Littérature scientifique sur le sujet « RPE in-Cell »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Sommaire
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « RPE in-Cell ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "RPE in-Cell"
Kuznetsova, Alla V., Alexander M. Kurinov et Maria A. Aleksandrova. « Cell Models to Study Regulation of Cell Transformation in Pathologies of Retinal Pigment Epithelium ». Journal of Ophthalmology 2014 (2014) : 1–18. http://dx.doi.org/10.1155/2014/801787.
Texte intégralMarrs, J. A., C. Andersson-Fisone, M. C. Jeong, L. Cohen-Gould, C. Zurzolo, I. R. Nabi, E. Rodriguez-Boulan et W. J. Nelson. « Plasticity in epithelial cell phenotype : modulation by expression of different cadherin cell adhesion molecules. » Journal of Cell Biology 129, no 2 (15 avril 1995) : 507–19. http://dx.doi.org/10.1083/jcb.129.2.507.
Texte intégralSzatmári-Tóth, Mária, Tanja Ilmarinen, Alexandra Mikhailova, Heli Skottman, Anu Kauppinen, Kai Kaarniranta, Endre Kristóf et al. « Human Embryonic Stem Cell-Derived Retinal Pigment Epithelium-Role in Dead Cell Clearance and Inflammation ». International Journal of Molecular Sciences 20, no 4 (20 février 2019) : 926. http://dx.doi.org/10.3390/ijms20040926.
Texte intégralDaniele, Elena, Lorenzo Bosio, Noor Ahmed Hussain, Barbara Ferrari, Stefano Ferrari, Vanessa Barbaro, Brian McArdle et al. « Denuded Descemet’s membrane supports human embryonic stem cell-derived retinal pigment epithelial cell culture ». PLOS ONE 18, no 2 (6 février 2023) : e0281404. http://dx.doi.org/10.1371/journal.pone.0281404.
Texte intégralKindzelskii, Andrei L., Victor M. Elner, Susan G. Elner, Dongli Yang, Bret A. Hughes et Howard R. Petty. « Toll-Like Receptor 4 (TLR4) of Retinal Pigment Epithelial Cells Participates in Transmembrane Signaling in Response to Photoreceptor Outer Segments ». Journal of General Physiology 124, no 2 (26 juillet 2004) : 139–49. http://dx.doi.org/10.1085/jgp.200409062.
Texte intégralVoisin, Audrey, Christelle Monville, Alexandra Plancheron, Emile Béré, Afsaneh Gaillard et Nicolas Leveziel. « Cathepsin B pH-Dependent Activity Is Involved in Lysosomal Dysregulation in Atrophic Age-Related Macular Degeneration ». Oxidative Medicine and Cellular Longevity 2019 (6 décembre 2019) : 1–15. http://dx.doi.org/10.1155/2019/5637075.
Texte intégralArai, Rei, Ayumi Usui-Ouchi, Yosuke Ito, Keitaro Mashimo, Akira Murakami et Nobuyuki Ebihara. « Effects of Secreted Mast Cell Mediators on Retinal Pigment Epithelial Cells : Focus on Mast Cell Tryptase ». Mediators of Inflammation 2017 (2017) : 1–10. http://dx.doi.org/10.1155/2017/3124753.
Texte intégralHellinen, Laura, Heidi Hongisto, Eva Ramsay, Kai Kaarniranta, Kati-Sisko Vellonen, Heli Skottman et Marika Ruponen. « Drug Flux Across RPE Cell Models : The Hunt for An Appropriate Outer Blood–Retinal Barrier Model for Use in Early Drug Discovery ». Pharmaceutics 12, no 2 (19 février 2020) : 176. http://dx.doi.org/10.3390/pharmaceutics12020176.
