Gotowa bibliografia na temat „Multipotency”
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Artykuły w czasopismach na temat "Multipotency"
Mrksich, Milan. "Multipotency retained". Nature Materials 10, nr 8 (22.07.2011): 559–60. http://dx.doi.org/10.1038/nmat3086.
Pełny tekst źródłaIstiaq, Arif, i Kunimasa Ohta. "Ribosome-Induced Cellular Multipotency, an Emerging Avenue in Cell Fate Reversal". Cells 10, nr 9 (1.09.2021): 2276. http://dx.doi.org/10.3390/cells10092276.
Pełny tekst źródłaIsmail, A. A., S. Wagner, H. Murua Escobar, S. Willenbrock, K. A. Sterenczak, M. T. Samy, A. M. Abd El-Aal, I. Nolte i P. Wefstaedt. "Effects of High-Mobility Group A Protein Application on Canine Adipose-Derived Mesenchymal Stem CellsIn Vitro". Veterinary Medicine International 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/752083.
Pełny tekst źródłaTeng, Chiao-Fang, Long-Bin Jeng i Woei-Cherng Shyu. "Role of Insulin-like Growth Factor 1 Receptor Signaling in Stem Cell Stemness and Therapeutic Efficacy". Cell Transplantation 27, nr 9 (8.06.2018): 1313–19. http://dx.doi.org/10.1177/0963689718779777.
Pełny tekst źródłaMiceli, Vitale, Mariangela Pampalone, Serena Vella, Anna Paola Carreca, Giandomenico Amico i Pier Giulio Conaldi. "Comparison of Immunosuppressive and Angiogenic Properties of Human Amnion-Derived Mesenchymal Stem Cells between 2D and 3D Culture Systems". Stem Cells International 2019 (18.02.2019): 1–16. http://dx.doi.org/10.1155/2019/7486279.
Pełny tekst źródłaJuliano, C. E., S. Z. Swartz i G. M. Wessel. "A conserved germline multipotency program". Development 137, nr 24 (23.11.2010): 4113–26. http://dx.doi.org/10.1242/dev.047969.
Pełny tekst źródłaXie, Meng, Dmitrii Kamenev, Marketa Kaucka, Maria Eleni Kastriti, Baoyi Zhou, Artem V. Artemov, Mekayla Storer i in. "Schwann cell precursors contribute to skeletal formation during embryonic development in mice and zebrafish". Proceedings of the National Academy of Sciences 116, nr 30 (8.07.2019): 15068–73. http://dx.doi.org/10.1073/pnas.1900038116.
Pełny tekst źródłaMalvicini, Ricardo, Diego Santa-Cruz, Natalia Pacienza i Gustavo Yannarelli. "OCT4 Silencing Triggers Its Epigenetic Repression and Impairs the Osteogenic and Adipogenic Differentiation of Mesenchymal Stromal Cells". International Journal of Molecular Sciences 20, nr 13 (3.07.2019): 3268. http://dx.doi.org/10.3390/ijms20133268.
Pełny tekst źródłaSwartz, S. Zachary, Celina E. Juliano, Tal Raz, Doron Lipson, Patrice Milos, Amro Hamdoun i Gary M. Wessel. "An ancient molecular circuit specifying multipotency". Developmental Biology 344, nr 1 (sierpień 2010): 514–15. http://dx.doi.org/10.1016/j.ydbio.2010.05.368.
Pełny tekst źródłaRahnama, Ruyan, i Challice L. Bonifant. "Engineering builds multipotency for iPSC-NKs". Blood 140, nr 23 (8.12.2022): 2414–16. http://dx.doi.org/10.1182/blood.2022017794.
Pełny tekst źródłaRozprawy doktorskie na temat "Multipotency"
Wetzig, Andrew R., i n/a. "Olfactory Stem Cells From Adult Rats". Griffith University. School of Biomolecular and Biomedical Science, 2007. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20070724.121953.
Pełny tekst źródłaWetzig, Andrew R. "Olfactory Stem Cells From Adult Rats". Thesis, Griffith University, 2007. http://hdl.handle.net/10072/366121.
