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Author Details
Full Name
Zhiguang Su
Affiliation
Guangzhou Sport University
ORCID
Career Start Year
2000
Papers
79
H Index
19
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36174906
Novel association of SNP rs2297828 in PRDM16 gene with predisposition to type 2 diabetes.
Gene
2023
37187876
Identifying the intervention mechanisms of polydatin in hyperuricemia model rats by using UHPLC-Q-Exactive Orbitrap mass spectroscopy metabonomic approach.
Front Nutr
2023
37310057
Liraglutide ameliorates hepatic steatosis via retinoic acid receptor-related orphan receptor α-mediated autophagy pathway.
IUBMB Life
2023
37000974
Nuclear factor-Y mediates pancreatic β-cell compensation by repressing reactive oxygen species-induced apoptosis under metabolic stress.
Chin Med J (Engl)
2023
36678850
Advances in the Study of Exosomes as Drug Delivery Systems for Bone-Related Diseases.
Pharmaceutics
2023
35308228
Cholesterol Sulfate Exerts Protective Effect on Pancreatic β-Cells by Regulating β-Cell Mass and Insulin Secretion.
Front Pharmacol
2022
33980692
Nuclear Factor-Y in Mouse Pancreatic β-Cells Plays a Crucial Role in Glucose Homeostasis by Regulating β-Cell Mass and Insulin Secretion.
Diabetes
2021
32593204
Effects of genetic variations in Acads gene on the risk of chronic obstructive pulmonary disease.
IUBMB Life
2020
33195204
Mitochondria-Associated Endoplasmic Reticulum Membranes in the Pathogenesis of Type 2 Diabetes Mellitus.
Front Cell Dev Biol
2020
30733709
Unraveling the Regulation of Hepatic Gluconeogenesis.
Front Endocrinol (Lausanne)
2019
35693877
Mutation spectrum in <i>GNAQ</i> and <i>GNA11</i> in Chinese uveal melanoma.
Precis Clin Med
2019
31585505
Deficiency in the short-chain acyl-CoA dehydrogenase protects mice against diet-induced obesity and insulin resistance.
FASEB J
2019
31209418
[Spectrometric analyses of larotaxel and larotaxel liposomes quantification by high performance liquid chromatography].
Beijing Da Xue Xue Bao Yi Xue Ban
2019
31205951
Effects of Genetic Variants of Nuclear Receptor Y on the Risk of Type 2 Diabetes Mellitus.
J Diabetes Res
2019
29530977
Regulation of hepatic gluconeogenesis by nuclear factor Y transcription factor in mice.
J Biol Chem
2018
27837431
Obesity-induced endoplasmic reticulum stress suppresses nuclear factor-Y expression.
Mol Cell Biochem
2017
28698385
Retinoic acid receptor-related orphan receptor α stimulates adipose tissue inflammation by modulating endoplasmic reticulum stress.
J Biol Chem
2017
28612522
[The Mechanisms of Trimetazidine Alleviating the Oxidative Stress in Adipose-derived Mesenchymal Stem Cells].
Sichuan Da Xue Xue Bao Yi Xue Ban
2017
26691988
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Nat Genet
2016
27744704
One-Step Self-Assembling Nanomicelles for Pirarubicin Delivery To Overcome Multidrug Resistance in Breast Cancer.
Mol Pharm
2016
27418000
Design and Validation of PEG-Derivatized Vitamin E Copolymer for Drug Delivery into Breast Cancer.
Bioconjug Chem
2016
27556492
Genetic Variants of Retinoic Acid Receptor-Related Orphan Receptor Alpha Determine Susceptibility to Type 2 Diabetes Mellitus in Han Chinese.
Genes (Basel)
2016
26806298
Genetic variants of CDH13 determine the susceptibility to chronic obstructive pulmonary disease in a Chinese population.
