Licheng Gong - Concepedia

Author

Licheng Gong

Union Hospital

Also Known As

Li-Cheng Gong, Licheng Gong

Publications

276

Citations

H-Index

Concepts

All Affiliations

Union Hospital Jilin University Union Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Peking Union Medical College Hospital

About

Licheng Gong is an author at Union Hospital specializing in medicine, epigenetics, and molecular medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	81
2	Cell Biology	2	2	65
3	Natural Sciences	1	1	45
4	Cellular Physiology	1	1	45
5	Immunology	1	1	20

Licheng Gong

Publications

259

Citations

H-Index

Page 1

	Year	Citations
Long Non-Coding RNA H19 Protects H9c2 Cells against Hypoxia-Induced Injury by Targeting MicroRNA-139 Licheng Gong, Haiming Xu, Gongliang Guo, Cellular Physiology and Biochemistry	2017	85
<i>Retracted</i>: Knockdown of long non‐coding RNA MEG3 protects H9c2 cells from hypoxia‐induced injury by targeting microRNA‐183 Licheng Gong, Haiming Xu, Chang Hong, Journal of Cellular Biochemistry H9c2 CellsMolecular BiologyCell DeathCardiac RegenerationGene 3	2017	45
Astragaloside IV Protects Rat Cardiomyocytes from Hypoxia-Induced Injury by Down-Regulation of miR-23a and miR-92a Licheng Gong, Hong Chang, Jingze Zhang, Cellular Physiology and Biochemistry	2018	45
RETRACTED ARTICLE: Quercetin supports cell viability and inhibits apoptosis in cardiocytes by down-regulating miR-199a Gongliang Guo, Licheng Gong, Liqun Sun, Artificial Cells Nanomedicine and Biotechnology	2019	35
Oridonin relieves hypoxia-evoked apoptosis and autophagy via modulating microRNA-214 in H9c2 cells Licheng Gong, Haiming Xu, Xiuli Zhang, Artificial Cells Nanomedicine and Biotechnology MitophagyH9c2 CellsApoptosisImmunologyCell Death	2019	20
Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly Licheng Gong, Binbin Wang, Jing Wang, European Journal of Medical Genetics Chinese FamilyHoxd13 GeneUnusual Clinical ManifestationsGenetic DisorderGenetics	2010	16
Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto’s thyroiditis Licheng Gong, Beihong Liu, Jing Wang, BMC Endocrine Disorders	2018	13

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