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Статті в журналах з теми "Singole cellule"
Andreula, C. F., A. M. N. Recchia-Luciani, A. Tarantino, V. Pavone, A. P. Garribba, R. De Blasi, and A. Carella. "I linfomi secondari del sistema nervoso centrale." Rivista di Neuroradiologia 7, no. 6 (December 1994): 883–93. http://dx.doi.org/10.1177/197140099400700605.
Повний текст джерелаAndreula, F. C., A. M. N. Recchia-Luciani, and L. Garofalo. "Linfomi del sistema nervoso centrale e Aids." Rivista di Neuroradiologia 10, no. 2_suppl (October 1997): 206. http://dx.doi.org/10.1177/19714009970100s292.
Повний текст джерелаOASA, Sho. "Report; Single Protein Dynamics in Cellulo 2014." Seibutsu Butsuri 54, no. 5 (2014): 280–82. http://dx.doi.org/10.2142/biophys.54.280.
Повний текст джерелаO. H. Abdelwahed, O. H. Abdelwahed, and M. El-Sayed Wahed. "Optimizing Single Layer Cellular Neural Network Simulator using Simulated Annealing Technique with Neural Networks." Indian Journal of Applied Research 3, no. 6 (October 1, 2011): 91–94. http://dx.doi.org/10.15373/2249555x/june2013/31.
Повний текст джерелаMiller, W., N. Abrosimov, I. Rasin, and D. Borissova. "Cellular growth of single crystals." Journal of Crystal Growth 310, no. 7-9 (April 2008): 1405–9. http://dx.doi.org/10.1016/j.jcrysgro.2007.11.046.
Повний текст джерелаAonuma, Yuki, Taiji Adachi, Mototsugu Tanaka, Masaki Hojo, Teruko Takano-Yamamoto, and Hiroshi Kamioka. "MECHANOSENSITIVITY OF A SINGLE OSTEOCYTE : DIFFERENCE IN CELL PROCESS AND CELL BODY(3A1 Cellular & Tissue Engineering & Biomaterials I)." Proceedings of the Asian Pacific Conference on Biomechanics : emerging science and technology in biomechanics 2007.3 (2007): S165. http://dx.doi.org/10.1299/jsmeapbio.2007.3.s165.
Повний текст джерелаO. H. Abdelwahed, O. H. Abdelwahed, and M. El-Sayed Wahed. "Optimizing Single-Layer Raster Cellular Neural Network Simulator Using Simulated Annealing Technique and RK4(2), RK4(3) and RK 6(4)." International Journal of Scientific Research 2, no. 6 (June 1, 2012): 108–12. http://dx.doi.org/10.15373/22778179/june2013/35.
Повний текст джерелаGe, Xiaohu, Meidong Huang, Jiaqi Chen, Hui Xu, Jing Xu, Wuxiong Zhang, and Yang Yang. "Wireless Single Cellular Coverage Boundary Models." IEEE Access 4 (2016): 3569–77. http://dx.doi.org/10.1109/access.2016.2582960.
Повний текст джерелаLee, J., J. Y. Sul, and J. H. Eberwine. "Single Cell/Cellular Subregion-Targeted Phototransfection." Cold Spring Harbor Protocols 2014, no. 9 (September 1, 2014): pdb.prot072421. http://dx.doi.org/10.1101/pdb.prot072421.
Повний текст джерелаLeake, M. C. "Analytical tools for single-molecule fluorescence imaging in cellulo." Phys. Chem. Chem. Phys. 16, no. 25 (2014): 12635–47. http://dx.doi.org/10.1039/c4cp00219a.
Повний текст джерелаДисертації з теми "Singole cellule"
Antoniolli, Francesca. "PROGETTAZIONE E CARATTERIZZAZIONE DI UN BIOSENSORE MEMS." Doctoral thesis, Università degli studi di Trieste, 2008. http://hdl.handle.net/10077/2755.
