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EmbryoGenetics
| EmbryoGenetics |
| Autore | Simón Carlos |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (176 p.) |
| Soggetto topico | Research and information: general |
| Soggetto non controllato |
advanced maternal age
aneuploidies aneuploidy apoptotic bodies Autosomal dominant polycystic kidney disease (ADPKD) blastocyst chromosomal abnormality combined preimplantation genetic testing DNA embryo embryo genetics embryos endometrium exosomes extracellular vesicles female age genetic diseases genetic testing genome editing genomic index implantation infertility male infertility microvesicles monogenic disease mosaicism multiplex PCR murine blastocysts next-generation sequencing NGS ovarian response perinatal care PGT-A PGT-P PGT-SR polygenic disease polygenic risk scoring preimplantation embryos preimplantation genetic testing Preimplantation genetic testing for aneuploidy assessment (PGT-A) Preimplantation genetic testing for monogenic disorders (PGT-M) relative risk reduction reproductive health segmental SNP array translocations uterus vitrification whole exome sequencing window of implantation |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557725303321 |
Simón Carlos
|
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Handbook of Genetic Diagnostic Technologies in Reproductive Medicine : Improving Patient Success Rates and Infant Health
| Handbook of Genetic Diagnostic Technologies in Reproductive Medicine : Improving Patient Success Rates and Infant Health |
| Autore | Simón Carlos |
| Edizione | [2nd ed.] |
| Pubbl/distr/stampa | Milton : , : Taylor & Francis Group, , 2022 |
| Descrizione fisica | 1 online resource (480 pages) |
| Disciplina |
618.1/78042
618.178042 |
| Altri autori (Persone) | RubioCarmen |
| Soggetto topico | Prenatal diagnosis |
| ISBN |
9781003024941
1003024947 9781000567410 1000567419 9781000567366 1000567362 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright Page -- Table of Contents -- Contributors -- Preface -- Chapter 1 The Brave New World of Genomics -- Chapter 2 Genetics at the Cell Level: The Human Cell Atlas -- Chapter 3 The Genetic Risk of a Couple Aiming to Conceive -- Chapter 4 Carrier Screening for Single-Gene Disorders -- Chapter 5 Meiotic Abnormalities in Infertile Males -- Chapter 6 Chromosomal Analysis of Sperm -- Chapter 7 Epigenetics in Sperm, Epigenetic Diagnostics, and Transgenerational Inheritance -- Chapter 8 Aneuploidy in Human Oocytes and Preimplantation Embryos -- Chapter 9 Epigenetics from Oocytes to Embryos -- Chapter 10 Embryo Kinetics and Aneuploidy -- Chapter 11 Preimplantation Genetic Testing of Aneuploidies (PGT-A) -- Chapter 12 Preimplantation Genetic Testing for Structural Rearrangements -- Chapter 13 Mosaicism in Preimplantation Embryos -- Chapter 14 Embryo Cell-Free DNA in the Culture Medium and Its Potential for Non-Invasive Aneuploidy Testing -- Chapter 15 Mitochondria and Embryo Viability -- Chapter 16 Preimplantation Genetic Diagnosis for Single Gene Disorders -- Chapter 17 Preimplantation Genetic Testing for Polygenic Disorders -- Chapter 18 Should Genome Editing Replace Embryo Selection Following PGT? -- Chapter 19 Molecular Diagnosis of Endometrial Receptivity -- Chapter 20 The Vaginal Microbiome -- Chapter 21 The Uterine Microbiota -- Chapter 22 Endometritis: New Times, New Opportunities -- Chapter 23 Decidualization Resistance: A New Condition Identified in Severe Preeclampsia -- Chapter 24 Advanced Cell Therapy for Asherman's Syndrome -- Chapter 25 Differential Genetic Diagnosis between Leiomyoma and Leiomyosarcoma -- Chapter 26 Non-Invasive Prenatal Testing (NIPT) -- Chapter 27 Advances in Non-Invasive Diagnosis of Single-Gene Disorders and Fetal Exome Sequencing.
Chapter 28 Chromosome Abnormalities in Human Pregnancy Loss: A Review of Cytogenetic and Molecular Analyses -- Chapter 29 Products of Conception: Current Methodologies and Clinical Applications -- Chapter 30 Mother and Embryo Cross Communication during Conception -- Chapter 31 Perinatal and Pediatric Outcome of Pregnancies Following PGT-M/SR/A -- Chapter 32 Genetic Counseling in Assisted Reproductive Technology -- Index. |
| Record Nr. | UNINA-9910772097003321 |
|
Simón Carlos
|
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| Milton : , : Taylor & Francis Group, , 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||