Guo Q - Search Results

1

Immune pathogenic response landscape of acute posterior multifocal placoid pigment epitheliopathy revealed by scRNA sequencing.

Liu J, Guo Q, Liu G, Wang W, Jin X, Hao B, Lei B. Liu J, et al. Among authors: guo q. Genes Immun. 2025 Jan 7. doi: 10.1038/s41435-024-00316-0. Online ahead of print. Genes Immun. 2025. PMID: 39774261

2

Mechanisms underlying morphological and functional changes of cilia in fibroblasts derived from patients bearing ARL3^T31A and ARL3^T31A/C118F mutations.

Zhang X, Yao S, Zhang L, Yang L, Yang M, Guo Q, Li Y, Wang Z, Lei B, Jin X. Zhang X, et al. Among authors: guo q. FASEB J. 2024 Mar 15;38(5):e23519. doi: 10.1096/fj.202301906R. FASEB J. 2024. PMID: 38457249

3

Preservation of Mitochondrial Function by SkQ1 in Skin Fibroblasts Derived from Patients with Leber's Hereditary Optic Neuropathy Is Associated with the PINK1/PRKN-Mediated Mitophagy.

Xu J, Li Y, Yao S, Jin X, Yang M, Guo Q, Qiu R, Lei B. Xu J, et al. Among authors: guo q. Biomedicines. 2024 Sep 4;12(9):2020. doi: 10.3390/biomedicines12092020. Biomedicines. 2024. PMID: 39335534 Free PMC article.

4

Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber's Hereditary Optic Neuropathy Patients.

Yao S, Zhou Q, Yang M, Li Y, Jin X, Guo Q, Yang L, Qin F, Lei B. Yao S, et al. Among authors: guo q. Front Mol Neurosci. 2022 Jul 13;15:920221. doi: 10.3389/fnmol.2022.920221. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35909448 Free PMC article.

5

A novel mutation located in the intermembrane space domain of AFG3L2 causes dominant optic atrophy through decreasing the stability of the encoded protein.

Yang L, Jin X, Li Y, Guo Q, Yang M, You Y, Yao S, Zhang X, Wang Z, Lei B. Yang L, et al. Among authors: guo q. Cell Death Discov. 2022 Aug 15;8(1):361. doi: 10.1038/s41420-022-01160-9. Cell Death Discov. 2022. PMID: 35970831 Free PMC article.

6

Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma.

Yang S, Li Y, Yang L, Guo Q, You Y, Lei B. Yang S, et al. Among authors: guo q. Front Med (Lausanne). 2023 Oct 12;10:1216427. doi: 10.3389/fmed.2023.1216427. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37901396 Free PMC article.

7

Mitochondrial functional impairment in ARL3-mutation related rod-cone dystrophy.

Zhang X, Yao S, Zhang L, Zhang B, Yang M, Guo Q, Xu J, Wang Z, Lei B, Jin X. Zhang X, et al. Among authors: guo q. FASEB Bioadv. 2024 Sep 9;6(11):555-564. doi: 10.1096/fba.2023-00138. eCollection 2024 Nov. FASEB Bioadv. 2024. PMID: 39512837 Free PMC article.

8

Phenotype Heterogeneity and the Association Between Visual Acuity and Outer Retinal Structure in a Cohort of Chinese X-Linked Juvenile Retinoschisis Patients.

Guo Q, Li Y, Li J, You Y, Liu C, Chen K, Li S, Lei B. Guo Q, et al. Front Genet. 2022 Mar 4;13:832814. doi: 10.3389/fgene.2022.832814. eCollection 2022. Front Genet. 2022. PMID: 35309139 Free PMC article.

9

Superoxide dismutase 2 ameliorates mitochondrial dysfunction in skin fibroblasts of Leber's hereditary optic neuropathy patients.

Zhou Q, Yao S, Yang M, Guo Q, Li Y, Li L, Lei B. Zhou Q, et al. Among authors: guo q. Front Neurosci. 2022 Aug 9;16:917348. doi: 10.3389/fnins.2022.917348. eCollection 2022. Front Neurosci. 2022. PMID: 36017189 Free PMC article.

10

Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy.

Zhen T, Li Y, Guo Q, Yao S, You Y, Lei B. Zhen T, et al. Among authors: guo q. Transl Vis Sci Technol. 2023 Oct 3;12(10):1. doi: 10.1167/tvst.12.10.1. Transl Vis Sci Technol. 2023. PMID: 37787991 Free PMC article.

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