Auswahl der wissenschaftlichen Literatur zum Thema „Cell division and cell death“
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Zeitschriftenartikel zum Thema "Cell division and cell death"
Maddox, Amy Shaub, und Jan M. Skotheim. „Cell cycle, cell division, cell death“. Molecular Biology of the Cell 30, Nr. 6 (15.03.2019): 732. http://dx.doi.org/10.1091/mbc.e18-12-0819.
Der volle Inhalt der QuelleColler, Hilary A., und Arshad Desai. „Cell cycle, cell division, and cell death“. Molecular Biology of the Cell 28, Nr. 6 (15.03.2017): 693–94. http://dx.doi.org/10.1091/mbc.e16-11-0793.
Der volle Inhalt der QuelleLewis, Mark. „Cell differentiation; Cell division, growth and death“. Current Opinion in Cell Biology 14, Nr. 6 (Dezember 2002): 671–72. http://dx.doi.org/10.1016/s0955-0674(02)00396-4.
Der volle Inhalt der QuelleYuan, Junying, und David Morgan. „Cell division, growth and death“. Current Opinion in Cell Biology 14, Nr. 6 (Dezember 2002): 673–75. http://dx.doi.org/10.1016/s0955-0674(02)00397-6.
Der volle Inhalt der QuelleKornbluth, Sally, und Jonathon Pines. „Cell division, growth and death“. Current Opinion in Cell Biology 15, Nr. 6 (Dezember 2003): 645–47. http://dx.doi.org/10.1016/j.ceb.2003.10.017.
Der volle Inhalt der QuelleReed, Steven I., und Joel H. Rothman. „Cell division, growth and death“. Current Opinion in Cell Biology 16, Nr. 6 (Dezember 2004): 599–601. http://dx.doi.org/10.1016/j.ceb.2004.10.002.
Der volle Inhalt der QuelleKaufmann, Scott, und Mike Tyers. „Cell division, growth and death“. Current Opinion in Cell Biology 17, Nr. 6 (Dezember 2005): 565–67. http://dx.doi.org/10.1016/j.ceb.2005.10.006.
Der volle Inhalt der QuelleEarnshaw, William C., und Yuri A. Lazebnik. „Cell division, growth and death“. Current Opinion in Cell Biology 18, Nr. 6 (Dezember 2006): 587–88. http://dx.doi.org/10.1016/j.ceb.2006.10.010.
Der volle Inhalt der QuelleJackson, Peter K., und Jan-Michael Peters. „Cell division, growth and death“. Current Opinion in Cell Biology 19, Nr. 6 (Dezember 2007): 646–48. http://dx.doi.org/10.1016/j.ceb.2007.11.001.
Der volle Inhalt der QuelleBarral, Yves, und Jürgen Knoblich. „Cell division, growth and death“. Current Opinion in Cell Biology 20, Nr. 6 (Dezember 2008): 647–49. http://dx.doi.org/10.1016/j.ceb.2008.10.007.
Der volle Inhalt der QuelleDissertationen zum Thema "Cell division and cell death"
Cheng, Jade. „Regulation of cell division and cell death by GRASP65“. Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.544414.
Der volle Inhalt der QuelleOtake, Andreia Hanada. „"Papel de dissialogangliosídios na proliferação e morte celular induzida de melanócitos e melanomas in vitro"“. Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/5/5155/tde-26052006-113740/.
Der volle Inhalt der QuelleDisialoganglioside GD3 and its derivatives are melanoma progression markers. To evaluate the possible roles of these molecules along melanoma progression, we have transfected the GD3 synthase gene (ST8Sia I) in a melanocyte cell line. Accumulation of GD3 did not confer any proliferative advantage to melanocytes. However, GD3 expression was associated with cell survival. The autonomic growth of melanomas is in part related to a constitutive activation of fibroblast growth factor dependent pathways. GD3 expression did not alter the proliferative response to either FGF-1 or FGF-2. However, GD3 and other membrane glycospingolipids modulate the motogenic activity of FGF-2. GD3 expression sensitizes melanocytes to chemotherapeutic agent-induced cell death, as cisplatin and vimblastin. On the other hand, GD3 turned melanocytes more resistant to temozolomide. Chemosensitization to vimblastin, but not to the other drugs, was dependent on the presence of GD3 within the cells, as shown by metabolic depletion of glycosphingolipids
Chalabi, Asma. „Processus d'analyse dynamique pour l'imagerie de cellules vivantes permettant la détection des réponses cellulaires aux anticancéreux, par traitement de l'image et du signal et apprentissage automatique profond“. Electronic Thesis or Diss., Université Côte d'Azur, 2024. http://www.theses.fr/2024COAZ6004.
