Добірка наукової літератури з теми "Embryogenesis; stem cell"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Embryogenesis; stem cell".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Embryogenesis; stem cell"
Cumano, Ana, and Isabelle Godin. "Pluripotent hematopoietic stem cell development during embryogenesis." Current Opinion in Immunology 13, no. 2 (April 2001): 166–71. http://dx.doi.org/10.1016/s0952-7915(00)00200-4.
Повний текст джерелаAiba, Kazuhiro, Mark Carter, Ryo Matoba, and Minoru Ko. "Genomic Approaches to Early Embryogenesis and Stem Cell Biology." Seminars in Reproductive Medicine 24, no. 5 (November 2006): 330–39. http://dx.doi.org/10.1055/s-2006-952155.
Повний текст джерелаGering, Martin, and Roger Patient. "Notch signalling and haematopoietic stem cell formation during embryogenesis." Journal of Cellular Physiology 222, no. 1 (January 2010): 11–16. http://dx.doi.org/10.1002/jcp.21905.
Повний текст джерелаWang, Han, Xie Luo, and Jake Leighton. "Extracellular Matrix and Integrins in Embryonic Stem Cell Differentiation." Biochemistry Insights 8s2 (January 2015): BCI.S30377. http://dx.doi.org/10.4137/bci.s30377.
Повний текст джерелаJakobsson, Lars, Johan Kreuger, and Lena Claesson-Welsh. "Building blood vessels—stem cell models in vascular biology." Journal of Cell Biology 177, no. 5 (May 29, 2007): 751–55. http://dx.doi.org/10.1083/jcb.200701146.
Повний текст джерелаVolotovski, I. D., D. A. Ermolenko, and N. I. Harokhava. "Epigenetic control of differentiation of mesenchymal stem cells. Stem cells differentiation in liver." Proceedings of the National Academy of Sciences of Belarus, Biological Series 65, no. 1 (February 11, 2020): 106–18. http://dx.doi.org/10.29235/1029-8940-2020-65-1-106-118.
Повний текст джерелаLong, Jeff A. "Specifying root/shoot stem cells during Arabidopsis embryogenesis." Developmental Biology 331, no. 2 (July 2009): 385–86. http://dx.doi.org/10.1016/j.ydbio.2009.05.010.
Повний текст джерелаParthibhan, S., M. Rao, J. A. Teixeira da Silva, and T. Kumar. "Somatic embryogenesis from stem thin cell layers of Dendrobium aqueum." Biologia plantarum 62, no. 3 (September 1, 2018): 439–50. http://dx.doi.org/10.1007/s10535-018-0769-4.
Повний текст джерелаTung, Hoang Thanh, Hoang Thi Van, Huynh Gia Bao, Le The Bien, Hoang Dac Khai, Vu Quoc Luan, Do Manh Cuong, Truong Hoai Phong, and Duong Tan Nhut. "Silver nanoparticles enhanced efficiency of explant surface disinfection and somatic embryogenesis in Begonia tuberous via thin cell layer culture." Vietnam Journal of Biotechnology 19, no. 2 (August 2, 2021): 337–47. http://dx.doi.org/10.15625/1811-4989/15872.
Повний текст джерелаTraver, David, Julien Bertrand, Albert Kim, Jennifer Cisson, and Emily Violette. "Hematopoietic Stem and Progenitor Cell Biology in the Zebrafish." Blood 108, no. 11 (November 16, 2006): 4160. http://dx.doi.org/10.1182/blood.v108.11.4160.4160.
Повний текст джерелаДисертації з теми "Embryogenesis; stem cell"
Poirier, Luc. "The degradation of the stem-loop binding protein at the late 2-cell stage of mouse embryogenesis /." Thesis, McGill University, 2003. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=80351.
Повний текст джерелаDe, Mot Laurane. "Mechanisms of cell differentiation during murine embryogenesis: model for specification in epiblast or primitive endoderm and experimental approach in embryonic stem cells." Doctoral thesis, Universite Libre de Bruxelles, 2013. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209375.
Повний текст джерелаDans la seconde partie de la thèse, effectuée dans le laboratoire d’O. Pourquié (Université de Strasbourg), nous avons étudié un processus de différenciation in vitro, par une approche expérimentale. Il s’agit de la différenciation des cellules souches embryonnaires (ES) en cellules de mésoderme paraxial, un tissu dont dérivent –au cours du développement embryonnaire– les cellules formant notamment les vertèbres, les côtes, la peau et les muscles squelettiques du dos.
