Genetics of bone biology and skeletal disease (Record no. 92368)

MARC details
000 -LEADER
fixed length control field 07209cam a2200649 i 4500
001 - CONTROL NUMBER
control field on1010494502
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20230822091134.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION
fixed length control field m d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr cnu|||unuuu
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 171107s2018 enk ob 001 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency N$T
066 ## - CHARACTER SETS PRESENT
Alternate G0 or G1 character set (S
019 ## -
-- 1057351252
-- 1057626780
-- 1066587378
-- 1162438393
-- 1235823758
-- 1294668611
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9780128041987
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 0128041986
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9780128041826
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 012804182X
035 ## - SYSTEM CONTROL NUMBER
System control number 1169197
-- (N$T)
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)1010494502
Canceled/invalid control number (OCoLC)1057351252
-- (OCoLC)1057626780
-- (OCoLC)1066587378
-- (OCoLC)1162438393
-- (OCoLC)1235823758
-- (OCoLC)1294668611
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number 2018 B-467
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number WE 225
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
049 ## - LOCAL HOLDINGS (OCLC)
Holding library MAIN
245 00 - TITLE STATEMENT
Title Genetics of bone biology and skeletal disease
Statement of responsibility, etc
Medium [E-Book]
250 ## - EDITION
Edition statement Second edition.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture London ;
-- Waltham, MA :
Name of producer, publisher, distributor, manufacturer Academic Press,
Date of production, publication, distribution, manufacture, or copyright notice [2018]
300 ## - PHYSICAL DESCRIPTION
Physical description 1 online resource
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
520 ## - ABSTRACT
Abstract "[This book] is aimed at students of bone biology and genetics and includes general introductory chapters on bone biology and genetics. More specific disease orientated chapters comprehensively summarize the clinical, genetic, molecular, animal model, molecular pathology, diagnostic, counseling, and treatment aspects of each disorder. The book is organized into five sections that each emphasize a particular theme, general background to bone biology, general background to genetics and epigenetics, disorders of bone and joint, parathyroid and related disorders, and vitamin D and renal disorders. The first section is specifically devoted to providing an overview of bone biology and structure, joint and cartilage biology, principles of endocrine regulation of bone, and the role of neuronal regulation and energy homeostasis. The second section reviews the principles and progress of medical genetics and epigenetics related to bone disease, including genome-wide association studies (GWAS), genomic profiling, copy number variation, prospects of gene therapy, pharmacogenomics, genetic testing and counseling, as well as the generation and utilizing of mouse models. The third section details advances in the genetics and molecular biology of bone and joint diseases, both monogenic and polygenic, as well as skeletal dysplasias, and rarer bone disorders. The fourth section highlights the central role of the parathyroids in calcium and skeletal homeostasis by reviewing the molecular genetics of: hyperparathyroidism, hypoparathyrodism, endocrine neoplasias, and disorders of the PTH and calcium-sensing receptors. The fifth section details molecular and cellular advances across associated renal disorders such as vitamin D and rickets."--Website publisher
590 ## - LOCAL NOTE (RLIN)
Local note WorldCat record variable field(s) change: 650
650 #0 - SUBJECT HEADINGS
Subject term Bones
General subdivision Diseases
-- Genetic aspects.
650 #0 - SUBJECT HEADINGS
Subject term Diseases
General subdivision Animal models.
650 #0 - SUBJECT HEADINGS
Subject term Mice.
650 12 - SUBJECT HEADINGS
Subject term Bone Diseases
General subdivision genetics
650 22 - SUBJECT HEADINGS
Subject term Bone and Bones
General subdivision physiology
650 22 - SUBJECT HEADINGS
Subject term Parathyroid Diseases
General subdivision genetics
650 22 - SUBJECT HEADINGS
Subject term Musculoskeletal Diseases
General subdivision genetics
650 22 - SUBJECT HEADINGS
Subject term Genetic Predisposition to Disease
650 22 - SUBJECT HEADINGS
Subject term Disease Models, Animal
650 22 - SUBJECT HEADINGS
Subject term Mice
700 1# - ADDED PERSONAL NAME
Added personal author Thakker, R. V.,
Relator term editor.
856 40 - ONLINE RESOURCE
Uniform Resource Identifier <a href="https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1169197">https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1169197</a>
Link text Kingston Hospital NHS Foundation Trust OpenAthens account holders click here for access
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Suppress in OPAC Do not Suppress in OPAC
588 0# - SOURCE OF DESCRIPTION NOTE
Source of description note Online resource; title from PDF title page (EBSCO, viewed November 7, 2017).
