FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

Background: Human reproductive disorders consist of frequently occurring dysfunctions including a broad range of phenotypes affecting fertility and women's health during pregnancy. Several female-related diseases have been associated with hypofertility/infertility phenotypes, such as recurrent...

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Autores:

Tipo de recurso:

Fecha de publicación:

2019

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/22618

Acceso en línea:

https://doi.org/10.1186/s10020-019-0104-3
https://repository.urosario.edu.co/handle/10336/22618

Palabra clave:

Complement component C3
Placental growth factor
Adult
Article
Bioinformatics
C3 gene
Colombian
Controlled study
Female
FOXD1 gene
Frenchman
Gene
Gene deletion
Gene identification
Gene mutation
Gene sequence
Genetic regulation
Genetic screening
Genetic transcription
Genetic variability
Genotype
Human
In vitro fertilization
In vitro study
Intrauterine growth retardation
Major clinical study
Pathogenesis
Plasmid
Plgf gene
Preeclampsia
Pregnancy disorder
Priority journal
Reimplantation
Repeated implantation failure
Sequence analysis

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