Rosenberg's molecular and genetic basis of neurological and psychiatric disease / (Record no. 2780532)

MARC details
000 -LEADER
fixed length control field 07609cam a2200937Ma 4500
001 - CONTROL NUMBER
control field ocn894609030
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220712001250.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION
fixed length control field m o d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
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008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 141021s2014 ne ob 001 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency UKMGB
Language of cataloging eng
Description conventions pn
Transcribing agency UKMGB
Modifying agency OCLCO
-- OCLCF
-- IDEBK
-- EBLCP
-- N$T
-- TEFOD
-- OCLCO
-- OCLCQ
-- TEFOD
-- OCLCO
-- OCLCQ
-- OCLCA
-- CUY
-- MERUC
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-- USU
-- ICG
-- OCLCO
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-- D6H
-- DKC
-- OCLCO
-- OCLCQ
-- RDF
-- OCLCQ
-- OCLCA
-- OCLCO
016 7# - NATIONAL BIBLIOGRAPHIC AGENCY CONTROL NUMBER
Record control number 016933102
Source Uk
016 7# - NATIONAL BIBLIOGRAPHIC AGENCY CONTROL NUMBER
Record control number 016931176
Source Uk
019 ## -
-- 894171500
-- 911047828
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9780124105492
Qualifying information (PDF ebook)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 0124105491
Qualifying information (PDF ebook)
029 1# - (OCLC)
OCLC library identifier AU@
System control number 000056029543
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)894609030
Canceled/invalid control number (OCoLC)894171500
-- (OCoLC)911047828
037 ## - SOURCE OF ACQUISITION
Stock number 785184
Source of stock number/acquisition MIL
037 ## - SOURCE OF ACQUISITION
Stock number E2BB10A8-0A1F-4050-87DE-3E59F3556520
Source of stock number/acquisition OverDrive, Inc.
Note http://www.overdrive.com
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number RC347
Item number .R674 2015eb
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number WL 140
Item number M7178r 2015
072 #7 - SUBJECT CATEGORY CODE
Subject category code HEA
Subject category code subdivision 039000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 014000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 022000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 112000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 045000
Source bisacsh
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.80442
Edition number 23
049 ## - LOCAL HOLDINGS (OCLC)
Holding library MAIN
130 0# - MAIN ENTRY--UNIFORM TITLE
Uniform title Molecular and genetic basis of neurological and psychiatric disease.
9 (RLIN) 1036482
245 10 - TITLE STATEMENT
Title Rosenberg's molecular and genetic basis of neurological and psychiatric disease /
Statement of responsibility, etc edited by Roger N. Rosenberg, Juan M. Pascual.
250 ## - EDITION STATEMENT
Edition statement Fifth edition.
264 #1 -
-- Amsterdam :
-- Academic Press,
-- 2014.
300 ## - PHYSICAL DESCRIPTION
Extent 1 online resource
336 ## -
-- text
-- txt
-- rdacontent
337 ## -
-- computer
-- c
-- rdamedia
338 ## -
-- online resource
-- cr
-- rdacarrier
588 0# -
-- CIP data; item not viewed.
500 ## - GENERAL NOTE
General note Preceded by Molecular and genetic basis of neurologic and psychiatric disease / editors, Roger N. Rosenberg [and others]. 4th ed. c2008.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note Front Cover; Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease; Copyright; Dedications; Contents; Preface to the Fifth Edition; Contributors; Section I: General Concepts and Tools; Chapter 1: Mendelian, Non-Mendelian, Multigenic Inheritance, and Epigenetics; Introduction; Mendelian traits; Mendel's Laws; Chromosomes and Genes; Mendelian Inheritance; Molecular Pathomechanisms of Mutations; Factors That Modify Classic Mendelian Inheritance Patterns; New Mutations, Mosaicism, and Somatic Mutations; Penetrance and Expressivity; Repeat expansion disorders.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Non-mendelian inheritanceMitochondrial Inheritance; Imprinting; Uniparental Disomy; Imprinting, UPD, and Genetic Disorders; Chromosomal and genomic disorders; Aneuploidy; lsochromosomes; Translocations; Intrachromosomal Rearrangements; Mechanisms for Formation of Chromosomal Rearrangements; Nonallelic homologous recombination (NAHR); Nonhomologous end joining (NHEJ); Fork stalling and template switching/microhomology-mediated break-induced replication (FoSTeS/MMBIR); How Chromosomal Rearrangements Confer Phenotypes; Assays for Chromosomal and Genomic Disorders; Multigenic inheritance.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Digenic InheritanceModifier Genes; Complex traits; Genetic Features of Complex Traits; Assessing Variation in the Human Genome; Genetic Variation and Complex Traits; Examples of Susceptibility Genes for Complex Traits; Epigenetics; DNA Methylation and Hydroxymethylation; Histone Modifications and Higher Order Chromatin Remodeling; Noncoding RNA Regulation; The human genome: High-throughput technologies; Conclusions; References; Chapter 2: Genotype-Phenotype Correlations; Introduction; Single phenotype: Multiple genes; Single gene: Multiple phenotypes; Neuronal/cellular selective vulnerability.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Highly variable systemic phenotypesPenetrance and age of onset; Conclusion and future directions; References; Chapter 3: Immunogenetics of Neurological Disease; Introduction; Epidemiological evidence for genetic susceptibility; Genetics of MS: Family-based investigations; The role of major histocompatibility complex genes; Other immune-related genes; The environment and immune-related genes; Conclusion; References; Chapter 4: Pharmacogenomic Approaches to the Treatment of Sporadic Alzheimer Disease using Cholinomimetic Agents; Introduction; Genetic risk factors and sporadic alzheimer disease.