880 0# - ALTERNATE GRAPHIC REPRESENTATION
Linkage 505-00/(S
a 1: GENERAL BACKGROUND TO GENETICS -- Chapter 2 -- Epigenetics -- Chapter 3 -- Genome-Wide Association Studies -- Chapter 4 -- Copy Number Variation -- Chapter 5 -- Genomic Profiling in Bone -- Chapter 6 -- Functional Genomics -- Chapter 7 -- Mouse Models: Approaches to Generate In Vivo Models for Hereditary Disorders of Mineral and Skeletal Homeostasis -- Chapter 8 -- Prospects of Gene Therapy for Skeletal Diseases -- Chapter 9 -- Pharmacogenetics and Pharmacogenomics of Osteoporosis: Personalized Medicine Outlook -- Chapter 10 -- Genetic Testing and Counseling -- 2: GENERAL BACKGROUND TO BONE BIOLOGY -- Chapter 11 -- Biology of Bone and Cartilage -- Chapter 12 -- Overview of Bone Structure and Strength -- Chapter 13 -- Overview of Joint and Cartilage Biology -- Chapter 14 -- Osteocyte Biology -- Chapter 15 -- Skeletal Stem Cells/Bone Marrow Stromal Cells -- Chapter 16 -- Osteoimmunology -- Chapter 17 -- Integrating Endocrine and Paracrine Influences on Bone; Lessons From Parathyroid Hormone and Parathyroid Hormone-Related Protein -- Chapter 18 -- Genetics of Bone Fat and Energy Regulation -- Chapter 19 -- The Cross Talk Between the Central Nervous System, Bone, and Energy Metabolism -- Chapter 20 -- Fetal Control of Calcium and Phosphate Homeostasis -- Chapter 21 -- Control of Mineral and Skeletal Homeostasis During Pregnancy and Lactation -- Chapter 22 -- Osteoporosis Genes Identified by Genome-Wide Association Studies -- Chapter 23 -- Osteogenesis Imperfecta -- Chapter 24 -- Osteoarthritis: Genetic Studies of Monogenic and Complex Forms -- Chapter 25 -- Genetics of Paget's Disease of Bone -- Chapter 26 -- Mendelian Disorders of RANKL/OPG/RANK/NF-(Sm(BB Signaling -- Chapter 27 -- Skeletal Dysplasias -- Chapter 28 -- Hypophosphatasia and How Alkaline Phosphatase Promotes Mineralization -- Chapter 29 -- Sclerosing Bone Disorders -- Chapter 30 -- Fibrodysplasia (Myositis) Ossificans Progressiva -- Chapter 31 -- Thyroid Hormone in Bone and Joint Disorders -- Chapter 32 -- Disorders and Mechanisms of Ectopic Calcification -- 4: PARATHYROID AND RELATED DISORDERS -- Chapter 33 -- Hyperparathyroidism -- Chapter 34 -- Hypoparathyroidism -- Chapter 35 -- Gs(Sa(B, Pseudohypoparathyroidism, Fibrous Dysplasia, and McCune-Albright Syndrome -- Chapter 36 -- Genetic Disorders Caused by Mutations in the PTH/PTHrP Receptor, its Ligands, and Downstream Effector Molecules -- Chapter 37 -- Genetically Determined Disorders of Extracellular Calcium (Cao2+) Sensing and Cao2+ Homeostasis -- Chapter 38 -- Multiple Endocrine Neoplasia Syndromes -- 5: VITAMIN D AND RENAL DISORDERS -- Chapter 39 -- Genetic Disorders Of Vitamin D Synthesis and Action -- Chapter 40 -- Heritable Renal Phosphate Wasting Disorders -- Chapter 41 -- Renal Fanconi Syndrome, Dent Disease, and Bartter Syndrome -- Chapter 42 -- Inherited Magnesium Disorders -- Chapter 43 -- Genetic Hypercalciuria: A Major Risk Factor in Kidney Stones
938 ## -
-- EBSCOhost
-- EBSC
-- 1169197
938 ## -
-- YBP Library Services
-- YANK
-- 14962858
994 ## -
-- 92
-- N$T
Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Shelving location Date acquired Source of acquisition Total Checkouts Date last seen Uniform Resource Identifier Price effective from Koha item type
        Stenhouse Library Stenhouse Library   28/11/2022 eBook EBSCO clinical collection   28/11/2022 https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1169197 28/11/2022 Electronic book
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