A screen for proteins that interact with PAX6: C-terminal mutations disrupt interaction with HOMER3, DNCL1 and TRIM11

BACKGROUND: The PAX6 protein is a transcriptional regulator with a key role in ocular and neurological development. Individuals with heterozygous loss-of-function mutations in the PAX6 gene have malformations of the eye and brain. Little is known about the interactions of PAX6 with other proteins, s...

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Detalles Bibliográficos
Autores principales: Cooper, Simon T, Hanson, Isabel M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1208879/
https://www.ncbi.nlm.nih.gov/pubmed/16098226
http://dx.doi.org/10.1186/1471-2156-6-43

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1208879/
https://www.ncbi.nlm.nih.gov/pubmed/16098226
http://dx.doi.org/10.1186/1471-2156-6-43

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