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武汉病毒研究所 [2]
复旦大学上海医学院 [2]
厦门大学 [1]
北京大学 [1]
上海神经科学研究所 [1]
武汉植物园 [1]
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期刊论文 [9]
会议论文 [1]
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Human Cytomegalovirus Immediate Early 1 Protein Causes Loss of SOX2 from Neural Progenitor Cells by Trapping Unphosphorylated STAT3 in the Nucleus
期刊论文
JOURNAL OF VIROLOGY, 2018, 卷号: 92, 期号: 17, 页码: 18
作者:
Luo, Min-Hua
;
Nevels, Michael
;
Paulus, Christina
;
Britt, William J.
;
Wang, Wei
收藏
  |  
浏览/下载:58/0
  |  
提交时间:2018/12/29
HCMV
IE1
neural progenitor cells
SOX2
STAT3
Human cytomegalovirus infection dysregulates neural progenitor cell fate by disrupting hes1 rhythm and down-regulating its expression
期刊论文
Virologica sinica, 2017, 卷号: 32, 期号: 3, 页码: 188-198
作者:
Liu, Xi-Juan
;
Jiang, Xuan
;
Huang, Sheng-Nan
;
Sun, Jin-Yan
;
Zhao, Fei
收藏
  |  
浏览/下载:37/0
  |  
提交时间:2019/05/08
Human cytomegalovirus (hcmv)
Neural progenitor cells (npcs)
Hes1 rhythm
Cell fate
Early-onset hearing loss reorganizes the visual and auditory network in children without cochlear implantation
期刊论文
NeuroReport, 2016, 卷号: 27, 期号: 3
作者:
Shi, Bin/57111333900[0]
;
Yang, Lizhuang/57104020200[1]
;
Liu, Ying/56457779400[2]
;
Zhao, Shuli/57111125500[3]
;
Wang, Ying/56681858000[4]
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/06
Auditory deprivation
Congenital deafness
Development
Functional connectivity
Hearing loss
Human cytomegalovirus infection dysregulates the localization and stability of nicd1 and jag1 in neural progenitor cells
期刊论文
Journal of virology, 2015, 卷号: 89, 期号: 13, 页码: 6792-6804
作者:
Li, Xiao-Jun
;
Liu, Xi-Juan
;
Yang, Bo
;
Fu, Ya-Ru
;
Zhao, Fei
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2019/05/09
Non-manifesting AHI1 truncations indicate localized loss-of-function tolerance in a severe Mendelian disease gene
期刊论文
human molecular genetics, 2015
Elsayed Solaf M
;
Phillips Jennifer B
;
Heller Raoul
;
Thoenes Michaela
;
Elsobky Ezzat
;
Nürnberg Gudrun
;
Nürnberg Peter
;
Seland Saskia
;
Ebermann Inga
;
Altmüller Janine
;
Thiele Holger
;
Toliat Mohammad
;
K?rber Friederike
;
Hu Xue-Jia
;
Wu Yun-Dong
;
Zaki Maha S
;
Abdel-Salam Ghada
;
Gleeson Joseph
;
Boltshauser Eugen
;
Westerfield Monte
;
Bolz Hanno J
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2015/11/13
First healthy baby born after PGD (preimplantation genetic diagnosis) - noninvasive haplotype screening in couples both carrying deafness gene GJB2 mutation
会议论文
31st Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology (ESHRE), JUN 14-17, 2015
作者:
Chen, Z.
;
Gao, Y.
;
Huang, S.
;
Yan, J.
;
Li, J.
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/31
congenital hearing loss
preimplantation genetic diagnosis
haplotyping
screening
GJB2 Gene
aneuploidy screening
Murine model for congenital CMV infection and hearing impairment
期刊论文
http://dx.doi.org/10.1186/1743-422X-8-70, 2011
Chen Juanjuan
;
Feng Yan
;
Chen Li
;
Liu Haizhi
;
Wang Ling
;
Wang Xinrong
;
Xiao Juan
;
Liu Tao
;
Yin Zongzhi
;
Chen Suhua
;
陈亮
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2013/12/12
CYTOMEGALO-VIRUS LABYRINTHITIS
CHILDREN
JAPAN
Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28
期刊论文
HUMAN MOLECULAR GENETICS, 2011, 卷号: 20, 期号: 16, 页码: 3213-3226
作者:
Du, Jiulin
收藏
  |  
浏览/下载:39/0
  |  
提交时间:2012/07/13
SEMICIRCULAR CANAL FORMATION
RECESSIVE DEAFNESS DFNB29
GRAINYHEAD-LIKE FACTOR
TRANSCRIPTION FACTOR
EPIDERMAL DIFFERENTIATION
DROSOPHILA-GRAINYHEAD
TIGHT JUNCTIONS
INNER-EAR
EXPRESSION
HEAD
A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family
期刊论文
LARYNGOSCOPE, 2006, 卷号: 116, 期号: 6
作者:
Wang, Qiu-Ju
;
Li, Qing-Zhong
;
Rao, Shao-Qi
;
Zhao, Ya-Li
;
Yuan, Hu
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/27
deaf-mutism
positional cloning
X-linked
missense mutation
molecular diagnosis
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