Laboratory Guide to the Methods in Biochemical Genetics
E-Book
Laboratory Guide to the Methods in Biochemical Genetics
This manual describes laboratory methodology for diagnosing inborn errors of metabolism. Each chapter is sufficiently detailed so as to be self-contained, thus enabling any individual to adopt the method in their own laboratory and obviating the need for additional methods of references. The book is unique in that it is the first of its kind to be published in the last 15 years, and individual chapters have been developed by experts in the field citing both established and 'cutting-edge' technology.
Thus, it is sufficiently up-to-date to be applicable to the field of inborn errors of metabolism for all readers and those interested in laboratory diagnosis.
Thus, it is sufficiently up-to-date to be applicable to the field of inborn errors of metabolism for all readers and those interested in laboratory diagnosis.
1;Foreword;52;Preface;73;Contents;94;List of Contributors;125;Abbreviations;176;1.1 Laboratory Strategies in Biochemical Genetics ;257;1.2 Quality Control and Quality Assurance in the Biochemical Genetic Laboratory;318;1.3 Simple Metabolic Screening Tests;479;1.4 Lactate, Pyruvate, Acetoacetate and 3-Hydroxybutyrate;5810;2.1 Amino Acids;7511;2.2 Homocysteine, S-adenosylmethionine and S-adenosylhomocysteine;11212;2.3 GABA, Homocarnosine, and ß-Alanine;13613;2.4 Pipecolic Acid;15014;3.1 Organic Acids;15715;3.2 Acylcarnitines, Including In Vitro Loading Tests;19016;3.3 Plasmalogens and Polyunsaturated Fatty Acids;22617;3.4 Very-Long-Chain Fatty Acids and Phytanic Acid;24018;3.5 Oxalate, Glycolate, Glycerate, Sulfate, and Citrate;25119;3.6 Glycerol and Glycerol Phosphates;26220;3.7 Biotinidase;26921;3.8 Mitochondrial Respiratory Chain;28122;4.1 Mucopolysaccharides;30323;4.2 Oligosaccharides;34124;4.3 Sialic Acid;35025;4.4 Glycosphingolipids;36526;4.5 Congenital Disorders of Glycosylation;39327;4.6 Enzymes and Metabolites of Carbohydrate Metabolism;43128;4.7 Polyols;48629;5.1 Diagnosis of Inherited Defects of Cholesterol Biosynthesis;49630;5.2 Lipoproteins;50931;5.3 Genetic Disorders of Steroid Metabolism Diagnosed by Mass Spectrometry;56132;5.4 Bile Acids;61833;6.1 Pterins and Related Enzymes;67634;6.2 Biogenic Amines;71335;6.3 Folates;72636;7.1 Screening for Disorders of Purine and Pyrimidine Metabolism Using HPLC-Electrospray Tandem Mass Spectrometry;73437;7.2 Creatine and its Metabolites;74738;7.3 Porphyrins, Porphobilinogen,and d-Aminolevulinic Acid;75839;7.4 Trimethylaminuria;78840;8.1 A Tandem Mass Spectrometry Primer for Metabolite Disease Detection;80041;8.2 Molecular Genetics: Mutation Analysis in the Diagnosis of Metabolic Disorders;81142;Subject Index;836
Blau, Nenad
Duran, Marinus
Gibson, K. M.
| ISBN | 9783540766988 |
|---|---|
| Artikelnummer | 9783540766988 |
| Medientyp | E-Book - PDF |
| Auflage | 2. Aufl. |
| Copyrightjahr | 2008 |
| Verlag | Springer-Verlag |
| Umfang | 860 Seiten |
| Sprache | Englisch |
| Kopierschutz | Adobe DRM |
