A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development.
第一作者:
Basile,Tarchini
第一单位:
The Jackson Laboratory, Bar Harbor, ME 04609, USA; Department of Medicine, Tufts University, Boston 02111, MA, USA; Graduate School of Biomedical Science and Engineering (GSBSE), University of Maine, Orono 04469, ME, USA. Electronic address: basile.tarchini@jax.org.
作者:
主题词
动物(Animals);COUP转录因子Ⅰ(COUP Transcription Factor I);聋(Deafness);内耳(Ear, Inner);增强子元件, 遗传学(Enhancer Elements, Genetic);女(雌)性(Female);基因缺失(Gene Deletion);基因表达调控, 发育期(Gene Expression Regulation, Developmental);基因敲除技术(Gene Knockout Techniques);人类(Humans);男(雄)性(Male);膜蛋白质类(Membrane Proteins);小鼠(Mice);小鼠, 近交C57BL(Mice, Inbred C57BL)
DOI
10.1016/j.ydbio.2018.09.011
PMID
30217595
发布时间
2024-06-10
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Developmental biology
153-164页
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