Auswahl der wissenschaftlichen Literatur zum Thema „Decellularized matrix“
Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an
Inhaltsverzeichnis
Machen Sie sich mit den Listen der aktuellen Artikel, Bücher, Dissertationen, Berichten und anderer wissenschaftlichen Quellen zum Thema "Decellularized matrix" bekannt.
Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.
Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.
Zeitschriftenartikel zum Thema "Decellularized matrix"
Hashemi, Javad, Ghasem Barati und Bahram Bibak. „Decellularized Matrix Bioscaffolds“. Pancreas 50, Nr. 7 (August 2021): 942–51. http://dx.doi.org/10.1097/mpa.0000000000001868.
Der volle Inhalt der QuelleHashemi, Javad, Ghasem Barati und Bahram Bibak. „Decellularized Matrix Bioscaffolds“. Pancreas 50, Nr. 7 (August 2021): 942–51. http://dx.doi.org/10.1097/mpa.0000000000001868.
Der volle Inhalt der QuelleNakamura, Naoko, Ai Ito, Tsuyoshi Kimura und Akio Kishida. „Extracellular Matrix Induces Periodontal Ligament Reconstruction In Vivo“. International Journal of Molecular Sciences 20, Nr. 13 (03.07.2019): 3277. http://dx.doi.org/10.3390/ijms20133277.
Der volle Inhalt der QuelleMeyer, Tanja, Serghei Cebotari, Gudrun Brandes, Dagmar Hartung, Frank Wacker, Monika Theis, Tim Kaufeld et al. „Decellularized Porcine Pericardium Enhances Autologous Vascularized Matrix as a Prosthesis for Left Ventricular Full-Wall Myocardial Reconstruction“. Prosthesis 5, Nr. 1 (01.02.2023): 113–29. http://dx.doi.org/10.3390/prosthesis5010010.
Der volle Inhalt der QuelleBelviso, Immacolata, Anna Maria Sacco, Domenico Cozzolino, Daria Nurzynska, Franca Di Meglio, Clotilde Castaldo und Veronica Romano. „Cardiac-derived extracellular matrix: A decellularization protocol for heart regeneration“. PLOS ONE 17, Nr. 10 (19.10.2022): e0276224. http://dx.doi.org/10.1371/journal.pone.0276224.
Der volle Inhalt der QuelleWu, Jinglei, Jiazhu Xu, Yihui Huang, Liping Tang und Yi Hong. „Regional-specific meniscal extracellular matrix hydrogels and their effects on cell–matrix interactions of fibrochondrocytes“. Biomedical Materials 17, Nr. 1 (23.12.2021): 014105. http://dx.doi.org/10.1088/1748-605x/ac4178.
Der volle Inhalt der QuelleLing, You, Weikang Xu, Lifeng Yang, Changyan Liang und Bin Xu. „Improved the biocompatibility of cancellous bone with compound physicochemical decellularization process“. Regenerative Biomaterials 7, Nr. 5 (30.08.2020): 443–51. http://dx.doi.org/10.1093/rb/rbaa024.
Der volle Inhalt der QuelleRashidi, Farina, Mahdi Mohammadzadeh, Arash Abdolmaleki, Asadollah Asadi und Mehrdad Sheikhlou. „Acellular carotid scaffold and evaluation the biological and biomechanical properties for tissue engineering“. Journal of Cardiovascular and Thoracic Research 16, Nr. 1 (13.03.2024): 28–37. http://dx.doi.org/10.34172/jcvtr.32899.
Der volle Inhalt der QuelleBrennan, Jordan, Michael L. Lu und Yunqing Kang. „A New Model of Esophageal Cancers by Using a Detergent-Free Decellularized Matrix in a Perfusion Bioreactor“. Bioengineering 10, Nr. 1 (11.01.2023): 96. http://dx.doi.org/10.3390/bioengineering10010096.
Der volle Inhalt der QuelleBobrova, M. M., L. A. Safonova, O. I. Agapova, A. E. Efimov und I. I. Agapov. „The analysis of the proliferative activity of cells on microparticles obtained from decellularized liver and kidney tissue“. Russian Journal of Transplantology and Artificial Organs 20, Nr. 4 (31.01.2019): 69–75. http://dx.doi.org/10.15825/1995-1191-2018-4-69-75.
Der volle Inhalt der QuelleDissertationen zum Thema "Decellularized matrix"
Shah, Mickey. „Cardiac Repair Using A Decellularized Xenogeneic Extracellular Matrix“. University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1542631193281779.
