Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice

During the analysis of a whole genome ENU mutagenesis screen for thrombosis modifiers, a spontaneous 8 base pair (bp) deletion causing a frameshift in exon 27 of the Nbeal2 gene was identified. Though initially considered as a plausible thrombosis modifier, this Nbeal2 mutation failed to suppress th...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:PLoS One
Main Authors: Tomberg, Kärt, Khoriaty, Rami, Westrick, Randal J., Fairfield, Heather E., Reinholdt, Laura G., Brodsky, Gary L., Davizon-Castillo, Pavel, Ginsburg, David, Di Paola, Jorge
Formato: Artigo
Idioma:Inglês
Publicado: Public Library of Science 2016
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4780761/
https://ncbi.nlm.nih.gov/pubmed/26950939
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0150852
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares