Shan Li
Lanzhou, 730070, China
Last Updated: 09/26/2026
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Found 22 publications
Optimal Nitrogen Application Strategies for Alfalfa Under Different Precipitation Patterns: Balancing Yield, Nitrogen Fertilizer Use Efficiency, and Soil Nitrogen Residue.
Journal: Plants (Basel, Switzerland)
Published: January 03, 2026
Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.
Journal: Molecular therapy. Nucleic acids
Published: December 10, 2025
Integrative pan-cancer analysis of UCP family and experimental validation identifies UCP2 as a potential therapeutic target for glioma.
Journal: Frontiers in cell and developmental biology
Published: July 09, 2025
UBE2C: a potential therapeutic target and prognostic biomarker for prostate cancer patients.
Journal: Functional & integrative genomics
Published: April 04, 2025
The role of SLC26A8 homozygous variants in male infertility and flagellum abnormalities.
Journal: Asian journal of andrology
Published: July 09, 2023
Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.
Journal: Biomolecules
Published: April 25, 2023
Association of aberrant brain network dynamics with gut microbial composition uncovers disrupted brain-gut-microbiome interactions in irritable bowel syndrome: Preliminary findings.
Journal: European journal of neurology
Published: November 29, 2022
Age-Related Differences of Cortical Topology Across the Adult Lifespan: Evidence From a Multisite MRI Study With 1427 Individuals.
Journal: Journal of magnetic resonance imaging : JMRI
Published: April 04, 2022
Spectrins and human diseases.
Journal: Translational research : the journal of laboratory and clinical medicine
Published: November 29, 2021
Brain age estimation using multi-feature-based networks.
Journal: Computers in biology and medicine
Published: October 27, 2021
Advance of research on Phelan-McDermid syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 06, 2021
A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.
Journal: Annals of hematology
Published: May 21, 2021
Last Updated: 09/26/2026