Xiujuan Wei
Hangzhou, 310059, China
Last Updated: 09/26/2026
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Found 14 publications
Nutrient stress-induced FTH1 safeguards redox balance and fuels pancreatic ductal adenocarcinoma growth while serving as a therapeutic target and diagnostic biomarker.
Journal: Cellular oncology (Dordrecht, Netherlands)
Published: December 29, 2025
Hepatocyte RAP1A Deletion Impairs Lipid Catabolism and Worsens Steatosis via Autophagy Activation.
Journal: Diabetes & metabolism journal
Published: May 01, 2025
β-hydroxybutyrate dehydrogenase promotes pancreatic cancer cell proliferation through regulation of the NAD+/NADH balance and mitochondrial acetylation.
Journal: The Journal of biological chemistry
Published: March 25, 2025
Identification of novel NDUFA3 variants in a patient with mitochondrial disorders.
Journal: Pediatric research
Published: March 13, 2025
Antioxidant capacity of the iron-sulfur cluster assembly protein IscU2 is mediated by aspartate metabolism to promote tumor survival.
Journal: The Journal of biological chemistry
Published: January 11, 2025
HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: November 18, 2020
4-Hydroxyphenylpyruvate Dioxygenase-Like Protein Promotes Pancreatic Cancer Cell Progression and Is Associated With Glutamine-Mediated Redox Balance.
Journal: Frontiers in oncology
Published: October 14, 2020
A novel mitochondrial m.14430A>G (MT-ND6, p.W82R) variant causes complex I deficiency and mitochondrial Leigh syndrome.
Journal: Clinical chemistry and laboratory medicine
Published: February 14, 2020
Mutations in TOMM70 lead to multi-OXPHOS deficiencies and cause severe anemia, lactic acidosis, and developmental delay.
Journal: Journal of human genetics
Published: September 06, 2019
Systematic analysis of a mitochondrial disease-causing ND6 mutation in mitochondrial deficiency.
Journal: Molecular genetics & genomic medicine
Published: September 03, 2019
Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency.
Journal: Human mutation
Published: June 01, 2019
Correction: A novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
Journal: Journal of human genetics
Published: September 30, 2018
Last Updated: 09/26/2026