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北京大学 [4]
复旦大学上海医学院 [4]
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南华大学 [1]
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期刊论文 [13]
其他 [1]
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浏览/检索结果:
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A novel model for the X-chromosome inactivation association on survival data
期刊论文
STATISTICAL METHODS IN MEDICAL RESEARCH, 2020, 卷号: 29, 期号: 5, 页码: 1305-1314
作者:
Han, Dongxiao
;
Hao, Meiling
;
Qu, Lianqiang
;
Xu, Wei
收藏
  |  
浏览/下载:37/0
  |  
提交时间:2020/06/30
Cox model
genetic association test
frailty model
right-censored survival data
X-chromosome association
X-chromosome inactivation
Silver Nanoparticles Compromise Female Embryonic Stem Cell Differentiation through Disturbing X Chromosome Inactivation
期刊论文
ACS NANO, 2019, 卷号: 13, 期号: 2, 页码: 2050-2061
作者:
Zhang, Jie
;
Chen, Yongjiu
;
Gao, Ming
;
Wang, Zhe
;
Liu, Rui
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2020/10/21
silver nanoparticles
embryonic stem cells
differentiation
X chromosome inactivation
imbalance
Changes in the position and volume of inactive X chromosomes during the G0/G1 transition
期刊论文
Chromosome Research, 2018, 卷号: 26, 期号: 3, 页码: 179-189
作者:
Lyu, Guoliang
;
Tan, Tan
;
Guan, Yiting
;
Sun, Lei
;
Liang, Qianjin*
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/27
G0/G1 transition
X chromosome inactivation
Xi movement
dimethylated histone H3 on lysine 9 (H3K9me2)
trimethylated histone H3 on lysine 27 (H3K27me3)
Detection of Turner syndrome using X-chromosome inactivation specific differentially methylated CpG sites: A pilot study
期刊论文
CLINICA CHIMICA ACTA, 2017, 卷号: 468
作者:
Zhang, Qiang
;
Guo, Xiaohong
;
Tian, Tian
;
Wang, Teng
;
Li, Qiaoli
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/05
Turner syndrome
X-chromosome inactivation
DNA methylation
X chromosome aneuploids
The State of Skewed X Chromosome Inactivation is Retained in the Induced Pluripotent Stem Cells from a Female with Hemophilia B
期刊论文
2017, 卷号: 26, 期号: 13, 页码: 1003-1011
作者:
Lyu Cuicui
;
Shen Jun
;
Zhang Jianping
;
Xue Feng
;
Liu Xiaofan
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2020/01/04
hemophilia B
X chromosome inactivation
induced pluripotent stem cells
XIST noncoding RNA
high-throughput nucleotide sequencing
Clonality assessment of adenomatoid tumor supports its neoplastic nature
期刊论文
HUMAN PATHOLOGY, 2016, 卷号: 48
作者:
Zhu, Hongguang
;
Wang, Wei
;
Zhu, Huiting
;
Wang, Jigang
;
Wang, Shuyang
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/05
Adenomatoid tumor
Clonality
Human androgen receptor gene
Laser capture microdissection
Mesothelial hyperplasia
X-chromosome inactivation
Clonal and genetic relationship between individual components of mucoepidermoid carcinoma: X-chromosome inactivation assay and microsatellite analysis
期刊论文
HUMAN PATHOLOGY, 2016, 卷号: 56
作者:
Wang, Wei
;
Zou, Bingqing
;
Zhu, Hongguang
;
Bao, Yun
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/06
Individual components
Heterogeneity
Laser-capture
microdissection
Loss of heterozygosity
Mucoepidermoid
carcinoma
X-chromosome
inactivation
Hallmarks of pluripotency
其他
2015-01-01
De Los Angeles, Alejandro
;
Ferrari, Francesco
;
Xi, Ruibin
;
Fujiwara, Yuko
;
Benvenisty, Nissim
;
Deng, Hongkui
;
Hochedlinger, Konrad
;
Jaenisch, Rudolf
;
Lee, Soohyun
;
Leitch, Harry G.
;
Lensch, M. William
;
Lujan, Ernesto
;
Pei, Duanqing
;
Rossant, Janet
;
Wernig, Marius
;
Park, Peter J.
;
Daley, George Q.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2017/12/03
EMBRYONIC STEM-CELLS
PRIMORDIAL GERM-CELLS
GROUND-STATE PLURIPOTENCY
X-CHROMOSOME INACTIVATION
DNA METHYLATION
TRANSCRIPTIONAL NETWORK
REGULATORY CIRCUITRY
ISOLATED BLASTOMERES
NAIVE PLURIPOTENCY
CULTURE-CONDITIONS
Association of skewed X chromosome inactivation and idiopathic recurrent spontaneous abortion: a systematic review and meta-analysis
期刊论文
REPRODUCTIVE BIOMEDICINE ONLINE, 2015, 卷号: 31, 期号: 2
作者:
Sui, Yilun
;
Chen, Qianqian
;
Sun, Xiaoxi
收藏
  |  
浏览/下载:1/0
  |  
提交时间:2019/12/19
chromosomal aneuploidy
idiopathic recurrent miscarriage
skewed X chromosome inactivation
X-linked mutations
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients
期刊论文
bmc medical genetics, 2014
Zhao, Ying
;
Zhang, Xiaoying
;
Bao, Xinhua
;
Zhang, Qingping
;
Zhang, Jingjing
;
Cao, Guangna
;
Zhang, Jie
;
Li, Jiarui
;
Wei, Liping
;
Pan, Hong
;
Wu, Xiru
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2015/11/10
CDKL5 mutations
Early-onset epileptic encephalopathy
X chromosome inactivation
ONSET INTRACTABLE EPILEPSY
X-CHROMOSOME INACTIVATION
CDKL5 MUTATIONS
RETT-SYNDROME
INFANTILE SPASMS
MENTAL-RETARDATION
SEVERE ENCEPHALOPATHY
FEMALE-PATIENTS
BOYS
SEIZURES
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