Cargando…
Absence of Vsx1 expression in the normal and damaged mouse cornea
PURPOSE: To examine the expression of visual system homeobox 1 (Vsx1) in the mouse cornea and its potential role in the corneal wound response pathway. METHODS: Expression of Vsx1 was examined by quantitative reverse-transcription PCR (qRT–PCR) in corneal tissue from developing and adult mice and fr...
Autores principales: | Watson, Tom, Chow, Robert L. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062518/ https://www.ncbi.nlm.nih.gov/pubmed/21437200 |
Ejemplares similares
-
VSX1 gene analysis in keratoconus
por: Tanwar, Mukesh, et al.
Publicado: (2010) -
VSX2 mutations in autosomal recessive microphthalmia
por: Reis, Linda M., et al.
Publicado: (2011) -
Analysis of VSX1 Variations in Brazilian Subjects with Keratoconus
por: da Silva, Dulceria Costa, et al.
Publicado: (2018) -
Vsx1 Transiently Defines an Early Intermediate V2 Interneuron Precursor Compartment in the Mouse Developing Spinal Cord
por: Francius, Cédric, et al.
Publicado: (2016) -
Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus
por: Saee-Rad, Samira, et al.
Publicado: (2011)