Повний текст джерелаNegli ultimi anni, le cellule sono state oggetto di studio approfondito e, in taluni casi, di esperimenti molto sofisticati. Tuttavia, benché si conosca molto circa la loro struttura, poche sono le informazioni sulla meccanica cellulare e sulla risposta cellulare agli stimoli meccanici. Le cellule, infatti, possono sentire forze meccaniche e convertirle in risposte biologiche, oppure, viceversa, è da tempo noto come segnali biologici e biochimici influenzino l’abilità cellulare nel sentire, generare e sopportare forze di tipo meccanico. Negli ultimi anni sono stati ideati e realizzati svariati meccanismi per l’applicazione di forze meccaniche su cellule e la rilevazione delle conseguenti deformazioni. Questi sistemi, però, presentano dei limiti: - la forza esercitata non è adeguata al fenomeno investigato; - lo studio viene effettuato su un’intera popolazione di cellule; - la forza è esercitata localmente e non sull’intera cellula. Il presente lavoro di tesi, avente come obiettivo primo lo sviluppo, la progettazione e la realizzazione di un dispositivo per la sollecitazione meccanica della singola cellula e la rilevazione delle conseguenti deformazioni, si è focalizzato sullo studio di dispositivi che potessero bypassare i suddetti limiti. La scelta è ricaduta nei Sistemi Micro Elettro Meccanici, dal momento che, oltre ad avere dimensioni compatibili con le caratteristiche cellulari ed assicurare modesti costi realizzativi ed operativi, garantiscono - la possibilità di applicare forze in un ampio range (pN-µN); - la possibilità di effettuare studi sulla singola cellula, ed in particolare su cellule aderenti; - la possibilità di stimolare l’intera cellula, e non soltanto una porzione locale di questa. La prima parte del lavoro è stata rivolta alla messa a punto di dispositivi che, concepiti in maniera analoga a quelle che sono le tradizionali macchine universali per test meccanici, potessero consentire l’ancoraggio della singola cellula su di una piattaforma di geometrie differenti a seconda che si volesse applicare una sollecitazione di trazione uniassiale, biassiale, pluriassiale oppure di taglio. Tali dispositivi tuttavia hanno riscontrato diverse problematiche quando operanti in soluzioni saline quali i medium cellulari. Sono stai quindi concepiti e sviluppati dei nuovi dispositivi che potessero bypassare le problematiche riscontrate con i primi: il MEMS è stato quindi sdoppiato su due outline di 2x2 mm, di cui una ospitante il motore per l’attuazione del dispositivo operante in aria l’altra ospitante la piattaforma per la collocazione della cellula in esame. Per completare il funzionamento di tali dispositivi è stata sviluppata e realizzata con successo una tecnica di collegamento di questi mediante una fibra di carbonio ancorata ai MEMS mediante wire bonding. Infine sono state acquisite e messe a punto la strumentazione e le tecniche che potessero consentire di operare con cellule viventi: è stato individuato un materiale tale da consentire un ancoraggio ottimale della cellula e con il quale si potesse funzionalizzate localmente la piattaforma per la cellula; è stato allestito un laboratorio per colture cellulari presso il Dipartimento dei Materiali e delle Risorse Naturali; è stata messa a punto una tecnica per la manipolazione di singole cellule; sono state infine eseguite alcune preliminari prove di trazione sulla singola cellula.
XX Ciclo
1979
Moussy, Alice. "Caractérisation des premières étapes de différenciation des cellules hématopoïétiques à l'échelle de la cellule unique." Thesis, Paris Sciences et Lettres (ComUE), 2017. http://www.theses.fr/2017PSLEP029/document.
Повний текст джерелаDespite intensively studies, the fundamental mechanisms of cell fate decision during cellular differentiation still remain unclear. The deterministic mechanisms, often based on studies of large cell populations, cannot explain the difference between individual cell fates choices placed in the same environment. The aim of my thesis work is to study the first steps of hematopoietic cell differentiation at the single cell level thanks to transcriptomic, proteomic and morphological analyses. Two differentiation models have been used: T regulatory lymphocytes and human cord blood-derived CD34+ cells. The behavior of individual cells following stimulation has been analyzed. Using time-lapse microscopy coupled to single cell molecular analyses, we could demonstrate that the cell fate choice is not a unique, programmed event. First, the cell reaches a metastable “multi-primed” state, which is characterized by a mixed lineage gene expression pattern. After transition through an “uncertain”, unstable state, characterized by fluctuations between two phenotypes, the cell reaches a stable state. Our observations are coherent with a stochastic model of cell fate decision. The differentiation is likely to be a spontaneous, dynamic, fluctuating and not a deterministic process. The cell fate decisions are taken by individual cells
MALLIA, SELENE. "La genomica su singola cellula rivela la gerarchia e l'architettura clonale nelle Neoplasie Mieloproliferative." Doctoral thesis, Università degli studi di Modena e Reggio Emilia, 2022. http://hdl.handle.net/11380/1278821.
