Neurogenetics - Info and Reading Options

"Neurogenetics" Table Of Contents:

• 1- Machine generated contents note: Preface
• 2- Color Plates
• 3- Contributors
• 4- PART I. QUANTITATIVE PCR
• 5- 1 Determination of Gene Dosage:
• 6- Utilization of Endogenous and Exogenous Internal Standards
• 7- Thomas W. Prior
• 8- 2 Semiquantitative PCR for the Detection of Exon Rearrangements in the Parkin Gene
• 9- Christoph B. Lucking and Alexis Brice
• 10- PART II. TRINUCLEOTIDE REPEAT DETECTION
• 11- 3 Detection of FMR1 Trinucleotide Repeat Expansion Mutations Using Southern Blot and PCR Methodologies
• 12- Jack Tarleton
• 13- 4 Extreme Expansion Detection in Spinocerebellar Ataxia Type 2 and Type 7
• 14- Karen Snow and Rong Mao
• 15- 5 Repeat Expansion Detection (RED) and the RED Cloning Strategy
• 16- Qiu-Ping Yuan, Kerstin Lindblad-Toh, and Martin Schalling
• 17- 6 Repeat Analysis Pooled Isolation and Detection (RAPID) Cloning of Microsatellite Expansions
• 18- Laura P. W. Ranum
• 19- 7 DIRECT Technologies for Molecular Cloning of Genes Containing
• 20- Expanded CAG Repeats
• 21- Kazuhiro Sanpei, Takeshi Ikeuchi, and Shoji Tsuji
• 22- 8 Antibody-Based Detection of CAG Repeat Expansion Containing Genes
• 23- Yvon Trottier
• 24- 9 Detection of Trinucleotide Repeat Containing Genes by Matrix-Assisted Laser Desorption/lonization (MALDI)
• 25- Mass Spectrometry
• 26- Chung-Hsuan Chen, Nicholas T. Potter, and Nelly T. Taranenko
• 27- 10 Fluorescence PCR and GeneScan Analysis for the Detection of CAG Repeat Expansions Associated with Huntington's Disease
• 28- Cindy L. Vnencak-Jones
• 29- PART III. SEQUENCE-BASED MUTATION DETECTION
• 30- 11 Molecular Detection of Galactosemia Mutations by PCR-ELISA
• 31- Kasinathan Muralidharan and Wei Zhang
• 32- 12 Denaturing High-Performance Liquid Chromatography and Sequence Analyses for MECP2 Mutations in Rett Syndrome
• 33- Inge M. Buyse and Benjamin B. Roa
• 34- 13 Multiplexed Fluorescence Analysis for Mutations Causing Tay-Sachs Disease
• 35- Tracy L. Stockley and Peter N. Ray
• 36- 14 Single-Strand Conformational Polymorphism Analysis (SSCP) and Sequencing for Ion Channel Gene Mutations
• 37- Kylie A. Scoggan and Dennis E. Bulman
• 38- 15 Pulse Field Gel Electrophoresis for the Detection of Facioscapulohumeral Muscular Dystrophy Gene Rearrangements
• 39- Luciano Felicetti and Giuliana Galluzzi
• 40- 16 Denaturing Gradient Gel Electrophoresis (DGGE) for Mutation Detection in Duchenne Muscular Dystrophy (DMD)
• 41- Luciana C. B. Dolinsky
• 42- 17 Genetic Diagnosis of Charcot-Marie-Tooth Disease
• 43- Frank Baas
• 44- 18 Analysis of Human Mitochondrial DNA Mutations
• 45- Antonio L. Andreu, Ramon Marti, and Michio Hirano
• 46- 19 Detection of Mitochondrial DNA Mutations Associated with Leber Hereditary Optic Neuropathy
• 47- Kasinathan Muralidharan
• 48- PART IV. MOLECULAR DETECTION OF IMPRINTED GENES
• 49- 20 PCR-Based Strategies for the Diagnosis of Prader-Willi/Angelman Syndromes
• 50- Milen Velinov and Edmund C. Jenkins
• 51- PART V. FLUORESCENCE IN SITU HYBRIDIZATION (FISH)
• 52- 21 Fluorescence In Situ Hybridization (FISH) for Identifying the Genomic Rearrangements Associated with Three Myelinopathies:
• 53- Charcot-Marie-Tooth Disease, Hereditary Neuropathy with Liability to Pressure Palsies, and Pelizaeus-Merzbacher Disease
• 54- Mansoor S. Mohammed and Lisa G. Shaffer
• 55- PART VI. IN VITRO EXPRESSION SYSTEMS AND STUDIES OF PROTEIN EXPRESSION AND FUNCTION
• 56- 22 Drosophila Models of Polyglutamine Diseases
• 57- H. Y. Edwin Chan and Nancy M. Bonini
• 58- 23 A Comparative Gene Expression Analysis of Emery-Dreifuss Muscular Dystrophy Using a cDNA Microarray
• 59- Toshifumi Tsukahara and Kiichi Arahata
• 60- 24 The COS-7 Cell In Vitro Paradigm to Study Myelin Proteolipid Protein 1 Gene Mutations
• 61- Alexander Gow
• 62- 25 In Vitro Expression Systems for the Huntington Protein
• 63- Shi-Hua Li and Xiao-Jiang Li
• 64- 26 Heterologous Expression of Ion Channels
• 65- Andrew R. Tapper and Alfred L. George, Jr.
• 66- 27 An Assay for Characterizing In Vitro the Kinetics of Polyglutamine Aggregation
• 67- Valerie Berthelier and Ronald Wetzel
• 68- 28 Characterization of Prion Proteins
• 69- Wenquan Zou, Monica Colucci, Pierluigi Gambetti,
• 70- and Shu G. Chen
• 71- 29 Detection of NF1 Mutations Utilizing the Protein Truncation Test (PTT)
• 72- Meena Upadhyaya, Michael Osborn, and David N. Cooper
• 73- 30 Application of the Protein Truncation Test (PTT) for the Detection of Tuberosis Sclerosis Complex Type 1 and 2 (TSC1 and TSC2) Mutations
• 74- Karin Mayer
• 75- 31 Development and Characterization of Antibodies that Immunoprecipitate the FMR1 Protein
• 76- Stephanie Ceman, Fuping Zhang, Tamika Johnson,
• 77- and Stephen T. Warren
• 78- 32 Immunological Methods for the Analysis of Protein Expression in Neuromuscular Diseases
• 79- Mariz Vainzof, Maria Rita Passos-Bueno, and Mayana Zatz.

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