Systematic Screening of Drosophila Deficiency Mutations for Embryonic Phenotypes and Orphan Receptor Ligands

This paper defines a collection of Drosophila deletion mutations (deficiencies) that can be systematically screened for embryonic phenotypes, orphan receptor ligands, and genes affecting protein localization. It reports the results of deficiency screens we have conducted that have revealed new axon...

Descripción completa

Detalles Bibliográficos
Autores principales: Wright, Ashley P., Fox, A. Nicole, Johnson, Karl G., Zinn, Kai
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924397/
https://www.ncbi.nlm.nih.gov/pubmed/20808815
http://dx.doi.org/10.1371/journal.pone.0012288

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924397/
https://www.ncbi.nlm.nih.gov/pubmed/20808815
http://dx.doi.org/10.1371/journal.pone.0012288

Ejemplares similares