Induction of apoptosis and inhibition of cell growth by tbx5 knockdown contribute to dysmorphogenesis in Zebrafish embryos

BACKGROUND: The tbx5 mutation in human causes Holt-Oram syndrome, an autosomal dominant condition characterized by a familial history of congenital heart defects and preaxial radial upper-limb defects. We report aberrant apoptosis and dormant cell growth over head, heart, trunk, fin, and tail of zeb...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Lu, Jenher, Tsai, Tzuchun, Choo, Sielin, Yeh, Shuyu, Tang, Renbing, Yang, Anhang, Lee, Hsinyu, Lu, Jennkan
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3199240/
https://ncbi.nlm.nih.gov/pubmed/21982178
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1423-0127-18-73
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares