Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA
Purpose of Review: This manuscript aims to review (for the first time) studies describing NGS sequencing of preeclampsia (PE) women’s DNA. Recent Findings: Describing markers for the early detection of PE is an essential task because, although associated molecular dysfunction begins early on during...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2020
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/23809
- Acceso en línea:
- https://doi.org/10.1007/s11906-020-01039-z
https://repository.urosario.edu.co/handle/10336/23809
- Palabra clave:
- Dna
Acvr2a gene
Allele
Ano9 gene
Dna sequencing
Environmental factor
Gene
Gene mutation
Genetic association
Genetic code
Genetic variation
High throughput sequencing
Human
Khdc3l gene
Maternal plasma
Molecular pathology
Nonhuman
Nrlp14 gene
Nrlp2 gene
Placenta development
Preeclampsia
Review
Tmtc1 gene
Tp53bp1 gene
Trim28 gene
Zfr2 gene
Genetic biomarker
Molecular medicine
Next-generation sequencing (ngs)
Preeclampsia
- Rights
- License
- Abierto (Texto Completo)