Cargando…
Screening for Copy Number Variations of the 15q13.3 Hotspot in CHRNA7 Gene and Expression in Patients with Migraines
Background: a migraine is a neurological disease. Copy number variation (CNV) is a phenomenon in which parts of the genome are repeated. We investigated the effects of the CNV and gene expression at the location 15q13.3 in the Cholinergic Receptor Nicotinic Alpha 7 Subunit (CHRNA7) gene, which we be...
Autores principales: | Özaltun, Mehmet Fatih, Geyik, Sırma, Yılmaz, Şenay Görücü |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929100/ https://www.ncbi.nlm.nih.gov/pubmed/34563047 http://dx.doi.org/10.3390/cimb43020078 |
Ejemplares similares
-
The holistic approach to the CHRNA7 gene,
hsa-miR-3158-5p, and 15q13.3 hotspot CNVs in
migraineurs
por: Yasin, Sedat, et al.
Publicado: (2023) -
Is Chromosome 15q13.3 Duplication Involving CHRNA7 Associated With Oral Clefts?
por: Xie, Yingjun
Publicado: (2015) -
Rapid-Onset Obesity Due to Impulsive Food-Seeking Behavior in a Puerto Rican Child With CHRNA7 15q13.3 Microdeletion
por: Jiménez, Brian L, et al.
Publicado: (2021) -
Chromosome 15q25 (CHRNA3-CHRNA5) Variation Impacts Indirectly on Lung Cancer Risk
por: Wang, Yufei, et al.
Publicado: (2011) -
A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity
por: Hasstedt, Sandra J., et al.
Publicado: (2015)