Pełny tekst źródłaThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Biomedical Sciences
Faculty of Science
Full Text
Wuidart, Aline. "Defining the mechanisms regulating the switch from multipotency to unipotency during mammary gland development". Doctoral thesis, Universite Libre de Bruxelles, 2018. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/264618.
Pełny tekst źródłaDoctorat en Sciences biomédicales et pharmaceutiques (Médecine)
info:eu-repo/semantics/nonPublished
McMurray, Rebecca Jane. "Nanoscale surfaces for the long-term maintenance of mesenchymal stem cell phenotype and multipotency". Thesis, University of Glasgow, 2011. http://theses.gla.ac.uk/3042/.
Pełny tekst źródłaGray, Simon Matthew. "PRC2-Mediated H3K27me3 Repression Promotes Effector CD8 + T Cell Terminal Differentiation and Loss of Multipotency". Thesis, Yale University, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10584947.
Pełny tekst źródłaElucidating how multipotent memory precursor (MP) cells maintain developmental plasticity and longevity to provide long-term immunity while most effector cells develop into terminally differentiated effector (TE) cells with limited survival is necessary for understanding immunological memory formation. We profiled active (H3K27Ac) and repressed (H3K27me3) chromatin states in naïve, MP and TE CD8+ T cells during viral infection, and observed increased H3K27me3 at numerous pro-memory and pro-survival genes in TE relative to MP cells, indicative of fate restriction, but permissive chromatin at both pro-memory and pro-effector genes in MP cells, indicative of multipotency. Deficiency in PRC2-mediated H3K27me3 deposition impaired clonal expansion and TE cell differentiation, but minimally impacted memory cell maturation. Abundant H3K27me3 deposition at pro-memory genes occurred relatively late during TE cell development in a FOXO1-regulated manner. These results outline a detailed temporal model for how effector T cells lose memory cell potential through selective epigenetic-silencing of pro-memory genes.
Cwinn, Matthew. "'Suppressor of fused' antagonizes hedgehog signaling and is required to maintain retinal progenitor cell identity and multipotency". Thesis, University of Ottawa (Canada), 2009. http://hdl.handle.net/10393/28214.
Pełny tekst źródłaChang, Eun Hyuk. "The role of polycomb repressive complex 2 in postnatal subventricular zone neural stem/progenitor cell self-renewal and multipotency". Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:1ddbd108-0256-4a4a-b40a-35818197ca39.
Pełny tekst źródłaKole, Denis. "Role of Fibroblast Growth Factor 2 in Maintenance of Multipotency in Human Dermal Fibroblasts Treated with Xenopus Laevis Egg Extract Fractions". Digital WPI, 2014. https://digitalcommons.wpi.edu/etd-dissertations/207.
Pełny tekst źródłaPhilip, Diana Liz. "The Influence of Synthetic Microenvironments in Determining Stem Cell Fate". University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1627669247178055.
Pełny tekst źródłaLoison-Robert, Ludwig. "Cellule souche gingivale : origine et multipotence". Thesis, Paris Est, 2016. http://www.theses.fr/2016PESC0083/document.
Pełny tekst źródłaGingiva is a natural regeneration model thanks to its "ad integrum" healing capability. Gingival fibroblasts are the main actors of this property. These cells, the main cellular component of the gingival connective tissue, regulate the inflammatory responses and healing process. This tissue contains, like many others, mesenchymal stem cells; which also partly explain these regenerative abilities. Moreover, as the gingiva is abundant and easily accessible, the use of these stem cells may interest cell therapy or in vitro model tissues responses. In this work, we demonstrated that Stem Cells Derived from Human Gingiva (SCHG) have common properties with neural crest adult stem cells. These cells can be called "stem cells" for their ability to self-renew, adhere to plastic and to differentiate. First, we have shown that the method and the culture products used for isolation of gingival fibroblasts from gingival biopsy had an influence on the obtained cells. Secondly, an analysis of in vitro clonal populations of gingival fibroblasts has shown that gingival fibroblasts are composed of subpopulations that express specific markers of stem cells and neural crests. In addition to their embryological origin, the study of their multipotency was also characterized after expansion and depending on the used additives. Finally, two examples of using these cells and dental pulp stem cells as a model to study the in vitro biocompatibility of biomaterials have been developed, mimicking oral mucosa or dentin reactions (reparative or reactional)
Książki na temat "Multipotency"
Harrison, Andrew James. Evidence of multipotency in immortalised cells derived from bone marrow stroma. Manchester: University of Manchester, 1996.