Doctorat en Sciences agronomiques et ingénierie biologique
info:eu-repo/semantics/nonPublished
Antonica, Francesco. "Modelling thyroid embryogenesis using embryonic stem cells." Doctoral thesis, Universite Libre de Bruxelles, 2013. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209551.
Повний текст джерелаFor the identification of new genes and molecular events controlling thyroid organogenesis it would be useful to develop an in vitro cellular model to recapitulate thyroid embryogenesis in a dish. Embryonic Stem Cells (ESCs) have recently emerged as system model to recapitulate the embryogenesis of several tissues in vitro.
Induced overexpression of defined transcription factors has been shown to have a directing effect on the differentiation of pluripotent stem cells into specific cell types. In this thesis I show that a transient overexpression of the transcription factors NKX2.1 and PAX8 is sufficient to direct the differentiation of murine ESCs into thyroid follicular cells (TFC) and promotes in vitro self- assembly of TFC into three-dimensional follicular structures, when associated to a subsequent thyrotropin (TSH) treatment. Cells differentiated by this protocol showed significant iodide organification activity, a hallmark of thyroid tissue function. Importantly, athyroid mice grafted with mESC-derived thyroid follicles show normalization of plasma T4 levels with concomitant decrease of plasma TSH. In addition, a full normalization of body temperature at 4 weeks after transplantation was observed. Together, these data clearly demonstrate that grafting of our mESC-derived thyroid cells rescues the hypothyroid state and triggers symptomatic recovery along with the normalization of plasma hormone concentrations. The high efficiency of TFC differentiation and follicle morphogenesis in our system will provide an unprecedented opportunity for future studies to decipher regulatory mechanisms involved in embryonic thyroid development, a major research need towards an improved understanding of the molecular mechanisms underlying congenital hypothyroidism, the most common congenital endocrine disorder in humans.
Doctorat en Sciences biomédicales et pharmaceutiques
info:eu-repo/semantics/nonPublished
Marshall, Carolyn Jean. "The origin and regulation of haematopoietic stem cells during mammalian embryogenesis." Thesis, City University London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.412734.
Повний текст джерелаHarrison, Sarah Ellys. "Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/275424.
Повний текст джерелаChoudhary, Meenakshi Khetaram. "Elucidating the role of Hyaluronan in early human embryogenesis and embryonic sten cell characterisation." Thesis, University of Newcastle Upon Tyne, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.506550.
Повний текст джерелаFei, Liwen. "Towards automating micropropagation: from cells to shoots to plants in one step." Digital WPI, 2015. https://digitalcommons.wpi.edu/etd-dissertations/195.
Повний текст джерелаPeralta, Oscar Alejandro. "Developmental Regulation of Prion Expression in Cattle and Mouse Embryonic Stem Cells." Diss., Virginia Tech, 2008. http://hdl.handle.net/10919/28584.
Повний текст джерелаPh. D.
Brock, Ryane Schmidt [UNESP]. "Retalho ósseo neo-fabricado de gálea e periósteo preenchido com células-tronco mesenquimais, plasma rico em plaquetas, pó de osso e ácido hialurônico: estudo em coelho." Universidade Estadual Paulista (UNESP), 2017. http://hdl.handle.net/11449/148751.
