Yinglong Gao
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Explore the profile of Yinglong Gao including associated specialties, affiliations and a list of published articles.
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10
Citations
114
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Recent Articles
1.
Wang C, Zhang L, Nie Z, Liang M, Liu H, Yi Q, et al.
JCI Insight
. 2024 Nov;
10(1.
PMID: 39561005
The degeneration of retinal ganglion cells (RGC) due to mitochondrial dysfunctions manifests optic neuropathy. However, the molecular components of RGC linked to optic neuropathy manifestations remain largely unknown. Here, we...
2.
Zheng D, Mao Y, Gao Y, He F, Ma J
iScience
. 2023 Jul;
26(7):107198.
PMID: 37485365
Nutrients are vital to cellular activities, yet it is largely unknown how individual cells respond to nutrient deprivation. Live imaging results show that unlike the removal of amino acids or...
3.
Zheng J, Bai X, Xiao Y, Ji Y, Meng F, Aishanjiang M, et al.
Mitochondrion
. 2020 Mar;
52:163-172.
PMID: 32169613
Mutations in the mitochondrial tRNAs have been reported to be the important cause of hearing loss. However, only a few cases have been identified thus far and the prevalence of...
4.
Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, et al.
Hum Mol Genet
. 2019 Jan;
28(9):1515-1529.
PMID: 30597069
Mitochondrial DNA (mtDNA) mutations have been associated with Leber's hereditary optic neuropathy (LHON) and their pathophysiology remains poorly understood. In this study, we investigated the pathophysiology of a LHON susceptibility...
5.
Ji Y, Qiao L, Liang X, Zhu L, Gao Y, Zhang J, et al.
Mol Med Rep
. 2017 Oct;
16(6):8997-9004.
PMID: 28990081
Mitochondrial (mt)DNA mutations have been revealed to be associated with Leber's hereditary optic neuropathy (LHON). The present study conducted clinical, genetic and molecular evaluations of two Han Chinese families. A...
6.
Ying Z, Zheng J, Cai Z, Liu L, Dai Y, Yao J, et al.
Protein Cell
. 2015 Sep;
6(11):844-8.
PMID: 26361786
No abstract available.
7.
Jiang P, Liang M, Zhang J, Gao Y, He Z, Yu H, et al.
Invest Ophthalmol Vis Sci
. 2015 Jul;
56(8):4778-88.
PMID: 26218905
Purpose: To investigate the prevalence and spectrum of mitochondrial ND4 mutations in subjects with Leber's hereditary optic neuropathy (LHON). Methods: A cohort of 1281 Chinese Han probands and 478 control...
8.
Zheng J, Ying Z, Cai Z, Sun D, He Z, Gao Y, et al.
PLoS One
. 2015 Jun;
10(6):e0128691.
PMID: 26043044
Mutations in Gap Junction Beta 2 (GJB2) have been reported to be a major cause of non-syndromic hearing loss in many populations worldwide. The spectrums and frequencies of GJB2 variants...
9.
Tang X, Zheng J, Ying Z, Cai Z, Gao Y, He Z, et al.
Mitochondrion
. 2015 May;
23:17-24.
PMID: 25968158
Mutations in the mitochondrial DNA have been associated with hearing loss. However, the prevalence and spectrum of mitochondrial tRNA mutations in hearing-impaired subjects are poorly understood. In this report, we...
10.
Xiao H, He Z, Gao Y, Yang Y, Zheng J, Cai Z, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
. 2015 Apr;
32(2):163-8.
PMID: 25863077
Objective: To identify secondary mutations associated with deafness in a Chinese family affected with deafness. Methods: The family has been subjected to clinical and molecular analyses, in addition with measurement...