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note Genetic risk factors, cholinergic dysfunction, and alzheimer diseaseApoE4 and cholinomimetic drugs in alzheimer disease; Experimental drugs and their relationship to the apoE4 allele; Acetylcholinesterase and butyrylcholinesterase genetic variants in dementia; Acknowledgements; References; Chapter 5: Application of Mouse Genetics to Human Disease: Generation and Analysis of Mouse Models; Generation and Analysis of Mouse Models; Introduction; Creating mouse models; Transgenesis; Gene Targeting; Random Mutagenesis; Phenotypic analysis of mouse models; Summary; References.
520 ## - SUMMARY, ETC.
Summary, etc " ... With this new edition the three key markets, research scientists, clinicians, and genetic counselors will all continue to benefit from the content. The research community will find great value in the coverage of genomics, animal models, and diagnostic methods along with a a better understanding of the clinical implications. Clinicians will rely on the coverage of the basic science of neurogenetics and the methods for evaluating patients with biochemical abnormalities or gene mutations. And genetic counselors will find this a comprehensive tutorial reference on the latest advances in the science, with links to genetic testing for specific diseases.
590 ## - LOCAL NOTE (RLIN)
Local note eBooks on EBSCOhost
Provenance (VM) [OBSOLETE] EBSCO eBook Subscription Academic Collection - Worldwide
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Nervous system
General subdivision Diseases
-- Molecular aspects.
9 (RLIN) 1036483
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Nervous system
General subdivision Diseases
-- Genetic aspects.
9 (RLIN) 1024933
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Molecular neurobiology.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Neurogenetics.
9 (RLIN) 679965
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Genetic disorders.
9 (RLIN) 147310
650 12 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Nervous System Diseases
General subdivision genetics
9 (RLIN) 1024934
650 22 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Mental Disorders
General subdivision genetics
9 (RLIN) 990428
650 22 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Genetic Diseases, Inborn
9 (RLIN) 881111
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Système nerveux
General subdivision Maladies
-- Aspect moléculaire.
9 (RLIN) 1036484
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Système nerveux
General subdivision Maladies
-- Aspect génétique.
9 (RLIN) 1024935
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Neurobiologie moléculaire.
9 (RLIN) 1036485
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Neurogénétique.
9 (RLIN) 944893
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Maladies génétiques.
9 (RLIN) 881115
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element HEALTH & FITNESS
General subdivision Diseases
-- General.
Source of heading or term bisacsh
9 (RLIN) 88045
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element MEDICAL
General subdivision Clinical Medicine.
Source of heading or term bisacsh
9 (RLIN) 91637
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element MEDICAL
General subdivision Diseases.
Source of heading or term bisacsh
9 (RLIN) 88037
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element MEDICAL
General subdivision Evidence-Based Medicine.
Source of heading or term bisacsh
9 (RLIN) 91638
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element MEDICAL
General subdivision Internal Medicine.
Source of heading or term bisacsh
9 (RLIN) 91639
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Molecular neurobiology.
Source of heading or term fast
-- (OCoLC)fst01024815
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Nervous system
General subdivision Diseases
-- Genetic aspects.
Source of heading or term fast
-- (OCoLC)fst01036107
9 (RLIN) 1024933
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Nervous system
General subdivision Diseases
-- Molecular aspects.
Source of heading or term fast
-- (OCoLC)fst01036114
9 (RLIN) 1036483
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Neurogenetics.
Source of heading or term fast
-- (OCoLC)fst01036353
9 (RLIN) 679965
655 #0 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
655 #4 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Rosenberg, Roger N.,
Relator term editor.
9 (RLIN) 601656
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pascual, Juan M.,
Relator term editor.
9 (RLIN) 601659
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Display text Print version
International Standard Book Number 9780124105294
Record control number (DNLM)101649357
-- (OCoLC)902835055
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=593413">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=593413</a>
938 ## -
-- EBL - Ebook Library
-- EBLB
-- EBL1826802
938 ## -
-- EBSCOhost
-- EBSC
-- 593413
938 ## -
-- ProQuest MyiLibrary Digital eBook Collection
-- IDEB
-- cis30008414
994 ## -
-- 92
-- INOPJ
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection code Home library Current library Date acquired Total Checkouts Date last seen Price effective from Koha item type
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