Повний текст джерелаSomatic mutations in Hematopoietic Stem Cells (HSCs) cause Myeloproliferative Neoplasms (MPNs), including Polycythemia Vera, Essential Thrombocythemia and Primary Myelofibrosis (PMF). PMF is a heterogeneous disorder consisting of bone marrow fibrosis, megakaryocyte hyperplasia and extramedullary hematopoiesis and is characterized by the worst prognosis among MPNs. About 15-20% of patients are unresponsive to conventional therapies and develop Acute Myeloid Leukemia (AML). In HSCs the main mutations, identified as “driver mutations” during MPNs pathogenesis, involve JAK2, CALR and MPL genes; in addition, many other genetic alterations contribute to the prognosis worsening and the development of AML. Disease progression and leukemic evolution in PMF results from an increase of the genomic complexity and clonal heterogeneity. Many studies confirmed that the mutational acquisition order affects the clinical outcome. However, the clonal architecture determining disease evolution and the clones guiding leukemic transformation are poorly understood. Recent studies demonstrate that single-cell (sc) genomics is a sensitive technique suitable to study clonal heterogeneity and to detect the evolution of the malignant cells in hematological neoplasms. For this reason, we used the sc-genomics approach to clarify the clonal complexity in PMF. Firstly, we developed a workflow for CD34+ Hematopoietic Stem Progenitor Cells (HSPCs) isolation from cord blood, fixation and immunostaining for CD34, in order to singularly separate the cells by DEP-array system (Menarini Silicon Biosystem) and to obtain a cell population suitable for sc-analysis. Then, we compared different whole genome amplification (WGA) protocols for single cells in order to obtain a uniform DNA amplification for Sanger sequencing and minimize allele drop out effect. Based on this method, we analyzed the CD34+ HSPCs of a PMF patient carrying JAK2V617F and other MPN frequent mutations. This patient was treated with JAK2-inhibitor Ruxolitinib but he was unresponsive to therapy and evolved to AML. In order to reconstruct the clonal hierarchy and architecture, we analyzed CD34+ cells during chronic phase (T1), the accelerated phase (T2) and the AML phase (T3). By means to sc-analysis, we established that TET2 was the first mutated gene, preceding JAK2 mutation, and this probably conferred a lower sensitivity to treatment. Moreover, we identified an increase of the allele burden of the TP53 mutation during disease progression, suggesting that TP53-mutated clones supported the accelerated (T2) phase. Interestingly, we already detected in T1 phase a small cell fraction, undetectable by bulk NGS and carrying the leukemogenic FLT3 mutation, probably driving the T3 phase. Finally, we characterized SRSF2 homozygous mutation that has not been described yet. Altogether our data demonstrate that sc-genomics is a promising method to uncover clonal heterogeneity in MPNs, highlighting the early occurrence of pro-leukemic mutations and to describe the real scenario of mutational events in hematological diseases.
Caccianini, Laura. "Imagerie de l'architecture dynamique de la chromatine dans la cellule unique." Thesis, Paris Sciences et Lettres (ComUE), 2019. https://tel.archives-ouvertes.fr/tel-02896692.
Повний текст джерелаChromatin structure and cellular function are tightly linked in the nucleus of mammalian cells. Disruption of chromatin spatial organisation dramatically affects the life of a cell and eventually leads to severe pathologies in entire organisms. Two nuclear factors, CTCF and Cohesin, have been found to play a crucial role in the regulation and maintenance of DNA architecture. Huge advancements have been made in the understanding of the mechanisms behind chromatin arrangement but the field is still lacking a dynamic picture at the single cell and single molecule level. This study provide this study provides insight into the dynamics of CTCF and Cohesin through single particle tracking of CTCF and Cohesin dynamics achieved with single molecule tracking in living mouse embryonic stem cells. The interplay between these two factors was studied by looking at Cohesin’s behaviour in the absence of CTCF and in the context of other biological alterations
Holt, Brian D. "Cellular Processing of Single Wall Carbon Nanotubes." Research Showcase @ CMU, 2014. http://repository.cmu.edu/dissertations/397.
