Cargando…
Both Positive and Negative Selection Pressures Contribute to the Polymorphism Pattern of the Duplicated Human CYP21A2 Gene
The human steroid 21-hydroxylase gene (CYP21A2) participates in cortisol and aldosterone biosynthesis, and resides together with its paralogous (duplicated) pseudogene in a multiallelic copy number variation (CNV), called RCCX CNV. Concerted evolution caused by non-allelic gene conversion has been d...
Autores principales: | Szabó, Julianna Anna, Szilágyi, Ágnes, Doleschall, Zoltán, Patócs, Attila, Farkas, Henriette, Prohászka, Zoltán, Rácz, Kárioly, Füst, George, Doleschall, Márton |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843699/ https://www.ncbi.nlm.nih.gov/pubmed/24312389 http://dx.doi.org/10.1371/journal.pone.0081977 |
Ejemplares similares
-
Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene
por: Bánlaki, Zsófia, et al.
Publicado: (2013) -
Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels
por: Doleschall, Márton, et al.
Publicado: (2014) -
Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation
por: Doleschall, Márton, et al.
Publicado: (2022) -
Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin‐like cell hyperplasia and autoimmune gastritis
por: Herold, Zoltan, et al.
Publicado: (2020) -
Role and function of granin proteins in diabetes mellitus
por: Herold, Zoltan, et al.
Publicado: (2021)