Literatura académica sobre el tema "Cellule vive"
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Artículos de revistas sobre el tema "Cellule vive"
Farhat, Raed, Ayman El-Seedy, Kamal El-Moussaoui, Marie-Claude Pasquet, Catherine Adolphe, Eric Bieth, Jeanne Languepin, Isabelle Sermet-Gaudelus, Alain Kitzis y Véronique Ladevèze. "Multi-physiopathological consequences of the c.1392G>T CFTR mutation revealed by clinical and cellular investigations". Biochemistry and Cell Biology 93, n.º 1 (febrero de 2015): 28–37. http://dx.doi.org/10.1139/bcb-2014-0042.
Texto completoSheng, Guojun. "Vive la difference". Cell Adhesion & Migration 4, n.º 3 (julio de 2010): 439. http://dx.doi.org/10.4161/cam.4.3.12642.
Texto completoWong, RaymondChing-Bong y Tu Nguyen. "Neuroregeneration using in vivo cellular reprogramming". Neural Regeneration Research 12, n.º 7 (2017): 1073. http://dx.doi.org/10.4103/1673-5374.211182.
Texto completoPeng, Tao y Howard C. Hang. "SORTing out cellular proteomes in vivo". Nature Biotechnology 32, n.º 5 (mayo de 2014): 445–46. http://dx.doi.org/10.1038/nbt.2898.
Texto completoTrani, Jose L., Howard K. Song, Susan M. Lerner, Hooman Noorchashm, Joseph W. Markmann, Jing Wang, Clyde F. Barker, Ali Naji y James F. Markmann. "IN VIVO CHARACTERIZATION OF CELLULAR XENOIMMUNITY". Transplantation 67, n.º 9 (mayo de 1999): S554. http://dx.doi.org/10.1097/00007890-199905150-00072.
Texto completoModo, Michel, Mathias Hoehn y Jeff W. M. Bulte. "Cellular MR Imaging". Molecular Imaging 4, n.º 3 (1 de julio de 2005): 153535002005051. http://dx.doi.org/10.1162/15353500200505145.
Texto completoBoppart, Stephan A., Brett E. Bouma, Costas Pitris, James F. Southern, Mark E. Brezinski y James G. Fujimoto. "In vivo cellular optical coherence tomography imaging". Nature Medicine 4, n.º 7 (julio de 1998): 861–65. http://dx.doi.org/10.1038/nm0798-861.
Texto completoRice, Andrew P. y Jason T. Kimata. "Cellular cofactors and HIV-1 infectionin vivo". Future Virology 1, n.º 3 (mayo de 2006): 337–47. http://dx.doi.org/10.2217/17460794.1.3.337.
Texto completoHornsby, P. J. "Cellular Senescence and Tissue Aging In Vivo". Journals of Gerontology Series A: Biological Sciences and Medical Sciences 57, n.º 7 (1 de julio de 2002): B251—B256. http://dx.doi.org/10.1093/gerona/57.7.b251.
Texto completoTréton, J. A. "Cellular aging, in vitro and in vivo". Aging Clinical and Experimental Research 5, n.º 4 (agosto de 1993): 291–97. http://dx.doi.org/10.1007/bf03324177.
Texto completoTesis sobre el tema "Cellule vive"
Mitri, Elisa. "Fabrication of microfluidic devices for studying living cells responding to external stimuli by FTIR vibrational spectroscopy". Doctoral thesis, Università degli studi di Trieste, 2014. http://hdl.handle.net/10077/9971.