Der volle Inhalt der QuelleMarengo, Kaitlyn A. „The Incorporation of Decellularized Cardiac ECM into Fibrin Microthreads“. Digital WPI, 2017. https://digitalcommons.wpi.edu/etd-theses/843.
Der volle Inhalt der QuelleYoung, Bethany M. „Novel Small Airway Model Using Electrospun Decellularized Lung Extracellular Matrix“. VCU Scholars Compass, 2016. http://scholarscompass.vcu.edu/etd/4273.
Der volle Inhalt der QuelleLi, Zhaoying. „Adaptive fabrication of biofunctional decellularized extracellular matrix niche towards complex engineered tissues“. Thesis, University of Cambridge, 2017. https://www.repository.cam.ac.uk/handle/1810/270349.
Der volle Inhalt der QuelleD'Angelo, Edoardo. „Decellularized colorectal cancer matrix as bioactive microenvironment for in vitro 3D cancer research“. Doctoral thesis, Università degli studi di Padova, 2018. http://hdl.handle.net/11577/3426811.
Der volle Inhalt der QuelleI modelli tumorali tridimensionali (3D) si stanno affacciando sul panorama scientifico con l’obiettivo primario di superare le limitazioni di colture cellulari convenzionali (2D) e modelli animali negli approcci di ricerca clinica. In questa tesi di dottorato, si descrive un innovativo approccio di ingegneria tissutale applicata alla ricerca oncologica mediante il quale, partendo da una biopsia tissutale decellularizzata, si genera un modello organo-tipico 3D bioattivo. Questo modello 3D, ricapitola, in vitro, l’ambiente ultra-strutturale del tessuto nativo come dimostrato da indagini istologiche, immunoistochimiche, di immunofluorescenza e di microscopia elettronica a scansione. L’analisi del proteoma e del secretoma mediante spettrometria di massa ha confermato una differente composizione stromale tra la mucosa colica sana decellularizzata e quella della controparte tumorale (CRC) in termini di proteine strutturali (Collagene 1A1, Collagene 1A2, Collagene 3A1) e di proteine secrete, come la Defensina alfa 3. Abbiamo dimostrato che le nostre matrici 3D mantengono le loro proprietà biologiche dopo il processo di decellularizzazione: mediante la CAM, abbiamo osservato un decremento del potenziale angiogenico della matrice decellularizzata di CRC comparata con la mucosa colica sana, causata da un effetto diretto della Defensina alfa 3. Inoltre, abbiamo dimostrato che dopo 5 giorni di ricellularizzazione con cellule HT-29 (linea stabilizzata di cancro del colon), le matrici tumorali 3D (comparate con le rispettive mucose coliche sane ed il metodo di coltura 2D) hanno indotto una sovra-espressione di IL-8, una chemochina a valle del pathway della Defensina alfa 3, che gioca un ruolo molto importante nella crescita e proliferazione tumorale. In conclusione, avendo dimostrato la capacità dei delle nostre matrici acellulari 3D di mucosa colica sana e CRC di mimare gli stimoli ultra-strutturali e biologici dei rispettivi tessuti nativi, crediamo che questo approccio possa essere un efficace strumento per migliorare il livello delle ricerche precliniche e nei test di screening di farmaci.
KC, Pawan. „Development of a Cardiac Patch with Decellularized Myocardial Tissue and Stem Cells“. University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1555413717363006.
Der volle Inhalt der QuelleHansen, Ryan. „Functional and Structural Analysis of Decellularized Liver Tissue Matrix, with Potential Applications in Cancer Tissue Engineering“. Case Western Reserve University School of Graduate Studies / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case1498650461817088.
Der volle Inhalt der QuelleMiyauchi, Yuya. „A novel three-dimensional culture system maintaining the physiological extracellular matrix of fibrotic model livers accelerates progression of hepatocellular carcinoma cells“. Kyoto University, 2018. http://hdl.handle.net/2433/232113.
Der volle Inhalt der QuelleTrignol, Aurélie. „The extracellular matrix as a biomaterial to optimize skeletal muscle regeneration“. Thesis, Lyon, 2019. http://www.theses.fr/2019LYSE1029.
