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Relevant bibliographies by topics / Mice Mice Mice Mice

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Academic literature on the topic 'Mice Mice Mice Mice'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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Journal articles on the topic "Mice Mice Mice Mice"

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Park, Woo Teak, and Byeong Cheol Lee. "The conceptual approach of MICE in daily lives: A case of MICE village." Journal & Article Management System 17, no. 1 (2021): 225–45. http://dx.doi.org/10.31927/asec.17.1.12.

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Seo, Min-Ryeong, Mi-Seong Kim, Yoo-Shik Yoon, and Na-Young Baek. "Market Segmentation of MICE Organizer by MICE City Marketing Awareness." Korea Trade Exhibition Review 15, no. 3 (2020): 95–113. http://dx.doi.org/10.16938/ijtfs.2020.15.3.095.

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Šlosárková, S., V. Híbalová, I. Literák, et al. "Experimental toxoplasmosis in hypoiodemic mice." Veterinární Medicína 47, No. 2 - 3 (2012): 67–74. http://dx.doi.org/10.17221/5806-vetmed.

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The hypothesis, that hypoiodemia of goats causes such a compromise of the immune system, which during subsequent Toxoplasma gondii infections results in clinically more pronounced signs of toxoplasmosis, was verifying in laboratory mouse. Hypoiodemic mice (fed by wheat and supplied by water), normoiodemic mice (fed by wheat and supplied by water containing 1.25 mg KI/l) and the majority of standard mice (fed by commercial grain mixture containing 0.83 mg I/kg) were experimentally infected with T. gondii oocysts or tachyzoites. The susceptibility to acute T. gondii infection was evaluated according to mortality rate. As a criterion of cell-mediated immune function has been chosen the spleen-lymphocyte transformation test (LTT). We observed no difference in LTT between hypoiodemic and normoiodemic mice infected with T. gondii oocysts or tachyzoites and no difference in mortality of both infected groups. Four days after the exposure to 100 tachyzoites of T. gondii (K24 strain), all experimentally infected groups of mice showed statistically significant decrease (P = 0.004) in spleen cells responsiveness to stimulation by all mitogens used &ndash; as compared to non-infected standard mice group. Reduced responsiveness of cells was probably caused by T. gondii infection itself &ndash; the relation to iodine deficiency has not been found.

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Jang, Mi-hwa. "How is Daegu perceived as a MICE destination? A Study on the Placeness of MICE Destination on Social Media." Korea Trade Exhibition Review 16, no. 1 (2021): 21–39. http://dx.doi.org/10.16938/ijtfs.2021.16.1.021.

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Mghamis, Munqith Mazin. "Effect of Prenatal Ketamine Exposure on GFAP Marker Expression in Mice Prefrontal Cortex Mice Prefrontal Cortex." International Journal of Psychosocial Rehabilitation 24, no. 4 (2020): 3936–44. http://dx.doi.org/10.37200/ijpr/v24i4/pr201507.

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Ryu, Jae Hee, and Byeong Cheol Lee. "Conceptualizing MICE Supporters’ Sharing Economy Activity." Journal & Article Management System 14, no. 1 (2018): 173–95. http://dx.doi.org/10.31927/asec.14.1.11.

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Choi, In-Ho. "Japanese MICE Promotion Utilizing Unique Venues." Korea Trade Exhibition Review 11, no. 3 (2016): 217–35. http://dx.doi.org/10.16938/ijtfs.2016.11.3.217.

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Safaeva, Sayyora, and Diyora Adilova. "Mice Tourism: Opportunities, Priorities, Problems, Prospects." American Journal of Applied Sciences 02, no. 11 (2020): 116–21. http://dx.doi.org/10.37547/tajas/volume02issue11-21.

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The MICE sector is one of the most significantly developing tourism industries in recent years. The growth of business tourism strongly affects not only the industry as a whole, but also the economy of the host country. However, with the development and greater popularization of MICE tourism, various difficulties arise. The research work will reveal the main opportunities, prospects and priorities for the development of the MICE tourism industry, as well as analyze the problematic aspects that MICE agencies face when organizing their activities.

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Кузнецова, Ольга, Olga Kuznetsova, Людмила Сильчева, et al. "Aspects on MICE-tourism and its management." Services in Russia and abroad 8, no. 2 (2014): 40–52. http://dx.doi.org/10.12737/3585.

