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"Offers a comprehensive examination of key advances in mouse genetic models throughout the twentieth century Features modern case studies connecting historic research to ongoing advances Authored by a thought-leader in the field"--
Mice --- Transgenic mice --- Genetic engineering --- History --- Transgenic animals --- House mice --- House mouse --- Mouse --- Mus musculus --- Rodents --- Transgenic mice. --- 1900-1999
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Acides nucléiques antisens --- Antisense nucleic acids --- Antisense nucleinezuren --- Genetic regulation --- Genetische regulatie --- Régulation génétique --- Antisense nucleic acids. --- Genetic regulation. --- DNA, Antisense. --- Gene Expression Regulation. --- RNA, Antisense. --- Dna, antisense. --- Gene expression regulation. --- Rna, antisense.
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Gonadal Disorders --- Sex Chromosome Disorders --- Sex Chromosomes --- Sexual Maturation --- Genetics, Biochemical --- Sexual disorders --- Sex differentiation disorders --- Developmental disabilities --- Sex chromosome abnormalities --- Generative organs --- genetics --- Genetic aspects --- Abnormalities --- Sex chromosome abnormalities. --- Genetics, Biochemical. --- Sex Chromosome Abnormalities --- Sex Maturation --- Genetic aspects. --- genetics. --- Troubles sexuels --- Troubles du développement --- Aspect génétique --- Aspect génétique. --- Genetics. --- Gonadal Disorders - genetics --- Sex Chromosome Disorders - genetics --- Sex Chromosomes - genetics --- Sexual Maturation - genetics --- Sexual disorders - Genetic aspects --- Sex differentiation disorders - Genetic aspects --- Developmental disabilities - Genetic aspects --- Generative organs - Abnormalities - Genetic aspects --- Troubles du développement --- Aspect génétique.
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Disorders that affect tissue differentiation, organogenesis, and morphogenesis constitute a significant proportion of human hereditary diseases. Until very recently, however, their genetic causes and pathogenesis have been unknown. Now, with the elucidation of the molecular pathways that govern developmental processes and with advances in gene identification, the genetic bases of an increasing number of human disorders of development are being discovered and the links between genotype and phenotype established. This extraordinary volume is the first to present in-depth analyses of the human syndromes of abnormal morphogenesis for which the responsible genes have been identified. Following a series of introductory chapters on the general principles of developmental biology, developmental genetics, and the development of individual tissues or organ systems, more than one hundred clinical genetic disorders are considered. The clinical chapters are organized into sections by defined developmental pathways or gene families, and each section is preceded by a general overview.; For each disorder the authors cover the disease-causing genes, the role of these genes in development as elucidated in model organisms, the human mutations that have been identified, and the developmental pathogenesis of the condition. Clinical descriptions, along with discussions of therapy and counselling, are provided. This book will be an invaluable resource for physicians, dentists, and other health professionals and for basic scientists interested in developmental processes and genetic perturbations that affect them. It is authoritative, clearly written, consistently organized, and attractively illustrated in colour.
Congenital Abnormalities --- Human Development --- Genetic Diseases, Inborn --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Growth and Development --- Behavior and Behavior Mechanisms --- Physiological Processes --- Diseases --- Psychiatry and Psychology --- Physiological Phenomena --- Phenomena and Processes --- Pathology --- Medicine --- Health & Biological Sciences --- Behavior And Behavior Mechanism --- Development and Growth --- Developmental Biology --- Disorders, Congenital --- Congenital Disorders --- Neonatal Diseases and Abnormalities --- Congenital Disorder --- Disorder, Congenital --- Physiological Concepts --- Physiological Phenomenon --- Physiological Process --- Concept, Physiological --- Concepts, Physiological --- Phenomena, Physiological --- Phenomenas, Physiological --- Phenomenon, Physiological --- Physiological Concept --- Process, Physiological --- Processes, Physiological --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Genetics, Medical --- Abnormalities, Congenital --- Defects, Congenital --- Birth Defects --- Congenital Defects --- Deformities --- Fetal Anomalies --- Fetal Malformations --- Abnormality, Congenital --- Anomaly, Fetal --- Birth Defect --- Congenital Abnormality --- Congenital Defect --- Defect, Birth --- Defect, Congenital --- Deformity --- Fetal Anomaly --- Fetal Malformation --- Malformation, Fetal --- Fetal Diseases --- Infant, Newborn, Diseases --- Teratogenesis --- Development, Human --- Humans --- Psychology, Developmental --- Psychiatry --- Congenital Abnormalities. --- Human Development. --- Genetic Diseases, Inborn. --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities. --- Growth and Development. --- Behavior and Behavior Mechanisms. --- Physiological Phenomena. --- Disease. --- Psychiatry.
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Congenital Abnormalities --- Developmental disabilities --- Developmental genetics. --- Genetic Diseases, Inborn --- Genetic disorders in children. --- Genetic disorders. --- Human Development. --- genetics. --- Genetic aspects.
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