Der volle Inhalt der QuelleSkeletal muscle exhibits high capacity for regeneration after an injury that relies on resident stem cells. Muscle regeneration is tightly regulated by both the immune response and other resident cells, as well as by cues from the local extracellular matrix (ECM), contributing to a coordinated repair process. Muscle ECM is a network of structural macromolecules with a large majority of collagens and trophic molecules such as glycosaminoglycans (GAGs). In the skeletal muscle tissue, ECM was overlooked due to its complex organization making investigations difficult. Muscle regenerative ability can be overtaken in large muscle wasting, such as in volumetric muscle loss (VML), leading to fibrosis formation and chronic inflammation. This type of injury predominantly occurs in traumatology and in war-wounded patients, with functional disability despite an optimal treatment. The use of biomaterials could provide the biochemical and physical cues that are missing in this pathologic repair. In this work we have focused on obtaining a biomaterial composed of skeletal muscle ECM. We have tested several decellularization protocols both to preserve the three-dimensional architecture of the muscle ECM and to completely remove cell components in order to avoid a deleterious immune response after implantation. However, the protocol did not allow the preservation of trophic molecules such as GAGs, in the scaffold.“ReGenerating Agents” (RGTA®) are functionally analogous of GAGs with a crucial property to resist enzymatic degradation. They function to restore a proper microenvironment for tissue healing with already a clinical application in skin and corneal repair. We have explored the effects of RGTA® in muscle regeneration using an in vivo model in mouse. At early time of regeneration (day 8), we performed histologic analysis. We showed that regenerating myofibers contained more nuclei in the treated animals, in favor of an increase of progenitor fusion, which has been validated in vitro in myogenic cultures. The number of capillaries was higher in favor of a better angiogenesis. Lipid droplets, a marker of impaired regeneration, were reduced by RGTA® administration. At later time of regeneration (day 28), capillary number was still improved in favor of a durable effect of RGTA® on angiogenesis. RGTA® could be incorporated into biomaterials and are particularly resistant in an inflammatory environment, such as that occurring after a VML injury. Chemokines and growth factors could also be added in ECM-based scaffolds to promote the migration of progenitors that are essential for myofiber neoformation. Therapeutic efficacy of these optimized biomaterials will require to be evaluated in an in vivo model of VML
Pouliot, Robert A. „DEVELOPMENT AND CHARACTERIZATION OF LUNG DERIVED EXTRACELLULAR MATRIX HYDROGELS“. VCU Scholars Compass, 2016. http://scholarscompass.vcu.edu/etd/4465.
Der volle Inhalt der QuelleBücher zum Thema "Decellularized matrix"
Yamaoka, Tetsuji, und Takashi Hoshiba, Hrsg. Decellularized Extracellular Matrix. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998.
Der volle Inhalt der QuelleYamaoka, Tetsuji, und Takashi Hoshiba. Decellularized Extracellular Matrix: Characterization, Fabrication and Applications. Royal Society of Chemistry, The, 2019.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Decellularized matrix"
Hoshiba, Takashi, und Tetsuji Yamaoka. „CHAPTER 1. Extracellular Matrix Scaffolds for Tissue Engineering and Biological Research“. In Decellularized Extracellular Matrix, 1–14. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00001.
Der volle Inhalt der QuelleYamaoka, Tetsuji. „CHAPTER 2. Preparation Methods for Tissue/Organ-derived dECMs – Effects on Cell Removal and ECM Changes“. In Decellularized Extracellular Matrix, 15–28. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00015.
Der volle Inhalt der QuelleHoshiba, T., N. Kawazoe und G. Chen. „CHAPTER 3. Preparation of Cultured Cell-derived Decellularized Matrix (dECM) – Factors Influencing dECM Formation and Its Ability“. In Decellularized Extracellular Matrix, 29–50. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00029.
Der volle Inhalt der QuelleMochitate, Katsumi, Reiko Nagano und Yukiko Toya-Nakajima. „CHAPTER 4. Bared Basement Membrane Substrata: Design, Cellular Assembly, Decellularization and Application to Tissue Regeneration and Stem Cell Differentiation“. In Decellularized Extracellular Matrix, 51–76. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00051.
Der volle Inhalt der QuelleMorimoto, Naoki, Atsushi Mahara und Tetsuji Yamaoka. „CHAPTER 5. A Novel Treatment for Giant Congenital Melanocytic Nevi Combining Inactivated Nevus Tissue by Pressurization and Cultured Epidermal Autograft“. In Decellularized Extracellular Matrix, 77–94. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00077.
Der volle Inhalt der QuelleScanameo, Alexandra, und Nicholas P. Ziats. „CHAPTER 6. Immune Responses to Decellularized Matrices“. In Decellularized Extracellular Matrix, 95–115. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00095.
Der volle Inhalt der QuelleDuran, Pamela, Marianna Alperin und Karen L. Christman. „CHAPTER 7. Decellularized Extracellular Matrix Hydrogels: Fabrication, Properties, Characterization, and Current Applications“. In Decellularized Extracellular Matrix, 116–38. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00116.