Texte intégralGupta, Santosh, Lyubomyr Lytvynchuk, Taras Ardan, Hana Studenovska, Georgina Faura, Lars Eide, Ljubo Znaor et al. « Retinal Pigment Epithelium Cell Development : Extrapolating Basic Biology to Stem Cell Research ». Biomedicines 11, no 2 (23 janvier 2023) : 310. http://dx.doi.org/10.3390/biomedicines11020310.
Texte intégralKamao, Hiroyuki, Atsushi Miki et Junichi Kiryu. « ROCK Inhibitor-Induced Promotion of Retinal Pigment Epithelial Cell Motility during Wound Healing ». Journal of Ophthalmology 2019 (19 juin 2019) : 1–10. http://dx.doi.org/10.1155/2019/9428738.
Texte intégralThèses sur le sujet "RPE in-Cell"
Spencer, Samantha A. « The Role of tfec in Zebrafish Neural Crest Cell and RPE Development ». VCU Scholars Compass, 2015. http://scholarscompass.vcu.edu/etd/3754.
Texte intégralGentles, Jeremy A., William G. Hornsby, Howard S. Gray, Jonathan A. Miller, Andy R. Dotterweich, Charles A. Stuart et Michael H. Stone. « Changes in Cell Free DNA During a College Soccer Season ». Digital Commons @ East Tennessee State University, 2015. https://dc.etsu.edu/etsu-works/3795.
Texte intégralPierro, Annalisa. « Protein structural dynamics in bacteria via nitroxide-based SDSL-EPR spectroscopy : from method improvements to in-cell studies ». Electronic Thesis or Diss., Aix-Marseille, 2021. http://theses.univ-amu.fr.lama.univ-amu.fr/211116_PIERRO_290xrxu60ryzjfl293g970fjmdnl_TH%20(1).pdf.
Texte intégralThe study of biomolecules in their native environment has been one of the main goals of structural biology in the last decade. As a result, we are assisting to a remarkable increase of new "in-cell" approaches, like Cryo-ET, FRET and NMR. Among these approaches, Site-Directed Spin Labeling (SDSL) coupled to Electron Paramagnetic Resonance (EPR) spectroscopy shows competitive and advantageous features to capture protein dynamics inside cells. In particular, nitroxide-based SDSL-EPR combines the advantages of high sensitivity and the lack of size constraints on the biomolecule of interest with the ability to capture protein structural transitions and interactions at physiological temperature. Despite the methodological advancements of the technique that have allowed the community to obtain increasingly relevant results, progresses still need to be done.In this work, the main limitation of nitroxide-based SDSL-EPR has been addressed. In the first time, we focused on the development of delivery methods to introduce the labeled protein in bacterial cells. Next, the stability of nitroxide labels in reducing environments and in-cell has been assessed, monitoring in parallel the viability of the cells during the EPR measurements. Thanks to the results achieved in this methodological part, we were able to study the structural dynamics of two flexible chaperone proteins directly in bacterial cells: NarJ from Escherichia coli and UreG from Sporosarcina pasteurii. Finally, to go further in understanding the impact of the cellular environment on the protein dynamics, the data obtained in cellular context were compared with those obtained in vitro or in a cell-mimicking environment
Guo, Shuangli. « ROLE OF REPLICATION PROTEIN A (RPA) AND PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) IN DNA MISMATCH REPAIR ». UKnowledge, 2005. http://uknowledge.uky.edu/gradschool_diss/258.
Texte intégralGuo, Shuangli. « Role of DNA replication proteina (RPA) and proliferating cell nuclear antigen (PCNA) in human DNA mismatch repair ». Lexington, Ky. : [University of Kentucky Libraries], 2005. http://lib.uky.edu/ETD/ukybioc2005d00284/etd.pdf.
Texte intégralTitle from document title page (viewed on November 7, 2005). Document formatted into pages; contains x, 3 p. : ill. Includes abstract and vita. Includes bibliographical references (p. 84-92).
