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- catalog alternative "Gamete and embryo mitochondria in humans".
- catalog contributor b11829234.
- catalog contributor b11829235.
- catalog contributor b11829236.
- catalog contributor b11829237.
- catalog contributor b11829238.
- catalog contributor b11829239.
- catalog contributor b11829240.
- catalog created "2000.".
- catalog date "2000".
- catalog date "2000.".
- catalog dateCopyrighted "2000.".
- catalog description "Includes bibliographical references and index.".
- catalog description "Origin and persistence of the mitochondrial genome -- Transcription and replication of mitochondrial DNA -- Genetic control of oxidative phosphorylation and experimental models of defects -- Genetic defects causing human mitochondrial respiratory chain disorders and disease -- Organismal effects of mitochondrial dysfuntion -- Practical problems in detecting abnormal mitochondrial function and genomes -- Morphological correlates of mitochondrial dysfunction in children -- In-vitro genetic modification of mitochondrial function -- Regulation of mitochondrial DNA copy number during spermatogenesis -- Fertilization and elimination of the paternal mitochondrial genome -- Evolutionary origin and consequences of uniparental mitochondrial inheritance -- Germline passage of mitochondria: quantitative considerations and possible embryological sequelae -- Mitochondrial morphology in human fetal and adult female germ cells -- Mitochondrial morphology during preimplantational human embryogenesis -- Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection? -- Intrafollicular influences on human oocyte developmental competence: perifollicular vascularity, oocyte metabolism and mitochondrial function -- Mitochondrial distribution and function in oocytes and early embryos -- Toxic effects of oxygen on early human embryo development -- Spontaneous and artificial changes in human ooplasmic mitochondria -- Mitochondrial ultrastructure in embryos after implantation -- Mitochondrial segregation in the developing embryo -- Transmission of the human mitochondrial genome -- Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults.".
- catalog extent "260 p. :".
- catalog identifier "0199224811".
- catalog isPartOf "Human reproduction (Oxford, England). Supplement ; v. 15, suppl. 2.".
- catalog isPartOf "Human reproduction ; vol. 15, supplement 2, July 2000".
- catalog issued "2000".
- catalog issued "2000.".
- catalog language "eng".
- catalog publisher "Oxford, U.K. : Published for the European Society for Human Reproduction and Embryology by Oxford University Press,".
- catalog subject "Embryo and Fetal Development genetics.".
- catalog subject "Fetal Development genetics.".
- catalog subject "Gametes Congresses.".
- catalog subject "Genome.".
- catalog subject "Human embryo Physiology Congresses.".
- catalog subject "Mitochondria Congresses.".
- catalog subject "Mitochondria.".
- catalog subject "QH 603 .M5 B751 2000".
- catalog subject "QH603.M5 B67 2000".
- catalog tableOfContents "Origin and persistence of the mitochondrial genome -- Transcription and replication of mitochondrial DNA -- Genetic control of oxidative phosphorylation and experimental models of defects -- Genetic defects causing human mitochondrial respiratory chain disorders and disease -- Organismal effects of mitochondrial dysfuntion -- Practical problems in detecting abnormal mitochondrial function and genomes -- Morphological correlates of mitochondrial dysfunction in children -- In-vitro genetic modification of mitochondrial function -- Regulation of mitochondrial DNA copy number during spermatogenesis -- Fertilization and elimination of the paternal mitochondrial genome -- Evolutionary origin and consequences of uniparental mitochondrial inheritance -- Germline passage of mitochondria: quantitative considerations and possible embryological sequelae -- Mitochondrial morphology in human fetal and adult female germ cells -- Mitochondrial morphology during preimplantational human embryogenesis -- Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection? -- Intrafollicular influences on human oocyte developmental competence: perifollicular vascularity, oocyte metabolism and mitochondrial function -- Mitochondrial distribution and function in oocytes and early embryos -- Toxic effects of oxygen on early human embryo development -- Spontaneous and artificial changes in human ooplasmic mitochondria -- Mitochondrial ultrastructure in embryos after implantation -- Mitochondrial segregation in the developing embryo -- Transmission of the human mitochondrial genome -- Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults.".
- catalog title "Gamete and embryo mitochondria in humans".
- catalog title "The bottleneck : gamete and embryo mitochondria in humans : proceedings of a Serono Symposia Australasia Symposium held in Sydney, Australia, May 7-8, 1999, in association with the 11th World Congress on In-Vitro Fertilization and Human Reproductive Genetics / edited by Robert P.S. Jansen.".
- catalog type "Conference proceedings. fast".
- catalog type "text".