Texto completoThe present PhD Thesis is about the development of new fabricative strategies to obtain microfluidic devices suitable for InfraRed MicroSpectroscopy (IRMS) studies on living cells in physiological environment and the demonstration of the screening and diagnostic capabilities of this technique for bio-medical applications. IRMS detects the vibrational pattern of molecules allowing the label-free characterization of the chemical profile of a biological specimen and its correlation with the sample morphology. Although powerful and versatile, this technique has been limited until recent years to the study of fixed or dried samples, in order to bypass the problem of water absorptions in the infrared spectral region. The use of microfabrication techniques for the production of Visible-Infrared (Vis-IR) transparent devices has recently opened an innovative approach, able to release some of the constrains encountered when dealing with living cells. Moreover, microfabrication is the best option to achieve long-range reproducibility of the optical path, which is mandatory for an accurate water subtraction in order to disclose cellular IR features. At first, we aimed to develop an IR-Vis transparent microfluidic chip with long-time stability in experimental conditions. The optical transparency was granted by the use of CaF2 or BaF2 as substrates, but their low surface energies imposed a challenge in order to establish reliable microfabrication protocols. With the introduction of a new strategy, that we refer to as “silicon-like”, based on the sputtering of a thin silicon layer onto the IR materials, it was possible to modify the surface properties of the substrates without changing their optical properties. These new substrates allowed the use of several common photo-resists as structural materials. The epoxy-based negative tone SU-8 was chosen for its chemical properties (resistance to solvents and watery media) and its long-term stability in experimental conditions. We established a new sealing protocol exploiting the optical properties of SU-8, able to create a chemical bonding between two already patterned layers of the polymer. It was thus possible to produce a new generation of fluidic chips, characterized by broadband transparency from mid-IR to UV and long-term stability in continuous flow conditions. Subsequently, the devices were employed to perform IRMS measurements on both adherent and circulating cells. In particular, we characterize the spectroscopic features associated to each stage of B16 cell cycle, the changes undergone in living MCF-7 upon exposure to hypo-osmotic and thermal stress and the apoptosis progression of U-937 cells, induced by growth factors removal and CCCP (Carbonyl Cyanide m-Chloro Phenylhydrazone) stimulation. All the studies had the intent to further verify the effectiveness of the microfluidic approach for both circulating and adherent living cells analysis and to prove the capabilities of IRMS as tool for the observation of biochemical processes undergone by live beings. For this reason, to validate the achieved results, a parallel analysis with a well established analytical technique such as the flow-cytometry was performed. The present Thesis demonstrates the capabilities of IRMS coupled with microfluidic technologies, as a diagnostic tool for bio-medical investigation of bio-medical applications. Thanks to the precise control of the cellular microenvironment, as well as its flexibility in terms of experimental design, IRMS could be seen as a new promising frontier for modern biology.
La presente tesi di dottorato concerne lo sviluppo di nuove strategie fabricative, volte all’ottenimento di dispositivi microfluidici per lo studio di cellule vive, in condizioni fisiologiche, tramite MicroSpettroscopia InfraRossa (MSIR). Inoltre intende dimostrare le potenzialità di questa tecnica analitica come mezzo di screening diagnostico in ambito bio-medico. La MSIR prevede la caratterizzazione di bio-molecole tramite l’acquisizione del loro spettro vibrazionale. A tale spettro viene poi associata un’immagine ottica, ottenendo quindi la correlazione tra il profilo morfologico di un campione e il suo contenuto chimico. Inoltre, l’uso della spettroscopia infrarossa permette una diretta analisi del campione senza l’uso di marcatori esterni o protocolli di fissazione. L’utilizzo di questa tecnica, sebbene molto potente e versatile, fino a pochi anni fa è stato limitato a campioni fissati o deidratati al fine di aggirare i problemi derivanti dal forte assorbimento delle molecole d’acqua nell’infrarosso, noti come “barriera di assorbimento dell’acqua”. L’utilizzo di tecniche di micro fabbricazione per la realizzazione di dispositivi trasparenti nelle regioni del visibile e dell’infrarosso ha permesso di sviluppare un nuovo e