Xiaoxu Zhao
Hangzhou, China
Last Updated: 09/26/2026
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Found 9 publications
Imaging supermolecular interactions of the pharmaceutical-cocrystal of apigenin-nicotinamide binding with serum albumin.
Journal: Turkish journal of chemistry
Published: April 09, 2022
Correction to: Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.
Journal: Orphanet journal of rare diseases
Published: December 08, 2021
Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.
Journal: Orphanet journal of rare diseases
Published: July 15, 2021
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.
Journal: The Journal of clinical investigation
Published: November 14, 2019
Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript.
Journal: Nucleic acids research
Published: February 02, 2019
Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNAAla mutation in cybrids.
Journal: International journal of biological sciences
Published: May 03, 2018
Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel.
Journal: Biomedical reports
Published: August 10, 2017
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
Journal: Human molecular genetics
Published: January 18, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026