Principles of Molecular Medicine
Humana Press Inc. (Verlag)
978-1-58829-202-5 (ISBN)
Genetics.- Mendelian Inheritance.- Nontraditional Inheritance.- Identifying Causal Genetic Factors.- Cancer Genetics and Molecular Oncology.- Pharmacogenetics.- Hemophilia as a Model Disease for Gene Therapy of Genetic Disorders.- Genetic Counseling.- Animal Models in Biomedical Research.- Ethical, Legal, and Social Implications.- Cardiology.- Congenital Heart Disease.- Inherited Cardiomyopathies.- Heart Failure.- Aortic Diseases.- Atherosclerotic Coronary Disease.- Lipid Metabolism and Coronary Artery Disease.- Hypertension.- Cardiac Hypertrophy.- Arrhythmias.- Genomics.- Cardiovascular Gene Therapy.- Pulmonary Diseases.- Idiopathic Interstitial Pneumonias.- Asthma.- Pulmonary Emphysema.- Pulmonary Hypertension.- Acute Lung Injury.- Primary Ciliary Dyskinesia.- Cystic Fibrosis.- Gene Therapy for Lung Diseases.- Sarcoidosis.- Disorders of Pulmonary Surfactant Homeostasis.- Endocrinology.- Mechanisms of Hormone Action.- Diabetes Mellitus.- Pituitary Function and Neoplasia.- Growth Hormone Deficiency Disorders.- Thyroid Disorders.- Disorders of the Parathyroid Gland.- Congenital Adrenal Hyperplasia.- Adrenal Diseases.- Multiple Endocrine Neoplasia Type 1.- Multiple Endocrine Neoplasia Type 2.- Disorders of Sex Determination and Differentiation.- Sex Chromosome Disorders.- Disorders of Pubertal Development.- Defects of Androgen Action.- Molecular Endocrinology of the Testis.- Ovarian Diseases.- Metabolic Disorders.- Gastrointestinal Regulation of Food Intake.- Cellular Regulation of Lipolysis.- Fat-Induced Insulin Resistance and Atherosclerosis.- Metabolic and Molecular Aspects of Sarcopenia.- Adipose Tissue Development and Metabolism.- Gastroenterology.- Hepatitis C.- Molecular Diagnostics in Hepatitis B.- Hereditary Hemochromatosis.- Pancreatic Exocrine Dysfunction.- Small and Large Bowel Dysfunction.- The Molecular Mechanisms of Helicobacter pylori-Associated Gastroduodenal Disease.- Nephrology.- Nitric Oxide Synthase and Cyclooxygenase in the Kidneys.- Hypertensionand Sodium Channel Turnover.- Nephrogenic Diabetes Insipidus st[Water and Urea Transport.- Glomerulonephritis and Smad Signaling.- Interstitial Nephritis.- The Pathophysiology of Acute Renal Failure.- Loss of Lean Body Mass in Uremia.- Mechanisms of Renal Allograft Rejection.- Musculoskeletal.- Muscle Development and Differentiation.- Skeletal Muscle Structure and Function.- Stem Cells and Muscle Regeneration.- Skeletal Muscle Hypertrophy and Response to Training.- Muscular Dystrophies.- Rhabdomyosarcomas.- Oncology.- Apoptosis.- Colorectal Cancer.- Breast Cancer.- Lung Cancer.- Discoveries and Frontiers in Prostate Cancer Translational Sciences.- Cutaneous Melanoma.- Applications of Gene Expression Profiling to the Study of Malignant Gliomas.- Acute Myeloid Leukemias.- Acute Lymphoblastic Leukemia.- Chronic Myelogenous Leukemia.- Non-Hodgkin’s Lymphoma and Chronic Lymphocytic Leukemia.- Multiple Myeloma.- HIV-1, AIDS, and Related Malignancies.- Hematology.- Disorders of the Red CellMembrane.- Paroxysmal Nocturnal Hemoglobinuria.- Iron Metabolism.- Correction of Genetic Blood Defects by Gene Transfer.- Bone Marrow Failure Syndromes.- Coagulation Disorders.- Advances in Transfusion Safety.- Immunology And Infectious Diseases.- Immunomodulation.- HIV Molecular Biology, Treatment Resistance.- Cellular and Molecular Aspects of Pneumonia.- Molecular Pathogenesis of Fungal Infections.- Dermatology.- Psoriasis.- Atopic Dermatitis.- Pemphigus Foliaceus, Pemphigus Vulgaris, Paraneoplastic Pemphigus, Bullous Pemphigoid, Herpes Gestationis, and Cicatricial Pemphigoid.- Systemic Lupus Erythematosus.- Systemic Sclerosis.- Diseases With Signaling and Transcriptional Abnormalities.- Genetic Skin Diseases With Neoplasia.- Melanoma and Nevi.- Disorders of Hypopigmentation.- Epidermolysis Bullosa.- Connective Tissue Disorders.- Genetic Epidermal Diseases.- Genetic Hair and Nail Defects.- Metabolic Genetic DisordersWith Prominent Skin Findings.- Heritable Conditions Affecting Tissues of the Oral Cavity.- Neurology.- The Genetic Basis of Human Cerebral Cortical Malformations.- Muscular Dystrophies.- Channelopathies of the Nervous System.- Charcot-Marie-Tooth Disease and Related Peripheral Neuropathies.- Amyotrophic Lateral Sclerosis and Related Motor Neuron Disorders.- Trinucleotide Repeat Disorders.- Parkinson’s Disease.- Genetics and Neurobiology of Alzheimer’s Disease and Frontotemporal Dementias.- Prion Diseases.- Narcolepsy and Other Neurological Sleep Disorders.- Neurofibromatosis 1 and 2.- Axonal Regeneration and Recovery From Chronic Central Nervous System Injury.- Psychiatry.- Molecular Mechanisms Regulating Behavior.- The Complex Genetics of Psychiatric Disorders.- Treating Depression.- Anxiety Disorders.- Trauma Spectrum Disorders.- Schizophrenia.- Disorders of Substance Abuse and Dependence.- Autism and Related Disorders.
Erscheint lt. Verlag | 20.6.2006 |
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Zusatzinfo | LIV, 1268 p. |
Verlagsort | Totowa, NJ |
Sprache | englisch |
Maße | 210 x 297 mm |
Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete |
Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
ISBN-10 | 1-58829-202-9 / 1588292029 |
ISBN-13 | 978-1-58829-202-5 / 9781588292025 |
Zustand | Neuware |
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