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The article highlights the issues of MICE-related business travel, such as business tourism, conference-, exhibition- and travel-study tourism. The authors consider the historical preconditions for business travel birth and development, as well as the peculiarities of incentive tourism and the types and purposes of incentive programmes. The article provides statistics concerning the current state of the MICE-industry, and a comprehensive aspect-by-aspect study of a sample offsite seminar management in the framework of business tourism.

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Kang, Hae-Sang, and Kang-Young Song. "Analysis on the Satisfaction by MICE Participants in Busan Metropolitan." Journal of the Korea Contents Association 10, no. 11 (2010): 414–23. http://dx.doi.org/10.5392/jkca.2010.10.11.414.

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Dissertations / Theses on the topic "Mice Mice Mice Mice"

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Holder, Ridley B. "Selecting for lean gain efficiency in mice using different seletion criteria /." free to MU campus, to others for purchase, 1996. http://wwwlib.umi.com/cr/mo/fullcit?p9737854.

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Byers, Shannon L. "Use of Inbred Strains of Mice to Study the Genetics and Biology of Sperm Function." Fogler Library, University of Maine, 2006. http://www.library.umaine.edu/theses/pdf/ByersSL2006.pdf.

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Bosk, Abigail. "Mating induced fos in forebrain neurons of female mice /." Norton, MA : Wheaton College, 2008. http://hdl.handle.net/10090/6013.

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Paterson, Andrew William James. "Mitochondrial abnormalities in PrP-null mice and Mecp2-null mice." Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/29313.

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Evidence of a mitochondrial abnormality in PrP-null mice was sought by extensive assessment of the morphological and functional characteristics of isolated brain mitochondria. Study of isolated mitochondrial suspensions by electron microscopy revealed that PrP-null mitochondria were larger and, when cristae density was quantitatively measured using a novel technique, to have a reduced cristae density when compared to controls. A significant increase in respiratory capacity was detected in PrP-null mitochondria when metabolising Complex I substrates, but not when electrons entered downstream of complex 1. This implicates Complex 1 as a site for pathological change. As recent studies of the Mecp2-null mouse model of Rett syndrome detected increased transcription of Uqcrc1 (a core subunit of Complex III), mitochondrial morphology and respiration were studied in Mecp2-null mice. Whilst electron microscopy did not reveal any gross alterations in mitochondrial size or cristae density, respiration measurements revealed a severe phenotype in symptomatic, but not presymptomatic, Mecp2-null mice. Mitochondrial coupling was considerably reduced in isolated brain mitochondria from Mecp2-null mice indicating reduced mitochondrial efficiency. This effect was accompanied by an increase in respiratory capacity through Complex III. In order to determine if the overexpression of Uqcrc1 was causative in the production of the observed increase in respiratory capacity, the respiration rates of N2A cells overexpressing Uqcrc1 were measured. As transfected N2A cells showed significantly increased respiration rates through Complex III, the up-regulation of Uqcrc1 may be causative in producing the respiratory capacity increase observed in the animal model. These results enhance the evidence for dysfunctional mitochondria in both PrP-null and Mecp2-null mouse models and are discussed in relation to other investigations of prion disease, Rett syndrome and other models of neurodegenerative disease.

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Braun, Stav. "Tracking multiple mice." Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/77001.

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Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2012.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references (p. 59-62).<br>Monitoring mouse social behaviors over long periods of time is essential for neurobehavioral analysis of social mouse phenotypes. Currently, the primary method of social behavioral plienotyping utilizes human labelers, which is slow and costly. In order to achieve the high throughput desired for scientific studies, social behavioral phenotyping must be automated. The problem of automation can be divided into two tasks; tracking and phenotyping. First, individual body parts of mice must be accurately tracked. This is achieved using shape context descriptors to obtain precise point to point correspondences between templates and mice in any frame of a video. This method provides for greater precision and accuracy than current state of the art techniques. We propose a means by which this tracking information can be used to classify social behaviors between mice.<br>by Stav Braun.<br>M.Eng.

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Chen, Xiaodi. "Identification, expression and characterization of Murine pepsinogen F /." free to MU campus, to others for purchase, 2000. http://wwwlib.umi.com/cr/mo/fullcit?p9998474.

