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Relevant bibliographies by topics / Biochemical Mice

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Academic literature on the topic 'Biochemical Mice'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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Journal articles on the topic "Biochemical Mice"

1

Leung, Gordon K., Walter K. Schmidt, Martin O. Bergo, et al. "Biochemical Studies ofZmpste24-deficient Mice." Journal of Biological Chemistry 276, no. 31 (2001): 29051–58. http://dx.doi.org/10.1074/jbc.m102908200.

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Choudhury, Chinmoy, Meenakshi Bawari, and G. D. Sharma G. D. Sharma. "Biochemical Screening of The Effect of a Plant Extract on Albino Mice Physiology." International Journal of Scientific Research 2, no. 8 (2012): 38–39. http://dx.doi.org/10.15373/22778179/aug2013/13.

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Calhoun, S. W., M. D. Engstrom, and I. F. Greenbaum. "Biochemical Variation in Pygmy Mice (Baiomys)." Journal of Mammalogy 70, no. 2 (1989): 374–81. http://dx.doi.org/10.2307/1381521.

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Sharma, Archana, Deepak Bhatnagar, and Rashmi Sisodia. "10 Ghz Microwaves Induced Biochemical, Learning and Memory Alterations in Swiss Albino Mice Brain." Indian Journal of Applied Research 4, no. 5 (2011): 1–5. http://dx.doi.org/10.15373/2249555x/may2014/215.

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Banchaabouchi, Mumna Al, Bart Marescau, Rudi D'Hooge, et al. "Biochemical and histopathological changes in nephrectomized mice." Metabolism 47, no. 3 (1998): 355–61. http://dx.doi.org/10.1016/s0026-0495(98)90271-2.

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Monfared, A. Louei. "Biochemical toxicity of phenol in treated mice." Toxicology Letters 196 (July 2010): S106. http://dx.doi.org/10.1016/j.toxlet.2010.03.378.

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Ukpo, GraceE, O. A. T. Ebuehi, and AA Kareem. "Evaluation of moxifloxacin-induced biochemical changes in mice." Indian Journal of Pharmaceutical Sciences 74, no. 5 (2012): 454. http://dx.doi.org/10.4103/0250-474x.108422.

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Cardona, Maria E., Elisabeth Norin, and Tore Midtvedt. "Biochemical Functions of Bacillus licheniformis in Gnotobiotic Mice." Microbial Ecology in Health and Disease 15, no. 1 (2003): 40–42. http://dx.doi.org/10.1080/08910600310012045.

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Tanu, Tanzina, Adiba Anjum, Momotaj Jahan, et al. "Antimony-Induced Neurobehavioral and Biochemical Perturbations in Mice." Biological Trace Element Research 186, no. 1 (2018): 199–207. http://dx.doi.org/10.1007/s12011-018-1290-5.

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Barbosa, Brenna De Sousa, Érika Almeida Praxedes, Mikael Almeida Lima, et al. "Haematological and Biochemical Profile of Balb-c Mice." Acta Scientiae Veterinariae 45, no. 1 (2017): 5. http://dx.doi.org/10.22456/1679-9216.80473.

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Background: Animal models are widely used in scientific research because of the ability to generate information from an organism like everything under a given experimental condition. Hematological and biochemical tests in laboratory animals are essential for the validation of several scientific studies. In addition, it standardizes physiological values for these animals according to their sex, age, lineage, environment, and nutritional status. The present work aims to establish reference values for biochemical and hematological standards in Balb/c mice, for males and females.Materials, Methods

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Dissertations / Theses on the topic "Biochemical Mice"

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Sokoloff, Dina. "Biochemical genetic studies on ganglioside biosynthesis in mice." Thesis, McGill University, 1987. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=63842.

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Le, Tissier Paul Roussel. "The biochemical genetics of purine catabolism in mice." Thesis, University of Reading, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236393.

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Asante, Emmanuel A. "Biochemical genetics of lipid metabolism in chickens and mice." Thesis, University of Edinburgh, 1988. http://hdl.handle.net/1842/11520.

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Xu, Yuekang. "Biochemical basis of B cell dysfunction in lyn kinase deficient mice /." Connect to thesis, 2003. http://eprints.unimelb.edu.au/archive/00002881.

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Thesis (Ph.D.)--University of Melbourne, The Walter & Eliza Hall Institute of Medical research, Dept. of Medical Biology, 2004.<br>Typescript (photocopy). Includes bibliographical references (leaves 161-190).

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Plattner, Florian. "Biochemical analysis of genetically-modified mice with learning and memory phenotypes." Thesis, University College London (University of London), 2006. http://discovery.ucl.ac.uk/1444677/.