Znajdź pełny tekst źródłaHoffman, Robert M., red. Multipotent Stem Cells of the Hair Follicle. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3786-8.
Pełny tekst źródłaBamba, Shigeki. Gut stem cells: Multipotent, clonogenic, and the origin of gastrointestinal cancer. New York: Nova Science Publishers, 2008.
Znajdź pełny tekst źródłaPearson, Mark Andrew. Investigation of molecular mechanisms involved in cytokine synergy in multipotent haemopoietic cells. Manchester: University of Manchester, 1996.
Znajdź pełny tekst źródłaReynolds, Brent A., i Loic P. Deleyrolle. Neural progenitor cells: Methods and protocols. New York: Humana Press, 2013.
Znajdź pełny tekst źródłaAmit, M., i Joseph Itskovitz-Eldor. Atlas of human pluripotent stem cells: Derivation and culturing. New York: Humana Press, 2012.
Znajdź pełny tekst źródłaHoffman, Robert M. Multipotent Stem Cells of the Hair Follicle: Methods and Protocols. Springer New York, 2016.
Znajdź pełny tekst źródłaHoffman, Robert M. Multipotent Stem Cells of the Hair Follicle: Methods and Protocols. Springer New York, 2018.
Znajdź pełny tekst źródłaReynolds, Brent A., i Loic P. Deleyrolle. Neural Progenitor Cells: Methods and Protocols. Humana Press, 2016.
Znajdź pełny tekst źródłaDeleyrolle, Loic P. Neural Progenitor Cells: Methods and Protocols. Springer, 2021.
Znajdź pełny tekst źródłaCzęści książek na temat "Multipotency"
Zipori, Dov. "Multipotency and Tissue-Specific Stem Cells". W Biology of Stem Cells and the Molecular Basis of the Stem State, 39–55. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60761-130-1_2.
Pełny tekst źródłaTeng, Yang D., Serdar Kabatas, Jianxue Li, Dustin R. Wakeman, Evan Y. Snyder i Richard L. Sidman. "Functional Multipotency of Neural Stem Cells and Its Therapeutic Implications". W Perspectives of Stem Cells, 255–70. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-3375-8_16.
Pełny tekst źródłaTeng, Yang D., Xiang Zeng, Inbo Han i Jaime E. Anderson. "Neural Stem Cells: Functional Multipotency and Spinal Cord Injury Research Protocols". W Working with Stem Cells, 311–29. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30582-0_18.
Pełny tekst źródłaJiang, Fang-Xu, i Grant Morahan. "Pancreas-Derived Multipotent Progenitors". W Regenerative Medicine - from Protocol to Patient, 345–62. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-27610-6_13.
Pełny tekst źródłaWolfe, Margaret, Alan Tucker, Roxanne L. Reger i Darwin J. Prockop. "Multipotent Stromal Cells (hMSCs)". W Human Adult Stem Cells, 45–72. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2269-1_2.
Pełny tekst źródłaVerfaillie, Catherine M. "Multipotent Adult Progenitor Cells: An Update". W Stem Cells: Nuclear Reprogramming and Therapeutic Applications, 55–65. Chichester, UK: John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/0470091452.ch5.
Pełny tekst źródłaPostovit, Lynne-Marie, Naira V. Margaryan, Elisabeth A. Seftor, Luigi Strizzi, Richard E. B. Seftor i Mary J. C. Hendrix. "Plasticity Underlying Multipotent Tumor Stem Cells". W Stem Cells and Cancer, 99–112. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-933-8_8.
Pełny tekst źródłaMotohashi, Tsutomu, i Takahiro Kunisada. "Melanoblasts as Multipotent Cells in Murine Skin". W Skin Stem Cells, 257–66. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/7651_2018_144.
Pełny tekst źródłaMotohashi, Tsutomu, i Takahiro Kunisada. "Melanoblasts as Multipotent Cells in Murine Skin". W Skin Stem Cells, 183–92. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-330-5_15.
