Purine and Pyrimidine Metabolism in Man VII

Lieferzeit: Lieferbar innerhalb 14 Tagen

53,49 

Part B: Structural Biochemistry, Pathogenesis, and Metabolism, Advances in Experimental Medicine and Biology 309B

ISBN: 1461577055
ISBN 13: 9781461577058
Herausgeber: R Angus Harkness/T B Elion/N Zöllner
Verlag: Springer Verlag GmbH
Umfang: xix, 393 S.
Erscheinungsdatum: 14.06.2012
Auflage: 1/2012
Produktform: Kartoniert
Einband: KT

InhaltsangabeB Structural Biochemistry, Pathogenesis and Metabolism.- D. Measurement of Purine and Pyrimidines in Tissues and Biological Fluids.- Capillary Electrophoresis for the Analysis of Cellular Nucleotides.- An Improved Screening Method for Inherited Disorders of Purine and Pyrimidine Metabolism by HPLC.- A Single HPLC System for the Evaluation of Purine and Pyrimidine Metabolites in Body Fluids.- Simple Method for the Quantitative Analysis of Dihydropyrimidine and N-Carbamyl-?-Aminoacids in Urine.- Diagnostic Potential of HPLC: Experimental and Clinical Trials.- Reference Values of Orotic Acid, Uracil and Pseudouridine in Urine.- Automated Quantitative Analysis for Orotidine and Uridine/Thymine in Urine by High-Performance Liquid Chromatography with Column Switching.- HPLC Assay of Uridine Monophosphate Synthase (UMPS) in Chorionic Villus Samples (CVS) and Erythrocytes (RBC).- A RP-HPLC Method for the Measurement of Guanine, Other Purine Bases and Nucleosides.- Some Aspects of Purine Nucleotide Metabolism in Human Lymphocytes. Before and after Infection with HIV-I Virus: Nucleotide Content.- Prenatal Diagnosis of Lesch-Nyhan Syndrome by Purine Analysis of Amniotic Fluid and Cordocentesis.- E. Structural Biochemistry.- Gene Therapy in Man and Mice: Adenosine Deaminase Deficiency, Ornithine Transcarbamylase Deficiency and Duchenne Muscular Dystrophy.- Regulation of the Human Adenosine Deaminase Gene by First Intron Sequences in a T-cell Enhancer.- Expression of the APRT Gene in an Adenovirus Vector System as a Model for Studying Gene Therapy.- Transcriptional Regulation of Ribonucleotide Reductase.- Mutational Basis of Adenine Phosphoribosyl-Transferase Deficiency.- Analysis of the Promoter Region of the CHO APRT Gene.- A Splice Mutation at the Adenine Phosphoribosyltransferase Locus Detected in a German Family.- Germline and Somatic Mutations Leading to Adenosine Phosphoribosyltransferase (APRT) Deficiency.- Long – Term Evolution of Type 1 Adenine Phosphoribosyltransferase (APRT) Deficiency.- A Strategy for the Creation of Mutations in Human HPRT-cDNA and the Expression of Recombinant Proteins in E. coli.- Molecular Analysis of Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in Japanese Patients.- Expression of Normal and Variant Human Hypoxanthine-Guanine Phosphoribosyltransferase in E. coli.- HPRT Gene Mutations in a Female Lesch-Nyhan Patient.- Molecular Analysis of Human HPRT Gene Deletions and Duplications.- Rat Hypoxanthine Phosphorbosyltranferase cDNA Cloning and Sequence Analysis.- Identification of Two Independent Japanese Mutant HPRT Genes Using the PCR Technique.- Identification of Distinct PRS1 Mutations in Two Patients with X-Linked Phosphoribosylpyrophosphate Synthetase Superactivity.- Human Phosphoribosylpyrophosphatase (PRS)2: an Independently Active, X Chromosome-Linked PRS Isoform.- Rescue of Lethal Purine Nucleoside Phosphorylase Mutation in the Mouse via a Second Locus Interaction.- Genetic Models of Purine Nucleoside Phosphorylase Deficiency in the Mouse.- A Genetic Defect in Muscle Phosphofructokinase Deficiency, a Typical Clinical Entity Presenting Myogenic Hyperuricemia.- 5?-Nucleotidase: an Overview of the Last Three Years.- Cytosolic Purine 5?-Nucleotidase from Chicken Heart: an Isozyme of the Liver Enzyme as Evidenced by Antibodies.- Amplification of T-cell Activity Induced by CD73 (Ecto 5?-Nucleotidase) Engagement.- Studies on the Structure and Biosynthesis of the Phosphatidyl-Inositol-Glycan Anchor and the Carbohydrate Side Chains of Human Placental Ecto 5?-Nucleotidase.- Diphosphonucleosides Are Indispensable Cofactors of AMP-Specific Cytoplasmic 5?-Nucleotidase Catalysed Reaction.- Adenosine Metabolising Enzymes in Bull and Human Spermatozoa.- Cytosolic 5?-Nucleotidase/Phosphotransferase of Human Colon Carcinoma.- Purine Nucleoside Phosphorylase: Allosteric Regulation of a Dissociating Enzyme.- Purine Nucleoside Phosphorylase of Bovine Liver Mitochondria.- Uridine and Purine Nucleoside Phos

Artikelnummer: 6450284 Kategorie:

Beschreibung

These two volumes record the scientific and clinical work presented at the VIIth International and 3rd European joint symposium on purine and pyrimidine metabolism in man held at the Bournemouth International Conference Centre, Bournemouth, UK, from 30th June to 5th July 1991. The series of international meetings at three yearly intervals have previously been held initially in 1973 in Israel, then Austria, Spain, the Netherlands, USA and Japan. The European Society for the Study of Purine and pyrimidine Metabolism in Man (ESSPPM) which has its own executive and some finance first met in switzerland in 1987, then in Germany in 1989. The steady evolution of the science in this series of meetings is intellectually satisfying; the subsequent clinical progress is emotionally and economically reassuring. As befits the position of purines and pyrimidines at the centre of biochemistry, there has been steady scientific development into molecular genetics and now onto developmental controls and biochemical pharmacology. The complexities of the immune system are being unravelled but an understanding of the human brain largely eludes us. Laboratory based scientists now predominate over those who work as clinical specialists in VIi rheumatology, immunology, oncology and paediatrics. However, there continue to be major clinical objectives since large sections are concerned with major causes of death like ATP depletion, cancer and now AIDS; the laboratory work is providing clinical solutions.

Das könnte Ihnen auch gefallen …