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BRD4 Targets the KEAP1-Nrf2-G6PD Axis and Suppresses Redox Metabolism in Small Cell Lung Cancer
期刊论文
ANTIOXIDANTS, 2022, 卷号: 11
作者:
Lv, Yang
;
Lv, Xiaotong
;
Zhang, Jiahui
;
Cao, Guozhen
;
Xu, Changzhi
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2022/05/16
small cell lung cancer
BRD4
KEAP1
Nrf2
pentose phosphate pathway
Rhubarb granule promotes diethylnitrosamine-induced liver tumorigenesis by activating the oxidative branch of pentose phosphate pathway via G6PD in rats
期刊论文
JOURNAL OF ETHNOPHARMACOLOGY, 2021, 卷号: 281
作者:
Huang, Hongwu
;
Liu, Zhenzhen
;
Qi, Xiaoru
;
Gao, Nailong
;
Chang, Jianguo
收藏
  |  
浏览/下载:57/0
  |  
提交时间:2021/11/15
Rhubarb
Hepatocarcinogenesis
Diethylnitrosamine
The pentose phosphate pathway
Glucose 6 phosphate dehydrogenase
Improvement of d-lactic acid productivity by introducing Escherichia coli acetyl-CoA synthesis pathway in engineered Saccharomyces cerevisiae
期刊论文
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2021, 页码: 11
作者:
Zhong, Wei
;
Yang, Maohua
;
Hao, Xuemi
;
Sharshar, Moustafa M.
;
Wang, Qinhong
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  |  
浏览/下载:16/0
  |  
提交时间:2021/08/31
d‐
lactic acid
acetylating acetaldehyde dehydrogenase
acetyl‐
CoA
metabolic engineering
Saccharomyces cerevisiae
Natural product 1,2,3,4,6-penta-O-galloyl-beta-D-glucopyranose is a reversible inhibitor of glyceraldehyde 3-phosphate dehydrogenase
期刊论文
ACTA PHARMACOLOGICA SINICA, 2021, 页码: 13
作者:
Li, Wen
;
Liao, Li-ping
;
Song, Ning
;
Liu, Yan-jun
;
Ding, Yi-luan
收藏
  |  
浏览/下载:80/0
  |  
提交时间:2021/06/11
glyceraldehyde 3-phosphate dehydrogenase
1,2,3,4,6-penta-O-galloyl-beta-D-glucopyranose
hydrogen deuterium exchange mass spectrometry
reversible inhibitor
glycolysis
Natural product 1,2,3,4,6-penta-O-galloyl-beta-D-glucopyranose is a reversible inhibitor of glyceraldehyde 3-phosphate dehydrogenase
期刊论文
ACTA PHARMACOLOGICA SINICA, 2021, 页码: 13
作者:
Li, Wen
;
Liao, Li-ping
;
Song, Ning
;
Liu, Yan-jun
;
Ding, Yi-luan
收藏
  |  
浏览/下载:81/0
  |  
提交时间:2021/06/11
glyceraldehyde 3-phosphate dehydrogenase
1,2,3,4,6-penta-O-galloyl-beta-D-glucopyranose
hydrogen deuterium exchange mass spectrometry
reversible inhibitor
glycolysis
Differentially expressed genes related to oxidoreductase activity and glutathione metabolism underlying the adaptation of Phragmites australis from the salt marsh in the Yellow River Delta, China
期刊论文
PEERJ, 2020, 卷号: 8, 页码: e10024
作者:
Zhang, Liwen
;
Chen, Lin
;
Lan, Siqun
;
Han, Guangxuan
;
Chen, Lin
收藏
  |  
浏览/下载:32/0
  |  
提交时间:2021/12/01
Transcriptome analysis
Salt stress
Glutathione metabolism
Phragmites australis
Yellow River Delta
Oxidoreductase activity
Common reed
Coastal wetland
Transcription factors
Differential gene expression
Elevated CO2 improves both lipid accumulation and growth rate in the glucose-6-phosphate dehydrogenase engineered Phaeodactylum tricornutum
期刊论文
MICROBIAL CELL FACTORIES, 2019, 卷号: 18, 期号: 1, 页码: 16
作者:
Wu, Songcui
;
Gu, Wenhui
;
Huang, Aiyou
;
Li, Yuanxiang
;
Kumar, Manoj
收藏
  |  
浏览/下载:201/0
  |  
提交时间:2020/01/03
Glucose-6-phosphate dehydrogenase
Overexpression
Antisense knockdown
CO2
Phaeodactylum tricornutum
Lipid accumulation
Algal growth rate
酿酒酵母产D-乳酸的代谢工程研究
学位论文
: 中国科学院大学, 2019
作者:
钟伟
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2020/06/17
D-乳酸,合成生物学,耐酸基因,乙酰化乙醛脱氢酶,酿酒酵母
The glucose-6-phosphate dehydrogenase Mahidol variant protects against uncomplicated Plasmodium vivax infection and reduces disease severity in a Kachin population from northeast Myanmar.
期刊论文
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2019, 卷号: 75
作者:
Yi Haoan
;
Li Hong
;
Liang Luxin
;
Wu Yanrui
;
Zhang Lu
收藏
  |  
浏览/下载:21/0
  |  
提交时间:2019/12/04
G6PD
Haplotype 1311T/93C
Kachin population
Mahidol variant
Malaria
Plasmodium vivax
A novel mutation of the ITGB2 gene in a Chinese Zhuang minority patient with leukocyte adhesion deficiency type 1 and glucose-6-phosphate dehydrogenase deficiency.
期刊论文
Gene, 2019, 卷号: 715
作者:
Zhang Yu
;
Yang Xiaotao
;
He Xiaoli
;
Liu Haifeng
;
Guo Pin
收藏
  |  
浏览/下载:37/0
  |  
提交时间:2019/12/04
Ethnic minority group
G6PD
ITGB2
Primary immunodeficiency disease
Rare genetic disorder
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