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Advances in Human Genetics 6
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. 1 Vitamin-Responsive Inherited Metabolic Disorders.- Vitamin Deficiency: Historical Perspective.- Vitamin Responsiveness or Dependency.- Genetic Control of Vitamin Metabolism.- Biochemical Role of Vitamins.- Effect of Mutation on Vitamin Function: Theoretic. N° de réf. du vendeur 4200466
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Advances in Human Genetics 6
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Advances in Human Genetics 6
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Springer US, Chapman And Hall/CRC Jan 2012, 2012
ISBN 10 : 1461582660
ISBN 13 : 9781461582663
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Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -1 Vitamin-Responsive Inherited Metabolic Disorders.- Vitamin Deficiency: Historical Perspective.- Vitamin Responsiveness or Dependency.- Genetic Control of Vitamin Metabolism.- Biochemical Role of Vitamins.- Effect of Mutation on Vitamin Function: Theoretical Possibilities.- Defects of Vitamin Transport and Coenzyme Synthesis.- Cobalamin (Vitamin B12).- Folic Acid.- Calciferol (Vitamin D).- Defects of Coenzyme-Dependent Apoenzymes.- Pyridoxine (Vitamin B6).- Biotin.- Thiamine (Vitamin B1).- Genetic Heterogeneity.- Clinical Panorama.- Mendelian Inheritance.- Prenatal Detection and Treatment.- Problems and Perspectives.- 2 Inherited Deficiency of Hypoxanthine-Guanine Phosphoribosyltransferase in X-Linked Uric Aciduria (the Lesch-Nyhan Syndrome and Its Variants).- Clinical Presentation.- Frequency.- Complete Syndrome.- Clinical Variants of the Syndrome.- Pathology.- Biochemical Characteristics.- Primary Enzyme Defect.- Secondary Enzyme Disturbances.- Properties of the Normal Enzyme.- Properties of the Mutant Enzyme.- Mechanism of Excessive Rate of Purine Synthesis.- Mechanism of Neurological Dysfunction.- Genetic Significance.- Genetic Heterogeneity.- X-Linked Inheritance.- Chemical Selection.- Somatic Cell Genetics.- Preventive Control through Prenatal Diagnosis.- Characteristics of the Heterozygous State.- Pharmacological Consequences of HPRT Deficiency.- Diagnosis of X-Linked Uric Aciduria.- Clinical Signs.- Laboratory Tests.- Heterozygote Detection.- Treatment.- General Measures.- Medications.- 3 Hereditary Hemolytic Anemia Due to Enzyme Defects of Glycolysis.- Glucose Utilization by the Red Cell.- Overall Regulation of Glycolysis.- Mass Action Ratio.- Effect of Cell Age on Metabolism.- Molecular Genetic Mechanisms of Enzyme Deficiency.- Expression of Enzyme Defects in the Red Cell and Other Tissues.- Hexokinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Glucosephosphate Isomerase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Phosphofructokinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Phosphoglycerate Kinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Pyruvate Kinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Other Defects of Glycolytic Enzymes in the Red Cells.- Triosephosphate Isomerase Deficiency.- Glyceraldehyde-3-phosphate Dehydrogenase Deficiency.- 2,3-Diphosphoglycerate Mutase Deficiency.- Lactate Dehydrogenase Deficiency.- 4 Population Structure of the ¿and Islands, Finland.- ¿and.- Location and Description.- History.- Population Composition.- Migration Analyses.- Kinship and Population Structure.- The Migration Matrix Model.- Matrimonial Migration in ¿and.- Parish Endogamy.- Prediction of Kinship from Matrimonial Migration Data.- Approach to Equilibrium.- Kinship Matrices.- Geographical Factors Affecting Migration Patterns.- Isolation by Distance.- Summary.- Topology of Population Structure.- 1750¿1799.- 1800¿1849.- 1850¿1899.- 1900¿1909.- 1910¿1919.- 1920¿1929.- 1930¿1939.- 1940¿1949.- 1900¿1949.- The Inclusion of Mariehamn.- Correlation between Coordinates.- Summary of Topology.- Discussion of Migration Analyses.- Biological Studies.- Genetic Analyses.- Geography and Genetic Structure.- Comparison of Genetic and Migration Inference.- Twinning in and around ¿and.- Ophthalmological Studies.- The ¿and Bleeder Syndrome (von Willebrand-J¿rgens).- 5 Population Genetics and Health Care Delivery: The Quebec Experience.- A Short History of French Canada.- A Consanguinity Study.- Objectives.- Demographic Aspect.- Sources and Material.- Results.- Discussion: Consanguinity and the Mean Coefficient Fw.- Conclusions and Decisions.- An Isolate Study.- Objectives.- Methods.- Results.- Conclusions and Decisions.- An Inbreeding Study.- Objectives.- M. N° de réf. du vendeur 9781461582663