Повний текст джерелаGeisler, Hubert. "Structuration d'hydrogels thermoactivables pour l'analyse de cellules uniques." Electronic Thesis or Diss., Université Paris sciences et lettres, 2020. http://www.theses.fr/2020UPSLS001.
Повний текст джерелаWe present in this work a new microfluidic technology aiming at isolating single cells by the use of thermoactuable polymers. One of the polymers we use is polyNIPAM, a polymer that can expand its volume by 400% in water when the temperature is set under 32°C and can shrink down when it is set over 34°C. We use this reversible swelling capability to open and close compartments embedded in a microfluidic chip.Grafting and structuring these hydrogel features relies on thiol-en click chemistry, initiated thermally or by UV irradiation. We have developed methods and microfabrication protocols in order to diversify the substrate materials (from glass to PDMS, COC, PMMA, etc), to expand the structures thickness range (from few microns to a tenth of microns) and to strengthen our knowledge regarding the fabrication impact on the hydrogel’s behavior. A robust protocol of photolithography has finally been worked on allowing the design of any type of 2D features on a large choice of substrates.One of the realistic applications detailed here is the development of microfluidic chips aiming at isolating single cells in hydrogel compartments. (confidential)
Boltyanskiy, Rostislav. "Mechanical Response of Single Cells to Stretch." Thesis, Yale University, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10160860.
Повний текст джерелаA living cell is a complex soft matter system far from equilibrium. While its components have definite mechanical properties such as stiffness and viscosity, cells consume energy to generate force and exhibit adaptation by modulating their mechanical properties through regulatory pathways. In this dissertation, we explore cell mechanics by stretching single fibroblast cells and simultaneously measuring their traction stresses. Upon stretch, there is a sudden, drastic increase in traction stresses, often followed by a relaxation over a time scale of about 1 minute. Upon release of stretch, traction stresses initially drop and often recover on a similar time scale of about 1 minute. We show that a minimal active linear viscoelastic model captures essential features of cell response to stretch. This model is most successful in describing the response of cells within the first 30 seconds of stretch. While perturbations of myosin and vinculin change quiescent traction stresses, they surprisingly have no significant impact on the stiffness or viscoelastic timescale of the cells. On longer time scales, cells may show an adaptive response to stretch that contradicts the minimal mechanical model. The probability of an adaptive response is significantly reduced by myosin de-activation and vinculin knockout. Therefore, we find that while vinculin and myosin are not important in determining passive mechanical properties of cells, such as stiffness and viscosity, they play a significant role in the adaptive mechanisms of cell response to stretch. To perform this work, we have built a novel micro stretching device compatible with live cell microscopy and developed a computational tool to analyze data from large traction stresses. Therefore, this dissertation's contribution is two-fold: (1) a novel experimental approach to explore the mechanics of living cells, and (2) a new model and framework for understanding the mechanical response of cells to stretch.
Pagliaro, Sarah Beatriz De Oliveira. "Transcriptional control induced by bcr-abl and its role in leukemic stem cell heterogeneity. Single-Cell Transcriptome in Chronic Myeloid Leukemia: Pseudotime Analysis Reveals Evidence of Embryonic and Transitional Stem Cell States Single Cell Transcriptome in Chronic Myeloid Leukemia (CML): Pseudotime Analysis Reveals a Rare Population with Embryonic Stem Cell Features and Druggable Intricated Transitional Stem Cell States A novel neuronal organoid model mimicking glioblastoma (GBM) features from induced pluripotent stem cells (iPSC) Experimental and integrative analyses identify an ETS1 network downstream of BCR-ABL in chronic myeloid leukemia (CML)." Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASQ032.
