Bibliografías temáticas / Cell state

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Literatura académica sobre el tema "Cell state"

Autor: Grafiati

Publicado: 1 de febrero de 2025

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Artículos de revistas sobre el tema "Cell state"

Holden, C. "STATE STEM CELL INITIATIVES: Most State Stem Cell Efforts Staying Afloat". Science 323, n.º 5922 (27 de marzo de 2009): 1660b—1661b. http://dx.doi.org/10.1126/science.323.5922.1660b.

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Mishra, Dharma Niranjan. "Clinico- haematological Profile of Sickle Cell Disease and Sickle Cell BetaThalassaemia in the State of Odisha". Journal of Medical Science And clinical Research 05, n.º 06 (12 de junio de 2017): 23062–69. http://dx.doi.org/10.18535/jmscr/v5i6.44.

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José Mendes de Seixas, Falcondes, Juan Paulo Robles Balestero, Claudiner Mendes de Seixas, Fernando Lessa Tofoli y Grover Victor Torrico-Bascopé. "Bridgeless boost PFC converter using the three-state switching cell". Eletrônica de Potência 17, n.º 2 (1 de mayo de 2012): 513–20. http://dx.doi.org/10.18618/rep.2012.2.513520.

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Aalam, Syed Mohammed Musheer, Kannan Vrindavan Manian, Sumitha Prameela Bharathan, Thiyagaraj Mayuranathan y Shaji Ramachandran Velayudhan. "Identification of Stable OCT4+NANOG− State in Somatic Cell Reprogramming". Cellular Reprogramming 18, n.º 6 (diciembre de 2016): 367–68. http://dx.doi.org/10.1089/cell.2016.0018.

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Pauklin, Siim y Ludovic Vallier. "The Cell-Cycle State of Stem Cells Determines Cell Fate Propensity". Cell 155, n.º 1 (septiembre de 2013): 135–47. http://dx.doi.org/10.1016/j.cell.2013.08.031.

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Pauklin, Siim y Ludovic Vallier. "The Cell-Cycle State of Stem Cells Determines Cell Fate Propensity". Cell 156, n.º 6 (marzo de 2014): 1338. http://dx.doi.org/10.1016/j.cell.2014.02.044.

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Lai, Dongmei, Yifei Chen, Fangyuan Wang, Lizhen Jiang y Chunsheng Wei. "LKB1 Controls the Pluripotent State of Human Embryonic Stem Cells". Cellular Reprogramming 14, n.º 2 (abril de 2012): 164–70. http://dx.doi.org/10.1089/cell.2011.0068.

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Smaglik, Paul. "Stem-cell state lines". Nature 429, n.º 6994 (junio de 2004): 905. http://dx.doi.org/10.1038/nj6994-905a.

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Venugopal, V. "Solid state electrochemical cell". Progress in Crystal Growth and Characterization of Materials 45, n.º 1-2 (enero de 2002): 139–41. http://dx.doi.org/10.1016/s0960-8974(02)00039-6.

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McNiven, M. A. "The solid state cell". Biology of the Cell 94, n.º 9 (diciembre de 2002): 555–56. http://dx.doi.org/10.1016/s0248-4900(02)01203-0.

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Tesis sobre el tema "Cell state"

Arévalo, Bautista Jazmine Paola. "The role of stat3 phosphorylation state in clear cell renal cell carcinoma (ccRCC)". Doctoral thesis, Universitat Autònoma de Barcelona, 2019. http://hdl.handle.net/10803/669570.

