位置：成果数据库 > 期刊 > 期刊详情页
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the devel
  • ISSN号：0964-6906
  • 期刊名称：Human Molecular Genetics
  • 时间：2012.12.12
  • 页码：5500-5510
  • 相关项目：Pur α调控rCGG重复序列引起的脆性X相关的震颤/共济失调综合症的分子机制研究
作者： Stephen T. Warren|Peng Jin|Ranhui Duan|Xuekun Li|
同期刊论文项目
Pur α调控rCGG重复序列引起的脆性X相关的震颤/共济失调综合症的分子机制研究
期刊论文 11
同项目期刊论文
Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neuro
MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm
Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration
A novel deletion to normal size in the sperm of a fragile X full mutation male
Attitude of medical school students in China towards genetic testing and counseling issues in FXS
Fragile X Syndrome in China: A Clinical Review
Correlation between FMR1 expression and clinical phenotype in discordant dichorionic-diamniotic mono
Fragile X Syndrome in China
Towards Understanding RNA-Mediated Neurological Disorders
脆性X综合征男性生殖系CGG重复不稳定性病例分析