Davoren, Jonathan M., et University of Lethbridge Faculty of Arts and Science. « Gene expression in a microspore-derived cell suspension culture of Brassica Napus exhibiting enhanced oil production ». Thesis, Lethbridge, Alta. : University of Lethbridge, Faculty of Arts and Science, 1997, 1997. http://hdl.handle.net/10133/345.
Texte intégralxxi, 256 leaves : ill. ; 28 cm.
Pourazadi, Ehsan. « Facile Synthesis of Boron-doped Graphitic Materials for Oxygen Reduction Purpose in Fuel Cell ». Thesis, The University of Sydney, 2016. http://hdl.handle.net/2123/16032.
Texte intégralWolk, Alyson M. « The Role of the Retinal Pigment Epithelium in Sorsby Fundus Dystrophy ». Case Western Reserve University School of Graduate Studies / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1606842751125309.
Texte intégralDu, Plessis Peter Clark. « Variations in radiosensitivity of breast cancer and normal breast cell lines using a 200MeV clinical proton beam ». Thesis, Cape Peninsula University of Technology, 2018. http://hdl.handle.net/20.500.11838/2970.
Texte intégralBackground: Breast cancer is one of the most commonly diagnosed among woman in South Africa, and a more resilient effort should be focused on treatment improvements. Worldwide, proton therapy is increasingly used as a radiation treatment alternative to photon therapy for breast cancer, mostly to decrease the risk for radiation-induced cardiovascular toxicity. This in vitro study aims to determine a better understanding of the radiosensitivity of both tumour and normal breast cell lines to clinical proton irradiation. In addition, we propose to investigate whether the increase in linear energy transfer (LET) towards the distal part of the proton beam results in an increase in relative biological effectiveness (RBE) for both cell lines. Methods: Malignant (MCF-7) and non-malignant (MCF-10A) breast cells were irradiated at different water equivalent depths in a 200 MeV proton beam at NRF iThemba LABS using a custom-made Perspex phantom: the entrance plateau, 3 points on the Bragg peak, the D80% and the D40%. A cytokinesis-block Micronucleus (CBMN) assay was performed and Micronuclei (MNi) were manually counted in binucleated cells (BNCs) using fluorescent microscopy. Reference dosimetry was carried out with a Markus chamber and irradiations were performed with a clinical proton beam generated at NRF iThemba LABS that was degraded to a R50 (half-value depths) range of 120 mm, with a field size of 10 cm x 10 cm and a 50 mm SOBP. The phantom could be adjusted to accommodate different perspex plates depending on the depth required within the proton beam. Cells were then exposed to 0.5, 1.0, 2.0, 3.0 and 4.0 Gy doses for each cell line independently and for each dose point. Results and Discussion: For the CBMN results, a program was developed on Matlab platform to calculate the 95% confidence ellipse on the co-variance parameters α and β. These values were determined by fitting the linear quadratic dose response curve to the average number of radiation induced MNi per 1000 BN cells. The ellipse region around a coordinate (the average MN frequency) for both MCF-7 and MCF-10A cells at the plateau region was defined by the mean estimate of the α-value and the β-value that were plotted on the X-axis and Y-axis respectively. The ratio of the two parameters, α/β, is a measure of the impact of fractionation to determine the biological effective dose. In fractionated proton therapy, the MCF10A cells will repair less between two fractions compared to the MCF7 cells. This is not an indication of therapeutic gain from a fractioned treatment protocol. For this reason, the hypofractionated stereotactic treatment protocols that can be applied with protons could be to the befit of the breast cancer patient. The above argument is based only on the radiosensitivity of the two cell lines exposed in the plateau region. Further analysis of the 95% confidence ellipse of both cell lines also showed a clear increase of the alpha value toward the distal portion of the beam and indicates an increase in energy transfer in this region. The gradual increase in α and β parameters with depth for protons for both cells is of clinical importance, since it implicates a non-homogeneous dose within the targeted area and an unwanted high dose behind the targeted area. Distal energy modulation could be investigated especially with larger breast tumours. RBE was calculated as the ratio of the dose at the different positions to the dose at the entrance plateau position (reference) to obtain an equal level of biological effect. A statistically significant difference in radiosensitivity could be observed between malignant and non-malignant cells at all positions (p<0.05). The variation in RBE was between 0.99 to 1.99 and 0.92 to 1.6 for the MCF-7 and MCF10A cell respectively. Conclusions: There is a variation in RBE along the depth-dose profile of a clinical proton beam. In addition, there is difference in radiosensitivity between the cancerous cells and the normal breast cells. While this study highlights a variation in sensitivity between cells it could be used by the modelling community to further develop biologically motivated treatment planning for proton therapy.