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STAT3 (signal transducer and activator of transcription 3) és un factor de transcripció latent que regula la transcripció de gens relacionats amb processos biològics essencials tals com: la diferenciació cel·lular, la proliferació, la migració, la inhibició de l’apoptosi i la supervivència. L’activació anormal d’STAT3 s’ha relacionat amb el desenvolupament d’aproximadament el 50% dels càncers humans, incloent el carcinoma renal de cèl·lula clara (ccRCC). Actualment, les propietats oncogèniques d’STAT3 s’atribueixen a la fosforilació del seu residu Tyr705; no obstant, recentment, la fosforilació de la Ser727 ha sorgit com un esdeveniment capaç d’amplificar l’activitat transcripcional d’STAT3, juntament a activitats no genòmiques que promouen el desenvolupament del càncer. El nostre grup va ser un dels pioners en assenyalar la importància de la fosforilació de la Ser727, demostrant que els nivells d’expressió de la pSer727 al nucli (en mostres de teixit de pacients de ccRCC) correlacionaven amb un mal pronòstic i una baixa supervivència global. Donat que el ccRCC és el subtipus histològic de carcinoma renal més prevalent i letal, i que els mecanismes subjacents al seu desenvolupament no han estat determinats fins el moment, l’objectiu d’aquest treball va ser elucidar el paper de l’estat de fosforilació d’STAT3 en el desenvolupament del ccRCC i, específicament, en estudiar la contribució de la pSer727 en la progressió tumoral. Amb aquesta finalitat, es varen generar fosfomutants simples i dobles d’STAT3 (Tyr705Phe, Ser727Ala, Ser727Asp, Tyr705Phe/Ser727Ala, i Tyr705Phe/Ser727Asp) que van ser transduïdes en línies cel·lulars humanes derivades de ccRCC (769-P i 786-O) per avaluar el seu comportament funcional, així com la conseqüent expressió gènica diferencial mitjançant l’anàlisi de microarray. Els nostres resultats han demostrat que les mutants d’STAT3 que contenien una substitució fosfomimètica de la Ser727 (Ser727Asp) promouen un fenotip pro-tumoral in vivo de manera independent a la Tyr705. A més, es descriu que l’estat de fosforilació global d’STAT3 determina l’expressió de diferents subconjunts de gens associats a diversos processos biològics, essent els gens dependents de la pSer727 els més relacionats amb processos característics amb el desenvolupament del càncer. En resum, aquest treball constitueix el primer anàlisi de quin és el paper de l’estat de fosforilació global d’STAT3 en el ccRCC, i demostra que la pSer727 activa la senyalització d’STAT3 a través de la transcripció d’un subconjunt específic de gens que són clínicament rellevants com potencials dianes terapèutiques i nous biomarcadors del ccRCC.
STAT3 (signal transducer and activator of transcription 3) es un factor de transcripción latente que regula la transcripción de genes relacionados con procesos biológicos esenciales, tales como: diferenciación celular, proliferación, migración, inhibición de la apoptosis y supervivencia. La activación anormal de STAT3 ha sido relacionada con el desarrollo de cerca del 50% de todos los cánceres humanos, incluyendo el carcinoma renal de célula clara (ccRCC). Actualmente, las propiedades oncogénicas de STAT3 se atribuyen a la fosforilación de su Tyr705; sin embargo, recientemente, la fosforilación de su Ser727 ha surgido como un evento capaz de amplificar la actividad transcripcional de STAT3, aunada a actividades no genómicas que promueven el desarrollo del cáncer. Nuestro grupo fue uno de los pioneros en señalar la importancia de la fosforilación de la Ser727, al demostrar que los niveles de expresión de pSer727 en el núcleo (en muestras de tejidos de pacientes con ccRCC) correlacionaban con un mal pronóstico y baja supervivencia global. Dado que el ccRCC es el subtipo histológico de carcinoma renal más prevalente y letal, y