Cheng Ai

Yiwu, 322000, China

Last Updated: 09/26/2026

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Found 10 publications

Optic neuropathy arising from the synergy between YARS2 and mitochondrial COX1 mutations.

Optic neuropathy arising from the synergy between YARS2 and mitochondrial COX1 mutations.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: November 10, 2025

Optic neuropathy arising from the synergy between YARS2 and mitochondrial COX1 mutations.

Optic neuropathy arising from the synergy between YARS2 and mitochondrial COX1 mutations.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: November 10, 2025

Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutation.

Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutation.

Journal: JCI insight

Published: November 07, 2024

PARP1 promotes tumor proliferation in lenalidomide-resistant multiple myeloma via the downregulation of microRNA-192-5p-AKT signaling.

PARP1 promotes tumor proliferation in lenalidomide-resistant multiple myeloma via the downregulation of microRNA-192-5p-AKT signaling.

Journal: Translational cancer research

Published: August 28, 2024

Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy.

Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy.

Journal: JCI insight

Published: April 25, 2024

Low‑dose venetoclax combined with azacitidine in older and frail patients with newly diagnosed acute myeloid leukaemia.

Low‑dose venetoclax combined with azacitidine in older and frail patients with newly diagnosed acute myeloid leukaemia.

Journal: Oncology letters

Published: October 31, 2023

Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation.

Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation.

Journal: Journal of biomedical science

Published: March 09, 2023

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

Journal: The Journal of clinical investigation

Published: November 14, 2019

Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism.

Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism.

Journal: Nucleic acids research

Published: January 25, 2019

Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel.

Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel.

Journal: Biomedical reports

Published: August 10, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026