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Recent advances in molecular genetics have enabled generation of sophisticated genetically-modified mouse models to study specific molecules and their biological function in vivo. Here, I investigated biochemical changes in two different genetically-modified mouse lines with previously described learning and memory phenotypes. Firstly, I analysed biochemical changes in a mouse line carrying a threonine to alanine point mutation at Thr286 of alpha Ca2+/calmoduline-dependent kinase II (aCaMKII), which disenables this phosphorylation site. Autophosphorylation at Thr286 switches aCaMKII into an au

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HuÌˆbner, Roland Karl Peter. "Chromosomal and biochemical variation in wild mice from Switzerland : relevance for models of chromosomal evolution in European house mice." Thesis, University of Oxford, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316879.

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Connelly, D. M. "A biochemical study of the relationship between ethanol consumption and Diabetes mellitus in mice." Thesis, University of Bristol, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375036.

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Healy, Charles E. "Immunologic, Hematologic, and Endocrine Responses to Subacute and Subchronic Exposures to Graded, Subanesthetic Levels of Nitrous Oxide in CD-1 Mice." DigitalCommons@USU, 1989. https://digitalcommons.usu.edu/etd/4651.

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Nitrous oxide (N2O) oxidizes vitamin B12. disrupting deoxyribonucleic acid (DNA) synthesis. Occupational exposures to subanesthetic levels of the gas have been documented that may result in suppressed proliferative cell activities. Male CD-I mice were exposed to 0, 50, 500, and 5000 parts of N2O per million parts of air (ppm) for 6 hr/day, 5 days/week for 2 and 13 weeks. Splenic lymphocytes were assayed for responsiveness to mitogens and for the ability to produce interleukin-2 (lL-2) . Tritiated-thymidine ([3H]-TdR) uptake was measured in CD-I splenic lymphocytes cultured in a mixed-lymphocyt

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Rivas, Traverso Francisco [Verfasser]. ""Morphologic, genetic, and biochemical characterisation of novel Heliobacter isolates from laboratory mice and tigers" / Francisco Rivas Traverso." Magdeburg : Universitätsbibliothek, 2011. http://d-nb.info/1051445523/34.

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Bettess, Michael David. "Purification, identification and characterisation of signals directing embryonic stem (ES) cell differentiation : a thesis submitted to the University of Adelaide for the degree of Doctor of Philosophy." Title page, contents and abstract only, 2001. http://web4.library.adelaide.edu.au/theses/09PH/09phb5644.pdf.

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Includes bibliographical references (leaves 142-168) Aim was the purification and identification of the early primitive ectoderm-like (EPL) cell induction signals within the medium conditioned by the human hepatocellular carcinoma cell line HepG2 and the localisation of the signals that induce EPL cell and primitive ectoderm formation.

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Books on the topic "Biochemical Mice"

1

Principles of biochemical toxicology. 3rd ed. Taylor & Francis, 2000.

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Dooren, Tom V. Biochemical & Immuno-histochemical Analysis of App-processing & Amyloid Pathology in Single & Multiple Transgenic Mice As Models for Alzheimer's Disease. Leuven Univ Pr, 2006.

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Numerical Methods for Chemical Engineering. Cambridge University Press, 2006.

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Beers, Kenneth J. Numerical Methods for Chemical Engineering: Applications in MATLAB. Cambridge University Press, 2006.

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Book chapters on the topic "Biochemical Mice"

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Stein, Lincoln D. "Of Mice and Men: Navigating Public Physical Mapping Databases." In Methods of Biochemical Analysis. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470110607.ch12.

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Snell, E. J. "Biochemical experiment on the blood of mice." In Applied Statistics. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-011-6946-2_21.

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Borràs, Miquel, Santiago Llacuna, Assumpta Górriz, and Jacint Nadal. "Hematological and Biochemical Parameters in Pollution-Exposed Mice." In Archives of Toxicology. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-46856-8_17.

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Nawashiro, Hiroshi, S. Huang, M. Brenner, K. Shima, and J. M. Hallenbeck. "ICP Monitoring Following Bilateral Carotid Occlusion in GFAP-Null Mice." In Intracranial Pressure and Brain Biochemical Monitoring. Springer Vienna, 2002. http://dx.doi.org/10.1007/978-3-7091-6738-0_69.

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Reddi, A. S., H. Wehner, M. Y. Khan, and R. A. Camerini-Davalos. "Kidney Disease in KK Mice: Structural, Biochemical and Functional Relationships." In Prediabetes. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5616-5_17.

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Mijares, Alfredo, Ludovic Verdot, Nicolas Peineau, Bernard Vray, Johan Hoebeke, and Jorge Argibay. "Antibodies from Trypanosoma cruzi infected mice recognize the second extracellular loop of the βl-adrenergic and M2-muscarinic receptors and regulate calcium channels in isolated cardiomyocytes." In Biochemical Regulation of Myocardium. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1289-5_12.

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Marshall, E. F., S. Dodds, E. Alderson, and M. Leitch. "Biochemical and behavioural study of tryptophan administration to mice treated neonatally with 5,7-dihydroxytryptamine." In Amino Acids. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_46.

