Suchergebnisse - (Person:"Zhang, Juanjuan")

PubPharm (5)

1

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy

enthalten in: Human molecular genetics | 2019

von Ji, Y. | Zhang, J. | Yu, J. | +18

2

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

3

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

enthalten in: Human molecular genetics | 2016

von Jiang, P. | Jin, X. | Peng, Y. | +16

4

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

enthalten in: Human molecular genetics | 2016

von Qu, J. | Wang, M. | Zhang, M. | +16

5

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

enthalten in: Human molecular genetics | 2015

von Jiang, P. | Jin, X. | Peng, Y. | +16

1
[1]