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Books on the topic 'In vivo characterization'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Karaskov, Elizabeta. In vivo characterization of ordered factor recruitment at CIITA inducible promoter IV. Ottawa: National Library of Canada, 2003.

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2

Müller, Rainer H. Colloidal carriers for controlled drug delivery and targeting: Modification, characterization, and in vivo distribution. Stuttgart: Wissenschaftliche Verlagsgesellschaft, 1991.

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3

Joshi, Mital. Development and characterization of a graded, in vivo, compressive, murine model of spinal cord injury. Ottawa: National Library of Canada, 2000.

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4

Kroeker, Randall Murray. In vivo characterization of NMR relaxation times. 1987.

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5

Juliette, Lisa Yvonne. In vivo and in vitro characterization of ammonia monooxygenase in Nitrosomonas europaea. 1995.

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6

Rahman, Mohammad Mohsin. In-vivo and in-vitro characterization of a human ependymoma-derived cell line. 1985.

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7

Griffiths, Emily Kathleen. Characterization of the in vivo roles of the adapter proteins ADAP and CBL-3. 2002.

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8

Characterization of rat glomerular epithelial cells in culture: A comparison to rat glomeruli in vivo. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.

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9

Dymarkowski, Steven. In Vivo Analysis & Characterization of Myocardial Ischemia & Infarction: Experimental Mri-Studies (Acta Biomedica Lovaniensia, 288). Leuven Univ Pr, 2003.

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10

Lahooti, Shahab. In vitro and in vivo characterization of genetically engineered cells microencapsulated in a HEMA-MMA copolymer. 1999.

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11

Portwine, Carol Ann. Identification and characterization of Li-Fraumeni syndrome families: Molecular and in vitro analysis and development of an in vivo model. 2002.

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12

Koller, Hannelore T. Multiple functional in vivo spacer rRNA gene promoters during early development and characterization of the intergenic spacer in the crustacean Artemia. 1987.

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13

In vivo characterization of R/S-and R-[11C]SKF 82957 as a D1 agonist radioligand for pet: Effect of drugs acting on the dopamine system. Ottawa: National Library of Canada, 1998.

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14

Glorieux, Griet, Nathalie Neirynck, Anneleen Pletinck, Eva Schepers, and Raymond Vanholder. Overview of uraemic toxins. Edited by Jonathan Himmelfarb. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0254_update_001.

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The uraemic syndrome is a complex mixture of organ dysfunctions attributed to the retention of a multitude of compounds that under normal conditions are excreted by healthy kidneys. Although important progress has been made in the identification and characterization of uraemic retention solutes and in the revealing of their pathophysiological effects, this knowledge remains far from complete. Data are discussed on general characteristics of specific uraemic retention solutes, on in vitro and in vivo biological effects and on available observational and interventional studies with respect to their removal and related patient outcome are discussed.

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15

Vassanelli, Stefano. Implantable neural interfaces. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199674923.003.0050.

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Establishing direct communication with the brain through physical interfaces is a fundamental strategy to investigate brain function. Starting with the patch-clamp technique in the seventies, neuroscience has moved from detailed characterization of ionic channels to the analysis of single neurons and, more recently, microcircuits in brain neuronal networks. Development of new biohybrid probes with electrodes for recording and stimulating neurons in the living animal is a natural consequence of this trend. The recent introduction of optogenetic stimulation and advanced high-resolution large-scale electrical recording approaches demonstrates this need. Brain implants for real-time neurophysiology are also opening new avenues for neuroprosthetics to restore brain function after injury or in neurological disorders. This chapter provides an overview on existing and emergent neurophysiology technologies with particular focus on those intended to interface neuronal microcircuits in vivo. Chemical, electrical, and optogenetic-based interfaces are presented, with an analysis of advantages and disadvantages of the different technical approaches.

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