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Advances in Human Genetics 6
Vendeur : Chiron Media, Wallingford, Royaume-Uni
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PF. Etat : New. N° de réf. du vendeur 6666-IUK-9781461582663
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Advances in Human Genetics 6
Edité par
Springer US, Springer New York Jan 2012, 2012
ISBN 10 : 1461582660
ISBN 13 : 9781461582663
Neuf
Taschenbuch
Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -1 Vitamin-Responsive Inherited Metabolic Disorders.- Vitamin Deficiency: Historical Perspective.- Vitamin Responsiveness or Dependency.- Genetic Control of Vitamin Metabolism.- Biochemical Role of Vitamins.- Effect of Mutation on Vitamin Function: Theoretical Possibilities.- Defects of Vitamin Transport and Coenzyme Synthesis.- Cobalamin (Vitamin B12).- Folic Acid.- Calciferol (Vitamin D).- Defects of Coenzyme-Dependent Apoenzymes.- Pyridoxine (Vitamin B6).- Biotin.- Thiamine (Vitamin B1).- Genetic Heterogeneity.- Clinical Panorama.- Mendelian Inheritance.- Prenatal Detection and Treatment.- Problems and Perspectives.- 2 Inherited Deficiency of Hypoxanthine-Guanine Phosphoribosyltransferase in X-Linked Uric Aciduria (the Lesch-Nyhan Syndrome and Its Variants).- Clinical Presentation.- Frequency.- Complete Syndrome.- Clinical Variants of the Syndrome.- Pathology.- Biochemical Characteristics.- Primary Enzyme Defect.- Secondary Enzyme Disturbances.- Properties of the Normal Enzyme.- Properties of the Mutant Enzyme.- Mechanism of Excessive Rate of Purine Synthesis.- Mechanism of Neurological Dysfunction.- Genetic Significance.- Genetic Heterogeneity.- X-Linked Inheritance.- Chemical Selection.- Somatic Cell Genetics.- Preventive Control through Prenatal Diagnosis.- Characteristics of the Heterozygous State.- Pharmacological Consequences of HPRT Deficiency.- Diagnosis of X-Linked Uric Aciduria.- Clinical Signs.- Laboratory Tests.- Heterozygote Detection.- Treatment.- General Measures.- Medications.- 3 Hereditary Hemolytic Anemia Due to Enzyme Defects of Glycolysis.- Glucose Utilization by the Red Cell.- Overall Regulation of Glycolysis.- Mass Action Ratio.- Effect of Cell Age on Metabolism.- Molecular Genetic Mechanisms of Enzyme Deficiency.- Expression of Enzyme Defects in the Red Cell and Other Tissues.- Hexokinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Glucosephosphate Isomerase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Phosphofructokinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Phosphoglycerate Kinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Pyruvate Kinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Other Defects of Glycolytic Enzymes in the Red Cells.- Triosephosphate Isomerase Deficiency.- Glyceraldehyde-3-phosphate Dehydrogenase Deficiency.- 2,3-Diphosphoglycerate Mutase Deficiency.- Lactate Dehydrogenase Deficiency.- 4 Population Structure of the ¿and Islands, Finland.- ¿and.- Location and Description.- History.- Population Composition.- Migration Analyses.- Kinship and Population Structure.- The Migration Matrix Model.- Matrimonial Migration in ¿and.- Parish Endogamy.- Prediction of Kinship from Matrimonial Migration Data.- Approach to Equilibrium.- Kinship Matrices.- Geographical Factors Affecting Migration Patterns.- Isolation by Distance.- Summary.- Topology of Population Structure.- 1750¿1799.- 1800¿1849.- 1850¿1899.- 1900¿1909.- 1910¿1919.- 1920¿1929.- 1930¿1939.- 1940¿1949.- 1900¿1949.- The Inclusion of Mariehamn.- Correlation between Coordinates.- Summary of Topology.- Discussion of Migration Analyses.- Biological Studies.- Genetic Analyses.- Geography and Genetic Structure.- Comparison of Genetic and Migration Inference.- Twinning in and around ¿and.- Ophthalmological Studies.- The ¿and Bleeder Syndrome (von Willebrand-J¿rgens).- 5 Population Genetics and Health Care Delivery: The Quebec Experience.- A Short History of French Canada.- A Consanguinity Study.- Objectives.- Demographic Aspect.- Sources and Material.- Results.- Discussion: Consanguinity and the Mean Coefficient Fw.- Conclusions and Decisions.- An Isolate Study.- Objectives.- Methods.- Results.- Conclusions and Decisions.- An Inbreeding Study.- Objectives.- Mater. N° de réf. du vendeur 9781461582663
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Advances in Human Genetics 6
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Advances in Human Genetics 6