innovativo approccio allo studio di campioni biologici tramite MSIR, superando le limitazioni connesse alla “barriera di assorbimento dell’acqua” e quindi alla manipolazione di sistemi viventi. Inoltre, l’approccio micro fabbricativo è la migliore strategia per ottenere una perfetta riproducibilità del cammino ottico, necessaria per sottrarre dallo spettro vibrazionale il contributo dell’acqua e ricavare quindi le caratteristiche spettrali delle cellule. Nella parte iniziale di questo lavoro di tesi, si è rivolta particolare attenzione allo sviluppo di nuovi dispositivi microfluidici trasparenti nel visibile e nell’infrarosso caratterizzati da una lunga stabilità nelle condizioni di misura. I substrati comunemente usati nella MSIR (fluoruro di calcio o bario, CaF2 e BaF2 rispettivamente) hanno una bassa energia superficiale che richiede lo sviluppo di nuovi protocolli fabbricativi per l’ottenimento dei dispositivi. Durante questo lavoro è stata proposta una nuova strategia operativa, chiamata “silicon-like”, che prevede la modifica delle proprietà superficiali dei materiali tramite la deposizione di un sottile strato di silicio sulle finestre ottiche. Lo strato di silicio provoca un incremento dell’energia superficiale del substrato senza alterarne le proprietà ottiche e permette l’uso dei comuni resist come materiali strutturali. Tra questi, si è deciso di utilizzare l’SU-8 una resina epossidica con tono negativo le cui proprietà chimico-fisiche (resistenza ai solventi e all’ambiente acquoso) e la sua stabilità nel tempo soddisfano i requisiti imposti dalle condizioni di misura. Infine è stato sviluppato un nuovo protocollo di chiusura per i dispositivi, sfruttando le proprietà ottiche dell’SU-8. Grazie a queste innovazioni è stato possibile sviluppare una nuova generazione di dispositivi microfluidici dotati di grande stabilità nel tempo e ottima trasparenza nelle regioni del visibile e infrarosso. Successivamente i dispositivi sono stati impiegati per condurre diversi studi sia su cellule circolanti che in adesione tramite MSIR. Nello specifico, sono state caratterizzate le caratteristiche spettrali che distinguono ciascuna fase del ciclo cellulare per le cellule B16, i cambiamenti nel contenuto chimico di cellule MCF-7 indotte da stress di tipo termico e osmotico e i riarrangiamenti cellulari subiti dai monociti (U937) durante la progressione attraverso l’apoptosi. Tutti questi studi avevano l’intento di dimostrare l’utilità dell’approccio microfluidico allo studio di cellule vive tramite MSIR e validare le potenzialità della MSIR come tecnica di indagine diagnostica per i processi biochimici in vivo. Per questo, parallelamente agli esperimenti MSIR sono stati condotti degli esperimenti di citofluorimetria, una tecnica di routine in ambito biologico. Questa tesi dimostra le potenzialità della MSIR accoppiata alla microfluidica come mezzo di indagine bio-medica. Grazie al preciso controllo dell’ambiente cellulare e alla flessibilità ottenibile in termini di design degli esperimenti MSIR può essere vista come una nuova frontiera per la biologia moderna.
XXVI Ciclo
1986
El, Ouali Hassan. "Détection immunocytochimique de la laminine in vivo et in vitro au niveau du tube séminifère de rat au cours de l'ontogenèse". Nancy 1, 1990. http://www.theses.fr/1990NAN10545.
Texto completoZucchini, Nicolas. "Etude in vivo des cellules dendritiques plasmacytoïdes murines à l'infection par le cytomégalovirus murin". Aix-Marseille 2, 2009. http://theses.univ-amu.fr.lama.univ-amu.fr/2009AIX22090.pdf.
Texto completoPlasmacytoid dentritic cells (pDC) are characterized by their ability to rapidly produce high levels of type I interferon (IFN-I) in response to many viruses, especially during in vivo infection by murine cytomegalovirus (MCMV). PDC also contribute to the production of other cytokines. However, their relativecontribution to these functions compared to other cells in unclear. In addtition, the overall role of pDC in the host resistance to viral infection is difficult to study rigorously, partly beacause of the lack beacause of a method for the effective and specific depletion of these cells in vivo. The expressions of IFN-I, IL-2 and TNF-a were examined by multiparameter flow cytometry identify the cellular souces and molecular mechanisms involved in the production if innate cytokines in various tissues early after infection by MCMV. Splenic pDC are the main source of innate cytokines early after infection been identified to regulate these functions. In order to obtain different mouse models designed for the rigorous study of pDC functions, we are about to generate mice that express CRE recombinase specifically in pDC
Kasprzyk, Laetitia. "Caractérisation du facteur de transmission ZBTB4 in vivo & in vitro". Paris 7, 2013. http://www.theses.fr/2013PA077098.
