Littérature scientifique sur le sujet « In vitro standardization »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « In vitro standardization ».
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 "In vitro standardization"
Yman, Lars. « Standardization of in vitro methods ». Allergy 56, s67 (avril 2001) : 70–74. http://dx.doi.org/10.1111/j.1398-9995.2001.00921.x.
Texte intégralGoggs, Robert, Antonio Borrelli, Benjamin M. Brainard, Daniel L. Chan, Armelle de Laforcade, Isabelle Goy-Thollot, Karl E. Jandrey et al. « Multicenter in vitro thromboelastography and thromboelastometry standardization ». Journal of Veterinary Emergency and Critical Care 28, no 3 (31 mars 2018) : 201–12. http://dx.doi.org/10.1111/vec.12710.
Texte intégralChander, NGopi. « Standardization of in vitro studies ». Journal of Indian Prosthodontic Society 16, no 3 (2016) : 227. http://dx.doi.org/10.4103/0972-4052.186399.
Texte intégralPooja, A., Sapna Panwar, A. K. Tiwari et Gunjeet Kumar. « Standardization of in vitro regeneration protocol in annual chrysanthemum ». Indian Journal of Horticulture 78, no 1 (2021) : 46–52. http://dx.doi.org/10.5958/0974-0112.2021.00007.4.
Texte intégralAhmad, Sayeed, Mhaveer Singh, MohammadA Khan, MasoodS Khan et SH Ansari. « Standardization and in vitro antioxidant activity of jatamansi rhizome ». Journal of Pharmacy and Bioallied Sciences 7, no 4 (2015) : 275. http://dx.doi.org/10.4103/0975-7406.168025.
Texte intégralMalvicini, R., D. Santa Cruz, C. Sanmartin, N. Pacienza et G. Yannarelli. « Bioassay standardization to assess exosomes antiinflammatory activity in vitro ». Cytotherapy 22, no 5 (mai 2020) : S24. http://dx.doi.org/10.1016/j.jcyt.2020.03.500.
Texte intégralMorosato, Federico, Francesco Traina et Luca Cristofolini. « Standardization of hemipelvis alignment for in vitro biomechanical testing ». Journal of Orthopaedic Research® 36, no 6 (19 décembre 2017) : 1645–52. http://dx.doi.org/10.1002/jor.23825.
Texte intégralKaur, Harpreet, Jaismeen Kaur et Bhagwant Singh Chahil. « in vitro protocol standardization for growth and rooting in strawberry ». Journal of Krishi Vigyan 9, no 1 (2020) : 193–201. http://dx.doi.org/10.5958/2349-4433.2020.00158.0.
Texte intégralSchendel, Dolores J., Rudolf Wank et Bo Dupont. « Standardization of the Human in vitro Cell-mediated Lympholysis Technique ». Tissue Antigens 13, no 2 (11 décembre 2008) : 112–20. http://dx.doi.org/10.1111/j.1399-0039.1979.tb01146.x.
Texte intégralSudha, V., K. L. Niraimathi, R. Lavanya, C. David Raj et P. Brindha. « Chemical Standardization and in vitro Cytotoxic Studies on Nellikai lehyam ». Asian Journal of Chemistry 26, no 12 (2014) : 3679–82. http://dx.doi.org/10.14233/ajchem.2014.17053.
Texte intégralThèses sur le sujet "In vitro standardization"
NUNES, Cristina Freitas. « Atividade virucida de um extrato etanólico de própolis verde in vitro e in vivo ». Universidade Federal de Pelotas, 2011. http://repositorio.ufpel.edu.br/handle/ri/2567.
Texte intégralCurrently, the drug industry looks for new drugs based on natural products, for the production of drugs more efficient, for which the microorganisms did not show resistance to both humans and animals. A natural product that has been the subject of intense pharmacological and chemical studies by scientists for the control of diseases is propolis, a resinous substance produced by honeybees from exudates collected from different parts of the plant, which has been used for centuries in popular medicine due to its therapeutic properties. Chemical studies revealed the complex chemical composition, identifying in some cases more than 300 components including various bioactive phenolic compounds responsible for the virucidal action. This work initially describes the standardization of an ethanol extract of green propolis (EEPV), where the chemicals were identified by high performance liquid chromatography (HPLC), phytochemical characterization by thin layer chromatography (TLC), soluble solids, content of phenolics and flavonoids and antioxidant activity by 2.2 diphenil picryl hydrazyl (DPPH). The EEPV was also evaluated in vitro and in vivo for their capacity lentogenic virucidal against a strain of the virus of Newcastle disease (NDV) at two different temperatures (22 and 37 ° C), 5 incubation periods (0, 1, 2, 4 and 8 hours) of NDV in five different concentrations of EEPV (4000μg/dose, 400μg/dose, 40μg/dose, and 4μg/dose 0μg/dose). The EEPV standard is within the standards required by the MAP, with high levels of phenolics and flavonoids (12.93 and 6.05% respectively) as shown by HPLC, which identified high concentrations of phenolic acids (p-coumaric acid, hydroxycinnamic acid diprenyl , cinâmino acid derivatives), which are assigned the antibacterial, antioxidant, antiviral and virucidal. This extract showed dose-dependent virucidal activity (4000μg/dose e 400μg/dose) and time of incubation with the virus (2 hour). The inhibitory activity of EEPV against the strain of NDV lentogenic found in the present study suggests the use of this extract as an alternative to fight the infection by this virus.