Der volle Inhalt der QuelleCell division and cell death are the main indicators to evaluate cancer drug action, and only their accurate measures can reveal the actual potency and efficacy of a compound. The detection of cell division and cell death events in live-cell assays has the potential to produce robust metrics of drug pharmacodynamics and return a more comprehensive understanding of tumor cells responses to cancer therapeutic combinations. Knowing precisely when a cell death or a cell division occurs in a live-cell experiment allows to study the relative contribution of different drug effects -such as cytotoxic or cytostatic effects, on a cell population. Yet, classical methods require dyes to measure cell viability as an end-point assay with whole population counts, where the proliferation rates can only be estimated when both viable and dead cells are labeled simultaneously.Live-cell imaging is a promising cell-based assay to determine drug efficacies, with the main limitation being the accuracy and depth of the analyses to detect and predict automatically cellular response phenotypes (cell death and division, which share some morphological features).This thesis introduces a method integrating deep learning using neural networks, and image and signal processing to perform dynamic image analyses of single-cell events in time-lapse microscopy experiments of drug pharmacological profiling. This method works by automatically tracking the cells, extracting radiometric and morphologic cell features, and analyzing the temporal evolution of these features for each cell so as to detect cellular events such as division and cell death, as well as acquiring signaling pathway dynamics.A case of study comprising the analyses of caspase-8 single-cell dynamics and other cell responses to cancer drugs is presented. The aim is to achieve automatically, at a large scale the necessary analyses to augment the phenotype prediction method available in the lab (Fateseq) and to apply it to various cancer cell lines of a human cancer cell line panel to improve our live-cell OMICS profiling approaches, and, in a longer term, to scale up pharmacological screening of new cancer drugs
Green, Katherine J. „The effect of acute exercise on T-lymphocyte function“. Thesis, Queensland University of Technology, 2002. https://eprints.qut.edu.au/36777/1/36777_Digitised%20Thesis.pdf.
Der volle Inhalt der QuellePat, Sze Wa. „Cell metabolism in cell death and cell growth“. HKBU Institutional Repository, 2007. http://repository.hkbu.edu.hk/etd_ra/775.
Der volle Inhalt der QuelleDix, Christina Lyn. „Adhesion-dependent cell division“. Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10044469/.
Der volle Inhalt der QuelleEllison, David William. „Cell proliferation, cell death, and differentiation in gliomas“. Thesis, University of Southampton, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.295912.
Der volle Inhalt der QuelleCrisby, Milita. „Cell death in atherosclerosis /“. Stockholm, 1998. http://diss.kib.ki.se/1998/91-628-3191-7/.
Der volle Inhalt der QuelleGorak-Stolinska, Patricia. „Activation induced cell death in human T cell subsets“. Thesis, King's College London (University of London), 2002. http://kclpure.kcl.ac.uk/portal/en/theses/activation-induced-cell-death-in-human-t-cell-subsets(eb708e24-eccb-42fc-8930-d62ddf6794c1).html.
Der volle Inhalt der QuelleRUNYAN, CHRISTOPHER MICHAEL. „The Role of Cell Death in Germ Cell Migration“. University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1210732680.
Der volle Inhalt der QuelleBücher zum Thema "Cell division and cell death"
Zirkin, Barry R., Hrsg. Germ Cell Development, Division, Disruption and Death. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4.
Der volle Inhalt der QuelleR, Zirkin B., Serono Symposia USA und Testis Workshop on Germ Cell Development, Division, Disruption, and Death (1997 : Baltimore, Md.), Hrsg. Germ cell development, division, disruption, and death. Norwell, Mass: Serono Symposia USA, 1998.
Den vollen Inhalt der Quelle findenP, Studzinski George, Hrsg. Cell growth, differentiation, and senescence: A practical approach. Oxford: Oxford University Press, 1999.
Den vollen Inhalt der Quelle findenOckner, Robert K. Integration of metabolism, energetics, and signal transduction: Unifying foundations in cell growth and death, cancer, atherosclerosis, and Alzheimer disease. New York: Kluwer Academic Publishers, 2004.
Den vollen Inhalt der Quelle findenMelino, Gerry. Cell death. Chichester, UK: Wiley-Blackwell, 2010.
