Coverart for item
The Resource The bottleneck : gamete and embryo mitochondria in humans, edited by Robert P.S. Jansen

The bottleneck : gamete and embryo mitochondria in humans, edited by Robert P.S. Jansen

Label
The bottleneck : gamete and embryo mitochondria in humans
Title
The bottleneck
Title remainder
gamete and embryo mitochondria in humans
Statement of responsibility
edited by Robert P.S. Jansen
Title variation
Gamete and embryo mitochondria in humans
Contributor
Subject
Genre
Language
eng
Cataloging source
MMU
Illustrations
illustrations
Index
index present
Literary form
non fiction
Nature of contents
bibliography
http://library.link/vocab/relatedWorkOrContributorDate
  • 1946-
  • 1999
  • 1999
http://library.link/vocab/relatedWorkOrContributorName
  • Jansen, Robert
  • European Society of Human Reproduction and Embryology
  • Serono Symposia Australasia Symposium
  • World Congress on In Vitro Fertilization & Human Reproductive Genetics
Series statement
Human Reproduction.
Series volume
15/2
http://library.link/vocab/subjectName
  • Mitochondria
  • Human embryo
  • Gametes
Label
The bottleneck : gamete and embryo mitochondria in humans, edited by Robert P.S. Jansen
Instantiates
Publication
Note
  • "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"--t.p
  • "Human reproduction, volume 15, supplement 2, July 2000."
  • "These proceedings were sponsored by the Ares-Serono Foundation and Serono Symposia Australasia"
Bibliography note
Includes bibliographical references and index
Carrier category
volume
Carrier category code
  • nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Contents
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
Control code
12787339
Dimensions
25 cm.
Extent
260 p.
Isbn
9780199224814
Media category
unmediated
Media MARC source
rdamedia
Media type code
  • n
Other physical details
ill.
Label
The bottleneck : gamete and embryo mitochondria in humans, edited by Robert P.S. Jansen
Publication
Note
  • "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"--t.p
  • "Human reproduction, volume 15, supplement 2, July 2000."
  • "These proceedings were sponsored by the Ares-Serono Foundation and Serono Symposia Australasia"
Bibliography note
Includes bibliographical references and index
Carrier category
volume
Carrier category code
  • nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Contents
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
Control code
12787339
Dimensions
25 cm.
Extent
260 p.
Isbn
9780199224814
Media category
unmediated
Media MARC source
rdamedia
Media type code
  • n
Other physical details
ill.

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