los mecanismos subyacentes a su desarrollo aún no han sido determinados, el objetivo de este trabajo fue elucidar el rol del estado de fosforilación de STAT3 en el desarrollo del ccRCC, y específicamente, en estudiar la contribución de la pSer727 en la progresión tumoral. Para ello, generamos fosfomutantes simples y dobles de STAT3 (Tyr705Phe, Ser727Ala, Ser727Asp, Tyr705Phe/Ser727Ala, y Tyr705Phe/Ser727Asp) que fueron transducidas en líneas celulares humanas derivadas de ccRCC (769-P y 786-O) para evaluar su comportamiento funcional, así como la consecuente expresión génica diferencial a través de un análisis de microarray. Nuestros resultados demostraron que las mutantes de STAT3 que contenían una substitución fosfomimética para la Ser727 (Ser727Asp) promueven un fenotipo pro-tumoral in vivo de forma independiente de la Tyr705. Además, describimos que el estado de fosforilación global de STAT3 determina la expresión de diferentes subconjuntos de genes asociados a distintos procesos biológicos, siendo los genes dependientes de la pSer727, los más relacionados con procesos característicos del desarrollo del cáncer. En resumen, este trabajo constituye el primer análisis acerca del rol del estado de fosforilación global de STAT3 en el ccRCC, y demuestra que la pSer727 activa la señalización de STAT3 a través de la transcripción de un subconjunto específico de genes que son clínicamente relevantes como potenciales dianas terapéuticas y nuevos biomarcadores para el ccRCC.
The signal transducer and activator of transcription 3 (STAT3) is a latent transcription factor that regulates downstream genes involved in essential biological processes such as cell differentiation, proliferation, migration, apoptosis inhibition, and survival. The aberrant activation of STAT3 has been related to the development of near 50% of all human cancers including clear cell renal cell carcinoma (ccRCC). To date, the oncogenic properties of STAT3 are attributed to the phosphorylation of its Tyr705, however, the phosphorylation of its Ser727 has recently emerged as an event that enhances STAT3 transcriptional activity, in addition to non-genomic activities that promote cancer development. Our group was one of the pioneers in bringing the Ser727 phosphorylation to light by demonstrating that nuclear pSer727 expression levels, in tissue samples of ccRCC patients, correlated with poor prognosis and low overall survival. Since ccRCC is the most prevalent and lethal histological subtype of renal cell carcinoma (RCC) and the molecular mechanisms behind its tumorigenesis remain unclear, we aimed to elucidate the role of STAT3 phosphorylation state in ccRCC development, and especially the contribution of pSer727 to tumor progression. For that purpose, we generated simple and double STAT3 phosphomutants (Tyr705Phe, Ser727Ala, Ser727Asp, Tyr705Phe/Ser727Ala, and Tyr705Phe/Ser727Asp) transduced in human-derived ccRCC cell lines (769-P and 786-O), and we evaluated their functional behavior as well as their differential gene expression through microarray analysis. Our data demonstrated that STAT3 mutants carrying a phosphomimetic substitution for Ser727 (Ser727Asp) promote a pro-tumoral phenotype in vitro in a Tyr705-independent manner. Moreover, we describe that the overall STAT3 phosphorylation state determines the expression of different subsets of target genes associated with distinct biological processes, being pSer727-dependent genes the most related to cellular hallmarks of cancer development. In summary, the present study constitutes the first analysis on the role of overall STAT3 phosphorylation state in ccRCC and demonstrates that pSer727 activates STAT3 signaling through transcription of a specific subset of target genes that are clinically relevant as potential therapeutic targets and novel biomarkers for ccRCC.

