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Libri sul tema "Gene Array"

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Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 20 febbraio 2023

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1

Muller, Hans-Joachim. Microarrays. Burlington, MA: Elsevier Academic Press, 2005.

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2

la, Fuente Alberto de. Gene network inference: Verification of methods for systems genetics data. Heidelberg: Springer, 2013.

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3

1966-, Scherer Andreas, a cura di. Batch effects and noise in microarray experiments, sources, and solutions. Chichester, West Sussex: J. Wiley, 2009.

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4

Muller, Hans-Joachim. Microarrays. Burlington, MA: Elsevier Academic Press, 2006.

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5

T, Kho Alvin, e Butte Atul J, a cura di. Microarrays for an integrative genomics. Cambridge, Mass: MIT Press, 2003.

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6

1965-, Blalock Eric M., a cura di. A beginner's guide to microarrays. Boston: Kluwer Academic Publishers, 2003.

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7

Al-mulla, Fahd. Formalin-fixed paraffin-embedded tissues: Methods and protocols. New York: Humana Press, 2011.

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8

1961-, Ye S., e Day Ian N. M, a cura di. Microarrays & microplates: Applications in biomedical sciences. Oxford: BIOS, 2003.

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9

Schena, Mark. Microarray analysis. Hoboken, NJ: Wiley-Liss, 2003.

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10

Beadchip molecular immunohematology: Toward routine donor and patient antigen profiling by DNA analysis. New York: Springer, 2011.

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11

Kacprzyk, Janusz. Fuzzy Systems in Bioinformatics and Computational Biology. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009.

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12

Hardiman, Gary. Microarray Innovations. Taylor & Francis Group, 2019.

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13

Hardiman, Gary. Microarray Innovations. Taylor & Francis Group, 2009.

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14

1966-, Hardiman Gary, a cura di. Microarray innovations: Technology and experimentation. Boca Raton: Taylor & Francis, 2008.

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15

Hardiman, Gary. Microarray Innovations: Technology and Experimentation. Taylor & Francis Group, 2009.

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16

Hardiman, Gary. Microarray Innovations: Technology and Experimentation. Taylor & Francis Group, 2009.

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17

Müller, Hans-Joachim, e Thomas Roeder. Microarrays (The Experimenter Series). Academic Press, 2005.

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18

Müller, Hans-Joachim, e Thomas Roeder. Microarrays (The Experimenter Series). Academic Press, 2005.

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19

(Editor), Alan R. Kimmel, e Brian Oliver (Editor), a cura di. DNA Microarrays Part A: Array Platforms & Wet-Bench Protocols, Volume 410 (Methods in Enzymology). Academic Press, 2006.

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20

(Editor), Alan R. Kimmel, e Brian Oliver (Editor), a cura di. DNA Microarrays Part A: Array Platforms & Wet-Bench Protocols, Volume 410 (Methods in Enzymology). Academic Press, 2006.

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21

Schena, M. DNA Microarrays (Methods Express) (Methods Express). Scion Publishing, 2007.

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22

Microarray Technology Through Applications. Taylor & Francis, 2007.

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23

F, Falciani, a cura di. Microarray technology through applications. New York: Taylor & Francis, 2007.

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24

Microarrays And Transcription Networks. Landes Bioscience, 2005.

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25

Do, Kim-Anh, Christophe Ambroise e Geoffrey J. McLachlan. Analyzing Microarray Gene Expression Data (Wiley Series in Probability and Statistics). Wiley-Interscience, 2004.

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26

Microarray technology through applications. New York, NY: Taylor & Francis, 2007.

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27

(Editor), Tuan D. Pham, Hong Yan (Editor) e Denis I. Crane (Editor), a cura di. Advanced Computational Methods for Biocomputing And Bioimaging. Nova Science Publishers, 2006.

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28

(Editor), Peng Liang, Jonathan Meade (Editor) e Arthur B. Pardee (Editor), a cura di. Differential Display Methods and Protocols (Methods in Molecular Biology). 2^a ed. Humana Press, 2005.

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29

Microarrays Methods and Applications (Nuts & Bolts series). Dna Press, 2003.

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30

Ulrike, Nuber, a cura di. DNA microarrays. New York, NY: Chapman&Hall/CRC, 2005.

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31

Peng, Liang, Meade Jonathan D e Pardee Arthur B. 1921-, a cura di. Differential display methods and protocols. 2^a ed. Totowa, N.J: Humana Press, 2005.

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32

R, Kimmel Alan, e Oliver B, a cura di. DNA microarrays. Amsterdam: Elsevier/Academic Press, 2006.

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33

Blalock, Eric M. Beginner's Guide to Microarrays. Springer, 2012.

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34

(Editor), Alan R. Kimmel, e Brian Oliver (Editor), a cura di. DNA Microarrays, Part B: Databases and Statistics, Volume 411 (Methods in Enzymology). Academic Press, 2006.

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35

Pardee, Arthur B., Peng Liang e Jonathan Meade. Differential Display Methods and Protocols. Humana Press, 2010.

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36

Harms, Matthew B., e Timothy M. Miller. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0027.

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Abstract (sommario):

Recent advances in sequencing technologies have dramatically expanded the number of genes associated with amyotrophic lateral sclerosis, including rare but highly penetrant causative mutations as well as common risk alleles. This chapter discusses these gene discoveries and how they have implicated a diverse array of biological pathways essential for motor neuron health and have begun to inform our understanding of ALS pathogenesis as a heterogeneous and multistep process. Insights from these discoveries are leading to a new generation of targeted therapies directed at specific genes and are poised to inform how patients with amyotrophic lateral sclerosis are evaluated and treated in the clinic.

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37

DNA Microarrays, Part B: Databases and Statistics, Volume 411 (Methods in Enzymology). Academic Press, 2006.