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Tsao, Jack W. "Wallerian degeneration in normal mice and in mutant C57BL/Wld mice." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260174.

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Verma, Sujeet. "Live plant and artificial plant settings are able to alleviate anxiety levels in mice an elevated plus-maze study /." Pullman, Wash. : Washington State University, 2009. http://www.dissertations.wsu.edu/Thesis/Spring2009/S_Verma_042409.pdf.

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Thesis (M.S. in horticulture)--Washington State University, May 2009.<br>Title from PDF title page (viewed on July 28, 2009). "Department of Horticulture and Landscape Architecture." Includes bibliographical references (p. 51-58).

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Rambau, Ramugondo Victor. "Molecular genetics of Rhabdomys subspecies boundaries : phylogeography of mitochondrial lineages and chromosomal fluorescence in situ hybridization." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53504.

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Thesis (PhD)--University of Stellenbosch, 2003.<br>ENGLISH ABSTRACT: The geographic genetic population structure and evolutionary history of the African four-striped mouse, Rhabdomys pumilio, was investigated using mitochondrial (mtDNA) cytochrome b gene (1140 bp) and control region (994 bp) sequences and a combination of cytogenetic banding techniques (G- and C-banding), and fluorescence in situ hybridization. Two cytotypes (2n = 46 and 2n = 48) were identified by cytogenetic analysis. No evidence of diploid number variation within populations was found nor were there differences in gross chromosome morphology, or subtle interchromosomal rearrangements at levels detected by ZOO-FISH. The comparative painting data (using the complete suite, N = 20, of Mus musculus chromosome specific painting probes) show that 10 mouse chromosomes have been retained as chromosomal arms, or intact chromosome blocks within the R. pumilio genome, six produced double signals, while the remaining four hybridized to three or more R. pumilio chromosomes. In total, the 20 mouse chromosome paints detected 40 segments of conserved synteny. Their analysis revealed eight R. pumilio specific contiguous segment associations, a further two that were shared by R. pumilio and other rodents for which comparable data are available, the Black (Rattus rattus) and Norwegian (Rattus nONegicus) rats, but not by the Chinese hamster, Cricetulus grise us. The results suggest that mouse chromosomes 1, 10, and 17 have undergone extensive rearrangements during genome evolution in the murids and may be useful markers for enhancing our understanding of the mode and tempo of chromosome evolution in rodents. Following initial studies using control region sequences, the phylogeographic appraisal of R. pumilio was done using cytochrome b gene sequences. Analyses based on a variety of analytical procedures resulted in the detection of two major mtDNA lineages that correspond roughly to the xeric and mesic biotic zones of southern Africa. One clade comprises specimens with 2n = 48, and the other representatives of two cytotypes (2n = 48 and 2n = 46). The mean sequence divergence (12.0%, range 8.3% -15.6%) separating the two mtDNA clades is comparable to among-species variation within murid genera suggesting their recognition as distinct species, the prior names for which would be R. dilecfus and R. pumilio. Low sequence divergences and the diploid number dichotomy within the mesic lineage support the recognition of two subspecies corresponding to R. d. dilecfus (2n = 46) and R. d. chakae (2n = 48). The data do not support subspecific division within the nominate, R. pumilio. Molecular dating places cladogenesis of the two putative species at less than 5 million years, a period characterised by extensive climatic oscillations which are thought to have resulted in habitat fragmentation throughout much of the species' range.<br>AFRIKAANSE OPSOMMING: Die geografiesebevolkingsstruktuur en evolusionêre verwantskappe binne die Afrika streepmuis, Rhabdoys pumilio, is ondersoek deur middel van mitochondriale ONS volgordebepaling van die geenfragment sitochroom b (1140 basispare) en die reguleerstreek (994 bp) in kombinasie met sitogenetiese tegnieke (G- en Cbandkleuring en f1uoreseerende in situ hibridisasie). Twee sitotipes (2n = 46 en 2n = 48) is geidentifiseer deur sitogenetiese analasie. Geen bewys van variasie in die 2n chromosoomgetal binne bevolkings is gevind nie. Verder is daar ook geen verskil in die morfologies struktuur van chromosome aanwesig binne bevolkings nie. Vergelykende data (verkry met behulp van die N = 20 Mus musculus chromosoomspesifiekepeilers) dui daarop dat 10 muis chromosome behoud gebly het as chromosoomarms of chromosoomblokke binne die R. pumilio genoom. Ses peilers het dubbel seine gelewer terwyl die oorblywende vier peilers gehibridiseer het aan drie of meer R. pumilio chromosome. In totaal het die 20 muischromosoomverwe 40 konserwatiewe segmente geidentifiseer. Die analise dui agt R. pumilio spesifieke aaneenlopende segmentassosiasies aan, met 'n addisionele twee wat deur R. pumilio en ander muisagtiges vir wie vergelykende data beskikbaar is, byvoorbeeld die swart (Rattus rattus) en Noorweegse (R. norvegicus) rot maar nie die Chinese hamster, Cricetulus grise us, gedeel word. Die resultate stel voor dat muischromosoom 1, 10 en 17 ekstensiewe herrangskikkings ondergaan het gedurende die genoom evolusie binne die Muridae en dat hulle waarskynlik waardevolle merkers kan wees om beide die patroon en tempo van chromosome evolusie in muisagtiges verder te kan verstaan. Die filogeografiese verwantskappe binne R. pumilio is ondersoek deur middel van ONS volgordebepalings van die reguleerstreek asook sitochroom b. Die resultate van hierdie studie het twee divergente mitochondriale ONS eenhede ontdek wat gekorreleer kan word met xeriese en mesiese klimaatsones binne suidelike Afrika. Een groep bestaan uit diere met 2n = 48, terwyl die ander genetiese groep twee sitotipes (2n = 46 en 2n= 48) insluit. 'n Gemiddelde genetiese divergensie van 12.0% (varieer tussen 8.3% - 15.5%) verdeel die twee mtDNS-groepe en is vergelykbaar met tussenspesievariasie binne ander muisagtige genera, wat moontlik daarop dui dat twee verskillende spesies teenwoordig is; die voorgestelde name is R. di/ectus en R. pumilio. Lae genetiese divergensie binne die mesiese groep versterk die moontlike teenwoordigheid van twee subspesies, R. d. di/ectus (2n = 46) en R. d. chakae (2n = 48). Die data verleen egter nie steun aan die divisie binne R. pumilio nie. Molekulêre datering van die twee spesies dui daarop dat die divergensie ten minste 5 miljoen jaar gelede plaasgevind het. Die periode was gekarakteriseer deur ekstensiewe klimaatsossilasies, wat gely het tot habitat fragmentasie in die spesie se verspreidingsgebied.