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Lu, Xibin y 盧希彬. "Quantitative characterization of mouse embryonic stem cell state transition". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/208049.

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Newman, Jamie Jennifer. "Regulation of gene expression and cell state in embryonic stem cells". Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/58526.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, June 2010.
"May 2010." Cataloged from PDF version of thesis.
Includes bibliographical references.
Cell state is established and maintained through the combined action of transcription factors, chromatin regulators and signaling pathways, which all contribute to a transcriptional regulatory circuitry. Embryonic stem (ES) cells are capable of self-renewal and can give rise to nearly all differentiated cell-types, making them an ideal system in which to address the challenges of understanding gene expression and cell state. Valuable insights into the control of cell state have been revealed by recent studies of the ES cell transcriptional regulatory circuitry. Here I present work contributing to the understanding of transcriptional regulatory mechanisms that control ES cell state, specifically signaling pathways and proteins that affect chromatin structure.
by Jamie J. Newman.
Ph.D.

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Calegari, Federico y Julieta Aprea. "Bioelectric State and Cell Cycle Control of Mammalian Neural Stem Cells". Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-185623.

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The concerted action of ion channels and pumps establishing a resting membrane potential has been most thoroughly studied in the context of excitable cells, most notably neurons, but emerging evidences indicate that they are also involved in controlling proliferation and differentiation of nonexcitable somatic stem cells. The importance of understanding stem cell contribution to tissue formation during embryonic development, adult homeostasis, and regeneration in disease has prompted many groups to study and manipulate the membrane potential of stem cells in a variety of systems. In this paper we aimed at summarizing the current knowledge on the role of ion channels and pumps in the context of mammalian corticogenesis with particular emphasis on their contribution to the switch of neural stem cells from proliferation to differentiation and generation of more committed progenitors and neurons, whose lineage during brain development has been recently elucidated.

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Calegari, Federico y Julieta Aprea. "Bioelectric State and Cell Cycle Control of Mammalian Neural Stem Cells". Sage-Hindawi, 2012. https://tud.qucosa.de/id/qucosa%3A27972.

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Orr, Simon Timothy. "Multinuclear solid-state NMR of fuel cell materials". Thesis, University of Warwick, 2010. http://wrap.warwick.ac.uk/35532/.

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This thesis describes the application of multinuclear solid-state NMR to three materials systems: first, components of polymer-based proton-exchange fuel cells including the fluoropolymer membranes (Chapter 4) and the precious metal supported catalysts (Chapter 5); secondly, the formation of a complex bismuth niobium aluminoborosilicate glass-ceramic with novel dielectric properties (Chapter 6); finally, platinum (II) dialkyldithiophosphates which belong to a class of compounds (metal dialkyldithiophosphates) some of which are used in mineral separation processing (Chapter 7). A full investigation into the effects of different conditions during sample preparation and 19F NMR experiments on fluoropolymer membranes recommended unmilled preparation, dry storage and magic angle spinning below 24 kHz for the study of structural differences between membranes. The application of 19F NMR to a range of commercial and experimental fluoropolymer membranes revealed that the equivalent weight does not affect the mobility of the polymer molecules such that can be detected by this technique. Calculations of equivalent weight from 19F NMR differed with quoted values by up to 14%. Discrepancies were smallest in the short sidechain polymers, as low as 3%. The assignment of spectra was invariant with sidechain structure apart from a change in the number of ester links. The presence or absence of oxygen affected chemical shielding even around nuclei separated by several bonds. Differences in 1H linewidths between membranes could not be interpreted without the control and comparison of manufacturing techniques. It is desirable to remove the necessity for organic solvents in membrane casting. However, membranes cast from aqueous solution do not possess the same properties as those from propanol. It had been proposed that rapid drying of water cast membranes would result in a structure more similar to those from organic solvent. 1H NMR revealed that the opposite is the case, rapid drying makes the ordinarily more inhomogeneous aqueous membranes even more so. The application of both 19F and 1H NMR revealed that the monomolecular layers of fluoropolymer deposited on the surface of fuel cell catalysts to aid proton conductivity are categorically different in nature to the same materials in the bulk state. 19F NMR suggests a polymer structure either more disordered, greatly less mobile or both. 1H NMR displayed water environments that could not be reconciled to the standard model of rapid exchange between bulk water and water associated with acid groups. Spectral differences caused by solvent and polymer loading were discussed. The first complete and quantitative Fourier transformed 195Pt NMR spectra of platinum fuel cell catalysts, acquired using a field sweeping method, are analysed for deviation from the cubooctohedral particle model and surface oxidation. A combination of 11B, 27Al and 29Si studies of the BN1 ceramic system after different temperature heat treatments confirmed much of the previous work on phase evolution. However, it was shown that kyanite does not make up a significant proportion of the material until heat treatment reaches 1000 ºC and that aluminium impurities in bismuthbiobate crystals appear to increase with treatment temperature. The nature and abundance of glassy phases in the system are explored for the first time. Field sweep 195Pt NMR was employed to characterise the 195Pt chemical shift anisotropy of five platinum (II) dialkyldithiophosphates complexes. Additionally the 31P chemical shift anisotropies of two of the complexes, previously unpublished are presented.

