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科研机构
中南大学 [15]
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期刊论文 [15]
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2016 [2]
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专题:中南大学
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Recycling of metals from pretreated waste printed circuit boards effectively in stirred tank reactor by a moderately thermophilic culture
期刊论文
Journal of Bioscience and Bioengineering, 2017, 卷号: 123, 期号: 6, 页码: 714-721
作者:
Xia, Ming-Chen
;
Wang, Ya-Ping
;
Peng, Tang-Jian
;
Shen, Li
;
Yu, Run-Lan
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2019/12/03
Waste printed circuit boards
Table separation
Bioleaching
Moderate thermophiles
Community structure
Amplified ribosomal DNA restriction analysis
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
期刊论文
AUTOPHAGY, 2016, 卷号: 12, 期号: 1, 页码: 1-222
作者:
Klionsky, Daniel J.*
;
Abdelmohsen, Kotb
;
Abe, Akihisa
;
Abedin, Md Joynal
;
Abeliovich, Hagai
收藏
  |  
浏览/下载:87/0
  |  
提交时间:2019/12/03
LC3
autolysosome
autophagosome
chaperone-mediated autophagy
flux
lysosome
macroautophagy
phagophore
stress
vacuole
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
期刊论文
Autophagy, 2016, 卷号: 12, 期号: 1, 页码: 1-222
作者:
Klionsky, Daniel J.*
;
Abdelmohsen, Kotb
;
Abe, Akihisa
;
Abedin, Md Joynal
;
Abeliovich, Hagai
收藏
  |  
浏览/下载:70/0
  |  
提交时间:2019/12/03
LC3
autolysosome
autophagosome
chaperone-mediated autophagy
flux
lysosome
macroautophagy
phagophore
stress
vacuole
Polygenic determinants of Parkinson's disease in a Chinese population
期刊论文
Neurobiology of Aging, 2015, 卷号: 36, 期号: 4, 页码: 1765.e1-1765.e6
作者:
Guo, Ji-Feng
;
Li, Kai
;
Yu, Ri-Li
;
Sun, Qi-Yin
;
Wang, Lei
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/12/03
Parkinson's disease
Gene polymorphism
Association analysis
Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases
期刊论文
Neuroscience letters, 2013, 卷号: 552, 页码: 40-45
作者:
Jun-Ling Wang
;
Xiao Mao
;
Zheng-Mao Hu
;
Jia-Da Li
;
Nan Li
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/12/03
BFIS
DNA
ICCA
Linkage analysis
PED
PKD
PNKD
PRRT2
Paroxysmal diseases
PxDs
benign familial infantile seizures
deoxyribonucleic acid
infantile convulsions and choreoathetosis
paroxysmal dyskinesis
paroxysmal exercise-induced dyskinesia
paroxysmal kinesigenic dyskinesias
paroxysmal non-kinesigenic dyskinesia
proline-rich transmembrane protein 2
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders
期刊论文
Neurobiology of Aging, 2013, 卷号: 34, 期号: 10, 页码: 2442.e11-2442.e17
作者:
Chen, Zhao
;
Wang, Jun-ling
;
Tang, Bei-sha
;
Sun, Zhan-fang
;
Shi, Yu-ting
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/12/03
Targeted gene sequencing
Exome sequencing
Autosomal recessive
Neurologic Mendelian disorders
Genetic diagnostic strategy
SUMO-1 Modification on K166 of PolyQ-Expanded aTaxin-3 Strengthens Its Stability and Increases Its Cytotoxicity
期刊论文
PLOS ONE, 2013, 卷号: 8, 期号: 1, 页码: e54214
作者:
Zhou, Ya-Fang
;
Liao, Shu-Sheng
;
Luo, Ying-Ying
;
Tang, Jian-Guang
;
Wang, Jun-Ling
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/03
SUMOylation,Immunoprecipitation,Lysine,Transfection,Ubiquitination,Subcellular localization,Apoptosis,Pathogenesis
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis
期刊论文
Biochemical and Biophysical Research Communications, 2013, 卷号: 430, 期号: 2, 页码: 780-786
作者:
Guan, Wen-Juan
;
Wang, Jun-Ling
;
Liu, Yu-Tao
;
Ma, Yan-Tao
;
Zhou, Ying
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/03
Apoptosis
Spinocerebellar ataxia 35 (SCA35)
Transglutaminase 6 (TG6)
Guidelines for the use and interpretation of assays for monitoring autophagy
期刊论文
Autophagy, 2012, 卷号: 8, 期号: 4, 页码: 445-544
作者:
Klionsky, Daniel J.*
;
Abdalla, Fabio C.
;
Abeliovich, Hagai
;
Abraham, Robert T.
;
Acevedo-Arozena, Abraham
收藏
  |  
浏览/下载:52/0
  |  
提交时间:2019/12/03
Autolysosome
Autophagosome
Flux
LC3
Lysosome
Phagophore
Stress
Vacuole
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
期刊论文
Brain, 2011, 卷号: 134, 期号: 12, 页码: 3490-3498
作者:
Wang, Jun-Ling
;
Cao, Li
;
Li, Xun-Hua
;
Hu, Zheng-Mao
;
Li, Jia-Da
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/12/03
proline-rich transmembrane protein 2
paroxysmal kinesigenic dyskinesias
whole-exome sequencing
linkage analysis
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