Shani, Saeideh. « The implication of cell-derived microvesicles in retinal pigment epithelium degeneration ». Thèse, 2018. http://hdl.handle.net/1866/22150.
Texte intégralLivres sur le sujet "RPE in-Cell"
Bengtsson, Staffan. Studies on structures and properties of soluble cell-well polysaccharides in rye and barley. Uppsala : Swedish University of Agricultural Sciences, Dept. of Food Science, 1991.
Trouver le texte intégralMonoclonal antibodies : Principles and practice : production and application of monoclonal antibodies in cell biology, biochemistry, and immunology. 2e éd. London : Academic Press, 1986.
Trouver le texte intégralRape in Holding Cell 6. Nazca Plains Corporation, The, 2011.
Trouver le texte intégralRape In Holding Cell 6. Nazca Plains Corporation, 2010.
Trouver le texte intégralSullivan, Kyle Michel. Rape in Holding Cell 6. KMSCB, 2014.
Trouver le texte intégralMcGough, Michael. A Field Guide to the Culture Wars. Greenwood Publishing Group, Inc, 2008. http://dx.doi.org/10.5040/9798400650796.
Texte intégralGlausser, Wayne. Entanglement. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190864170.003.0001.
Texte intégralTallacchini, Mariachiara. Medical Technologies and EU Law : The Evolution of Regulatory Approaches and Governance. Oxford University Press, 2017. http://dx.doi.org/10.1093/acprof:oso/9780198807216.003.0002.
Texte intégralIzzedine, Hassan, et Victor Gueutin. Drug-induced acute tubulointerstitial nephritis. Sous la direction de Adrian Covic. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0084.
Texte intégralSnyder, Jeremy. Exploiting Hope. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780197501252.001.0001.
Texte intégralChapitres de livres sur le sujet "RPE in-Cell"
Qin, Suofu. « Roles for AMP-Activated Protein Kinase in RPE Cell Function ». Dans Retinal Degenerative Diseases, 745–51. Boston, MA : Springer US, 2011. http://dx.doi.org/10.1007/978-1-4614-0631-0_95.
Texte intégralRashid, Alia, Shagun K. Bhatia, Karina I. Mazzitello, Micah A. Chrenek, Qing Zhang, Jeffrey H. Boatright, Hans E. Grossniklaus, Yi Jiang et John M. Nickerson. « RPE Cell and Sheet Properties in Normal and Diseased Eyes ». Dans Retinal Degenerative Diseases, 757–63. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17121-0_101.
Texte intégralKhristov, Vladimir, Arvydas Maminishkis, Juan Amaral, Aaron Rising, Kapil Bharti et Sheldon Miller. « Validation of iPS Cell-Derived RPE Tissue in Animal Models ». Dans Retinal Degenerative Diseases, 633–40. Cham : Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-75402-4_77.
Texte intégralYamada, H., N. Ogata, C. Yamamoto, M. Miyashiro, M. Uyama et A. Del Monte. « Localization of bFGF in wound healing process of RPE cell in vitro ». Dans Documenta Ophthalmologica Proceedings Series, 89–93. Dordrecht : Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5137-5_13.
