Littérature scientifique sur le sujet « Mousse PU »
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 « Mousse PU ».
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 "Mousse PU"
Madrange, L., P. Ehabouryi, O. Ferrandon, M. Mazeti et J. Rodeaud. « Étude de la formation et de la stabilité des mousses chimiques de surface de la Vienne ». Revue des sciences de l'eau 6, no 3 (12 avril 2005) : 315–35. http://dx.doi.org/10.7202/705178ar.
Texte intégralChristians, Jean-François. « Redécouverte de Schistostega pennata (Hedwig) F. Weber et D. Mohr (Schistostegaceae, Bryophyta) dans le massif du Pilat (Loire, France) ». Bulletin mensuel de la Société linnéenne de Lyon 84, no 7 (2015) : 215–25. http://dx.doi.org/10.3406/linly.2015.17768.
Texte intégralThomas, Marc, Emmanuel Discamps, Mathieu Lejay, Xavier Muth et Jean-Guillaume Bordes. « Os qui roule n’amasse pas mousse. Une expérimentation sur le tri différentiel des vestiges lithiques et osseux dans un écoulement turbulent ». Paléo 33 (2023) : 146–63. http://dx.doi.org/10.4000/1296o.
Texte intégralHwang, Cheol Kyu, Chun Sung Kim, Hack Sun Choi, Scott R. McKercher et Horace H. Loh. « Transcriptional Regulation of Mouse μ Opioid Receptor Gene by PU.1 ». Journal of Biological Chemistry 279, no 19 (3 mars 2004) : 19764–74. http://dx.doi.org/10.1074/jbc.m400755200.
Texte intégralGerasimo, P., C. Duserre et H. Metivier. « Biological Behaviour of Pu Administered to Animals as Pu-Standard LICAM(C) Complex : Therapeutical Attempts to Decrease Pu Kidney Burden ». Human Toxicology 5, no 5 (septembre 1986) : 309–18. http://dx.doi.org/10.1177/096032718600500503.
Texte intégralZhou, Jing, Bo Li, Jun Wu, Fuhong He, Qiang Li, Xiaomei Yan, Yue Zhang et al. « Essential Role for PU.1 in MEIS1 Activation and MLL Fusion Leukemia »,. Blood 118, no 21 (18 novembre 2011) : 3466. http://dx.doi.org/10.1182/blood.v118.21.3466.3466.
Texte intégralStaber, Philipp B., Pu Zhang, Min Ye, Gang Huang, Boris Bartholdy, Annalisa DiRuscio, Alexander K. Ebralidze et Daniel G. Tenen. « Autoregulation of the Transcription Factor PU.1 Via Its Evolutionarily Conserved Upstream Regulatory Element Is Critical in Adult Mouse Hematopoiesis. » Blood 114, no 22 (20 novembre 2009) : 1468. http://dx.doi.org/10.1182/blood.v114.22.1468.1468.
Texte intégralBonfield, Tracey L., Baisakhi Raychaudhuri, Anagha Malur, Susamma Abraham, Bruce C. Trapnell, Mani S. Kavuru et Mary Jane Thomassen. « PU.1 regulation of human alveolar macrophage differentiation requires granulocyte-macrophage colony-stimulating factor ». American Journal of Physiology-Lung Cellular and Molecular Physiology 285, no 5 (novembre 2003) : L1132—L1136. http://dx.doi.org/10.1152/ajplung.00216.2003.
Texte intégralMak, Ka Sin, Alister P. W. Funnell, Richard C. M. Pearson et Merlin Crossley. « PU.1 and Haematopoietic Cell Fate : Dosage Matters ». International Journal of Cell Biology 2011 (2011) : 1–6. http://dx.doi.org/10.1155/2011/808524.
Texte intégralGhisi, Margherita, Mark D. McKenzie, Ethan P. Oxley, Emilia Simankowicz, Cynthia Liu, Aleksandar Dakic, Stephen L. Nutt, Matthew E. Ritchie, Johannes Zuber et Ross A. Dickins. « Uncovering Key Downstream Effectors of PU.1 Tumor Suppression in Acute Myeloid Leukemia ». Blood 128, no 22 (2 décembre 2016) : 2698. http://dx.doi.org/10.1182/blood.v128.22.2698.2698.
Texte intégralThèses sur le sujet "Mousse PU"
Njeugna, Yotchou Nicole Suzie. « Contribution au développement et à l'industrialisation d'un système non-tissé 3D ». Phd thesis, Université de Haute Alsace - Mulhouse, 2009. http://tel.archives-ouvertes.fr/tel-00487989.
Texte intégralJaussaud, Quentin. « Génération in situ d’isocyanates par décarboxylation d’acides oxamiques pour l’élaboration de matériaux polyuréthanes ». Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0139.
Texte intégralThis PhD work focus on the synthesis of polyurethanes through the in situ generation of isocyanates, using pathways with lower toxicity compared to the classical approach involving the direct use of isocyanates. The oxidative decarboxylation of oxamic acids leading to the formation of isocyanates was, first, carried out by thermal activation using a hypervalent iodine as an oxidant. A kinetic study on model reactions in the presence of alcohol, combined with computational modeling, notably revealed a catalytic effect of acetic acid, a by-product of the reaction, on the formation of urethane bonds. The CO2 generated by this reaction, leading to the formation of isocyanates, was then exploited for the synthesis of cross-linked polyurethane foams. The effects of various parameters, such as the nature of the monomers or the reaction temperature, on the morphology and properties of the obtained foams were thereafter studied. This activation reaction of oxamic acids was then carried out by light irradiation in the presence of a photocatalyst, allowing the production of polyurethane films. Modifying the components of the reaction mixture enabled the development of homogeneous formulations, particularly by changing the nature of the hypervalent iodine used. Finally, the synthesis of urethanes and polyurethanes from 1,4,2-dioxazol-5-ones was explored. After optimizing the catalytic conditions for generating isocyanates through the opening of these heterocycles, the generated CO2 was exploited for the production of polyurethane foams
Vafiadès, Virginie. « Caractérisations microstructurale et mécanique de mousses de nickel à cellules ouvertes pour batteries de véhicules hybrides ». Paris, ENMP, 2004. http://www.theses.fr/2004ENMP1199.
