Gotowa bibliografia na temat „Cell division and cell death”
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Artykuły w czasopismach na temat "Cell division and cell death"
Maddox, Amy Shaub, i 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.
Pełny tekst źródłaColler, Hilary A., i 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.
Pełny tekst źródłaLewis, Mark. "Cell differentiation; Cell division, growth and death". Current Opinion in Cell Biology 14, nr 6 (grudzień 2002): 671–72. http://dx.doi.org/10.1016/s0955-0674(02)00396-4.
Pełny tekst źródłaYuan, Junying, i David Morgan. "Cell division, growth and death". Current Opinion in Cell Biology 14, nr 6 (grudzień 2002): 673–75. http://dx.doi.org/10.1016/s0955-0674(02)00397-6.
Pełny tekst źródłaKornbluth, Sally, i Jonathon Pines. "Cell division, growth and death". Current Opinion in Cell Biology 15, nr 6 (grudzień 2003): 645–47. http://dx.doi.org/10.1016/j.ceb.2003.10.017.
Pełny tekst źródłaReed, Steven I., i Joel H. Rothman. "Cell division, growth and death". Current Opinion in Cell Biology 16, nr 6 (grudzień 2004): 599–601. http://dx.doi.org/10.1016/j.ceb.2004.10.002.
Pełny tekst źródłaKaufmann, Scott, i Mike Tyers. "Cell division, growth and death". Current Opinion in Cell Biology 17, nr 6 (grudzień 2005): 565–67. http://dx.doi.org/10.1016/j.ceb.2005.10.006.
Pełny tekst źródłaEarnshaw, William C., i Yuri A. Lazebnik. "Cell division, growth and death". Current Opinion in Cell Biology 18, nr 6 (grudzień 2006): 587–88. http://dx.doi.org/10.1016/j.ceb.2006.10.010.
Pełny tekst źródłaJackson, Peter K., i Jan-Michael Peters. "Cell division, growth and death". Current Opinion in Cell Biology 19, nr 6 (grudzień 2007): 646–48. http://dx.doi.org/10.1016/j.ceb.2007.11.001.
Pełny tekst źródłaBarral, Yves, i Jürgen Knoblich. "Cell division, growth and death". Current Opinion in Cell Biology 20, nr 6 (grudzień 2008): 647–49. http://dx.doi.org/10.1016/j.ceb.2008.10.007.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaOtake, 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/.
Pełny tekst źródłaDisialoganglioside 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.
Pełny tekst źródłaCell 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.
Pełny tekst źródłaPat, Sze Wa. "Cell metabolism in cell death and cell growth". HKBU Institutional Repository, 2007. http://repository.hkbu.edu.hk/etd_ra/775.
Pełny tekst źródłaDix, Christina Lyn. "Adhesion-dependent cell division". Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10044469/.
Pełny tekst źródłaEllison, 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.
Pełny tekst źródłaCrisby, Milita. "Cell death in atherosclerosis /". Stockholm, 1998. http://diss.kib.ki.se/1998/91-628-3191-7/.
Pełny tekst źródłaGorak-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.
Pełny tekst źródłaRUNYAN, 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.
Pełny tekst źródłaKsiążki na temat "Cell division and cell death"
Zirkin, Barry R., red. 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.
Pełny tekst źródłaR, Zirkin B., Serono Symposia USA i Testis Workshop on Germ Cell Development, Division, Disruption, and Death (1997 : Baltimore, Md.), red. Germ cell development, division, disruption, and death. Norwell, Mass: Serono Symposia USA, 1998.
Znajdź pełny tekst źródłaP, Studzinski George, red. Cell growth, differentiation, and senescence: A practical approach. Oxford: Oxford University Press, 1999.
Znajdź pełny tekst źródłaOckner, 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.
Znajdź pełny tekst źródłaMelino, Gerry. Cell death. Chichester, UK: Wiley-Blackwell, 2010.
Znajdź pełny tekst źródłaWu, Hao, red. Cell Death. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9302-0.
Pełny tekst źródłaGerry, Melino, i Vaux David, red. Cell death. Chichester, West Sussex: John Wiley & Sons, 2010.
Znajdź pełny tekst źródłaCaillaud, Marie-Cécile, red. Plant Cell Division. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1744-1.
Pełny tekst źródłaMacieira-Coelho, Alvaro, red. Asymmetric Cell Division. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-69161-7.
Pełny tekst źródłaCaillaud, Marie-Cécile, red. Plant Cell Division. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3142-2.
Pełny tekst źródłaCzęści książek na temat "Cell division and cell death"
Campisi, Judith. "Cell Senescence and Aging". W 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.
Pełny tekst źródłaKnudson, C. Michael, Kenneth S. K. Tung i Stanley J. Korsmeyer. "Molecular Regulation of Testicular Cell Death". W 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.
Pełny tekst źródłaSwerdloff, Ronald S., YanHe Lue, Christina Wang, Tripathi Rajavashisth i Amiya Sinha Hikim. "Hormonal Regulation of Germ Cell Apoptosis". W 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.
Pełny tekst źródłaTanaka, Hiromitsu, i Yoshitake Nishimune. "Cloning and Characterization of Genes Specifically Expressed in Germ Line Cells". W 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.
Pełny tekst źródłaHabener, Joel F., Philip B. Daniel i William H. Walker. "Expression of Activator and Repressor Isoforms of Transcription Factor CREB During Spermatogenesis". W 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.