Повний текст джерелаApproved for entry into archive by LUIZA DE MENEZES ROMANETTO (luizamenezes@reitoria.unesp.br) on 2017-02-09T20:00:55Z (GMT) No. of bitstreams: 1 brock_rs_dr_bot.pdf: 138052465 bytes, checksum: f5b517e489dbadd6cf6b83fbef881ecd (MD5)
Made available in DSpace on 2017-02-09T20:00:55Z (GMT). No. of bitstreams: 1 brock_rs_dr_bot.pdf: 138052465 bytes, checksum: f5b517e489dbadd6cf6b83fbef881ecd (MD5) Previous issue date: 2017-01-31
As deformidades craniofaciais decorrentes de traumas, ressecções de tumores ou malformações congênitas são freqüentes na prática médica e o tratamento destas necessitam de cirurgia reparadora, com técnicas especializadas e profissionais qualificados para corrigir os defeitos e proporcionar melhor qualidade de vida, aprimorar a fala, respiração, mastigação e deglutição. Há diversas técnicas descritas para corrigir os defeitos ósseos, cada uma com vantagens e desvantages, escolhidas de acordo com o tipo de deformidade. Este estudo avaliou a formação óssea em um retalho tubular vascularizado, gáleo-periostal, enriquecido com o uso de pó de osso, plasma rico em plaquetas, células-tronco mesenquimais e ácido hialurônico, em coelhos, que tenha capacidade de substituir o enxerto ósseo nas reconstruções, principalmente nos defeitos faciais. No estudo, utilizou-se 98 coelhos divididos em doze grupos, submetidos à cirurgia para confecção do retalho em calota craniana. Foram realizados retalhos tubulares com o periósteo voltado para dentro e preenchidos com pó de osso, plasma rico em plaquetas (PRP), células-tronco mesenquimais (CTM) e ácido hialurônico. O Grupo 1 não foi manipulado. No Grupo 2 foi realizado o retalho tubular e mantido vazio. O Grupo 3 teve o retalho preenchido com pó de osso, no Grupo 4 o retalho foi mantido vazio. O Grupo 5 teve o retalho preenchido com PRP. No Grupo 6 o retalho foi preenchido com PRP e pó de osso. O Grupo 7 foi preenchido com CTM. O Grupo 8 teve o retalho preenchido com CTM e pó de osso. O Grupo 9 teve o retalho preenchido com CTM e PRP. No Grupo 10, o retalho tubular foi preenchido com PRP, CTM e pó de osso. O Grupo 11 foi mantido vazio e o Grupo 12 foi preenchido com ácido hialurônico. Os resultados foram avaliados através de métodos de imagem e avaliação histológica. Os resultados demonstraram que, no modelo experimental utilizado, os grupos com apenas periósteo, isto é, retalho tubular vazio, apresentaram formação óssea pequena e irregular. No grupo com PRP também houve a formação óssea irregular e imatura. Quando o PRP foi associado ao pó de osso houve uma formação mais regular e organizada. O grupo com célula-tronco mesenquimal também apresentou formação óssea, com características teciduais organizadas, próprias do tecido ósseo maduro. Quando associada ao pó de osso e ao PRP, as características histológicas apresentaram-se com tecido organizado, regular, maduro com células bem formadas e organizadas. O uso de materiais com fatores de crescimento celular ósseo melhoram a qualidade e organização do tecido neoformado. Quanto maior o número de fatores de enriquecimento usados, melhores foram os resultados quanto a qualidade tecidual neoformada.
Craniofacial deformities caused by traumas, tumor ressections or congenital malformation are frequent in medical practice, and their treatment with reconstructive surgeries are common, especially in plastic surgery, which aim to provide the patients with better quality of life and functional improvement of speach, breathing, chewing and swallowing. Many different techniques are described to correct bone defects. They have advantages and disadvantages, chosen according to the type of deformity. This study evaluated a vascularized galeal and periosteum flap filled with bone fragments, platelet rich plasma, mesenchymal stem cells and hyaluronic acid, using rabbits, which could possibily substitute the bone graft in reconstructive surgery, especially for facial defects. It was an experimental study, with 98 rabbits divided into twelve groups, submitted to a surgical procedure to construct a calvaria flap. A tubular flap with the periosteum inside was constructed and filled with bone fragments, platelet rich plasma (PRP), mesenchymal stem cells (MSC) and hyaluronic acid. Group 1 was not manipulated. In Group 2, the tubular flap was maintained empty. Group 3 had the flap filled with bone fragments, in Grupo 4 the flap was maintained empty. Group 5 had the flap filled with PRP. In Group 6 the flap was filled with PRP and bone fragments. The Group 7 was filled with MSC. Group 8 had the flap filled with MSC and bone fragments. The Group 9 had the flap filled with MSC and PRP. In Group 10, the tubular flap was filled with PRP, MSC and bone fragments.The Group 11 was maintained empty and Group 12 was filled with hyaluronic acid. The results were evaluated using image methods and histological analysis. The results demonstrated that, in the experimental model used, the groups with only periosteum, this is the empty tubular flap, presented small and irregular bone formation. In the group with PRP, it also had irregular and imature bone formation. When the PRP was associated to bone fragments it had a more regular and organized formation. The group with mesenchymal stem cell also presented bone formation, with organized tissue characteristics, proper of mature osseous tissue. When associated to bone fragments and PRP, the histological characteristics presented organized, regular, mature tissue with organized and well formed cells. The use of materials with osseous cellular growth factors improves the quality and organization of the neoformed tissue. The more enrichment factor used, the better the neoformed tissue quality result was.
