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科研机构
北京大学 [3]
中南大学 [2]
厦门大学 [1]
上海药物研究所 [1]
昆明植物研究所 [1]
中国科学院大学 [1]
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期刊论文 [11]
其他 [1]
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Allosteric Inhibitors of SHP2: An Updated Patent Review (2015-2020)
期刊论文
CURRENT MEDICINAL CHEMISTRY, 2021, 卷号: 28, 期号: 19, 页码: 3825-3842
作者:
Wu, Jingwei
;
Zhang, Huan
;
Zhao, Guilong
;
Wang, Runling
收藏
  |  
浏览/下载:65/0
  |  
提交时间:2021/08/17
SHP2 inhibitor
PTPN11 gene
allosteric
cancer
combination therapy
clinical trial
A novel RIT1 mutation causes deterioration of Noonan syndrome-associated cardiac hypertrophy
其他
2019-01-01
作者:
Cai, Jingjing
;
Li, Hongliang
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
BRaf signaling principles unveiled by large-scale human mutation analysis with a rapid lentivirus-based gene replacement method
期刊论文
GENES & DEVELOPMENT, 2017
Lim, Chae-Seok
;
Kang, Xi
;
Mirabella, Vincent
;
Zhang, Huaye
;
Bu, Qian
;
Araki, Yoichi
;
Hoang, Elizabeth T.
;
Wang, Shiqiang
;
Shen, Ying
;
Choi, Sukwoo
;
Kaang, Bong-Kiun
;
Chang, Qiang
;
Pang, Zhiping P.
;
Huganir, Richard L.
;
Zhu, J. Julius
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2017/12/03
BRaf
cancer
CFC syndrome
neurodevelopmental disorder
synaptic transmission
LONG-TERM POTENTIATION
AMPA RECEPTOR TRAFFICKING
FACIO-CUTANEOUS SYNDROME
SYNAPTIC PLASTICITY
NOONAN SYNDROME
CANCER-THERAPY
MOUSE MODELS
RAS
ACTIVATION
DISORDERS
Plasiatine, an Unprecedented Indole-Phenylpropanoid Hybrid from Plantago asiatica as a Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2
期刊论文
SCIENTIFIC REPORTS, 2016, 卷号: 6, 期号: 1, 页码: 24945
作者:
Gao, Zhong-Hua
;
Shi, Yi-Ming
;
Qiang, Zhe
;
Wang, Xia
;
Shang, Shan-Zhai
收藏
  |  
浏览/下载:78/0
  |  
提交时间:2016/08/22
Braf gene: from human cancers to developmental syndromes
期刊论文
Saudi journal of biological sciences, 2015, 卷号: 22, 期号: 4, 页码: 359-373
作者:
Hussain, Muhammad Ramzan Manwar
;
Baig, Mukhtiar
;
Mohamoud, Hussein Sheik Ali
;
Ulhaq, Zaheer
;
Hoessli, Daniel C.
收藏
  |  
浏览/下载:35/0
  |  
提交时间:2019/05/10
Braf gene
Ras-raf overactivation
Cancers
Developmental syndromes
Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11
期刊论文
Molecular Cytogenetics, 2014, 卷号: 7, 期号: 1, 页码: 28
作者:
Chen, Jin-Lan
;
Zhu, Xin
;
Zhao, Tian-Li
;
Wang, Jian
;
Yang, Yi-Feng
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/03
10q25.2 deletion
12q24 duplication
CNV
Congenital heart defect
Copy number variation
Noonan syndrome
PTPN11
RASopathy
SHOC2
Regulation of the HDM2-p53 pathway by ribosomal protein L6 in response to ribosomal stress
期刊论文
核酸研究, 2014
Bai, Dongmei
;
Zhang, Jinfang
;
Xiao, Weichun
;
Zheng, Xiaofeng
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2015/11/13
MDM2-P53 PATHWAY
NOONAN-SYNDROME
FEEDBACK LOOP
P53 RESPONSE
INHIBITION
L11
ACTIVATION
CANCER
TRANSLATION
GROWTH
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
期刊论文
cell, 2013
Willsey, A. Jeremy
;
Sanders, Stephan J.
;
Li, Mingfeng
;
Dong, Shan
;
Tebbenkamp, Andrew T.
;
Muhle, Rebecca A.
;
Reilly, Steven K.
;
Lin, Leon
;
Fertuzinhos, Sofia
;
Miller, Jeremy A.
;
Murtha, Michael T.
;
Bichsel, Candace
;
Niu, Wei
;
Cotney, Justin
;
Ercan-Sencicek, A. Gulhan
;
Gockley, Jake
;
Gupta, Abha R.
;
Han, Wenqi
;
He, Xin
;
Hoffman, Ellen J.
;
Klei, Lambertus
;
Lei, Jing
;
Liu, Wenzhong
;
Liu, Li
;
Lu, Cong
;
Xu, Xuming
;
Zhu, Ying
;
Mane, Shrikant M.
;
Lein, Ed S.
;
Wei, Liping
;
Noonan, James P.
;
Roeder, Kathryn
;
Devlin, Bernie
;
Sestan, Nenad
;
State, Mat
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2015/11/11
SPECTRUM DISORDERS
NOVO MUTATIONS
GENES
RISK
CNVS
Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome
期刊论文
American Journal of Medical Genetics Part A, 2012, 卷号: 158A, 期号: 8, 页码: 1918-1923
作者:
Luo, Cheng
;
Yang, Yi-Feng
;
Yin, Bang-Liang
;
Chen, Jin-Lan
;
Huang, Can
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/03
Noonan syndrome
Noonan syndrome with multiple lentigines
RAF1
PTPN11
duplication 3p25.2
SNP array
dosage sensitive gene
copy number variation
CNV
congenital heart defect
无权访问的条目
期刊论文
作者:
Huang, Heng
;
Jin, Ting
;
He, Jing
;
Ding, QiuRong(丁秋蓉)
;
Xu, Daqian
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2015/08/25
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