Cargando…
Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice
BACKGROUND: Loss-of-function mutations in TBC1D20 cause Warburg Micro syndrome 4 (WARBM4), which is an autosomal recessive syndromic disorder characterized by eye, brain, and genital abnormalities. Blind sterile (bs) mice carry a Tbc1d20-null mutation and exhibit cataracts and testicular phenotypes...
Autores principales: | Park, Anna Kyunglim, Liegel, Ryan P, Ronchetti, Adam, Ebert, Allison D, Geurts, Aron, Sidjanin, Duska J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266191/ https://www.ncbi.nlm.nih.gov/pubmed/25476608 http://dx.doi.org/10.1186/s12863-014-0135-2 |
Ejemplares similares
-
Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice
por: Liang, Lina, et al.
Publicado: (2011) -
Gene Targeting in NOD Mouse Embryos Using Zinc-Finger Nucleases
por: Chen, Yi-Guang, et al.
Publicado: (2014) -
Alkylglycerone phosphate synthase (AGPS) deficient mice: Models for rhizomelic chondrodysplasia punctata type 3 (RCDP3) malformation syndrome
por: Liegel, Ryan P., et al.
Publicado: (2014) -
Heritable Targeted Gene Disruption in Zebrafish Using Designed Zinc Finger Nucleases
por: Doyon, Yannick, et al.
Publicado: (2008) -
Zinc-finger nuclease mediated disruption of Rag1 in the LEW/Ztm rat
por: Zschemisch, Nils-Holger, et al.
Publicado: (2012)