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Neurogenetics : (Record no. 8411)

MARC details
000 -LEADER
fixed length control field	06019cam a22003494a 4500
001 - CONTROL NUMBER
control field	12775537
003 - CONTROL NUMBER IDENTIFIER
control field	OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field	20200226163346.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field	020515s2003 njua b 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number	2002068584
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number	0896039900 (alk. paper)
040 ## - CATALOGING SOURCE
Original cataloging agency	DLC
Transcribing agency	DLC
Modifying agency	DLC
042 ## - AUTHENTICATION CODE
Authentication code	pcc
050 00 - LIBRARY OF CONGRESS CALL NUMBER
Classification number	QP356.22
Item number	.N485 2003
082 00 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number	616.042 POT
Edition number	21
245 00 - TITLE STATEMENT
Title	Neurogenetics :
Remainder of title	methods and protocols /
Statement of responsibility, etc.	edited by Nicholas T. Potter.
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc.	Totowa, N.J. :
Name of publisher, distributor, etc.	Humana Press,
Date of publication, distribution, etc.	c2003.
300 ## - PHYSICAL DESCRIPTION
Extent	xiii, 390 p. :
Other physical details	ill. (some col.) ;
Dimensions	26 cm.
490 1# - SERIES STATEMENT
Series statement	Methods in molecular biology ;
Volume/sequential designation	v. 217
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note	Includes bibliographical references and index.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note	Machine generated contents note: Preface -- Color Plates -- Contributors -- PART I. QUANTITATIVE PCR -- 1 Determination of Gene Dosage: -- Utilization of Endogenous and Exogenous Internal Standards -- Thomas W. Prior -- 2 Semiquantitative PCR for the Detection of Exon Rearrangements in the Parkin Gene -- Christoph B. Lucking and Alexis Brice -- PART II. TRINUCLEOTIDE REPEAT DETECTION -- 3 Detection of FMR1 Trinucleotide Repeat Expansion Mutations Using Southern Blot and PCR Methodologies -- Jack Tarleton -- 4 Extreme Expansion Detection in Spinocerebellar Ataxia Type 2 and Type 7 -- Karen Snow and Rong Mao -- 5 Repeat Expansion Detection (RED) and the RED Cloning Strategy -- Qiu-Ping Yuan, Kerstin Lindblad-Toh, and Martin Schalling -- 6 Repeat Analysis Pooled Isolation and Detection (RAPID) Cloning of Microsatellite Expansions -- Laura P. W. Ranum -- 7 DIRECT Technologies for Molecular Cloning of Genes Containing -- Expanded CAG Repeats -- Kazuhiro Sanpei, Takeshi Ikeuchi, and Shoji Tsuji -- 8 Antibody-Based Detection of CAG Repeat Expansion Containing Genes -- Yvon Trottier -- 9 Detection of Trinucleotide Repeat Containing Genes by Matrix-Assisted Laser Desorption/lonization (MALDI) -- Mass Spectrometry -- Chung-Hsuan Chen, Nicholas T. Potter, and Nelly T. Taranenko -- 10 Fluorescence PCR and GeneScan Analysis for the Detection of CAG Repeat Expansions Associated with Huntington's Disease -- Cindy L. Vnencak-Jones -- PART III. SEQUENCE-BASED MUTATION DETECTION -- 11 Molecular Detection of Galactosemia Mutations by PCR-ELISA -- Kasinathan Muralidharan and Wei Zhang -- 12 Denaturing High-Performance Liquid Chromatography and Sequence Analyses for MECP2 Mutations in Rett Syndrome -- Inge M. Buyse and Benjamin B. Roa -- 13 Multiplexed Fluorescence Analysis for Mutations Causing Tay-Sachs Disease -- Tracy L. Stockley and Peter N. Ray -- 14 Single-Strand Conformational Polymorphism Analysis (SSCP) and Sequencing for Ion Channel Gene Mutations -- Kylie A. Scoggan and Dennis E. Bulman -- 15 Pulse Field Gel Electrophoresis for the Detection of Facioscapulohumeral Muscular Dystrophy Gene Rearrangements -- Luciano Felicetti and Giuliana Galluzzi -- 16 Denaturing Gradient Gel Electrophoresis (DGGE) for Mutation Detection in Duchenne Muscular Dystrophy (DMD) -- Luciana C. B. Dolinsky -- 17 Genetic Diagnosis of Charcot-Marie-Tooth Disease -- Frank Baas -- 18 Analysis of Human