Texte intégralHazim, Roni, Mei Jiang, Julian Esteve-Rudd, Tanja Diemer, Vanda S. Lopes et David S. Williams. « Live-Cell Imaging of Phagosome Motility in Primary Mouse RPE Cells ». Dans Retinal Degenerative Diseases, 751–55. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17121-0_100.
Texte intégralSkottman, Heli. « RPE and Stem Cell Therapy ». Dans Retinal Pigment Epithelium in Health and Disease, 249–63. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28384-1_14.
Texte intégralDetrick, Barbara, et John J. Hooks. « The RPE Cell and the Immune System ». Dans Retinal Pigment Epithelium in Health and Disease, 101–14. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28384-1_6.
Texte intégralBen M’Barek, Karim, Walter Habeler, Florian Regent et Christelle Monville. « Developing Cell-Based Therapies for RPE-Associated Degenerative Eye Diseases ». Dans Pluripotent Stem Cells in Eye Disease Therapy, 55–97. Cham : Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28471-8_3.
Texte intégralHazim, Roni A., et David S. Williams. « Cell Culture Analysis of the Phagocytosis of Photoreceptor Outer Segments by Primary Mouse RPE Cells ». Dans Methods in Molecular Biology, 63–71. New York, NY : Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7720-8_4.
Texte intégralKuhns, Stefanie, Alice Dupont Juhl, Zeinab Anvarian, Daniel Wüstner, Lotte B. Pedersen et Jens S. Andersen. « Endogenous Tagging of Ciliary Genes in Human RPE1 Cells for Live-Cell Imaging ». Dans Methods in Molecular Biology, 147–66. New York, NY : Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3507-0_9.
Texte intégralActes de conférences sur le sujet "RPE in-Cell"
Delori, François C. « Fluorophotometer for Noninvasive Measurement of RPE Lipofuscin ». Dans Noninvasive Assessment of the Visual System. Washington, D.C. : Optica Publishing Group, 1992. http://dx.doi.org/10.1364/navs.1992.tuc3.
Texte intégralKelly, Michael W., et Charles P. Lin. « Microcavitation and cell injury in RPE cells following short-pulsed laser irradiation ». Dans BiOS '97, Part of Photonics West, sous la direction de Steven L. Jacques. SPIE, 1997. http://dx.doi.org/10.1117/12.275473.
Texte intégralGlickman, Randolph D., Meena Vendal, Mary Ann Gonzalez et Neeru Kumar. « Intracellular photochemical reactions in the RPE cell exhibit a wavelength dependence that resembles the action spectrum of melanin ». Dans BiOS '99 International Biomedical Optics Symposium, sous la direction de Steven L. Jacques, Gerhard J. Mueller, Andre Roggan et David H. Sliney. SPIE, 1999. http://dx.doi.org/10.1117/12.349992.
Texte intégralBrinkmann, Ralf, Jan Roegener, Charles P. Lin, Johann Roider, Reginald Birngruber et Gereon Huettmann. « Selective RPE photodestruction : mechanism of cell damage by pulsed-laser irradiance in the ns to μm time regime ». Dans BiOS '99 International Biomedical Optics Symposium, sous la direction de Steven L. Jacques, Gerhard J. Mueller, Andre Roggan et David H. Sliney. SPIE, 1999. http://dx.doi.org/10.1117/12.350041.
Texte intégralPatel, Gaurav, Hitesh Tekchandani et Shrish Verma. « Intermediate Generation Selection Attention and Multi-scale Feature Aggregation for segmentation of cell regions in RPE implant absorbance images ». Dans 2020 IEEE 17th India Council International Conference (INDICON). IEEE, 2020. http://dx.doi.org/10.1109/indicon49873.2020.9342342.
Texte intégralSchüle, Georg, Elke Joachimmeyer, Carsten Framme, Johann Roider, Reginald Birngruber et Ralf Brinkmann. « Optoacoustic detection of selective RPE cell damage during µs-laser irradiation ». Dans European Conference on Biomedical Optics. Washington, D.C. : Optica Publishing Group, 2001. http://dx.doi.org/10.1364/ecbo.2001.4433_92.