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Thayer, Kristina A. "Prenatal exposure to low doses of estrogen : reproductive effects in male and female mice and implications for regulation of endocrine disrupting environmental chemicals /." free to MU campus, to others for purchase, 1999. http://wwwlib.umi.com/cr/mo/fullcit?p9951127.

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Books on the topic "Mice Mice Mice Mice"

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Gagne, Tammy. Mice. T.F.H. Publications, 2012.

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Reece, Gordon. Mice. Pan, 2012.

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Reece, Gordon. Mice. Viking, 2011.

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Nikoleski, Vančo. Mice. Detska radost, 1998.

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ill, Ehlert Lois, ed. Mice. Beach Lane Books, 2012.

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Astrop, Caroline. Mice. Crocodile Books, 1989.

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Spilsbury, Louise. Mice. Heinemann Library, 2006.

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Mice. Grolier, 2008.

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Frankel, Julie E. Mice. Childrens Press, 1986.

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Spilsbury, Louise. Mice. Heinemann Library, 2006.

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Book chapters on the topic "Mice Mice Mice Mice"

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Banks, Ron E., Julie M. Sharp, Sonia D. Doss, and Deborah A. Vanderford. "Mice." In Exotic Small Mammal Care and Husbandry. John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119265405.ch6.

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Lee, Jinsoo, and Kaye Chon. "MICE." In Encyclopedia of Tourism. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-01669-6_407-1.

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Lee, Jinsoo, and Kaye Chon. "MICE." In Encyclopedia of Tourism. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-01384-8_407.

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Roman, Steven. "Mice." In Understanding Personal Computer Hardware. Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4684-6419-1_11.

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Löffler-Mang, Martin. "Optical Mice." In Optische Sensorik. Vieweg+Teubner Verlag, 2011. http://dx.doi.org/10.1007/978-3-8348-8308-7_21.

