skip to main content
Idioma:
Tipo de recurso Mostra resultados com: Mostra resultados com: Índice

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

Robert Jansen 1946-; European Society of Human Reproduction and Embryology; Serono Symposia Australasia Symposium (1999 Sydney, N.S.W.); World Congress on in Vitro Fertilization & Human Reproductive Genetics (11th 1999 Sydney, N.S.W.)

Oxford, UK Published for the European Society for Human Reproduction and Embryology by Oxford University Press 2000

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (611-013 B751 )(Acessar)

  • Título:
    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
  • Autor: Robert Jansen 1946-; European Society of Human Reproduction and Embryology; Serono Symposia Australasia Symposium (1999 Sydney, N.S.W.); World Congress on in Vitro Fertilization & Human Reproductive Genetics (11th 1999 Sydney, N.S.W.)
  • Assuntos: Mitochondria -- Congresses; Human embryo -- Physiology -- Congresses; Gametes -- Congresses; Embryo and Fetal Development -- genetics; Genome; Mitochondria; EMBRIOLOGIA HUMANA (CONGRESSOS); MITOCÔNDRIAS (CONGRESSOS); GAMETAS (CONGRESSOS); DESENVOLVIMENTO FETAL (CONGRESSOS)
  • Notas: Includes bibliographical references and index
  • Descrição: 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
  • Editor: Oxford, UK Published for the European Society for Human Reproduction and Embryology by Oxford University Press
  • Data de criação/publicação: 2000
  • Formato: 260 p ill 25 cm.
  • Idioma: Inglês
Links
Voltar para lista de resultados
Resultado  1 AvançarIr para próxima página

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.