Storer, Mekayla 1981. "Investigating the roles of cellular senescence in embryogenesis and aging." Doctoral thesis, Universitat Pompeu Fabra, 2014. http://hdl.handle.net/10803/289617.
Повний текст джерелаLa senescencia celular es una forma irreversible de paro proliferativo ligado históricamente a la supresión tumoral y al envejecimiento. Sin embargo, estudios recientes han demostrado que también juega un papel en complejos procesos biológicos como reparación tisular, promoción tumoral y desórdenes relacionados con la edad. Estos nuevos conocimientos están redefiniendo nuestra visión de la senescencia celular, no tanto como un proceso estático sino como un fenotipo colectivo compuesto por una compleja red de programas efectores. El resultado biológico de estos programas efectores varía dependiendo del contexto celular y la naturaleza del estrés. Aquí, hemos investigado el papel funcional de la senescencia en dos contextos antagónicos: primero, en la población de células madre del epidermis durante el proceso de envejecimiento, y segundo, durante el desarrollo embrionario. Hemos demostrado que la población de células madre del folículo piloso que expresan queratina 15 aumenta en número en función de la edad, pero presenta una disminución de la capacidad funcional y una incapacidad de tolerar el estrés. Si bien no hemos encontrado ninguna evidencia de que las células madre que expresan queratina 15 entren directamente a senescencia, hemos identificado un desequilibrio en la vía de señalización de Jak-Stat alrededor de las células madre, posiblemente procedente de células senescentes extrínsecas que inhiben la función de las células madre. Estos descubrimientos sugieren que el declive de las células madre epidérmicas contribuye al envejecimiento del tejido y que puede estar dirigido por la senescencia extrínseca. Por otra parte, también hemos descrito el proceso celular de la senescencia como un mecanismo normal en el desarrollo embrionario de los mamíferos, específicamente en la cresta ectodérmica apical (AER) y en la placa del techo del tubo neural. Cabe notar que la senescencia del desarrollo es estrictamente dependiente de p21. Así, los ratones deficientes de p21 presentan defectos en la senescencia embrionaria, el mantenimiento del AER y la formación de las extremidades. Además, hemos visto que hay un solapamiento importante en la expresión génica de la senescencia del desarrollo y la senescencia inducida por oncogenes en los adultos, sugiriendo una similitud en la función. Asimismo, hemos descubierto que el mesénquima subyacente actúa como instructor de la senescencia, y que el destino de las células senescentes es entrar en apoptosis y ser eliminadas por el sistema inmunitario. Estos hallazgos indican que la senescencia también tiene lugar en estados no patológicos y que juega un papel instructivo durante el desarrollo embrionario. Hacen pensar que la senescencia podría haber evolucionado inicialmente como un mecanismo del desarrollo que fue adaptándose para su papel en la vida adulta.
Книги з теми "Embryogenesis; stem cell"
Atwood, Craig. Embryonic stem cells: The hormonal regulation of pluripotency and embryogenesis. Rijeka, Croatia: InTech, 2011.
Знайти повний текст джерелаAtwood, Craig, ed. Embryonic Stem Cells: The Hormonal Regulation of Pluripotency and Embryogenesis. InTech, 2011. http://dx.doi.org/10.5772/589.
Повний текст джерелаMelchers, Fritz. Lymphoid Organogenesis. Springer, 2012.
Знайти повний текст джерелаLymphoid Organogenesis: Proceedings of the Workshop Held at the Basel Institute for Immunology 5th-6th November 1999 (Current Topics in Microbiology and Immunology). Springer, 2000.
Знайти повний текст джерелаMelchers, Fritz. Lymphoid Organogenesis: Proceedings of the Workshop Held at the Basel Institute for Immunology 5th-6th November 1999. Springer London, Limited, 2012.
Знайти повний текст джерелаЧастини книг з теми "Embryogenesis; stem cell"
Yagui-Beltrán, Adam, Biao He, and David M. Jablons. "Wnt Signaling in Cancer: From Embryogenesis to Stem Cell Self-Renewal." In Stem Cells and Cancer, 39–57. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-933-8_4.