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Bryan, Andrea K. (Andrea Kristine). "Cell State Identication by Mass, Density, and volume". Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/67071.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biological Engineering, 2011.
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from student submitted PDF version of thesis.
Includes bibliographical references (p. 119-124).
Cell size is often overlooked in the drive to define molecular mechanisms, but as a basic physical property it is an integrator of the cell's metabolic rate and indicator of cell fate. Development of the Suspended Microchannel Resonator (SMR), a microfluidic mass measurement system, enables femtogram cell mass resolution, and the resistive pulse (Coulter) technique provides high-speed electronic readout of cell volume. With these tools, we developed four methods to measure cell density, the ratio of mass to volume. We first measure the average density of cell populations using the SMR and a Coulter counter. We observe that cell density increases prior to bud formation at the G1/S transition of budding yeast, which is consistent with previous measurements using density gradient centrifugation. To investigate the origin of this density increase, we use the SMR to measure buoyant mass in high density media and monitor relative density changes of growing yeast cells. We find that the density increase requires energy, function of the protein synthesis regulator TOR, passage through START, and an intact actin cytoskeleton. These techniques are suitable for most non-adherent cells and subcellular particles to characterize cell growth in a variety of applications. We next develop two platforms to measure single-cell mass, volume, and density. These properties are calculated from two SMR buoyant mass measurements, each in different density fluids. These measurements are achieved by serially connecting two SMR structures through a microchannel with an intermediate T-junction, such that a cell is measured by each SMR in different density fluids. Similar measurements can also be made with one SMR by reversing the SMR fluid flow after a cell is measured-each cell re-enters the SMR in a higher density fluid for a second measurement. We find that the intrinsic cell-to-cell density variation is nearly 100-fold smaller than the mass or volume variation, and by simultaneously measuring density and mass, we identify distinct subpopulations of diseased and healthy cells that are indistinguishable by mass or volume alone.
by Andrea K. Bryan.
Ph.D.

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Fonseca, Aaron James. "State-Space Randles Cell Model for Instrument Calibration". Thesis, North Dakota State University, 2020. https://hdl.handle.net/10365/31790.

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It is desirable to calibrate electrochemical impedance spectroscopy (EIS) instrumentation using a Randles circuit. This presents a challenge as realistic loads, simulated by this circuit, contain theoretical components (Warburg elements) that are difficult to model. This thesis proposes a state-space solution to this problem and explores the process of realizing a digital high-accuracy approximation of a Randles circuit for the purposes of verifying and calibrating EIS instrumentation. Using Valsa, Dvo{\v r}{\'a}k, and Friedl's network approximation of a Warburg element, a collection of state-space relations describing the impedance of a Randles circuit are derived. From these equations the process of realizing a digital system is explored; this includes a discussion on methods of discretization, an overview of the challenges of realizing digital filters, and an analysis of the effects that finite word-length has on the accuracy of the model when using fixed-point hardware.

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Wang, Peng. "Some improvements in state/parameter estimation using the cell-to-cell mapping technique /". The Ohio State University, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486402544591959.

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McBride, Jared Adam. "Steady State Configurations of Cells Connected by Cadherin Sites". BYU ScholarsArchive, 2016. https://scholarsarchive.byu.edu/etd/6023.