Der volle Inhalt der QuelleDas, Sanskrita, Anthony Safaa Mukhtar, Jinah Jang und Jin-Hyung Shim. „CHAPTER 8. Decellularized Extracellular Matrix as Bioink for 3D-Bioprinting“. In Decellularized Extracellular Matrix, 139–62. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00139.
Der volle Inhalt der QuelleHwang, Mintai P., und Kwideok Park. „CHAPTER 9. Mechanical Property Tunable dECM and Their Regenerative Applications“. In Decellularized Extracellular Matrix, 163–78. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00163.
Der volle Inhalt der QuelleHodde, J. P. „CHAPTER 10. Use of Small Intestinal Submucosa dECM in Tissue Engineering and Regenerative Medicine“. In Decellularized Extracellular Matrix, 179–98. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015998-00179.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Decellularized matrix"
Shchotkina, Nataliia V., Anatoliy A. Sokol, Glib I. Yemets, Oleksandr Yu Galkin, Liudmyla V. Dolinchuk, Iryna M. Skorokhod, Olena V. Shepeleva, Nadiia M. Rudenko und Iliia M. Yemets. „Microarchitectonic of Decellularized Bovine Pericardium Matrix“. In The 7th World Congress on New Technologies. Avestia Publishing, 2021. http://dx.doi.org/10.11159/icbb21.167.
Der volle Inhalt der QuelleTas, S., D. A. Bölükbas, H. N. Alsafadi, I. A. Da Silva, M. M. De Santis, E. Rehnberg, I. Tamargo, S. Mohlin, S. Lindstedt und D. E. Wagner. „Decellularized extracellular matrix hydrogels for human airway organoid culture“. In ERS Lung Science Conference 2021 abstracts. European Respiratory Society, 2021. http://dx.doi.org/10.1183/23120541.lsc-2021.101.
Der volle Inhalt der QuelleKuhlin, B., J. Kern, D. Gvaramia, N. Rotter, H. Tritschler, Y. Jakob, L. Körber, R. Breiter und RE Brenner. „Detection of matrix metalloproteinases after seeding a decellularized extracellular matrix with chondrogenic progenitor cells“. In Abstract- und Posterband – 90. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Digitalisierung in der HNO-Heilkunde. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1686890.
Der volle Inhalt der QuelleGvaramia, D., J. Kern, Y. Jakob, L. Huber und N. Rotter. „The Response of Primary Human Macrophages to Decellularized Cartilage Extracellular Matrix“. In Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1711446.
Der volle Inhalt der QuellePrice, AP, TR Metz und A. Panoskaltsis-Mortari. „Decellularized Lung as a 3-D Matrix for Bioengineering the Lung.“ In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5382.
Der volle Inhalt der QuelleGvaramia, D., J. Kern, Y. Jakob, L. Huber, J. Kzhyshkowska und N. Rotter. „The Response of Primary Human Macrophages to Decellularized Cartilage Extracellular Matrix“. In 100 JAHRE DGHNO-KHC: WO KOMMEN WIR HER? WO STEHEN WIR? WO GEHEN WIR HIN? Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1728945.
Der volle Inhalt der QuelleZhao, Shijia, Linxia Gu, James M. Hammel und Haili Lang. „Mechanical Characterization of the Decellularized Porcine Small Intestinal Submucosa Extracellular Matrix“. In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-65640.
Der volle Inhalt der QuelleSinem, Tas, Deniz A. Bölükbas, Hani N. Alsafadi, Iran An Da Silva, Martina M. De Santis, Emil Rehnberg, Isabel Tamargo, Sophie Mohlin, Sandra Lindstedt und Darcy E. Wagner. „LSC - 2021 - Decellularized extracellular matrix hydrogels for human airway organoid culture“. In ERS International Congress 2021 abstracts. European Respiratory Society, 2021. http://dx.doi.org/10.1183/13993003.congress-2021.oa1614.
Der volle Inhalt der QuelleWirtzfeld, L. A., E. S. L. Berndl und M. C. Kolios. „Ultrasonic characterization of extra-cellular matrix in decellularized murine kidney and liver“. In 2015 IEEE International Ultrasonics Symposium (IUS). IEEE, 2015. http://dx.doi.org/10.1109/ultsym.2015.0170.
Der volle Inhalt der QuelleGodin, Lindsay M., Andrew P. Price und Angela Panoskaltsis-Mortari. „Characterization Of Decellularized Lung Matrix After FITC-Induced Lung Injury In Mice“. In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a1030.
Der volle Inhalt der Quelle