Повний текст джерелаGenevière, Anne-Marie, Antoine Aze, Yasmine Even, Maria Imschenetzky, Clara Nervi, and Luigi Vitelli. "Cell Dynamics in Early Embryogenesis and Pluripotent Embryonic Cell Lines: From Sea Urchin to Mammals." In Stem Cells in Marine Organisms, 215–44. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2767-2_9.
Повний текст джерелаMuramatsu, Hisako, Peng Zou, and Takashi Muramatsu. "Stem Cells and Midkine." In Midkine: From Embryogenesis to Pathogenesis and Therapy, 203–10. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4234-5_18.
Повний текст джерелаJames, Daylon, Marco Seandel, and Shahin Rafii. "Endothelial Ontogeny During Embryogenesis: Role of Cytokine Signaling Pathways." In Regulatory Networks in Stem Cells, 319–28. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-227-8_27.
Повний текст джерелаZon, Leonard I. "Derivation of Adult Stem Cells during Embryogenesis." In The Harvey Lectues, 117–32. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470593042.ch6.
Повний текст джерелаSamoilina, N. L., A. L. Medvinsky, O. I. Gan, and T. E. Manakova. "Hemopoietic Stem Cells in Embryogenesis of the Mouse." In Modern Trends in Human Leukemia IX, 106–9. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76829-3_20.
Повний текст джерелаDoetschman, T., A. Gossler, and R. Kemler. "Blastocyst-Derived Embryonic Stem Cells as a Model for Embryogenesis." In Future Aspects in Human In Vitro Fertilization, 187–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71412-2_27.
Повний текст джерелаIrene Yan, C. Y., Felipe M., Tatiane Y., Jos Antonio O. Turri, and Mirian A. F. Hayashi. "Gene Expression in Embryonic Neural Development and Stem Cell Differentiation." In Embryogenesis. InTech, 2012. http://dx.doi.org/10.5772/38067.
Повний текст джерелаTsuji-Tamura, Kiyomi, Hiroshi Sakamoto, and Minetaro Ogaw. "ES Cell Differentiation as a Model to Study Cell Biological Regulation of Vascular Development." In Embryonic Stem Cells: The Hormonal Regulation of Pluripotency and Embryogenesis. InTech, 2011. http://dx.doi.org/10.5772/14101.
Повний текст джерелаOrtuno-Sahagun, Daniel, Argelia E., Antoni Camins, and Merce Pallas. "Embryonic Neural Stem Cell Differentiation to Aldynoglia Induced by Olfactory Bulb Ensheathing Cell-Conditioned Medium." In Embryonic Stem Cells: The Hormonal Regulation of Pluripotency and Embryogenesis. InTech, 2011. http://dx.doi.org/10.5772/15239.
Повний текст джерелаТези доповідей конференцій з теми "Embryogenesis; stem cell"
Engle, DD, J. Lin, B. Spike, S. Cheung, and G. Wahl. "Abstract PD02-02: Characterization of Mammary Stem Cells during Embryogenesis." In Abstracts: Thirty-Third Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 8‐12, 2010; San Antonio, TX. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/0008-5472.sabcs10-pd02-02.
Повний текст джерелаSpike, Benjamin T., Dannielle D. Engle, Jennifer C. Lin, Justin La, Samantha K. Cheung, and Geoffrey M. Wahl. "Abstract 1015: Mammary stem cells increase late in embryogenesis, facilitating their characterization and revealing links to breast cancer." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-1015.
Повний текст джерелаLonardo, Enza, Patrick C. Hermann, Maria-Theresa Mueller, Irene Miranda-Lorenzo, and Christopher Heeschen. "Abstract B45: Embryogenesis meets tumorigenesis: Nodal/activin signaling drives self-renewal and invasiveness of pancreatic cancer stem cells." In Abstracts: Second AACR International Conference on Frontiers in Basic Cancer Research--Sep 14-18, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.fbcr11-b45.
Повний текст джерелаKruithof, E. KO, W. D. Schleuning, and F. Bachman. "PLASMINOGEN ACTIVATOR INHIBITOR BIOCHEMICAL AND CLINICAL ASPECTS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644764.
Повний текст джерела