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Many cells employ cadherin complexes (c-sites) on the cell membrane to attach to neighboring cells, as well as integrin complexes (i-sites) to attach to a substrate in order to accomplish cell migration. This paper analyzes a model for the motion of a group of cells connected by c-sites. We begin with two cells connected by a single c-site and analyze the resultant motion of the system. We find that the system is irrotational. We present a result for reducing the number of c-sites in a system with c-sites between pairs of cells. This greatly simplifies the general system, and provides an exact solution for the motion of a system of two cells and several c-sites.Then a method for analyzing the general cell system is presented. This method involves 0-row-sum, symmetric matrices. A few results are presented as well as conjectures made that we feel will greatly simplify such analyses. The thesis concludes with the proposal of a framework for analyzing a dynamic cell system in which stochastic processes govern the attachment and detachment of c-sites.

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Más fuentes

Libros sobre el tema "Cell state"

Sammes, Nigel, Alevtina Smirnova y Oleksandr Vasylyev, eds. Fuel Cell Technologies: State and Perspectives. Berlin/Heidelberg: Springer-Verlag, 2005. http://dx.doi.org/10.1007/1-4020-3498-9.

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M, Sammes Nigel, Smirnova Alevtina, Vasylyev Oleksandr y North Atlantic Treaty Organization, eds. Fuel cell technologies: State and perspectives. Dordrecht: Springer, 2005.

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Empire State Stem Cell Board. Empire state stem cell board strategic plan. Albany, N.Y: New York State Dept. of Health, 2008.

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William, Negendank y Edelmann Ludwig, eds. The state of water in the cell. AMF O'Hare, Chicago, IL, U.S.A: Scanning Microscopy International, 1988.

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Gallagher, Helen Christine. Regulation of neural cell adhesion molecule polysialylation state. Dublin: University College Dublin, 1998.

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Blake, Levitt B. y Berkshire-Litchfield Environmental Council, eds. Cell towers: Wireless convenience or environmental hazard? : proceedings of the "Cell Towers Forum", State of the Science/State of the Law, December 2, 2000. Markham, Ont: Safe Goods/New Century Pub., 2001.

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Gupta, Dharmendra K., José M. Palma y Francisco J. Corpas, eds. Redox State as a Central Regulator of Plant-Cell Stress Responses. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-44081-1.

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Herrmann, Heinz. Cell biology: An inquiry into the nature of the living state. Cambridge: Harper & Row, 1989.

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Auditor, Missouri State, ed. Management of cellular telephones at state agencies. [Jefferson City, Mo.]: Missouri State Library, 2001.

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Pezeshki, Peyman. Use of cell cycle analysis in early state estimation and process control. Birmingham: University of Birmingham, 2002.

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Capítulos de libros sobre el tema "Cell state"

Hsu, C. S. "Cell State Space and Simple Cell Mapping". En Cell-to-Cell Mapping, 85–97. New York, NY: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4757-3892-6_4.

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Tsuchiya, Masa, Alessandro Giuliani y Paul Brazhnik. "From Cell States to Cell Fates: Control of Cell State Transitions". En Methods in Molecular Biology, 137–62. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3577-3_9.

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Hsu, C. S. "Other Topics of Study Using the Cell State Space Concept". En Cell-to-Cell Mapping, 331–34. New York, NY: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4757-3892-6_14.

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Hime, Gary R. y Helen E. Abud. "The Stem Cell State". En Transcriptional and Translational Regulation of Stem Cells, 1–4. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6621-1_1.

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Sequeira, C. A. C. "D.C. Methods of Cell Characterization Part II: Definition of Full Cell/Battery Parameters". En Solid State Batteries, 241–60. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5167-9_16.

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Abraham, K. M. "Non-Electrical Techniques of Cell Characterization". En Solid State Batteries, 283–96. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5167-9_18.

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Willkomm, Lena y Wilhelm Bloch. "State of the Art in Cell–Cell Fusion". En Methods in Molecular Biology, 1–19. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2703-6_1.

