.1.

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Tek, Sumeyra, Brandy A. Vincent, Christopher A. Baker, Ashley N. Tran, and Kelly L. Nash. "Upconversion nanoparticles for photobiomodulation of neuronal cells." In Colloidal Nanoparticles for Biomedical Applications XIV, edited by Wolfgang J. Parak and Marek Osiński. SPIE, 2019. http://dx.doi.org/10.1117/12.2512255.

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Battistoni, Silvia, Victor Erokhin, Nicola Cornella, Tatiana Berzina, Paolo Macchi, and Salvatore Iannotta. "Analysis of PANI biocompatibility with neuronal cells." In 2015 International Conference on Memristive Systems (MEMRISYS). IEEE, 2015. http://dx.doi.org/10.1109/memrisys.2015.7378403.

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Me´ndez-Rojas, Miguel A., Claudia Cravioto Guzman, and Oscar Arias-Carrion. "Synthesis and Chemical Functionalization of Ferromagnetic Nanoparticles to Manipulate Stem Cells Using External Magnetic Fields." In ASME 2007 5th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2007. http://dx.doi.org/10.1115/icnmm2007-30188.

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The human brain is able to respond to several situations that promotes neural survivance, growth and neuronal cells regeneration. The potential of stem cells from the subventricular zone to be used for neuronal cell substitution has been widely studied. However, migration of endogen or transplanted cells is random, not efficient and with a very low survivance rate. The use of ferromagnetic nanoparticles may be of interest to guide the stem cells to the desired site using external fields. In this project, we have synthesized ferromagnetic nanoparticles (magnetite) with an average diameter of 10–12 nm, and functionalized with folic acid-flourosceine (with an average yield of 60–70%) in order to induce their entry into rat neuronal precursor cells in vivo and in vitro. The efficiency of cellular incorporation was low in vitro, observing clustering of the nanoparticles at the cytoplasm membrane. During the in vivo tests, no incorporation of nanoparticles was detected. Several results and perspectives are discussed in this work.
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Kleiman, Ross, Michelle Previtera, Sharan Parikh, Devendra Verma, Rene Schloss, and Noshir Langrana. "The Effects of Extracellular Matrix Proteins and Stiffness on Neuronal Cell Adhesion." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53596.

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Spinal cord injuries have spurred research interests in finding ways to repair or replace damaged neurons. We are looking to find novel ways to promote proliferation and differentiation of stem cells in order to replace damaged spinal cord neurons. While previous studies have shown that the mechanical properties of the cellular environment influence proliferation and differentiation, these studies have only been performed on polyacrylamide and agarose gels (1, 2). Collagen gels provide the opportunity to promote neuronal precursor cell (NPCs) proliferation and differentiation in a more natural environment by utilizing the mechanical properties of the gel. In this study, we examine the effects of 2D collagen matrices of varying stiffness on proliferation and differentiation of rat, spinal cord NPCs in order to create a more biocompatible tissue-engineered platform.
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Li, Lulu, Alexander Davidovich, Jennifer Schloss, Uday Chippada, Rene Schloss, Noshir Langrana, and Martin Yarmush. "Control of Neural Lineage Differentiation in an Alginate Encapsulation Microenvironment via Cellular Aggregation." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206496.

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Cell replacement therapies, which utilize renewable stem cell sources, hold tremendous potential to treat a wide range of degenerative diseases. Although many studies have established techniques to successfully differentiate stem cells into different mature cell lineages, their practicality is limited by the lack of control during the differentiation process and low yields of differentiated cells. In order to address these issues, we have previously established a murine embryonic stem cell alginate-poly-L-lysine microencapsulation differentiation system [1]. We demonstrated that ES cell differentiation could be mediated by cell-cell aggregation in the encapsulation microenvironment. We have demonstrated that both cell aggregation and hepatocyte functions, such as urea and albumin secretions, as well as increased expression of cytokeratin 18 and cyp4507a, occur concomitantly with surface E-cadherin expression [2]. In the present studies, we assessed the feasibility of inducing neuronal lineage differentiation in the alginate microenvironment by incorporating soluble inducers, such as retinoic acid, into the permeable microcapsule system. We demonstrated decreased cell aggregation and enhanced neuronal lineage differentiation with the expression of various neuronal specific markers, including neurofilament, A2B5, O1 and glial fibrillary acidic protein (GFAP). In addition, we demonstrated that, by blocking the cell aggregation using anti-E-cadherin antibody, encapsulated cells increased neuronal marker expression at a later stage of the encapsulation, even in the absence of retinoic acid. In conjunction with the mechanical and physical characterizations of the alginate crosslinking network, we show that 2.2% alginate concentration is most conducive to neuronal differentiation from embryonic stem cells in the presence of retinoic acid.
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Reports on the topic "Neuronal cells"

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Dr. Husni Elbahesh, Dr Husni Elbahesh. Does Zika virus suppress the antiviral host response in neuronal cells? Experiment, April 2016. http://dx.doi.org/10.18258/6968.

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Pattabiraman, Nagarajan, Carolyn Chambers, Ayesha Adil, and Gregory E. Garcia. Identification of Small Molecules against Botulinum Neurotoxin B Binding to Neuronal Cells at Ganglioside GT1b Binding Site with Low to Moderate Affinity. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada612876.

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Carvey, Paul M. Cytokine Induction of Dopamine Neurons from Progenitor Cells. Fort Belvoir, VA: Defense Technical Information Center, October 2000. http://dx.doi.org/10.21236/ada391417.

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Polt, Robin. Enzyme Inhibitors of Cell-Surface Carbohydrates: Insects as Model Systems for Neuronal Development and Repair Mechanisms. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada397723.

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Polt, Robin. Enzyme Inhibitors of Cell-Surface Carbohydrates: Insects as Model Systems for Neuronal Development and Repair Mechanisms. Fort Belvoir, VA: Defense Technical Information Center, July 2000. http://dx.doi.org/10.21236/ada382533.

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Wynshaw-Boris, Anthony. Testing Brain Overgrowth and Synaptic Models of Autism Using NPCs and Neurons from Patient-Derived iPS Cells. Fort Belvoir, VA: Defense Technical Information Center, October 2014. http://dx.doi.org/10.21236/ada613860.

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Bergey, Gregory K. Mechanisms of Action of Clostridial Neurotoxins on Dissociated Mouse Spinal Cord Neurons in Cell Culture. Fort Belvoir, VA: Defense Technical Information Center, September 1991. http://dx.doi.org/10.21236/ada244092.

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Zigmond, Michael J., Amanda Smith, and Anthony Liou. The Impact of Exercise on the Vulnerability of Dopamine Neurons to Cell Death in Animal Models of Parkinson's Disease. Fort Belvoir, VA: Defense Technical Information Center, July 2008. http://dx.doi.org/10.21236/ada501105.

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