Texto completoThe ZBTBs transcription factors play an important role in the organism. These factors are indeed involved in development, as well as in several processes that may lead to tumorigenesis. Three of these ZBTB factors, named Kaiso, ZBTB4 and ZBTB38, also belong to a protein family able to bind methylated DNA (MBP) and also implicated in essential cellular mechanisms. The goal of my graduate work was to initiate the characterization of one of these ZBTB-MBP protein, ZBTB4, by generating a mouse model. The preliminary results on the study of the mice phenotype, carrying an inhibitory mutation of the Zbtb4 gene, showed that the mice are viable, fertile, but display an overall lower weight, especially for three organs in particular : the brain, the heart and the kidneys. They also display a behavior trouble, with an increased tendency to anxiety. In parallel of this in vivo approach, an in vitro study of ZBTB4 showed results in favor to a tumor suppressor role. This work could thus give clues concerning the role of ZBTB4 in the organism
Breart, Béatrice. "Caractérisation du comportement des cellules NK in vivo". Nice, 2005. http://www.theses.fr/2005NICE4042.
Texto completoNatural killer (nk) cells are major actor of innate immunity, however their role in the immune system as their mechanism of activation and their cellular interactions are still poorly understood. During this ph. D, we have studied the nk cell behavior in course of the intracellular parasite leishmania major infection. Primary we have shown that, after parasite inoculation, nk cells are first recruited in the draining lymph node where they are activated and produce ifn-g, by a mechanism involving cd4+ cells, and are then detected in the lesion site three days after infection. We have also schown that nk cells, low motile cells, are localized in a strategic area of the lymph node, where the initiation of adaptativ immune response takes place, in close contact and in interaction with dc and t lymphocytes. These data suggest that nk cells have an activ role in the control of immune response. Finally we caracterize a new cell population which express classical marker of dc, cd11c and the nk cell marker, cd49b. This population is in fact a sub-population of nk cells which, in term of recruitment and activity, behave as nk cd11c-nk cells in course of l. Majors infection. In conclusion, our results identify, for the first time, an interaction in vivo between nk cell and dc and constitute a necessary prelude of further nk cell study in vivo
Maamar, Hédia. "Etude in vivo du système cellulolytique de Clostridium cellulolyticum : caractérisation du premier mutant d'insertion cipC". Aix-Marseille 1, 2003. http://www.theses.fr/2003AIX11034.
Texto completoDalle, Prisca. "Système intégré pour l'encapsulation monocouche de cellules". Thesis, Grenoble, 2012. http://www.theses.fr/2012GRENS036/document.
Texto completoEpileptic seizures arise from pathological synchronization of neuronal ensemble.Seizures originating from primary motor cortex are often pharmacoresistant, and many times unsuitable for respective surgery because of location of epileptic focus in eloquent area. Basal ganglia play important role in seizure propagation. Micro electrode recordings performed during previous studies indicated that input structures of basal ganglia such as GPe, Putamen and Subthalamic nucleus (STN) are strongly modified during seizures. For example the mean firing rate of neurons of the STN and Putamen increased and the percentage of oscillatory neurons synchronized with the ictal EEG was higher during seizures as compared to interictal periods. Pilot studies in humans have shown the possible beneficial effect of chronic DBS applied to STN in treatment of pharmacoresistant motor seizures. Our study was aimed at studying the therapeutic effect of electrical stimulation of input structures of basal ganglia . We first developed a stable, predictable primate model of focal motor epilepsy by intracortical injection of penicillin and we documented it's pharmacoresistence. We then stereotactically implanted DBS electrodes in the STN and Putamen. The stimulator was embedded at the back of the animals. Subthreshold electrical stimulations at 130 Hz were applied to STN. Stimulator was turned ON when penicillin was injected. Sham stimulation at 0 volt was used as a control situation, each monkey being its own control. The time course, number and duration of seizures occurring in each epochs of 1 h were compared during ON and sham stimulation periods. Each experimental session lasted