Texte intégralZhang, Xiongjun, Jun Zhang, Dengsheng Wu, Jiangang Zheng, Mingzhong Li, Kuixing Zheng, Jingqin Su et Feng Jing. « Progress of rep-rate plasma Pockels cell technology in RCLF ». Dans SPIE LASE, sous la direction de Abdul A. S. Awwal, A. Mike Dunne, Hiroshi Azechi et Brian E. Kruschwitz. SPIE, 2011. http://dx.doi.org/10.1117/12.876549.
Texte intégralRuby, Douglas S., Saleem Zaidi, S. Narayanan, Satoshi Yamanaka et Ruben Balanga. « RIE-Texturing of Industrial Multicrystalline Silicon Solar Cells ». Dans ASME 2003 International Solar Energy Conference. ASMEDC, 2003. http://dx.doi.org/10.1115/isec2003-44003.
Texte intégralZhao, Yu, Ignas Niemegeers et Sonia Heemstra de Groot. « Power Allocation in mmWave Cell-F ree Massive MIMO with User Mobility Using Deep Learning ». Dans 2020 IEEE 20th International Conference on Communication Technology (ICCT). IEEE, 2020. http://dx.doi.org/10.1109/icct50939.2020.9295936.
Texte intégralChitakudige, Ramachandra, Sarat Kumar Dash et A. M. Khan. « Deprocessing Methodologies for Detection of IBC and Cell-to-Cell Shorts in Submicron DRAM ». Dans ISTFA 2012. ASM International, 2012. http://dx.doi.org/10.31399/asm.cp.istfa2012p0383.
Texte intégralRapports d'organisations sur le sujet "RPE in-Cell"
Carpita, Nicholas C., Ruth Ben-Arie et Amnon Lers. Pectin Cross-Linking Dynamics and Wall Softening during Fruit Ripening. United States Department of Agriculture, juillet 2002. http://dx.doi.org/10.32747/2002.7585197.bard.
Texte intégralManulis, Shulamit, Christine D. Smart, Isaac Barash, Guido Sessa et Harvey C. Hoch. Molecular Interactions of Clavibacter michiganensis subsp. michiganensis with Tomato. United States Department of Agriculture, janvier 2011. http://dx.doi.org/10.32747/2011.7697113.bard.
Texte intégralPrusky, Dov, Noel T. Keen et Stanley Freeman. Elicitation of Preformed Antifungal Compounds by Non-Pathogenic Fungus Mutants and their Use for the Prevention of Postharvest Decay in Avocado Fruits. United States Department of Agriculture, janvier 1996. http://dx.doi.org/10.32747/1996.7570573.bard.
Texte intégralFriedmann, Michael, Charles J. Arntzen et Hugh S. Mason. Expression of ETEC Enterotoxin in Tomato Fruit and Development of a Prototype Transgenic Tomato for Dissemination as an Oral Vaccine in Developing Countries. United States Department of Agriculture, mars 2003. http://dx.doi.org/10.32747/2003.7585203.bard.
Texte intégralSengupta-Gopalan, Champa, Shmuel Galili et Rachel Amir. Improving Methionine Content in Transgenic Forage Legumes. United States Department of Agriculture, février 2001. http://dx.doi.org/10.32747/2001.7580671.bard.
Texte intégralFahima, Tzion, et Jorge Dubcovsky. Map-based cloning of the novel stripe rust resistance gene YrG303 and its use to engineer 1B chromosome with multiple beneficial traits. United States Department of Agriculture, janvier 2013. http://dx.doi.org/10.32747/2013.7598147.bard.
Texte intégralHovav, Ran, Peggy Ozias-Akins et Scott A. Jackson. The genetics of pod-filling in peanut under water-limiting conditions. United States Department of Agriculture, janvier 2012. http://dx.doi.org/10.32747/2012.7597923.bard.
Texte intégral