Screening for mutations of the FOXO4 gene in premature ovarian failure patients
FOXO4 constitutes a coherent candidate gene associated with premature ovarian failure (POF) pathogenesis. This study sequenced the coding and exon-flanking regions of this gene in a panel of 116 POF patients and 143 controls of Tunisian origin. In both groups, the IVS2 + 41T > G sequence variant...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2012
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22923
- Acceso en línea:
- https://doi.org/10.1016/j.rbmo.2011.11.017
https://repository.urosario.edu.co/handle/10336/22923
- Palabra clave:
- Foxo4 protein
Transcription factor
Unclassified drug
Article
Controlled study
Dna flanking region
Exon
Female
Female infertility
Gene expression
Gene mutation
Genetic screening
Genetic variability
Human
Major clinical study
Nucleotide sequence
Open reading frame
Pathogenesis
Polymerase chain reaction
Premature ovarian failure
Promoter region
Sequence analysis
Tunisia
Adult
Dna mutational analysis
Female
Gene frequency
Humans
Mutation
Open reading frames
Primary ovarian insufficiency
Transcription factors
Tunisia
Female infertility
Foxo4
Premature ovarian failure
dna
genetic
Promoter regions
Sequence analysis
- Rights
- License
- Abierto (Texto Completo)