Mitochondrial DNA Mutations -- Antonio L. Andreu, Ramon Marti, and Michio Hirano -- 19 Detection of Mitochondrial DNA Mutations Associated with Leber Hereditary Optic Neuropathy -- Kasinathan Muralidharan -- PART IV. MOLECULAR DETECTION OF IMPRINTED GENES -- 20 PCR-Based Strategies for the Diagnosis of Prader-Willi/Angelman Syndromes -- Milen Velinov and Edmund C. Jenkins -- PART V. FLUORESCENCE IN SITU HYBRIDIZATION (FISH) -- 21 Fluorescence In Situ Hybridization (FISH) for Identifying the Genomic Rearrangements Associated with Three Myelinopathies: -- Charcot-Marie-Tooth Disease, Hereditary Neuropathy with Liability to Pressure Palsies, and Pelizaeus-Merzbacher Disease -- Mansoor S. Mohammed and Lisa G. Shaffer -- PART VI. IN VITRO EXPRESSION SYSTEMS AND STUDIES OF PROTEIN EXPRESSION AND FUNCTION -- 22 Drosophila Models of Polyglutamine Diseases -- H. Y. Edwin Chan and Nancy M. Bonini -- 23 A Comparative Gene Expression Analysis of Emery-Dreifuss Muscular Dystrophy Using a cDNA Microarray -- Toshifumi Tsukahara and Kiichi Arahata -- 24 The COS-7 Cell In Vitro Paradigm to Study Myelin Proteolipid Protein 1 Gene Mutations -- Alexander Gow -- 25 In Vitro Expression Systems for the Huntington Protein -- Shi-Hua Li and Xiao-Jiang Li -- 26 Heterologous Expression of Ion Channels -- Andrew R. Tapper and Alfred L. George, Jr. -- 27 An Assay for Characterizing In Vitro the Kinetics of Polyglutamine Aggregation -- Valerie Berthelier and Ronald Wetzel -- 28 Characterization of Prion Proteins -- Wenquan Zou, Monica Colucci, Pierluigi Gambetti, -- and Shu G. Chen -- 29 Detection of NF1 Mutations Utilizing the Protein Truncation Test (PTT) -- Meena Upadhyaya, Michael Osborn, and David N. Cooper -- 30 Application of the Protein Truncation Test (PTT) for the Detection of Tuberosis Sclerosis Complex Type 1 and 2 (TSC1 and TSC2) Mutations -- Karin Mayer -- 31 Development and Characterization of Antibodies that Immunoprecipitate the FMR1 Protein -- Stephanie Ceman, Fuping Zhang, Tamika Johnson, -- and Stephen T. Warren -- 32 Immunological Methods for the Analysis of Protein Expression in Neuromuscular Diseases -- Mariz Vainzof, Maria Rita Passos-Bueno, and Mayana Zatz.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element	Neurogenetics
Form subdivision	Laboratory manuals.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element	Genetic disorders
General subdivision	Diagnosis
Form subdivision	Laboratory manuals.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name	Potter, Nicholas T.
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title	Methods in molecular biology (Clifton, N.J.) ;
Volume/sequential designation	v. 217.
856 41 - ELECTRONIC LOCATION AND ACCESS
Materials specified	Table of contents
Uniform Resource Identifier	<a href="http://www.loc.gov/catdir/toc/fy033/2002068584.html">http://www.loc.gov/catdir/toc/fy033/2002068584.html</a>
856 42 - ELECTRONIC LOCATION AND ACCESS
Materials specified	Book review (E-STREAMS)
Uniform Resource Identifier	<a href="http://www.e-streams.com/es0606/es0606_2540.html">http://www.e-streams.com/es0606/es0606_2540.html</a>
856 42 - ELECTRONIC LOCATION AND ACCESS
Materials specified	Publisher description
Uniform Resource Identifier	<a href="http://www.loc.gov/catdir/enhancements/fy0825/2002068584-d.html">http://www.loc.gov/catdir/enhancements/fy0825/2002068584-d.html</a>
906 ## - LOCAL DATA ELEMENT F, LDF (RLIN)
a	7
b	cbc
c	orignew
d	1
e	ocip
f	20
g	y-gencatlg
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme	Dewey Decimal Classification
Koha item type	Reference text books

Holdings
Withdrawn status	Lost status	Source of classification or shelving scheme	Damaged status	Not for loan	Collection code	Home library	Current library	Date acquired	Total Checkouts	Full call number	Barcode	Date last seen	Price effective from	Koha item type
		Dewey Decimal Classification			R-30/1	All India Institute of Speech and Hearing	All India Institute of Speech and Hearing	26/02/2020		616.042 POT	15659	26/02/2020	26/02/2020	Reference text books