Human reproductive and prenatal genetics /
Human Reproductive and Prenatal Genetics presents the latest material from a detailed molecular, cellular and translational perspective. Considering its timeliness and potential international impact, this all-inclusive and authoritative work is ideal for researchers, students, and clinicians worldwi...
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| Language: | English |
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London :
Academic Press, an imprint of Elsevier,
[2019]
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| Online Access: | ScienceDirect |
Table of Contents:
- Part I: Reproductive tract development and gametogenesis. Developmental genetics of the male reproductive system
- Genetics and genomics of early gonad development
- Genetics of meiotic chromosome dynamics and fertility
- Effects of aging on sperm chromatin
- In vitro spermatogenesis from pluripotent stem cells
- Developmental genetics of the female reproductive tract
- The molecular genetics of oogenesis
- Epigenetic control of oocyte development
- RNA binding protein networks and translational regulation in oocytes
- Translational regulation of gene expression during oogenesis and preimplantation embryo development
- MicroRNAs in gametes and preimplantation embryos: clinical implications
- Part II: Embryo implantation, placenta development and pregnancy. Transcriptomics of the human endometrium and embryo implantation
- Epigenetic modifications in the human placenta
- MicroRNAs in pregnancy: implications for basic research and clinical management
- Genetics and genomics of preterm birth
- The intergenerational effects on fetal programming
- Part III: Infertility and assisted reproductive technology . Genetic testing in male infertility
- Genetics and genomics of endometriosis<U+0006>
- Genetics and genomics of primary ovarian insufficiency
- Genetics of polycystic ovary syndrome
- Genetics and genomics of recurrent pregnancy loss
- Human genetics and assisted reproduction in endometriosis
- Uterine transplantation
- Part IV: Preimplantation/prenatal genetic diagnosis and screening. Epidemiology and genetics of human aneuploidy
- Next-generation sequencing for gene panels and clinical exomes
- Chromosomal microarrays and exome sequencing for diagnosis of fetal abnormalities
- Noninvasive prenatal testing for genetic diseases
- Noninvasive prenatal testing by cell-free DNA: technology, biology, clinical utility, and limitations
- Prenatal diagnosis and treatment of genetic steroid disorders
- Application of gene-editing technologies in embryos and their potential for gene therapy.