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Pioglitazone reversed the fructose-programmed astrocytic glycolysis and oxidative phosphorylation of female rat offspring
Chih Wei Wu
, Chun Ying Hung
, Hajime Hirase
, You Lin Tain
, Wei Chia Lee
, Julie Y.H. Chan
, Mu Hui Fu
, X. Lee Wei Chen
, Wen Chung Liu
, Chih Kuang Liang
, Ying Hao Ho
, Yu Chih Kung
, Steve Leu
, X. Kay L.H. Wu
*
*
此作品的通信作者
醫學系
Chang Gung Memorial Hospital
RIKEN
Saitama University
University of Copenhagen
Chang Gung University
Veterans General Hospital-Kaohsiung Taiwan
Meiho University
National Tainan Junior College of Nursing
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期刊稿件
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同行評審
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引文 斯高帕斯(Scopus)
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Medicine and Dentistry
Child
100%
Female
100%
Fructose
100%
Oxidative Phosphorylation
100%
Glycolysis
100%
Pioglitazone
100%
High-Fructose Diet
100%
Infant
28%
Glucose Metabolism
28%
Brain
28%
Lactic Acid
28%
Water-Electrolyte Imbalance
14%
Phosphotransferase
14%
Energy Metabolism
14%
Cell Type
14%
Neuron
14%
Metabolism
14%
Lactation
14%
Astrocyte
14%
Pregnancy
14%
Mitochondrial Respiration
14%
Cell Metabolism
14%
Postnatal Development
14%
Primary Culture
14%
Western Blot
14%
Adenosine Triphosphate
14%
Respiratory Chain
14%
Brain Metabolism
14%
Gene Dosage
14%
Phosphatidylinositide
14%
Insulin Receptor Substrate 1
14%
Fetus Development
14%
Glucose Transporter 1
14%
Mitochondrial Transcription Factor A
14%
Insulin Receptor
14%
Neuroscience
Pioglitazone
100%
Oxidative Phosphorylation
100%
Glycolysis
100%
Fructose
100%
Female Rats
100%
Glucose
25%
Insulin Receptor
25%
Mitochondrial DNA
12%
Kinase
12%
Astrocyte
12%
Mitochondrial Respiration
12%
Metabolic Pathway
12%
Adenosine Triphosphate
12%
Energy Metabolism
12%
Phosphatidylinositide
12%
Electron Transport Chain
12%
Brain Metabolism
12%
Gene Dosage
12%
Glucose Transporter 1
12%
Mitochondrial Transcription Factor A
12%