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38

Kinsman, Stephen L. Spina Bifida and Related Conditions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0077.

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The term “spinal dysraphism” encompasses the broadest array of the conditions known as the neural tube defects. The open neural tube defects (spina bifida aperta and cystica) include both disorders of primary and/or secondary neuralation and are best defined as myelomeningocele complex (MMC) due to their protean nervous system manifestations beyond the spinal lesion. Closed spinal dysraphisms (so-called spina bifida occulta) include lipomatous lesions, forms of tethered spinal cord, sinus tracts, and forms of split spinal cord (diastematomyelia). Both genetic and environmental etiologies have been identified. Gene-environment and gene-gene interactions are also important in the pathobiology of these conditions.

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39

E, Burczynski Michael, a cura di. An introduction to toxicogenomics. Boca Raton, FL: CRC Press, 2003.

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40

(Editor), Stuart Handwerger, e Bruce Aronow (Editor), a cura di. Genomics in Endocrinology: DNA Microarray Analysis in Endocrine Health and Disease (Contemporary Endocrinology). Humana Press, 2007.

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41

Handwerger, Stuart, e Bruce J. Aronow. Genomics in Endocrinology: DNA Microarray Analysis in Endocrine Health and Disease. Humana, 2014.

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42

Day, I. n. m. Microarrays and Microplates: Applications in Biomedical Sciences (Advanced Methods). Garland Science, 2003.

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43

Handwerger, Stuart, e Bruce J. Aronow. Genomics in Endocrinology: DNA Microarray Analysis in Endocrine Health and Disease. Humana Press, 2007.

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44

Q, Wang John, a cura di. Drugs of abuse: Neurological reviews and protocols. Totowa, N.J: Humana Press, 2003.

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45

(Editor), Daniel H. Geschwind, e Jeffrey P. Gregg (Editor), a cura di. Microarrays for the Neurosciences: An Essential Guide (Cellular and Molecular Neuroscience). The MIT Press, 2002.

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46

Schena, Mark. Microarray Analysis. Wiley-Liss, 2002.

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47

Canli, Turhan, a cura di. The Oxford Handbook of Molecular Psychology. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780199753888.001.0001.

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Abstract (sommario):

Determining the biological bases for behavior—and the extent to which we can observe and explain their neural underpinnings—requires a bold, broadly defined research methodology. The interdisciplinary entries in this handbook are organized around the principle of “molecular psychology,” which unites cutting-edge research from such wide-ranging disciplines as clinical neuroscience and genetics, psychology, behavioral neuroscience, and neuroethology. For the first time in a single volume, leaders from diverse research areas present their work in which they use molecular approaches to investigate social behavior, psychopathology, emotion, cognition, and stress in healthy volunteers, patient populations, and an array of nonhuman species including nonhuman primates, rodents, insects, and fish. Chapters draw on molecular methods covering candidate genes, genome-wide association studies, copy number variations, gene expression studies, and epigenetics while addressing the ethical, legal, and social issues to emerge from this new and exciting research approach.

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48

Brüne, Martin. Textbook of Evolutionary Psychiatry and Psychosomatic Medicine. Oxford University Press, 2016. http://dx.doi.org/10.1093/med:psych/9780198717942.001.0001.

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Abstract (sommario):

Psychiatry and psychosomatic medicine are concerned with medical conditions affecting the brain, mind, and behaviour in manifold ways. Traditional approaches have focused on a restricted array of potential causes of psychiatric and psychosomatic conditions, including adverse experiences such as trauma, neglect, or abuse, genetic vulnerability, and epigenetic regulation of gene expression. While essential for the understanding of mental disorders, these approaches have disregarded pertinent questions such as why the human mind is vulnerable to dysfunction at all. This Textbook of Evolutionary Psychiatry and Psychosomatic Medicine seeks to find answers to these questions by emphasizing an evolutionary perspective on psychiatric and psychosomatic conditions. It explains how the human brain/mind has been shaped by natural and sexual selection; why adaptations to environmental conditions in our evolutionary past may nowadays work in suboptimal ways; and how human cognition, emotions, and behaviour can be scientifically framed to improve our understanding of how people try to attain important biosocial goals pertaining to one’s status in society, mating, eliciting and providing care, and maintaining rewarding relationships. The evolutionary topics relevant to the understanding of psychiatric and psychosomatic conditions include the concepts of genetic plasticity, life-history theory, stress regulation, and immunological aspects. In addition, it is argued that an evolutionary framework is necessary to understand how psychotherapy and psychopharmacology work to improve the lives of patients with psychiatric and psychosomatic disorders.

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49

New approaches to molecular diagnostics: Identification of differentially expressed genes in breast cancer cell lines using cDNA aray hybridization and sequence analysis. Ottawa: National Library of Canada, 1998.

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50

Crosbie, Christopher. Revenge Tragedy and Classical Philosophy on the Early Modern Stage. Edinburgh University Press, 2019. http://dx.doi.org/10.3366/edinburgh/9781474440264.001.0001.

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Abstract (sommario):

This book discovers within early modern revenge tragedy the surprising shaping presence of a wide array of classical philosophies not commonly affiliated with the genre. By recovering the pervasive influence of Aristotelian faculty psychology on The Spanish Tragedy, Aristotelian ethics on Titus Andronicus, Lucretian atomism on Hamlet, Galenic pneumatics on Antonio’s Revenge and Epictetian Stoicism on The Duchess of Malfi, this book reveals how the very atmospheres and ontological assumptions of revenge tragedy exert their own kind of conditioning dramaturgical force. The book also revitalises our understanding of how the Renaissance stage, even at its most lurid, functions as a unique space for the era’s practical, vernacular engagement with received philosophy.

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