uptoo 6 hours,We also studied preventive high frequency stimulation of STN and subthershold low frequency stimulation of Putamen with 5 Hz and 20 Hz in the same model .Finally we studied combined effects of high frequency STN and low frequency Putamen stimulation in one monkey Results: Data was analysed from 1572 seizures in 30 experiments in three monkeys for chronic STN stimulation , 454 seizures in 10 experiments in one moneky during preventive STN stimulation ,289 seizures from 14 experiments in two monkeys during LFS putamen stimulation and 477 seizures from 10 sessions during combined STN and Putamen stimulation in one monkey The best results were observed during chronic STN stimulation The occurrence of first seizure was significantly delayed as compared to sham situation. Total time spent in focal seizures was significantly reduced by ≥69% on an average (p ≤0.05) after STN stimulation, due to a significant decrease in the number of seizures especially so during the first 3 hours after stimulation. The duration of individual seizures reduced moderately. Bipolar and monopolar stimulation modes were equally effective Preventive HFS STN (in one specimen) was not found to be superior to acute stimulation. LFS Putamen alone was effective but mainly in first two hours of stimulation .In a combined HFS STN and LFS Putamen stimulation the effect of stimulation in terms of seizure control was modest and poor compared to HFS STN alone or LFS Putamen alone. This study provides original data in primates showing the potential therapeutic effect of chronic HFS-STN DBS to treat focal motor seizures . A discussion explaining these
De, Smedt Thibaut. "Maturation et apoptose des cellules dendritiques in vivo". Doctoral thesis, Universite Libre de Bruxelles, 1998. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212028.
Texto completoPezzella, Francesca Maria. "Studio ex vivo di rigenerazione epatica:valutazione biologico funzionale". Thesis, Università degli Studi di Catania, 2011. http://hdl.handle.net/10761/233.
Texto completoMesenchymal stem cells can represent a therapeutic alternative to organ transplantation in the treatment of liver diseases.This animal model study investigated liver function parameters (GOT, GPT, ALP) at different timepoints after organ regeneration with MSCs after CCL4-induced necrosis compared with normal organ regeneration controls.Hepatic functional recovery was significantively smaller in rats treated with stem cells compared with controls.These data demonstrated that the use of MSCs may ameliorate the treatment of hepatic desease
Nicolini, Benedetta <1981>. "Effetto della combinazione di cellule CD4+CD25+, cellule staminali emopoietiche CD34+e ATG nella prevenzione della risposta alloreattiva delle cellule T in vitro ed in vivo". Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2011. http://amsdottorato.unibo.it/3557/1/nicolini_benedetta_tesi_dottorato.pdf.
Texto completoLibros sobre el tema "Cellule vive"
Hoffman, Robert M., ed. In Vivo Cellular Imaging Using Fluorescent Proteins. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-797-2.
Texto completoIn vivo migration of immune cells. Boca Raton, Fla: CRC Press, 1987.
Buscar texto completoIn vivo cellular imaging using fluorescent proteins: Methods and protocols. New York: Humana Press, 2012.
Buscar texto completo1951-, Imhof Beat A., Berrih-Aknin Sonia 1955-, Ezine Sophie 1954- y International Conference on Lymphatic Tissues and Germinal Centers in Immune Reactions (10th : 1990 : Compiègne, France), eds. Lymphatic tissues and in vivo immune responses. New York: M. Dekker, 1991.
Buscar texto completoFerrick, David A. Transgenic mice as a in vivo model for self reactivity. Austin: R.G. Landes Co., 1994.
Buscar texto completoMorowitz, Harold J. Beginnings of cellular life: Metabolism recapitulatesbiogenesis. New Haven: Yale University Press, 1992.
Buscar texto completoCelle qui monte du désert: Récit d'une conversion. Paris: Médiaspaul, 2015.
Buscar texto completoBiology of normal proliferating cells in vitro: Relevance for in vivo aging. Basel: Karger, 1988.
Buscar texto completoBeginnings of cellular life: Metabolism recapitulates biogenesis. New Haven: Yale University Press, 1992.
Buscar texto completoVision: Quand la quête d'aujourd'hui était celle d'hier. Rouyn-Noranda, Québec: ABC de l'édition, 2010.
Buscar texto completoCapítulos de libros sobre el tema "Cellule vive"
London, Robert E. "In Vivo 2H NMR Studies of Cellular Metabolism". En In Vivo Spectroscopy, 277–306. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4757-9477-9_6.