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Setter, Michael P. "A Warning for the Wagner Polarization Cell". En Solid State Microbatteries, 419–22. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2263-2_26.

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Jossen, Valentin, Regine Eibl, Gilles Broccard y Dieter Eibl. "Single-Use Systems in Biopharmaceutical Manufacture: State of the Art and Recent Trends". En Cell Engineering, 3–38. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-45669-5_1.

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Tonezzer, M., D. Gutierrez y D. Vincenzi. "Luminescent Solar Concentrators - State of the Art and Future Perspectives". En Solar Cell Nanotechnology, 293–315. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118845721.ch12.

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Actas de conferencias sobre el tema "Cell state"

Acharya, Sayan, Aditya Ganguly, Ram Sarkar y Abin Jose. "Cell Cycle State Prediction Using Graph Neural Networks". En 2024 IEEE International Conference on Image Processing (ICIP), 2916–22. IEEE, 2024. http://dx.doi.org/10.1109/icip51287.2024.10648030.

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Schwickert, David, Skirmantas Alisauskas, Nick Kschuev, Anne-Laure Calendron, Ayhan Tajalli Seifi, Giovanni Cirmi, Stefan Düsterer et al. "Sub-15 fs Jitter After Multi-Pass Cell Pulse Compression at the Beamline FL23 of the FLASH Facility". En Advanced Solid State Lasers, AW1A.4. Washington, D.C.: Optica Publishing Group, 2024. https://doi.org/10.1364/assl.2024.aw1a.4.

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Resumen

The temporal stability of laser pulses after a high-energy compression stage using a multi-pass cell with transport beamline was investigated, resulting in correctable ~1 ps long-term drift, and 11 fs residual jitter (10 s integration).

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Kang, Jungmyung, Keonhee Cho, Sekeon Kim, Giseok Kim, Hyunjun Kim, Dongwook Seo, Sangyeop Baeck, Seiseung Yoon y Seong-Ook Jung. "A 14nm SRAM Using NMOS Header Assist Cell for Improved Write Ability and Reduced Cell Retention Leakage". En 2024 IEEE European Solid-State Electronics Research Conference (ESSERC), 669–72. IEEE, 2024. http://dx.doi.org/10.1109/esserc62670.2024.10719479.

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Wang, Ziyao, Warunya Röder, Tobias Heuermann, Philipp Gierschke, Yi Zhang, Maximilian Karst, Mathias Lenski, Lucas Eisenbach, Jan Rothhardt y Jens Limpert. "Multipass cell for mJ-level, sub-two cycle nonlinear pulse compression with >100W average power at 1.9 µm". En Advanced Solid State Lasers, AW1A.7. Washington, D.C.: Optica Publishing Group, 2024. https://doi.org/10.1364/assl.2024.aw1a.7.

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In this work, we present a nonlinear post-compression with an average power exceeding 100 W based on a gas-filled multipass cell providing sub-two-cycle pulses. It is enabled by a thulium-doped fiber chirped-pulsed amplification system.

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Kraak, M., J. M. Koopmans y R. Nouta. "Cell Layout Library Parameterization". En 11th European Solid State Circuits Conference. IEEE, 1985. http://dx.doi.org/10.1109/esscirc.1985.5468100.

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Huang, Liang-Chi, Pen-Yi Chu, Ko-Cheng Lu, Wei-Cheng Kang, Bo-Hsun Juan, Tzu-Yin Chen, Bi-Xian Wu y Tzu-Hsuan Chang. "Logic Cell of CFET Based on Double-Cell-Height to Enhance Intra-Cell Connectivity". En 2024 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2024. http://dx.doi.org/10.7567/ssdm.2024.ps-01-03.

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Engelborghs, Yves, Marijke Somers y Hilde De Bruyn. "A pressure jump relaxation study of microtubules showing dynamic instability at steady state". En The living cell in four dimensions. AIP, 1991. http://dx.doi.org/10.1063/1.40583.

