Juanjuan Zhang

Wenzhou, 325027, China

Last Updated: 09/26/2026

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Found 36 publications

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

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

Published: May 11, 2026

Progressive mitochondrial and autophagic dysfunction during RGC development driven by a LHON-associated mitochondrial tRNAThr mutation.

Progressive mitochondrial and autophagic dysfunction during RGC development driven by a LHON-associated mitochondrial tRNAThr mutation.

Journal: Cellular signalling

Published: May 09, 2026

Leber's hereditary optic neuropathy-associated ND1 3733G>C mutation ameliorates the mitochondrial quality control and cellular homeostasis.

Leber's hereditary optic neuropathy-associated ND1 3733G>C mutation ameliorates the mitochondrial quality control and cellular homeostasis.

Journal: The Journal of biological chemistry

Published: May 26, 2025

Mechanism of BNIP3-mediated mitophagy in m.3635G>A related Leber hereditary optic neuropathy

Mechanism of BNIP3-mediated mitophagy in m.3635G>A related Leber hereditary optic neuropathy

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 11, 2025

Defective post-transcriptional modification of tRNA disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.

Defective post-transcriptional modification of tRNA disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.

Journal: The Journal of biological chemistry

Published: May 13, 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

Dysregulation of mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutation.

Dysregulation of mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutation.

Journal: Gene

Published: March 23, 2024

Clinical and genetic analysis of essential hypertension with CYB gene m.15024G>A mutation.

Clinical and genetic analysis of essential hypertension with CYB gene m.15024G>A mutation.

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: August 29, 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

Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy.

Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy.

Journal: Human molecular genetics

Published: November 29, 2022

Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.

Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.

Journal: Mitochondrion

Published: March 08, 2022

Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy.

Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy.

Journal: Human molecular genetics

Published: March 01, 2022

Showing 1-12 of 36

Last Updated: 09/26/2026