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Taschenbuch. Etat : Neu. Druck auf Anfrage Neuware - Printed after ordering - 1 Vitamin-Responsive Inherited Metabolic Disorders.- Vitamin Deficiency: Historical Perspective.- Vitamin Responsiveness or Dependency.- Genetic Control of Vitamin Metabolism.- Biochemical Role of Vitamins.- Effect of Mutation on Vitamin Function: Theoretical Possibilities.- Defects of Vitamin Transport and Coenzyme Synthesis.- Cobalamin (Vitamin B12).- Folic Acid.- Calciferol (Vitamin D).- Defects of Coenzyme-Dependent Apoenzymes.- Pyridoxine (Vitamin B6).- Biotin.- Thiamine (Vitamin B1).- Genetic Heterogeneity.- Clinical Panorama.- Mendelian Inheritance.- Prenatal Detection and Treatment.- Problems and Perspectives.- 2 Inherited Deficiency of Hypoxanthine-Guanine Phosphoribosyltransferase in X-Linked Uric Aciduria (the Lesch-Nyhan Syndrome and Its Variants).- Clinical Presentation.- Frequency.- Complete Syndrome.- Clinical Variants of the Syndrome.- Pathology.- Biochemical Characteristics.- Primary Enzyme Defect.- Secondary Enzyme Disturbances.- Properties of the Normal Enzyme.- Properties of the Mutant Enzyme.- Mechanism of Excessive Rate of Purine Synthesis.- Mechanism of Neurological Dysfunction.- Genetic Significance.- Genetic Heterogeneity.- X-Linked Inheritance.- Chemical Selection.- Somatic Cell Genetics.- Preventive Control through Prenatal Diagnosis.- Characteristics of the Heterozygous State.- Pharmacological Consequences of HPRT Deficiency.- Diagnosis of X-Linked Uric Aciduria.- Clinical Signs.- Laboratory Tests.- Heterozygote Detection.- Treatment.- General Measures.- Medications.- 3 Hereditary Hemolytic Anemia Due to Enzyme Defects of Glycolysis.- Glucose Utilization by the Red Cell.- Overall Regulation of Glycolysis.- Mass Action Ratio.- Effect of Cell Age on Metabolism.- Molecular Genetic Mechanisms of Enzyme Deficiency.- Expression of Enzyme Defects in the Red Cell and Other Tissues.- Hexokinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Glucosephosphate Isomerase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Phosphofructokinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Phosphoglycerate Kinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Pyruvate Kinase Deficiency.- Clinical Spectrum.- Biochemical Considerations.- Genetic Considerations.- Other Defects of Glycolytic Enzymes in the Red Cells.- Triosephosphate Isomerase Deficiency.- Glyceraldehyde-3-phosphate Dehydrogenase Deficiency.- 2,3-Diphosphoglycerate Mutase Deficiency.- Lactate Dehydrogenase Deficiency.- 4 Population Structure of the ¿and Islands, Finland.- ¿and.- Location and Description.- History.- Population Composition.- Migration Analyses.- Kinship and Population Structure.- The Migration Matrix Model.- Matrimonial Migration in ¿and.- Parish Endogamy.- Prediction of Kinship from Matrimonial Migration Data.- Approach to Equilibrium.- Kinship Matrices.- Geographical Factors Affecting Migration Patterns.- Isolation by Distance.- Summary.- Topology of Population Structure.- 1750¿1799.- 1800¿1849.- 1850¿1899.- 1900¿1909.- 1910¿1919.- 1920¿1929.- 1930¿1939.- 1940¿1949.- 1900¿1949.- The Inclusion of Mariehamn.- Correlation between Coordinates.- Summary of Topology.- Discussion of Migration Analyses.- Biological Studies.- Genetic Analyses.- Geography and Genetic Structure.- Comparison of Genetic and Migration Inference.- Twinning in and around ¿and.- Ophthalmological Studies.- The ¿and Bleeder Syndrome (von Willebrand-J¿rgens).- 5 Population Genetics and Health Care Delivery: The Quebec Experience.- A Short History of French Canada.- A Consanguinity Study.- Objectives.- Demographic Aspect.- Sources and Material.- Results.- Discussion: Consanguinity and the Mean Coefficient Fw.- Conclusions and Decisions.- An Isolate Study.- Objectives.- Methods.- Results.- Conclusions and Decisions.- An Inbreeding Study.- Objectives.- Material.- Result. N° de réf. du vendeur 9781461582663
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Advances in Human Genetics 6
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Etat : New. Series: Advances in Human Genetics. Num Pages: black & white illustrations, bibliography. BIC Classification: MFN; WM; WNCF. Category: (G) General (US: Trade). Dimension: 229 x 152 x 21. Weight in Grams: 540. . 2012. Paperback / so. . . . . N° de réf. du vendeur V9781461582663
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Advances in Human Genetics 6
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Advances in Human Genetics 6
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Springer-Verlag New York Inc., 2012
ISBN 10 : 1461582660
ISBN 13 : 9781461582663
Neuf
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