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Lapotko, Dmitry, Tat'yana Romanovskaya y Elena Gordiyko. "Photothermal response of live cell depends upon cell metabolic state". En International Symposium on Biomedical Optics, editado por Alexander A. Oraevsky. SPIE, 2002. http://dx.doi.org/10.1117/12.469854.

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Kim, Y. J., J. G. Kang, B. Lee, G. S. Cho, S. K. Park y W. Y. Choi. "Abnormal Cell-to-Cell Interference of NAND Flash Memory". En 2013 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2013. http://dx.doi.org/10.7567/ssdm.2013.a-1-2.

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Wang, Lei. "Harnessing Synthetic Biology to Sense and Guide Cell-State Transitions". En International Conference on Cell Science and Regenerative Medicine, 56. United Research Forum, 2024. https://doi.org/10.51219/urforum.2024.lei-wang.

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Informes sobre el tema "Cell state"

Smyrl, W. H., B. B. Owens y H. S. White. Exploratory cell research and fundamental processes study in solid state electrochemical cells. Office of Scientific and Technical Information (OSTI), junio de 1990. http://dx.doi.org/10.2172/6396835.

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Steven Shaffer, Sean Kelly, Subhasish Mukerjee, David Schumann, Gail Geiger, Kevin Keegan, John Noetzel y Larry Chick. SOLID STATE ENERGY CONVERSION ALLIANCE DELPHI SOLID OXIDE FUEL CELL. Office of Scientific and Technical Information (OSTI), diciembre de 2003. http://dx.doi.org/10.2172/834990.

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Steven Shaffer, Sean Kelly, Subhasish Mukerjee, David Schumann, Gail Geiger, Kevin Keegan y Larry Chick. SOLID STATE ENERGY CONVERSION ALLIANCE DELPHI SOLID OXIDE FUEL CELL. Office of Scientific and Technical Information (OSTI), mayo de 2004. http://dx.doi.org/10.2172/825673.

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Kurtz, Jennifer, Sam Sprik y Genevieve Saur. State-of-the-Art Fuel Cell Voltage Durability Status (Presentation). Office of Scientific and Technical Information (OSTI), junio de 2012. http://dx.doi.org/10.2172/1045057.

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Nguyen Minh. Solid State Energy Conversion Alliance (SECA) Solid Oxide Fuel Cell Program. Office of Scientific and Technical Information (OSTI), julio de 2006. http://dx.doi.org/10.2172/915745.

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Unknown. SOLID STATE ENERGY CONVERSION ALLIANCE (SECA) SOLID OXIDE FUEL CELL PROGRAM. Office of Scientific and Technical Information (OSTI), junio de 2003. http://dx.doi.org/10.2172/821427.

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Nguyen Minh y Jim Powers. SOLID STATE ENERGY CONVERSION ALLIANCE (SECA) SOLID OXIDE FUEL CELL PROGRAM. Office of Scientific and Technical Information (OSTI), octubre de 2003. http://dx.doi.org/10.2172/821428.

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Blekhman, David. HYDROGEN AND FUEL CELL EDUCATION AT CALIFORNIA STATE UNIVERSITY, LOS ANGELES. Office of Scientific and Technical Information (OSTI), septiembre de 2011. http://dx.doi.org/10.2172/1025719.

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Kurtz, Jennfier, Huyen Dinh, Chris Ainscough y Genevieve Saur. State-of-the-art Fuel Cell Voltage Durability Status: 2015 Composite Data Products. Office of Scientific and Technical Information (OSTI), mayo de 2015. http://dx.doi.org/10.2172/1226475.

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Kurtz, J., S. Sprik, G. Saur, M. Peters, M. Post y C. Ainscough. State-of-the-Art Fuel Cell Voltage Durability Status: Spring 2013 Composite Data Products. Office of Scientific and Technical Information (OSTI), mayo de 2013. http://dx.doi.org/10.2172/1080110.

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