Texto completoFrischknecht, Freddy, Rogerio Amino, Blandine Franke-Fayard, Chris Janse, Andrew Waters y Robert Ménard. "Imaging Parasites in Vivo". En Imaging Cellular and Molecular Biological Functions, 345–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71331-9_12.
Texto completoFlaherty, Lynne, John M. Harlan y Robert K. Winn. "Blockade of Leukocyte Adhesion in in Vivo Models of Inflammation". En Cellular Adhesion, 153–66. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2466-3_9.
Texto completoMiller, Sandra K. y Gabriel A. Elgavish. "Shift-Reagent-Aided 23Na NMR Spectroscopy in Cellular, Tissue, and Whole-Organ Systems". En In Vivo Spectroscopy, 159–240. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4757-9477-9_4.
Texto completoVan der Gouw, Lex. "Tracking and Traceability". En Quality Management and Accreditation in Hematopoietic Stem Cell Transplantation and Cellular Therapy, 83–88. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-64492-5_10.
Texto completoChan, Justin, Jayant P. Menon, Rohit Mahajan y Rahul Jandial. "In Vivo Imaging of Cellular Transplants". En Frontiers in Brain Repair, 1–12. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-5819-8_1.
Texto completoAndes, David R. "In Vivo Candida Device Biofilm Models". En Candida albicans: Cellular and Molecular Biology, 93–113. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-50409-4_7.
Texto completoHenschler, R., J. Winkler, D. Möbest, A. Spyridonidis, W. Lange y R. Mertelsmann. "Recent Developments in the Ex Vivo Manipulation of Hematopoietic Cells from Bone Marrow and Blood". En Cellular Therapy, 37–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-662-03509-2_3.
Texto completoFriedman, Mark T., Kamille A. West, Peyman Bizargity, Kyle Annen, H. Deniz Gur y Timothy Hilbert. "Serendipity, C’est La Vie". En Immunohematology, Transfusion Medicine, Hemostasis, and Cellular Therapy, 437–41. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-14638-1_59.
Texto completoBraun, Christina, Robert Knüppel, Jorge Perez-Fernandez y Sébastien Ferreira-Cerca. "Non-radioactive In Vivo Labeling of RNA with 4-Thiouracil". En Ribosome Biogenesis, 199–213. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2501-9_12.
Texto completoActas de conferencias sobre el tema "Cellule vive"
Zwick, H., B. E. Stuck, W. R. Elliott, D. J. Lund, S. T. Schuschereba y G. Li. "An Animal Model for In-Vivo Characterization of Laser Induced Retinal cellular Pathology and Recovery Processes". En In Vivo optical Imaging at the NIH. Washington, D.C.: Optica Publishing Group, 1999. http://dx.doi.org/10.1364/ivoi.1999.msi31.
Texto completoBoppart, Stephen A., Wolfgang Drexler, Uwe Morgner, Franz X. Kärtner y James G. Fujimoto. "Ultrahigh Resolution and Spectroscopic OCT Imaging of Cellular Morphology and Function". En In Vivo optical Imaging at the NIH. Washington, D.C.: Optica Publishing Group, 1999. http://dx.doi.org/10.1364/ivoi.1999.msi56.
Texto completoGoldschmidt, Ezequiel, Meghan Schneck, David Gau, Aidan Dadey, Bruno L., Zhipeng Li, Sally Wenzel, Eric Wang, Carl Snyderman y Paul Garnder. "Regenerated Oxidized Cellulose (Surgicel) Induces Nasal Epithelial Necrosis In Vivo by Acidifying the Cellular Environment". En 29th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1679506.
Texto completoOraevsky, Alexander, Elena V. Savateeva, Alexander A. Karabutov, Brent Bell, Richard Johnigan, Jay P. Pasricha y Massoud Motamedi. "Application of the confocal opto-acoustic tomography in detection of squamous epithelial carcinoma at early stages". En In Vivo optical Imaging at the NIH. Washington, D.C.: Optica Publishing Group, 1999. http://dx.doi.org/10.1364/ivoi.1999.dis153.