Повний текст джерелаChronic myeloid leukemia is a clonal hematopoietic malignancy, characterized by the acquisition of the t (9;22) translocation leading to Ph1 chromosome and its counterpart BCR-ABL oncogene, in a very primitive hematopoietic stem cell. CML is a model of targeted therapies as the proof of concept of the feasibility of targeting the tyrosine kinase (TK) activity BCR-ABL using TK inhibitors (TKI) has been shown to lead to major responses and remissions. However, the current problems encountered in these therapies are primitive leukemic stem cells resistance and their persistence which is thought to be related to the heterogeneity of the stem cells at diagnosis leading to clonal selection of cells resisting to TKI therapies. I have applied the technology of single cell transcriptome analysis to CML cells using a panel of genes involved in different pathways combined with trajectory inference analysis to the gene expression pattern. The results showed a transitional stem cell states including embryonic genes identified in CML cells at diagnosis which could contribute to LSC resistance and persistence. Furthermore, the oncoprotein Bcr-Abl is the constitutively active tyrosine kinase produced by the chimeric BCR-ABL gene in chronic myeloid leukemia (CML). The transcriptional targets of Bcr-Abl in leukemic cells have not been extensively studied. A transcriptome experiment using the hematopoietic UT7 cell line expressing BCR-ABL, has identified the overexpression of eukaryotic elongation factor kinase 2 (eEF2K) which plays a major role in the survival of cells upon nutrient deprivation. Overall, the data suggest that overexpression of eEF2K in CML is associated with an increased sensitivity to nutrient-deprivation
Simon-Desbois, Linda. "Development of a microfluidic device for single cell transcriptome analysis." Thesis, Lille 2, 2013. http://www.theses.fr/2013LIL2S007.
Повний текст джерелаIn the post-genomic era, it is now critical to characterize living organisms at the singlecell level. CAGE (Cap Analysis of Gene Expression) is a technology developed by agroup of RIKEN instituteto get genome-wide profile of gene expression. It can beused for profiling of gene expression and identifying the TSS (transcription start site)to analyze promoters architecture. By using the CAGE technology, it could be foundthat different tissues and families of genes differentially use distinct types ofpromoters. Applying CAGE technology against single cells is an ideal way tounderstand life phenomenon based on genome and will have a major impact inbiology. To address this, a novel platform to manipulate single cell and analyze itsown transcriptome with higher precision and efficiency is required.This project aims to develop a microfluidic platform to realize the protocol of CAGEtechnology against single cells with higher-throughput and sensitivity overconventional microtube-based way. For this, we encapsulated single cells inmicrodroplets, lysed them, and performed RT reaction in order to sequence andanalyze their transcriptome
Chen, Peng. "Single cell assays of exocytosis /." free to MU campus, to others for purchase, 2002. http://wwwlib.umi.com/cr/mo/fullcit?p3074384.
Повний текст джерелаКниги з теми "Singole cellule"
Single-molecule cellular biophysics. Cambridge: Cambridge University Press, 2012.
Знайти повний текст джерелаChemical cytometry: Ultrasensitive analysis of single cells. Weinheim: Wiley-VCH, 2010.
Знайти повний текст джерелаSako, Yasushi. Cell Signaling Reactions: Single-Molecular Kinetic Analysis. Dordrecht: Springer Science+Business Media B.V., 2011.
Знайти повний текст джерелаSardin, Marie-Neige. Celle qui dit non. Paris: Œuvre, 2011.
Знайти повний текст джерела1961-, Duijn Bert van, and Wiltink Anneke 1961-, eds. Signal transduction--single cell techniques. Berlin: Springer, 1998.
Знайти повний текст джерелаThe diversity of life: From single cells to multicellular organizations. Oxford: Heinemann Library, 2003.
Знайти повний текст джерелаSnedden, Robert. The diversity of life: From single cells to multicellular organisms. Chicago, Ill: Heinemann Library, 2008.
Знайти повний текст джерелаArnaud, Chauvière, Preziosi Luigi, and Verdier Claude 1962-, eds. Cell mechanics: From single scale-based models to multiscale modeling. Boca Raton: Chapman & Hall/CRC, 2009.
Знайти повний текст джерелаArnaud, Chauvière, Preziosi Luigi, and Verdier Claude, eds. Cell mechanics: From single scale-based models to multiscale modeling. Boca Raton: Chapman & Hall/CRC, 2009.
Знайти повний текст джерелаLuigi, Preziosi, and Verdier Claude, eds. Cell mechanics: From single scale-based models to multiscale modeling. Boca Raton: Chapman & Hall/CRC, 2009.
Знайти повний текст джерелаЧастини книг з теми "Singole cellule"
De Keijzer, Sandra, B. Ewa Snaar-Jagalska, Herman P. Spaink, and Thomas Schmidt. "Single-Molecule Imaging of Cellular Signaling." In Single Molecules and Nanotechnology, 107–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-73924-1_5.