Acta Pharmacol Sin
2016
24498989
CETP Gene may be Associated with Advanced Age-Related Macular Degeneration in the Chinese Population.
Ophthalmic Genet
2015
26301885
Effects of adiponectin polymorphisms on the risk of advanced age-related macular degeneration.
Biomarkers
2015
26308894
Corrigendum: Lanosterol reverses protein aggregation in cataracts.
Nature
2015
26045367
Reveal genes functionally associated with ACADS by a network study.
Gene
2015
26200341
Lanosterol reverses protein aggregation in cataracts.
Nature
2015
25921655
Salidroside protects retinal endothelial cells against hydrogen peroxide-induced injury via modulating oxidative status and apoptosis.
Biosci Biotechnol Biochem
2015
24286382
Association of five genetic variants with chronic obstructive pulmonary disease susceptibility and spirometric phenotypes in a Chinese Han population.
Respirology
2014
25111685
Malattia leventinese/Doyne honeycomb retinal dystrophy in a chinese family with mutation of the EFEMP1 gene.
Retina
2014
24943193
Genetic variations in RORα are associated with chronic obstructive pulmonary disease.
J Hum Genet
2014
24615081
Association of XRCC5 polymorphisms with COPD and COPD-related phenotypes in the Han Chinese population: a case-control cohort study.
Genet Mol Res
2014
24583012
Identification of insulin as a novel retinoic acid receptor-related orphan receptor α target gene.
FEBS Lett
2014
23441113
Genetic analysis of the forkhead transcriptional factor 2 gene in three Chinese families with blepharophimosis syndrome.
Mol Vis
2013
24171171
Advanced systems biology methods in drug discovery and translational biomedicine.
Biomed Res Int
2013
23868022
RAD51 gene is associated with advanced age-related macular degeneration in Chinese population.
Clin Biochem
2013
22199362
Essential role of ELOVL4 protein in very long chain fatty acid synthesis and retinal function.
J Biol Chem
2012
23209832
Genetic variations in ADIPOQ gene are associated with chronic obstructive pulmonary disease.
PLoS One
2012
22796760
Association between fibroblast growth factor 7 and the risk of chronic obstructive pulmonary disease.
Acta Pharmacol Sin
2012
22875704
Complement factor H genotypes impact risk of age-related macular degeneration by interaction with oxidized phospholipids.
Proc Natl Acad Sci U S A
2012
22274563
Characterization of Bglu3, a mouse fasting glucose locus, and identification of Apcs as an underlying candidate gene.
Physiol Genomics
2012
22049084
High temperature requirement factor A1 (HTRA1) gene regulates angiogenesis through transforming growth factor-β family member growth differentiation factor 6.
J Biol Chem
2012
22022387
Identification of Soat1 as a quantitative trait locus gene on mouse chromosome 1 contributing to hyperlipidemia.
PLoS One
2011
20562441
Untangling HDL quantitative trait loci on mouse chromosome 5 and identifying Scarb1 and Acads as the underlying genes.
J Lipid Res
2010
20833975
Sequence variation at multiple loci influences red cell hemoglobin concentration.
Blood
2010
18988887
Farp2 and Stk25 are candidate genes for the HDL cholesterol locus on mouse chromosome 1.
Arterioscler Thromb Vasc Biol
2009
19799071
[A study on the haplotype of the solute carrier family 11 member 1 gene in Tibetan patients with pulmonary tuberculosis in China].
Zhonghua Jie He He Hu Xi Za Zhi
2009
19436067
Four additional mouse crosses improve the lipid QTL landscape and identify Lipg as a QTL gene.
J Lipid Res
2009
18772481
Genetic basis of HDL variation in 129/SvImJ and C57BL/6J mice: importance of testing candidate genes in targeted mutant mice.
J Lipid Res
2009
1 - 50 of 79
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The University of Texas at Austin
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University of California San Diego
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Guangzhou Women and Children's Medical Center, Guangzhou Medical University
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