Den vollen Inhalt der Quelle findenWu, Hao, Hrsg. Cell Death. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9302-0.
Der volle Inhalt der QuelleGerry, Melino, und Vaux David, Hrsg. Cell death. Chichester, West Sussex: John Wiley & Sons, 2010.
Den vollen Inhalt der Quelle findenCaillaud, Marie-Cécile, Hrsg. Plant Cell Division. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1744-1.
Der volle Inhalt der QuelleMacieira-Coelho, Alvaro, Hrsg. Asymmetric Cell Division. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-69161-7.
Der volle Inhalt der QuelleCaillaud, Marie-Cécile, Hrsg. Plant Cell Division. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3142-2.
Der volle Inhalt der QuelleBuchteile zum Thema "Cell division and cell death"
Campisi, Judith. „Cell Senescence and Aging“. In Germ Cell Development, Division, Disruption and Death, 121–29. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_12.
Der volle Inhalt der QuelleKnudson, C. Michael, Kenneth S. K. Tung und Stanley J. Korsmeyer. „Molecular Regulation of Testicular Cell Death“. In Germ Cell Development, Division, Disruption and Death, 140–49. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_14.
Der volle Inhalt der QuelleSwerdloff, Ronald S., YanHe Lue, Christina Wang, Tripathi Rajavashisth und Amiya Sinha Hikim. „Hormonal Regulation of Germ Cell Apoptosis“. In Germ Cell Development, Division, Disruption and Death, 150–64. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_15.
Der volle Inhalt der QuelleTanaka, Hiromitsu, und Yoshitake Nishimune. „Cloning and Characterization of Genes Specifically Expressed in Germ Line Cells“. In Germ Cell Development, Division, Disruption and Death, 3–10. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_1.
Der volle Inhalt der QuelleHabener, Joel F., Philip B. Daniel und William H. Walker. „Expression of Activator and Repressor Isoforms of Transcription Factor CREB During Spermatogenesis“. In Germ Cell Development, Division, Disruption and Death, 96–104. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_10.
Der volle Inhalt der QuelleBraun, Robert E. „Repression and Activation of Protamine mRNA Translation During Murine Spermatogenesis“. In Germ Cell Development, Division, Disruption and Death, 105–17. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_11.
Der volle Inhalt der QuelleChen, Haolin, Lindi Luo und Barry R. Zirkin. „Testicular Aging: Leydig Cells and Spermatogenesis“. In Germ Cell Development, Division, Disruption and Death, 130–39. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_13.
Der volle Inhalt der QuelleSharpe, Richard M., Jane S. Fisher, Philippa T. K. Saunders, Gregor Majdic, Mike R. Millar, Priyanke Parte, Jeffrey B. Kerr und Katie J. Turner. „Estrogen Effects on Development and Function of the Testis“. In Germ Cell Development, Division, Disruption and Death, 167–77. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_16.
Der volle Inhalt der QuelleKelce, William R., und Elizabeth M. Wilson. „Developmental Effects and Molecular Mechanisms of Environmental Antiandrogens“. In Germ Cell Development, Division, Disruption and Death, 178–89. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_17.
Der volle Inhalt der QuelleRobaire, Bernard, und Barbara F. Hales. „Targets of Chemotherapeutic Drug Action in Testis and Epididymis“. In Germ Cell Development, Division, Disruption and Death, 190–201. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-2206-4_18.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Cell division and cell death"
Li, Zhehan, David Grace und Paul Mitchell. „Cell division, migration and death for energy efficient 5G ultra-small cell networks“. In 2014 IEEE Globecom Workshops (GC Wkshps). IEEE, 2014. http://dx.doi.org/10.1109/glocomw.2014.7063554.
Der volle Inhalt der QuelleBeeharry, Neil, Xijun Zhu, Vignish Murali, Mitchell R. Smith und Timothy Yen. „Abstract A147: Pixantrone induces cell death through mitotic perturbations and subsequent aberrant cell divisions in solid tumor cell lines.“ In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Oct 19-23, 2013; Boston, MA. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1535-7163.targ-13-a147.
Der volle Inhalt der QuelleKraning-Rush, Casey M., Shawn P. Carey und Cynthia A. Reinhart-King. „Molded Collagen Microchannels for the Study of Cancer Cell Invasion“. In ASME 2012 10th International Conference on Nanochannels, Microchannels, and Minichannels collocated with the ASME 2012 Heat Transfer Summer Conference and the ASME 2012 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/icnmm2012-73093.
