Pitx2 Regulates Procollagen Lysyl Hydroxylase (Plod) Gene Expression: Implications for the Pathology of Rieger Syndrome

The Rieger syndrome is an autosomal dominant disease characterized by ocular, craniofacial, and umbilical defects. Patients have mutations in PITX2, a paired-bicoid homeobox gene, also involved in left/right polarity determination. In this study we have identified a family of genes for enzymes respo...

Descripción completa

Detalles Bibliográficos
Autores principales: Hjalt, Tord A., Amendt, Brad A., Murray, Jeffrey C.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196000/
https://www.ncbi.nlm.nih.gov/pubmed/11157981

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196000/
https://www.ncbi.nlm.nih.gov/pubmed/11157981

Ejemplares similares