Повний текст джерелаHuang, Howard, Constantinos B. Papadias, and Sivarama Venkatesan. "Single-user MIMO." In MIMO Communication for Cellular Networks, 35–78. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-77523-4_2.
Повний текст джерелаShinde, Ashwini, Srabani Kar, Moeto Nagai, Fan-Gang Tseng, and Tuhin Subhra Santra. "Light-Induced Cellular Delivery and Analysis." In Handbook of Single Cell Technologies, 1–29. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-10-4857-9_4-1.
Повний текст джерелаShinde, Ashwini, Srabani Kar, Moeto Nagai, Fan-Gang Tseng, and Tuhin Subhra Santra. "Light-Induced Cellular Delivery and Analysis." In Handbook of Single-Cell Technologies, 3–30. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-10-8953-4_4.
Повний текст джерелаPatsch, Katherin, Shannon M. Mumenthaler, and Daniel Ruderman. "Image-Based Tracking of Heterogeneous Single-Cell Phenotypes." In Cellular Heterogeneity, 47–63. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7680-5_3.
Повний текст джерелаNavas-Moreno, Maria, and James W. Chan. "Laser Tweezers Raman Microspectroscopy of Single Cells and Biological Particles." In Cellular Heterogeneity, 219–57. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7680-5_13.
Повний текст джерелаKwon, Jungeun Sarah, Xia Wang, and Guang Yao. "Study Quiescence Heterogeneity by Coupling Single-Cell Measurements and Computer Modeling." In Cellular Quiescence, 287–99. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7371-2_20.
Повний текст джерелаSanchez-Adams, Johannah, and Kyriacos A. Athanasiou. "Biomechanical Characterization of Single Chondrocytes." In Cellular and Biomolecular Mechanics and Mechanobiology, 247–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/8415_2010_20.
Повний текст джерелаBrun, Caroline E., Yu Xin Wang, and Michael A. Rudnicki. "Single EDL Myofiber Isolation for Analyses of Quiescent and Activated Muscle Stem Cells." In Cellular Quiescence, 149–59. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7371-2_11.
Повний текст джерелаBarteneva, Natasha S., and Ivan A. Vorobjev. "Heterogeneity of Metazoan Cells and Beyond: To Integrative Analysis of Cellular Populations at Single-Cell Level." In Cellular Heterogeneity, 3–23. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7680-5_1.
Повний текст джерелаТези доповідей конференцій з теми "Singole cellule"
Liu, Yu-San, Yonghua Luo, John O. Baker, Yining Zeng, Michael E. Himmel, Steve Smith, and Shi-You Ding. "A single molecule study of cellulase hydrolysis of crystalline cellulose." In BiOS, edited by Jörg Enderlein, Zygmunt K. Gryczynski, and Rainer Erdmann. SPIE, 2010. http://dx.doi.org/10.1117/12.840975.
Повний текст джерелаCoskun, Ulas C., Matthew L. Ferguson, Alexander Vallmitjana, Huynh Anh, Julianna Goelzer, Yuansheng Sun, Shih-Chu J. Liao, Sunil Shah, Enrico Gratton, and Beniamino Barbieri. "Nano-resolution in vivo 3D orbital tracking system to study cellular dynamics and bio-molecular processes." In Single Molecule Spectroscopy and Superresolution Imaging XIII, edited by Ingo Gregor, Rainer Erdmann, and Felix Koberling. SPIE, 2020. http://dx.doi.org/10.1117/12.2546690.
Повний текст джерелаMandyam, Giridhar D. "Single-Sideband OFDM for Cellular Systems." In 2006 Fortieth Asilomar Conference on Signals, Systems and Computers. IEEE, 2006. http://dx.doi.org/10.1109/acssc.2006.355064.
Повний текст джерелаChen, Fei. "Abstract IA02: Slide-seq: A platform for understanding cellular circuits in tissue." In Abstracts: AACR Virtual Special Conference on Tumor Heterogeneity: From Single Cells to Clinical Impact; September 17-18, 2020. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.tumhet2020-ia02.
Повний текст джерелаWu, Catherine J. "Abstract IA11: Detecting and targeting cellular heterogeneity of the lymphoid blood malignancies." In Abstracts: AACR Virtual Special Conference on Tumor Heterogeneity: From Single Cells to Clinical Impact; September 17-18, 2020. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.tumhet2020-ia11.
Повний текст джерелаAshlock, Daniel, and Sharon McNicholas. "Single parent generalization of cellular automata rules." In 2012 IEEE Congress on Evolutionary Computation (CEC). IEEE, 2012. http://dx.doi.org/10.1109/cec.2012.6256126.
Повний текст джерелаKaufmann, Rainer, Paul Lemmer, Manuel Gunkel, Yanina Weiland, Patrick Müller, Michael Hausmann, David Baddeley, Roman Amberger, and Christoph Cremer. "SPDM: single molecule superresolution of cellular nanostructures." In SPIE BiOS: Biomedical Optics, edited by Jörg Enderlein, Zygmunt K. Gryczynski, and Rainer Erdmann. SPIE, 2009. http://dx.doi.org/10.1117/12.809109.
Повний текст джерелаLin, C. M., C. C. Tseng, C. L. Chen, and Andrew M. Wo. "Hydrodynamic single-cell trapping for cellular assays." In TRANSDUCERS 2009 - 2009 International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2009. http://dx.doi.org/10.1109/sensor.2009.5285399.
Повний текст джерелаBabaee, Sahab, Babak Haghpanah Jahromi, Amin Ajdari, Hamid Nayeb-Hashemi, and Ashkan Vaziri. "Mechanical Properties of Open-Cell Cellular Structures With Rhombic Dodecahedron Cells." In ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-39924.
Повний текст джерелаDahan, Maxime. "Probing Cellular Events with Single Quantum Dot Imaging." In Laser Science. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/ls.2009.lsthb4.
Повний текст джерелаЗвіти організацій з теми "Singole cellule"
Harmon, Jennifer. Cotton Versus Bacterial Cellulose: A Comparison of Single Ply Yarns. Ames (Iowa): Iowa State University. Library, January 2019. http://dx.doi.org/10.31274/itaa.8789.
Повний текст джерелаHiddessen, A. SINGLE-CELL LEVEL INVESTIGATION OF CYTOSKELETAL/CELLULAR RESPONSE TO EXTERNAL STIMULI. Office of Scientific and Technical Information (OSTI), February 2007. http://dx.doi.org/10.2172/902301.
Повний текст джерелаSun, Lina, Yanan Han, Hua Wang, Huanyu Liu, Shan Liu, Hongbin Yang, Xiaoxia Ren, and Ying Fang. MicroRNAs as Potential Biomarkers for the Diagnosis of Inflammatory Bowel Disease: A Systematic Review and Meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, February 2022. http://dx.doi.org/10.37766/inplasy2022.2.0027.
Повний текст джерелаBarg, Rivka, Erich Grotewold, and Yechiam Salts. Regulation of Tomato Fruit Development by Interacting MYB Proteins. United States Department of Agriculture, January 2012. http://dx.doi.org/10.32747/2012.7592647.bard.
Повний текст джерелаLapidot, Moshe, and Vitaly Citovsky. molecular mechanism for the Tomato yellow leaf curl virus resistance at the ty-5 locus. United States Department of Agriculture, January 2016. http://dx.doi.org/10.32747/2016.7604274.bard.
Повний текст джерелаGafni, Yedidya, and Vitaly Citovsky. Molecular interactions of TYLCV capsid protein during assembly of viral particles. United States Department of Agriculture, April 2007. http://dx.doi.org/10.32747/2007.7587233.bard.
Повний текст джерелаChejanovsky, Nor, and Bruce A. Webb. Potentiation of Pest Control by Insect Immunosuppression. United States Department of Agriculture, January 2010. http://dx.doi.org/10.32747/2010.7592113.bard.
Повний текст джерелаSharon, Amir, and Maor Bar-Peled. Identification of new glycan metabolic pathways in the fungal pathogen Botrytis cinerea and their role in fungus-plant interactions. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7597916.bard.
Повний текст джерелаHansen, Peter J., Zvi Roth, and Jeremy J. Block. Improving oocyte competence in dairy cows exposed to heat stress. United States Department of Agriculture, January 2014. http://dx.doi.org/10.32747/2014.7598163.bard.
Повний текст джерелаTzfira, Tzvi, Michael Elbaum, and Sharon Wolf. DNA transfer by Agrobacterium: a cooperative interaction of ssDNA, virulence proteins, and plant host factors. United States Department of Agriculture, December 2005. http://dx.doi.org/10.32747/2005.7695881.bard.
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