Der volle Inhalt der QuelleNgo, Angela, Disha Sardana und Ivica Ico Bukvic. „Sonifying 2d Cellular Behavior Using Cellular Stethoscope“. In ICAD 2022: The 27th International Conference on Auditory Display. icad.org: International Community for Auditory Display, 2022. http://dx.doi.org/10.21785/icad2022.015.
Der volle Inhalt der QuelleHashimoto, Shigehiro. „Oblique Micro Grooves on Bottom Wall of Flow Channel to Sort Cells“. In ASME 2020 Fluids Engineering Division Summer Meeting collocated with the ASME 2020 Heat Transfer Summer Conference and the ASME 2020 18th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/fedsm2020-20096.
Der volle Inhalt der QuelleHenkels, Julia A., und Evan A. Zamir. „A Novel Biomimetic Model for Studying Mechanics of Embryonic Morphogenesis and Differentiation“. In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19608.
Der volle Inhalt der QuelleHebeisen, Jason, Timothy M. Adams und Douglas Munson. „Sustained Pressure Test Results for Surface Scratches in PE4710, Cell Classification 445574C High Density Polyethylene Pipe Material“. In ASME 2019 Pressure Vessels & Piping Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/pvp2019-93071.
Der volle Inhalt der QuelleRichardson, William J., Dennis D. van der Voort und James E. Moore. „A Device to Subject Cells to Longitudinal Stretch Gradients on a Tube In Vitro“. In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80941.
Der volle Inhalt der QuelleMaeda, Noriyoshi, und Tetsuo Shoji. „Failure Probability Analysis by Probabilistic Fracture Mechanics Based on FRI SCC Model“. In ASME 2010 Pressure Vessels and Piping Division/K-PVP Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/pvp2010-25917.
Der volle Inhalt der QuelleAdams, Timothy M., Jason Hebeisen, Jie Wen und Douglas Munson. „Development of Crack Growth Curves and Correlation to Sustained Pressure Test Results for Cell Classification 445574C High Density Polyethylene Pipe Material“. In ASME 2013 Power Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/power2013-98078.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Cell division and cell death"
Baker, Nicholas E. Cell Proliferation, Cell Death, and Size Regulation. Fort Belvoir, VA: Defense Technical Information Center, Oktober 1998. http://dx.doi.org/10.21236/adb248354.
Der volle Inhalt der QuelleDistelhorst, Clark W. Programmed Cell Death in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 1995. http://dx.doi.org/10.21236/ada300581.
Der volle Inhalt der QuelleDistelhorst, Clark W. Programmed Cell Death in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, Oktober 1997. http://dx.doi.org/10.21236/ada340671.
Der volle Inhalt der QuelleChung, Leland W. K. Accelerated Tumor Cell Death by Anglogenic Modifiers. Fort Belvoir, VA: Defense Technical Information Center, August 2005. http://dx.doi.org/10.21236/ada441865.
Der volle Inhalt der QuelleDrews, Gary, N. Programmed Cell Death During Female Gametophyte Development. Office of Scientific and Technical Information (OSTI), September 2004. http://dx.doi.org/10.2172/1014978.
Der volle Inhalt der QuelleChung, Leland W., Chia-Ling Hsieh, Michael Bradley und Mitchell H. Sokoloff. Accelerated Tumor Cell Death by Angiogenic Modifiers. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada403672.
Der volle Inhalt der QuelleTyler, Kenneth L. Mechanisms of Virus-Induced Neural Cell Death. Fort Belvoir, VA: Defense Technical Information Center, März 2005. http://dx.doi.org/10.21236/ada435392.
Der volle Inhalt der QuelleChung, Leland W. Accelerated Tumor Cell Death by Angiogenic Modifiers. Fort Belvoir, VA: Defense Technical Information Center, August 2003. http://dx.doi.org/10.21236/ada418654.
Der volle Inhalt der QuelleKornbluth, Sally. Metabolic Regulation of Ovarian Cancer Cell Death. Fort Belvoir, VA: Defense Technical Information Center, Juli 2012. http://dx.doi.org/10.21236/ada570124.
Der volle Inhalt der QuelleTyler, Kenneth L. Mechanisms of Virus-Induced Neural Cell Death. Fort Belvoir, VA: Defense Technical Information Center, September 2003. http://dx.doi.org/10.21236/ada419455.
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