Atualmente, a indústria farmacêutica busca novos medicamentos com base em produtos naturais, visando à produção de fármacos mais eficientes, para os quais os microrganismos não apresentem resistência, tanto para humanos quanto para animais. Um dos produtos naturais que tem sido objeto de intensos estudos farmacológicos e químicos por cientistas para o controle de enfermidades é a própolis, uma substância resinosa produzida por abelhas melíferas a partir de exsudatos coletados em diferentes partes das plantas, que tem sido utilizada durante séculos na medicina popular devido as suas propriedades terapêuticas. Estudos químicos revelaram a complexa composição da própolis, identificando em alguns casos mais de 300 componentes, incluindo vários compostos bioativos fenólicos responsáveis pela ação virucida. Este trabalho inicialmente descreve a padronização de um extrato etanólico de própolis verde (EEPV), onde foram identificados os compostos químicos por cromatografia liquida de alta eficiência (CLAE), caracterização fitoquímica por cromatografia em camada delgada (CCD), teor de sólidos solúveis, teor de fenóis e flavonóides totais e atividade antioxidante por 2,2 diphenil picril hidrazil(DPPH). O EEPV foi avaliado também in vitro e in vivo, quanto a sua capacidade virucida contra uma cepa lentogênica do vírus da doença de Newcastle (NDV) em duas temperaturas distintas (22 e 37°C), 5 períodos de incubação (0, 1, 2, 4 e 8 horas) do NDV em 5 concentrações de EEPV distintos (4000μg/dose, 400μg/dose, 40μg/dose, 4μg/dose e 0μg/dose). O EEPV padronizado está dentro dos padrões requisitados pelo MAPA, com altos níveis de fenóis e flavonóides totais (12.93 e 6,05% respectivamente), comprovado por CLAE, o qual identificou altas concentrações de ácidos fenólicos (ácido p-cumárico, ácido diprenil hidroxicinâmico, derivados do ácido cinâmino), os quais são atribuídos as propriedades antibacteriana, antioxidante, antiviral e virucida. Este extrato apresentou atividade virucida dependente da dose (4000μg/dose, 400μg/dose) e do tempo de incubação com o vírus (2 horas). A atividade inibitória do EEPV contra a cepa lentogênica de NDV, encontrada no presente estudo sugere a utilização deste extrato como uma alternativa no combate a infecções por este vírus.
LUCO, DAYANE P. « Padronização de técnicas de isolamento de células de Langerhans imaturas e desenvolvimento de um modelo tridimensional de pele humana para testes de sensibilidade in vitro ». reponame:Repositório Institucional do IPEN, 2014. http://repositorio.ipen.br:8080/xmlui/handle/123456789/23179.
Texte intégralMade available in DSpace on 2014-12-19T17:52:28Z (GMT). No. of bitstreams: 0
Dissertação (Mestrado em Tecnologia Nuclear)
IPEN/D
Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
STANCO, DEBORAH. « Toward personalized medicine : human adipose-derived stem cells (ASCs) and xenogenic-free media as enabling tools in tendon tissue engineering strategies ». Doctoral thesis, Politecnico di Torino, 2020. http://hdl.handle.net/11583/2839845.
Texte intégralLivres sur le sujet "In vitro standardization"
S, Ambesi-Impiombato F., et Perrild H, dir. FRTL-5 today : Proceedings of the First International Workshop on Characterization and Standardization of an In Vitro Thyroid Cell System, Udine, Italy, 26-28 October 1988. Amsterdam : Excerpta Medica, 1989.
Trouver le texte intégralChapitres de livres sur le sujet "In vitro standardization"
Stacey, Glyn N., et Thomas Hartung. « Availability, Standardization and Safety of Human Cells and Tissues for Drug Screening and Testing ». Dans Drug Testing in vitro, 229–50. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/9783527609611.ch9.
