Cargando…
Somatic clones heterozygous for recessive disease alleles of BMPR1A exhibit unexpected phenotypes in Drosophila
The majority of mutations studied in animal models are designated as recessive based on the absence of visible phenotypes in germline heterozygotes. Accordingly, genetic studies primarily rely on homozygous loss-of-function to determine gene requirements, and a conceptually-related ‘two-hit model’ r...
Autores principales: | Akiyama, Takuya, User, Sırma D, Gibson, Matthew C |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963922/ https://www.ncbi.nlm.nih.gov/pubmed/29745898 http://dx.doi.org/10.7554/eLife.35258 |
Ejemplares similares
-
Autosomal Recessive Rod-Cone Dystrophy Associated With Compound Heterozygous Variants in ARL3 Gene
por: Fu, Leming, et al.
Publicado: (2021) -
Novel compound heterozygous variants in the USH2A gene associated with autosomal recessive retinitis pigmentosa without hearing loss
por: Huang, Yanxia, et al.
Publicado: (2023) -
Mga Modulates Bmpr1a Activity by Antagonizing Bs69 in Zebrafish
por: Sun, Xiaoyun, et al.
Publicado: (2018) -
Novel CLCN7 compound heterozygous mutations in intermediate autosomal recessive osteopetrosis
por: Okamoto, Nana, et al.
Publicado: (2017) -
Molecular mechanism of estrogen–estrogen receptor signaling
por: Yaşar, Pelin, et al.
Publicado: (2016)