Texto completoWin, Zaw, Geoffrey D. Vrla, Emily N. Sevcik y Patrick W. Alford. "Microfluidic Device for Spatial Control of Cell Seeding in Engineered Tissues". En ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14510.
Texto completoZawadzki, Robert J., Suman Pilli, Dae Yu Kim, Sandra Balderas-Mata, Arlie G. Capps y John S. Werner. "Three-dimensional cellular resolution in-vivo retinal imaging". En Bio-Optics: Design and Application. Washington, D.C.: OSA, 2011. http://dx.doi.org/10.1364/boda.2011.bma3.
Texto completoPorter, Jason. "In vivo cellular imaging of the rodent retina". En Frontiers in Optics. Washington, D.C.: OSA, 2009. http://dx.doi.org/10.1364/fio.2009.fthq3.
Texto completoLeforestier, Claire. "Fontaines narratives de Jean GIono". En XXV Coloquio AFUE. Palabras e imaginarios del agua. Valencia: Universitat Politècnica València, 2016. http://dx.doi.org/10.4995/xxvcoloquioafue.2016.3039.
Texto completoBoppart, Stephen A., Gary J. Tearney, Brett E. Bouma, James G. Fujimoto y Mark E. Brezinski. "Optical Coherence Tomography of Embryonic Morphology During Cellular Differentiation". En Advances in Optical Imaging and Photon Migration. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/aoipm.1996.cit231.
Texto completoNg, Colin y Amrinder Nain. "Cellular Dynamics on Aligned Fibrous PLGA Scaffolds". En ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-54014.
Texto completoInformes sobre el tema "Cellule vive"
Eldar, Avigdor y Donald L. Evans. Streptococcus iniae Infections in Trout and Tilapia: Host-Pathogen Interactions, the Immune Response Toward the Pathogen and Vaccine Formulation. United States Department of Agriculture, diciembre de 2000. http://dx.doi.org/10.32747/2000.7575286.bard.
Texto completoMendez, Juan y Bruce Stillman. Investigation of the Causes of Breast Cancer at the Cellular Level: Isolation of In Vivo Binding Sites of the Human Origin Recognition Complex. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2001. http://dx.doi.org/10.21236/ada398164.
Texto completoMendez, Juan y Bruce Stillman. Investigation of the Causes of Breast Cancer at the Cellular Level: Isolation of In Vivo Binding Sites of the Human Origin Recognition Complex. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2002. http://dx.doi.org/10.21236/ada409474.
Texto completoMendez, Juan y Bruce Stillman. Investigation of the Causes of Breast Cancer at the Cellular Level: Isolation of In Vivo Binding Sites of the Human Origin Recognition Complex. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2000. http://dx.doi.org/10.21236/ada390687.
Texto completoDavidson, Irit, Hsing-Jien Kung y Richard L. Witter. Molecular Interactions between Herpes and Retroviruses in Dually Infected Chickens and Turkeys. United States Department of Agriculture, enero de 2002. http://dx.doi.org/10.32747/2002.7575275.bard.
Texto completoFromm, A., Avihai Danon y Jian-Kang Zhu. Genes Controlling Calcium-Enhanced Tolerance to Salinity in Plants. United States Department of Agriculture, marzo de 2003. http://dx.doi.org/10.32747/2003.7585201.bard.
Texto completoSchuster, Gadi y David Stern. Integrated Studies of Chloroplast Ribonucleases. United States Department of Agriculture, septiembre de 2011. http://dx.doi.org/10.32747/2011.7697125.bard.
Texto completoSukenik, Assaf, Paul Roessler y John Ohlrogge. Biochemical and Physiological Regulation of Lipid Synthesis in Unicellular Algae with Special Emphasis on W-3 Very Long Chain Lipids. United States Department of Agriculture, enero de 1995. http://dx.doi.org/10.32747/1995.7604932.bard.
Texto completoBarash, Itamar y Robert Rhoads. Translational Mechanisms Governing Milk Protein Levels and Composition. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7696526.bard.
Texto completoHansen, Peter J., Zvi Roth y Jeremy J. Block. Improving oocyte competence in dairy cows exposed to heat stress. United States Department of Agriculture, enero de 2014. http://dx.doi.org/10.32747/2014.7598163.bard.
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