Pełny tekst źródłaBraun, Robert E. "Repression and Activation of Protamine mRNA Translation During Murine Spermatogenesis". W 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.
Pełny tekst źródłaChen, Haolin, Lindi Luo i Barry R. Zirkin. "Testicular Aging: Leydig Cells and Spermatogenesis". W 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.
Pełny tekst źródłaSharpe, Richard M., Jane S. Fisher, Philippa T. K. Saunders, Gregor Majdic, Mike R. Millar, Priyanke Parte, Jeffrey B. Kerr i Katie J. Turner. "Estrogen Effects on Development and Function of the Testis". W 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.
Pełny tekst źródłaKelce, William R., i Elizabeth M. Wilson. "Developmental Effects and Molecular Mechanisms of Environmental Antiandrogens". W 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.
Pełny tekst źródłaRobaire, Bernard, i Barbara F. Hales. "Targets of Chemotherapeutic Drug Action in Testis and Epididymis". W 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.
Pełny tekst źródłaStreszczenia konferencji na temat "Cell division and cell death"
Li, Zhehan, David Grace i Paul Mitchell. "Cell division, migration and death for energy efficient 5G ultra-small cell networks". W 2014 IEEE Globecom Workshops (GC Wkshps). IEEE, 2014. http://dx.doi.org/10.1109/glocomw.2014.7063554.
Pełny tekst źródłaBeeharry, Neil, Xijun Zhu, Vignish Murali, Mitchell R. Smith i Timothy Yen. "Abstract A147: Pixantrone induces cell death through mitotic perturbations and subsequent aberrant cell divisions in solid tumor cell lines." W 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.
Pełny tekst źródłaKraning-Rush, Casey M., Shawn P. Carey i Cynthia A. Reinhart-King. "Molded Collagen Microchannels for the Study of Cancer Cell Invasion". W 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.
Pełny tekst źródłaNgo, Angela, Disha Sardana i Ivica Ico Bukvic. "Sonifying 2d Cellular Behavior Using Cellular Stethoscope". W 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.
Pełny tekst źródłaHashimoto, Shigehiro. "Oblique Micro Grooves on Bottom Wall of Flow Channel to Sort Cells". W 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.
Pełny tekst źródłaHenkels, Julia A., i Evan A. Zamir. "A Novel Biomimetic Model for Studying Mechanics of Embryonic Morphogenesis and Differentiation". W ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19608.
Pełny tekst źródłaHebeisen, Jason, Timothy M. Adams i Douglas Munson. "Sustained Pressure Test Results for Surface Scratches in PE4710, Cell Classification 445574C High Density Polyethylene Pipe Material". W ASME 2019 Pressure Vessels & Piping Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/pvp2019-93071.
Pełny tekst źródłaRichardson, William J., Dennis D. van der Voort i James E. Moore. "A Device to Subject Cells to Longitudinal Stretch Gradients on a Tube In Vitro". W ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80941.
Pełny tekst źródłaMaeda, Noriyoshi, i Tetsuo Shoji. "Failure Probability Analysis by Probabilistic Fracture Mechanics Based on FRI SCC Model". W ASME 2010 Pressure Vessels and Piping Division/K-PVP Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/pvp2010-25917.
Pełny tekst źródłaAdams, Timothy M., Jason Hebeisen, Jie Wen i Douglas Munson. "Development of Crack Growth Curves and Correlation to Sustained Pressure Test Results for Cell Classification 445574C High Density Polyethylene Pipe Material". W ASME 2013 Power Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/power2013-98078.
Pełny tekst źródłaRaporty organizacyjne na temat "Cell division and cell death"
Baker, Nicholas E. Cell Proliferation, Cell Death, and Size Regulation. Fort Belvoir, VA: Defense Technical Information Center, październik 1998. http://dx.doi.org/10.21236/adb248354.
Pełny tekst źródłaDistelhorst, Clark W. Programmed Cell Death in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1995. http://dx.doi.org/10.21236/ada300581.
Pełny tekst źródłaDistelhorst, Clark W. Programmed Cell Death in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, październik 1997. http://dx.doi.org/10.21236/ada340671.
Pełny tekst źródłaChung, Leland W. K. Accelerated Tumor Cell Death by Anglogenic Modifiers. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2005. http://dx.doi.org/10.21236/ada441865.
Pełny tekst źródłaDrews, Gary, N. Programmed Cell Death During Female Gametophyte Development. Office of Scientific and Technical Information (OSTI), wrzesień 2004. http://dx.doi.org/10.2172/1014978.
Pełny tekst źródłaChung, Leland W., Chia-Ling Hsieh, Michael Bradley i Mitchell H. Sokoloff. Accelerated Tumor Cell Death by Angiogenic Modifiers. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2001. http://dx.doi.org/10.21236/ada403672.
Pełny tekst źródłaTyler, Kenneth L. Mechanisms of Virus-Induced Neural Cell Death. Fort Belvoir, VA: Defense Technical Information Center, marzec 2005. http://dx.doi.org/10.21236/ada435392.
Pełny tekst źródłaChung, Leland W. Accelerated Tumor Cell Death by Angiogenic Modifiers. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2003. http://dx.doi.org/10.21236/ada418654.
Pełny tekst źródłaKornbluth, Sally. Metabolic Regulation of Ovarian Cancer Cell Death. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2012. http://dx.doi.org/10.21236/ada570124.
Pełny tekst źródłaTyler, Kenneth L. Mechanisms of Virus-Induced Neural Cell Death. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2003. http://dx.doi.org/10.21236/ada419455.
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