Pełny tekst źródłaZhao, Weian, Debanjan Sarkar, James Ankrum, Sean Hall, Weili Loh, Wei Suong Teo i Jeffrey M. Karp. "Therapeutic Applications of Mesenchymal Stem/Multipotent Stromal Cells". W Stem Cells & Regenerative Medicine, 195–218. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-860-7_12.
Pełny tekst źródłaStreszczenia konferencji na temat "Multipotency"
Trella, Emanuele. "Abstract A016: Multipotency of a CD40L-expressing recombinant vaccinia virus". W Abstracts: Second CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; September 25-28, 2016; New York, NY. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/2326-6066.imm2016-a016.
Pełny tekst źródłaVan Dyke, William S., Ozan Akkus i Eric Nauman. "Murine Osteochondral Stem Cells Express Collagen Type I More Strongly on PDMS Substrates Than on Tissue Culture Plastic". W ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14272.
Pełny tekst źródłaKolosova, Irina, Daniel J. Angelini, Chunling Fan, John Skinner i Roger A. Johns. "Hypoxia-Induced Mitogenic Factor Stimulates Proliferation And Migration Maintaining The Multipotency Of Mesenchymal Stem Cells". W American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a1238.
Pełny tekst źródłaKosak, Oliver, Felix Bohn, Felix Keller, Hella Ponsar i Wolfgang Reif. "Ensemble Programming for Multipotent Systems". W 2019 IEEE 4th International Workshops on Foundations and Applications of Self* Systems (FAS*W). IEEE, 2019. http://dx.doi.org/10.1109/fas-w.2019.00037.
Pełny tekst źródłaYuan, Lin, Naoya Sakamoto, Guanbin Song i Masaaki Sato. "Migration of Human Mesenchymal Stem Cells is Stimulated by Low Shear Stress via MAPK Signaling". W ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80056.
Pełny tekst źródłaSerdukov, Yu V., А. Yu Adamovich, V. K. Shadrina i D. B. Nizheharodava. "THE COMPARISON OF MULTIPOTENT MESENCHYMAL STROMAL CELLS IN DONORS OF DIFFERENT AGE GROUPS". W SAKHAROV READINGS 2021: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute of Belarusian State University, 2021. http://dx.doi.org/10.46646/sakh-2021-2-111-114.
Pełny tekst źródłaSvirskaya, A. V., M. A. Yakauleva, D. B. Nizheharodava i M. M. Zafranskaya. "EFFECT OF HYPOXIA ON IMMUNOMODULATORY PROPERTIES OF MULTIPOTENT MESENCHYMAL STROMAL CELLS". W SAKHAROV READINGS 2022: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute of Belarusian State University, 2022. http://dx.doi.org/10.46646/sakh-2022-2-94-97.
Pełny tekst źródłaTsao, Chia-Wen, Meng-Zhi Chiang i Yu-Che Cheng. "Effects of Chemical and Physical Shear-Stress Stimulation of Human Placenta-Derived Multipotent Stem Cells in Microchannel". W ASME 2013 11th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icnmm2013-73194.
Pełny tekst źródłaAbdelalim, Essam, Idil Aigha, Ahmed Elsayed i Bushra Memon. "Generation of a Novel Population of Pancreatic Multipotent Progenitor Cells Expressing NKX61". W Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2018. http://dx.doi.org/10.5339/qfarc.2018.hbpd291.
Pełny tekst źródłaAbdelalim, Essam, Idil I. Aigha, Ahmed K. Elsayed i Bushra Memon. "Generation of a Novel Population of Pancreatic Multipotent Progenitor Cells Expressing NKX61". W Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2018. http://dx.doi.org/10.5339/qfarc.2018.hbpp291.
Pełny tekst źródłaRaporty organizacyjne na temat "Multipotency"
Selsted, Michael E. Structure and Design of Multipotent Peptide Microbicides. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1988. http://dx.doi.org/10.21236/ada199085.
Pełny tekst źródłaWilson, Cindy A. Signaling from a Novel Receptor Tyrosine Kinase and the Control of Multipotent Mammary Progenitor Cells. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2006. http://dx.doi.org/10.21236/ada492622.
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