Suchergebnisse - (Person:"Zhang, Juanjuan")

PubPharm (23)

1

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

enthalten in: Journal of biomedical science | 2023

von Wang, J. | Ji, Y. | Ai, C. | +5

2

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

enthalten in: Human molecular genetics | 2023

von Chen, J. | Chen, C. | Chen, J. | +7

3

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

enthalten in: Human molecular genetics | 2022

von Liang, M. | Ji, Y. | Zhang, L. | +6

4

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

enthalten in: Mitochondrion | 2022

von Ji, Y. | Zhang, J. | Liang, M. | +5

5

Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy

enthalten in: Investigative ophthalmology & visual science | 2021

von Zhang, J. | Ji, Y. | Chen, J. | +7

6

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy

enthalten in: The Journal of biological chemistry | 2020

von Ji, Y. | Zhang, J. | Lu, Y. | +9

7

Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagy

enthalten in: Human molecular genetics | 2018

von Zhang, J. | Ji, Y. | Lu, Y. | +4

8

Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigrees

enthalten in: Molecular medicine reports | 2017

von Ji, Y. | Qiao, L. | Liang, X. | +8

9

A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis

enthalten in: Scientific reports | 2017

von Zhang, J. | Liu, X. | Liang, X. | +11

10

Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees

enthalten in: Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis | 2017

von Xie, S. | Zhang, J. | Sun, J. | +9