Texte intégralThe nickel foam production at NiTECH starts with a 10 microns thick coating of nickel onto an open-cell polyurethane foam. The major aim of this study is to reduce the costs of production. For that purpose, the thermal degradation of the polyurethane foam is studied by thermogravimetric analysis and involves three superimposed phenomena. Afterwards, the three phenomena are separated and the thermal degradation is modeled. The dependence of the mechanical behavior of nickel foams upon grain size is studied. The foam walls being very thin, the result is compared with that of nickel foils. Once the microstructure becomes "bamboo", the yield strength remains constant. A mechanical model is finally presented incorporating the grain size effect. Besides, an other application of nickel foam could be found in the fuel cells operating at high temperatures. Tensile creep tests were carried out and the creep parameters were estimated experimentally and incorporated in two mechanical models
Olme, Carl-Henrik Axel. « Role and functional consequences of PU.1 transcriptional factor loss and mutations in a mouse model of radiation-induced acute myeloid leukaemia ». Thesis, Imperial College London, 2011. http://hdl.handle.net/10044/1/9122.
Texte intégral李淑貞. « The effect of Pu-Chung-I-Chi-Tang and its associated crude drugs on Glutathione homeostasis in mouse livers ». Thesis, 2000. http://ndltd.ncl.edu.tw/handle/67939120662716052427.
Texte intégral國立臺灣大學
藥學研究所
88
Pu-Chung-I-Chi-Tang (abbreviated as PCICT) was an herbal formula developed by the renowned medical expert Lee, Tung-Yuan back in 1180-1251, which composed of Hedysarum polybotrys, Panax ginseng, Bupleurum chinense, Cimicifuga foetida, Atractylodes macrocephala, Angelica sinensis, Glycyrrhiza uralensis and Citrus reticulata. The formula has the functions of liver protection, overall fortification and enhancement of immunity defense mechanism, inhibition of tumor growth, and enhancement of chemotherapeutic effects. Clinically, it is applied in treatments of hepatitis, intestinal tuberculosis, gastroptosis, cold, flu, tuberculosis, anemia, various malignant tumors and neurasthenia. Glutathione is constituted by three types of amino acids; its bio-synthesis and metabolism inside the human body is generally regulated by enzyme system in -glutamyl cycle. The vital enzymes that participate in the cycle are as follows: -glutamylcysteine synthetase and glutathione synthetase, which controls the bio-synthesis of glutathione; glutathione reductase and glutathione peroxidase, which regulates redox cycle and is endowed with the function of biochemical protection, while glutathione S-transferase controls physical metabolism and detoxification. Glutathione has wide ranging biological rejuvenating properties; the most critical biological functions involve: anti-oxidation defense mechanism, detoxification, regulation in oxidation-reduction related message conveyance system, regulations in immunity reactions, cancer resistance, and chemotherapeutic agents. With respect to anti-oxidation, detoxification, liver protection, cell regulation, immunity build-up, and cancer prevention, PCICT shares the same biochemical function as glutathione. This study primarily investigates the relation between PCICT and glutathione in biochemical system; the concentration of glutathione and the activities of related enzymes have been analyzed, and through their relations in -glutamyl cycle and the biochemical potencies manifested, the effects of PCICT on -glutamyl cycle is elucidated. The result of this study reveals that PCICT drives up the concentration of glutathione; both Panax ginseng and Bupleurum chinense possess anti-oxidation effect; Bupleurum chinense, Angelica sinensis, Cimicifuga foetida and Atractylodes macrocephala can regulates redox cycle, while Hedysarum polybotrys, Bupleurum chinense, Angelica sinensis, Cimicifuga foetida and Atractylodes macrocephala induces synthesis of glutathione. Summarizing these results, it was established that PCICT and the related herbs are indeed endowed with specific bio-activities and anti-oxidation effects.
Livres sur le sujet "Mousse PU"
1820-1898, Taschereau E. A., et Église catholique. Archidiocèse de Québec. Archevêque (1870-1898 : Taschereau), dir. Circulaire au clergé : Comme j'ai pu le constater, le fléau de "la mouche à patate" continue a faire des ravages dans nos campagnes .. [S.l : s.n., 1986.
Trouver le texte intégralChapitres de livres sur le sujet "Mousse PU"
Zou, Gang-Ming, Meredith A. Thompson et Mervin C. Yoder. « RNAi Knockdown of Transcription Factor Pu.1 in the Differentiation of Mouse Embryonic Stem Cells ». Dans Methods in Molecular Biology, 127–36. Totowa, NJ : Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-536-7_10.
Texte intégralActes de conférences sur le sujet "Mousse PU"
Solomon, Lauren A., Stephen K. h. Li, Jan Piskorz, Li S. Xu et Rodney P. DeKoter. « Abstract 2098 : Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line ». Dans Proceedings : AACR 106th Annual Meeting 2015 ; April 18-22, 2015 ; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-2098.
Texte intégralde Cidrac, L., L. Radoï, R. Pecorari et T. Nguyen. « Tumeur à cellules géantes : à propos d’un cas récidivant et agressif à localisation mandibulaire ». Dans 66ème Congrès de la SFCO. Les Ulis, France : EDP Sciences, 2020. http://dx.doi.org/10.1051/sfco/20206603021.
Texte intégral