Cargando…
Embryonic defence mechanisms against glucose-dependent oxidative stress require enhanced expression of Alx3 to prevent malformations during diabetic pregnancy
Oxidative stress constitutes a major cause for increased risk of congenital malformations associated to severe hyperglycaemia during pregnancy. Mutations in the gene encoding the transcription factor ALX3 cause congenital craniofacial and neural tube defects. Since oxidative stress and lack of ALX3...
Autores principales: | García-Sanz, Patricia, Mirasierra, Mercedes, Moratalla, Rosario, Vallejo, Mario |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428206/ https://www.ncbi.nlm.nih.gov/pubmed/28341857 http://dx.doi.org/10.1038/s41598-017-00334-1 |
Ejemplares similares
-
Zebrafish models of alx-linked frontonasal dysplasia reveal a role for Alx1 and Alx3 in the anterior segment and vasculature of the developing eye
por: Yoon, Baul, et al.
Publicado: (2022) -
Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene
por: McGonnell, Imelda M, et al.
Publicado: (2011) -
Abstract 107: Requirement Of ALX1 Homeobox Transcription Factor In Craniofacial Development
por: PINI, Jonathan, et al.
Publicado: (2018) -
Alx1 Deficient Mice Recapitulate Craniofacial Phenotype and Reveal Developmental Basis of ALX1-Related Frontonasal Dysplasia
por: Iyyanar, Paul P. R., et al.
Publicado: (2022) -
Dopamine D(2)R is Required for Hippocampal-dependent Memory and Plasticity at the CA3-CA1 Synapse
por: Espadas, Isabel, et al.
Publicado: (2020)