Texte intégralRaja, Pavan M. V., Ghislaine Lacroix, Jacques-Aurélien Sergent, Frédéric Bois, Andrew R. Barron, Enrico Monbelli et Dan Elgrabli. « Nanotoxicology : Role of Physical and Chemical Characterization and RelatedIn Vitro,In Vivo, andIn SilicoMethods ». Dans Metrology and Standardization of Nanotechnology, 363–80. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527800308.ch23.
Texte intégralLima-Filho, José Vitor, et Rossana de Aguiar Cordeiro. « In Vitro and In Vivo Antibacterial and Antifungal Screening of Natural Plant Products : Prospective Standardization of Basic Methods ». Dans Springer Protocols Handbooks, 275–91. New York, NY : Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8636-7_17.
Texte intégralSchmitt, K., S. Rosenkranz, F. Platzer, G. Jagarzewskj, M. Kästner, A. Schroda, R. Seitz et J. Dodt. « Standardization of the Thrombin-Fibrinogen Clotting Time (TFCT) — An In Vitro Test on Thrombogenicity of Prothrombin Complex Concentrates (PCCs) ». Dans 28. Hämophilie-Symposion Hamburg 1997, 125–34. Berlin, Heidelberg : Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59915-6_17.
Texte intégralEkwall, Bjorn, et Frank A. Barile. « Standardization and Validation ». Dans Introduction to In Vitro Cytotoxicology, 189–208. CRC Press, 2019. http://dx.doi.org/10.1201/9780429275487-11.
Texte intégralBhatt, Deepa, M. K. Tripathi, M. Vidhya Sankar, Sushma Tiwari, Mohini Sharma, Niraj Tripathi et Sharad Tiwari. « Standardization of In-vitro Regeneration Protocol in Gerbera jamesonii Bolus Ex Hooker F. » Dans Current Topics in Agricultural Sciences Vol. 7, 105–21. Book Publisher International (a part of SCIENCEDOMAIN International), 2022. http://dx.doi.org/10.9734/bpi/ctas/v7/2303b.
Texte intégralBorziak, Kirill, Irena Parvanova et Joseph Finkelstein. « Introducing a Platform for Integrating and Sharing Stem Cell Research Data ». Dans Studies in Health Technology and Informatics. IOS Press, 2021. http://dx.doi.org/10.3233/shti210186.
Texte intégral« Good cell culture practice : good laboratory practice in the cell culture laboratory for the standardization and quality assurance of in vitro studies ». Dans Cell Culture Models of Biological Barriers, 138–46. CRC Press, 2002. http://dx.doi.org/10.1201/9780203219935-14.
Texte intégralOliver, Anthony R. « Laboratory Quality Control and Accreditation ». Dans Tutorial Topics in Infection for the Combined Infection Training Programme. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198801740.003.0019.
Texte intégralActes de conférences sur le sujet "In vitro standardization"
Singhera, G. K., T. Guo, J. M. Leung et D. R. Dorscheid. « Standardization of Airway Epithelial 3D Culture for In Vitro Studies ». Dans American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a1300.
Texte intégralSilva, Andréa, Tamiris Azamor, Leonardo Batista-Silva, Nathalia Benigno, Thyago Calvo, Camilla Bayma, Denise Matos et Milton Moraes. « Standardization of an in vitro assay for the evaluation of a candidate yellow fever vaccine ». Dans IV International Symposium on Immunobiologicals & VII Seminário Anual Científico e Tecnológico. Instituto de Tecnologia em Imunobiológicos, 2019. http://dx.doi.org/10.35259/isi.sact.2019_32551.
Texte intégralHoppensteadt, D., J. Fareed, J. M. Walenga, R. M. Emnuele et A. Racanelli. « DIFFERENT LOW MOLECULAR WEIGHT HEPARINS (LMWHs) ARE NOT IDENTICAL IN THE IN VITRO SCREENING REGARDLESS OF POTENCY ADJUSTMENT ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643227.
Texte intégralZwagerman, Ralph. « Development of ISO18363-4 / AOCS Cd29f-2021 : A new standardized method to quantify MCPDE and GE in edible oils ». Dans 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/dqcb6439.
Texte intégralSuor-Cherer, S., H. Bui Thi Quynh et P. Caillis. « Standardization of an in vitro spectrophotometric method for the evaluation of the ammonia-binding properties of plant extracts rich in saponins ». Dans 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399745.
Texte intégralWehmeier, A., et W. Schneider. « FACTORS AFFECTING PLATELET VOLUME ANALYSIS ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643538.
Texte intégral