Fengxia Li
Shanghai, 200032, China
Last Updated: 09/26/2026
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Found 12 publications
Nicotinamide n-methyltransferase inhibitor synergizes with sodium-glucose cotransporter 2 inhibitor to protect renal tubular epithelium in experimental models of type 2 diabetes mellitus.
Journal: Journal of diabetes and its complications
Published: August 16, 2024
Hepatocyte growth factor attenuates high glucose-disturbed mitochondrial dynamics in podocytes by decreasing ARF6-dependent DRP1 translocation.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: May 11, 2023
Long non-coding RNA FENDRR suppresses cancer-associated fibroblasts and serves as a prognostic indicator in colorectal cancer.
Journal: Translational oncology
Published: May 04, 2023
Correction: Heparanase promotes endothelial-to-mesenchymal transition in diabetic glomerular endothelial cells through mediating ERK signaling.
Journal: Cell death discovery
Published: March 10, 2022
NAD+ Anabolism Disturbance Causes Glomerular Mesangial Cell Injury in Diabetic Nephropathy.
Journal: International journal of molecular sciences
Published: February 21, 2022
Heparanase promotes endothelial-to-mesenchymal transition in diabetic glomerular endothelial cells through mediating ERK signaling.
Journal: Cell death discovery
Published: October 09, 2021
Dysbiosis of urine microbiota in obstructive urinary retention patients revealed by next-generation sequencing.
Journal: Annals of clinical microbiology and antimicrobials
Published: September 11, 2020
Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: December 04, 2019
Circular RNA sequencing indicates circ-IQGAP2 and circ-ZC3H6 as noninvasive biomarkers of primary Sjögren's syndrome.
Journal: Rheumatology (Oxford, England)
Published: September 18, 2019
Correction: Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 02, 2019
Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 30, 2019
Elevated CCL19/CCR7 Expression During the Disease Process of Primary Sjögren's Syndrome.
Journal: Frontiers in immunology
Published: December 08, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026