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Functional Genomics and Proteomics in the Clinical Neurosciences

Specificaties
Gebonden, blz. | Engels
Elsevier Science | e druk, 2006
ISBN13: 9780444518538
Rubricering
Elsevier Science e druk, 2006 9780444518538
Onderdeel van serie Progress in Brain Research
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Samenvatting

The purpose of this work is to familiarize neuroscientists with the available tools for proteome research and their relative abilities and limitations. To know the identities of the thousands of different proteins in a cell, and the modifications to these proteins, along with how the amounts of both of these change in different conditions would revolutionize biology and medicine. While important strides are being made towards achieving the goal of global mRNA analysis, mRNA is not the functional endpoint of gene expression and mRNA expression may not directly equate with protein expression. There are many potential applications for proteomics in neuroscience: determination of the neuro-proteome, comparative protein expression profiling, post-translational protein modification profiling and mapping protein-protein interactions, to name but a few. Functional Genomics and Proteomics in Clinical Neuroscience will comment on all of these applications, but with an emphasis on protein expression profiling. This book combines the basic methodology of genomics and proteomics with the current applications of such technologies in understanding psychiatric illnesses.

Specificaties

ISBN13:9780444518538
Taal:Engels
Bindwijze:Gebonden

Inhoudsopgave

<p>List of Contributors</p> <p>Foreword</p> <p>Functional Genomics and Proteomics in the Clinical Neurosciences</p> <p>Tissue preparation and banking</p> <p>Introduction</p> <p>Identifying subjects</p> <p>Collection and harvesting tissue</p> <p>Documenting</p> <p>RNA integrity</p> <p>Protein integrity</p> <p>Conclusions</p> <p>Functional genomic methodologies</p> <p>Introduction</p> <p>Input sources of RNA</p> <p>Gene expression profiling: toward an informed choice</p> <p>Level of sensitivity to detect the molecules of interest</p> <p>Magnitude of expression-level changes in the brain</p> <p>Minimum starting material for functional genomic analysis</p> <p>Verification of expression-profiling analysis</p> <p>Conventional methods of analyzing gene expression: Northern hybridization</p> <p>qPCR</p> <p>Serial analysis of gene expression (SAGE)</p> <p>Massive parallel signature sequencing (MPSS)</p> <p>Total analysis of gene expression (TOGA)</p> <p>Sequencing by hybridization (SBH)</p> <p>Microarray platforms</p> <p>Analyzing massive datasets</p> <p>Regional and single cell assessment</p> <p>RNA amplification strategies: aRNA amplification</p> <p>Additional considerations</p> <p>Conclusions</p> <p>Methods for proteomics in neuroscience</p> <p>Introduction</p> <p>Subcellular fractionation</p> <p>Expression proteomics</p> <p>Functional proteomics</p> <p>Mass spectrometry</p> <p>Protein arrays</p> <p>Conclusion</p> <p>Functional genomics and proteomics in the clinical neurosciences: data mining and bioinformatics</p> <p>Introduction</p> <p>Experimental methods</p> <p>Data analysis</p> <p>Statistical analysis and pattern classification</p> <p>Microarray case study</p> <p>Interpretation and validation</p> <p>Reproducibility of microarray studies: concordance of current analysis methods</p> <p>Introduction</p> <p>The data analysis pipeline</p> <p>Assessment of data quality</p> <p>Performance comparison</p> <p>Validation</p> <p>Implications for data mining</p> <p>Summary and conclusions</p> <p>The genomics of mood disorders</p> <p>Introduction</p> <p>Genetics of mood disorders: the progress</p> <p>Neurobiological and neuroanatomical substrates of severe mood disorders</p> <p>The pathophysiology of