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Mitochondrial Disorders

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Cover of 'Mitochondrial Disorders'

Table of Contents

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    Book Overview
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    Chapter 1 Mitochondrial DNA Mutations: An Overview of Clinical and Molecular Aspects
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    Chapter 2 Nuclear gene defects in mitochondrial disorders.
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    Chapter 3 Diagnostic Challenges of Mitochondrial Disorders: Complexities of Two Genomes
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    Chapter 4 Biochemical Analyses of the Electron Transport Chain Complexes by Spectrophotometry
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    Chapter 5 Measurement of Mitochondrial Oxygen Consumption Using a Clark Electrode
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    Chapter 6 Mitochondrial Respiratory Chain: Biochemical Analysis and Criterion for Deficiency in Diagnosis
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    Chapter 7 Assays of Pyruvate Dehydrogenase Complex and Pyruvate Carboxylase Activity
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    Chapter 8 Assessment of Thymidine Phosphorylase Function: Measurement of Plasma Thymidine (and Deoxyuridine) and Thymidine Phosphorylase Activity.
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    Chapter 9 Measurement of Mitochondrial dNTP Pools.
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    Chapter 10 Measurement of Oxidized and Reduced Coenzyme Q in Biological Fluids, Cells, and Tissues: An HPLC-EC Method
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    Chapter 11 Assay to Measure Oxidized and Reduced Forms of CoQ by LC–MS/MS
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    Chapter 12 Morphological Assessment of Mitochondrial Respiratory Chain Function on Tissue Sections
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    Chapter 13 Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Diagnostic Tool for the Detection of Assembly Defects in the Enzyme Complexes of Oxidative Phosphorylation
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    Chapter 14 Radioactive Labeling of Mitochondrial Translation Products in Cultured Cells
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    Chapter 15 Transmitochondrial cybrids: tools for functional studies of mutant mitochondria.
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    Chapter 16 Fluorescence-Activated Cell Sorting Analysis of Mitochondrial Content, Membrane Potential, and Matrix Oxidant Burden in Human Lymphoblastoid Cell Lines
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    Chapter 17 Molecular Profiling of Mitochondrial Dysfunction in Caenorhabditis elegans.
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    Chapter 18 Analysis of Common Mitochondrial DNA Mutations by Allele-Specific Oligonucleotide and Southern Blot Hybridization
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    Chapter 19 Sequence analysis of the whole mitochondrial genome and nuclear genes causing mitochondrial disorders.
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    Chapter 20 Utility of Array CGH in Molecular Diagnosis of Mitochondrial Disorders
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    Chapter 21 Quantification of mtDNA Mutation Heteroplasmy (ARMS qPCR)
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    Chapter 22 Measurement of mitochondrial DNA copy number.
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    Chapter 23 Determination of the Clinical Significance of an Unclassified Variant
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Title
Mitochondrial Disorders
Published by
Humana Press, January 2012
DOI 10.1007/978-1-61779-504-6
ISBNs
978-1-61779-503-9, 978-1-61779-504-6, 978-1-4939-5950-1
Editors

Lee-Jun C. Wong, Ph.D.

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X Demographics

The data shown below were collected from the profiles of 4 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 174 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 174 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 6 3%
Researcher 2 1%
Student > Ph. D. Student 2 1%
Professor 1 <1%
Student > Doctoral Student 1 <1%
Other 1 <1%
Unknown 161 93%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 4%
Agricultural and Biological Sciences 1 <1%
Immunology and Microbiology 1 <1%
Economics, Econometrics and Finance 1 <1%
Medicine and Dentistry 1 <1%
Other 1 <1%
Unknown 162 93%