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Shin, Kyung-Ok, Jin A. Yoon, and Kyung-Soon Choi. "The Effect on Blood Biochemical Factors of a ICR-Mice in a High-Fat Diet with Taurine 20%." In Advances in Experimental Medicine and Biology. Springer Netherlands, 2017. http://dx.doi.org/10.1007/978-94-024-1079-2_77.

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Frasier, Mark, Shanti Frausto, Daniel Lewicki, Lawrence Golbe, and Benjamin Wolozin. "Dissecting the Biochemical Pathways Mediated by Genes Implicated in Parkinson’s Disease: Induction of DJ-1 Expression in A30P α-Synuclein Mice." In Advances in Alzheimer’s and Parkinson’s Disease. Springer US, 2008. http://dx.doi.org/10.1007/978-0-387-72076-0_11.

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Klein, Robert, Judith S. Tischler, Martin Mühling, and Michael Schlömann. "Bioremediation of Mine Water." In Advances in Biochemical Engineering/Biotechnology. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/10_2013_265.

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Conference papers on the topic "Biochemical Mice"

1

Patlolla, Anita K., Britney McGinnis, and Paul Tchouwou. "Abstract 4381:Biochemical and histopathological evaluation of mice exposed to functionalized single-walled carbon nanotube." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4381.

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Xia, Daozong, Jiaqi Guan, Yeping Ruan, and Xinfen Yu. "Notice of Retraction: Effects of Lead in Drinking Water on Biochemical Alterations in Multi-Organs of Mice." In 2011 5th International Conference on Bioinformatics and Biomedical Engineering. IEEE, 2011. http://dx.doi.org/10.1109/icbbe.2011.5781427.

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Peterson, Sherket B., Zannatul Ferdous, Magnus Höök, and K. Jane Grande-Allen. "Decorin Deficient Cells Demonstrate Increased Proliferation and Altered Phenotypic Properties." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176043.

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Decorin (DCN), a class I member of the small leucine-rich proteoglycan (SLRP) family, is composed of a protein core of approximately 40kDa [1, 2] substituted with a single glycosaminoglycan (GAG) chain of chondroiton/dermatan sulfate on the N-terminal site [3]. DCN has been reported to interact with collagen [4,5] via its core protein, influence collagen fibrillogenesis [6], and inhibit the growth rates of various cell types when added exogenously to cell cultures [5,6]. There has recently been growing interest and studies in DCN related research using the knockout (KO) mice model which provid

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Ahmed, Ahmed Hamid, Raghad Hazem Alabbasy, and Zinah Ibrahim Khaleel. "The protective role of aqueous extract of grape seeds Vitis vinifera in some biochemical parameters and histological changes in methionine for liver, kidney and heart in mice (Mus musculus)." In 2ND INTERNATIONAL CONFERENCE ON MATERIALS ENGINEERING & SCIENCE (IConMEAS 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0000450.

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Alieva, Zamira O., Matvej V. Kanevskiy, Anna A. Galitskaya, et al. "Physico-chemical and biochemical approaches to assessing the development of precancerous pathologies of the gastrointestinal tract during their modeling in mice with complex effects of stress factors of different nature." In Saratov Fall Meeting 2015, edited by Elina A. Genina, Valery V. Tuchin, Vladimir L. Derbov, et al. SPIE, 2016. http://dx.doi.org/10.1117/12.2225478.

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Hunter, N. R., I. R. MacGregor, J. Dawes, and D. S. Pepper. "MICROCARRIER CULTURE OF HUMAN ENDOTHELIAL CELL TYPES - A SOURCE OF METABOLITES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643348.

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The production of human endothelial cell secretory products in amounts sufficient for biochemical studies is largely restricted by the culture growth area. Conventional flat bed systems yield at best 20-30 x 106 cells per 180cm2 culture flask. To overcome this problem, cells may be grown on Cytodex 3 microcarriers allowing large numbers of cells to be grown and conditioned in small culture volumes. A typical microcarrier unit will contain 200-300 x 106 cells and may be expanded in excess of 1000 x 106 cells at confluence. High viability (95%) and recovery (70-80%) in sub-culturing of microcarr

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Post, Sijranke, Martijn Nawijn, Antoon van Oosterhout, and Irene H. Heijink. "Different Biochemical Properties Of House Dust Mite Induce Divergent Epithelial And Inflammatory Responses." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a1444.

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Seror, Jasmine, Nir Kampf, Alice Maroudas, and Jacob Klein. "Nanotribological Investigation of the Role of Proteoglycans in Biolubrication." In ASME 2008 9th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2008. http://dx.doi.org/10.1115/esda2008-59390.

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Articular joints in human body are uniquely efficient lubrication systems. While the cartilage surfaces slide past each other under physiological working conditions (pressure of tens of atmospheres and shear rates up to 106 – 107 Hz), the friction coefficient (μ) achieves extremely low values (down to 0.001) never successfully reached by mechanical prosthetic devices. Friction studies on polymer brushes attached to surfaces have recently demonstrated (17) their ability to reduce friction between the rubbing surfaces to extremely low values by means of the hydrated ions and the charges on the p

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