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Fang, Wei-Ta. "MICE Industry." In Tourism in Emerging Economies. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2463-9_10.

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Mitchell, William J., and John R. Steel. "Squashed Mice." In Fine Structure and Iteration Trees. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-21903-4_4.

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Baker, Darren J. "Hypomorphic Mice." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-974-1_13.

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Lo, Lilian H., and Vincent W. Keng. "Transgenic Mice." In Encyclopedia of Gerontology and Population Aging. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-69892-2_967-1.

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Poluektova, Larisa Y., and Edward Makarov. "Humanized Mice." In Springer Protocols Handbooks. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8794-4_33.

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Conference papers on the topic "Mice Mice Mice Mice"

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Soler, Paul. "MICE Results." In The 20th International Workshop on Neutrinos. Sissa Medialab, 2019. http://dx.doi.org/10.22323/1.341.0015.

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Torun, Yağmur. "MICE Status." In NEUTRINO FACTORIES AND SUPERBEAMS: 5th International Workshop on Neutrino Factories and Superbeams; NuFact 03. AIP, 2004. http://dx.doi.org/10.1063/1.1818383.

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Soler, F. J. P., Daniel Kaplan, Maury Goodman, and Zack Sullivan. "Status of MICE." In NEUTRINO FACTORIES, SUPERBEAMS, AND BETA BEAMS: 11th International Workshop on Neutrino Factories, Superbeams and Beta Beams—NuFact09. AIP, 2010. http://dx.doi.org/10.1063/1.3399320.

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Schulz, Claus-Dieter. "The MICE project." In the second ACM international conference. ACM Press, 1994. http://dx.doi.org/10.1145/192593.197414.

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Perner-Wilson, Hannah, and Leah Buechley. "Handcrafting textile mice." In the 8th ACM Conference. ACM Press, 2010. http://dx.doi.org/10.1145/1858171.1858257.

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Bonesini, Maurizio. "MICE and NuStorm." In Neutrino Oscillation Workshop. Sissa Medialab, 2019. http://dx.doi.org/10.22323/1.337.0031.

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Zisman, Michael S., Osamu Yasuda, Naba Mondal, and Chihiro Ohmori. "MICE Construction Status." In NEUTRINO FACTORIES, SUPERBEAMS AND BETABEAMS: 9th International Workshop on Neutrino Factories, Superbeams, and Betabeams. AIP, 2008. http://dx.doi.org/10.1063/1.2898965.

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Isley, Vicky, and Paul Smith. "Dreams of Mice." In C&C '15: Creativity and Cognition. ACM, 2015. http://dx.doi.org/10.1145/2757226.2757366.

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Ólafsdóttir, Hildur, Tron A. Darvann, Bjarne K. Ersbøll, et al. "Craniofacial statistical deformation models of wild-type mice and Crouzon mice." In Medical Imaging, edited by Josien P. W. Pluim and Joseph M. Reinhardt. SPIE, 2007. http://dx.doi.org/10.1117/12.697406.

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Milenkovic, Maria, and Roland Alo. "Of mice and children." In Posters and short talks of the 1992 SIGCHI conference. ACM Press, 1992. http://dx.doi.org/10.1145/1125021.1125076.

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Reports on the topic "Mice Mice Mice Mice"

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Fry, R. J. M. Mice, myths, and men. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/41272.

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Witte H. and S. Plate. Partial Return Yoke for MICE. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1108553.

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Wong, Kwok-Kin. MPD in Telomerase Null Mice. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada587644.

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Roderick, T. H. Improved mutagen testing systems in mice. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6732389.

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Segall, Jeffrey. Analysis of Metastasis in Transgenic Mice. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada384861.

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Neuffer, D., D. Summers, T. Mohayai, P. Snopok, and C. Rogers. Use of Wedge Absorbers in MICE. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1354869.

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Bennett, L. M., and Roger Wiseman. The Development of BRCA2-Deficient Mice. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada414587.

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Green, Michael A. The Cryogenic refrigeration system for MICE. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/926451.

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Green, Michael A. The superconducting solenoid magnets for MICE. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/926743.

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Segall, Jeffrey E. Analysis of Metastasis in Transgenic Mice. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada403427.

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