severe mood disorders: insights from recent gene profiling studies</p> <p>Clues from animal models</p> <p>Concluding remarks</p> <p>Transcriptome alterations in schizophrenia: disturbing the functional architecture of the dorsolateral prefrontal cortex</p> <p>Dysfunction of the DLPFC in schizophrenia</p> <p>Types of transcriptome alterations in the DLPFC in schizophrenia</p> <p>Causes of transcriptome alterations in the DLPFC in schizophrenia</p> <p>Consequences of transcriptome alterations in the DLPFC in schizophrenia</p> <p>Conclusions</p> <p>Strategies for improving sensitivity of gene expression profiling: regulation of apoptosis in the limbic lobe of schizophrenics and bipolars</p> <p>Introduction</p> <p>Conclusions</p> <p>Assessment of genome and proteome profiles in cocaine abuse</p> <p>Introduction</p> <p>Neuroanatomy of cocaine addiction</p> <p>Functional genomics</p> <p>Proteomics</p> <p>Conclusion</p> <p>Neuronal gene expression profiling: uncovering the molecular biology of neurodegenerative disease</p> <p>Introduction</p> <p>Alzheimer's disease</p> <p>Determination of RNA within senile plaques and neurofibrillary tangles in AD</p> <p>Single cell gene array analysis of hippocampal senile plaques in AD</p> <p>Single cell gene analysis of hippocampal NFTs in AD</p> <p>Regional gene expression profiling in the hippocampus in AD</p> <p>Regional gene expression profiling in frontal and temporal neocortex in AD</p> <p>Regional gene expression profiling in other AD-related brain regions</p> <p>Single cell analysis of cholinergic basal forebrain (CBF) neurons in AD</p> <p>Single cell profiling of galanin hyperinnervated CBF neurons in AD</p> <p>Summary of gene expression profiling in AD</p> <p>Parkinson's disease</p> <p>Regional gene profiling of the substantia nigra in PD</p> <p>Gene expression profiling of Lewy body-containing SNpc neurons in PD</p> <p>Summary of gene expression profiling in PD</p> <p>Schizophrenia</p> <p>Regional gene expression profiling in frontal cortex in schizophrenia</p> <p>Single cell gene profiling in the entorhinal cortex in schizophrenia</p> <p>Multiple sclerosis</p> <p>Gene profiling in multiple sclerosis</p> <p>Creutzfeld–Jakob disease</p> <p>Gene profiling in the aged brain</p> <p>Single cell profiling of aged CA1 and CA3 hippocampal neurons</p> <p>Gene regulation during the course of normal aging within the frontal cortex</p> <p>Conclusions</p> <p>Abbreviations</p> <p>Epileptogenesis-related genes revisited</p> <p>Introduction</p> <p>Methods</p> <p>Results and discussion</p> <p>Concluding remarks</p> <p>Abbreviations</p> <p>Functional genomics of sex hormone-dependent neuroendocrine systems: specific and generalized actions in the CNS</p> <p>Neural and genomic mechanisms for female mating behaviors</p> <p>From lordosis to sexual arousal to generalized CNS arousal</p> <p>From generalized CNS arousal to specific forms of arousal</p> <p>Molecular biology of histamine receptors in CNS</p> <p>α1B-Noradrenergic receptor signaling</p> <p>μ and δ opioid receptor signaling</p> <p>Summary and outlook</p> <p>Abbreviations</p> <p>Implications for the practice of psychiatry</p> <p>Introduction</p> <p>Proteomics</p> <p>mRNA expression arrays (expressomics)</p> <p>Whole genome SNP association studies</p> <p>Use of convergent evidence</p> <p>Future directions</p> <p>Human brain evolution</p> <p>Anatomical evolution</p> <p>Protein sequence evolution</p> <p>Gene expression evolution</p> <p>Theory of gene expression evolution</p> <p>Adaptive human brain evolution</p> <p>Conclusion</p> <p>Subject Index</p> <p>Erratum to Progress in Brain Research Vol. 158 Functional Genomics and Proteomics in the Clinical Neurosciences Scott E. Hemby and Sabine Bahn</p>
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        Functional Genomics and Proteomics in the Clinical Neurosciences