Guo Q - Search Results

1

Influence of Model Evolution and System Roles on ChatGPT's Performance in Chinese Medical Licensing Exams: Comparative Study.

Ming S, Guo Q, Cheng W, Lei B. Ming S, et al. Among authors: guo q. JMIR Med Educ. 2024 Aug 13;10:e52784. doi: 10.2196/52784. JMIR Med Educ. 2024. PMID: 39140269 Free PMC article.

2

Autosomal Recessive Rod-Cone Dystrophy Associated With Compound Heterozygous Variants in ARL3 Gene.

Fu L, Li Y, Yao S, Guo Q, You Y, Zhu X, Lei B. Fu L, et al. Among authors: guo q. Front Cell Dev Biol. 2021 Mar 4;9:635424. doi: 10.3389/fcell.2021.635424. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33748123 Free PMC article.

3

High-Resolution Image Analysis Reveals a Decrease in Lens Thickness and Cone Density in a Cohort of Young Myopic Patients.

Xin X, Guo Q, Ming S, Liu C, Wang Z, Lei B. Xin X, et al. Among authors: guo q. Front Med (Lausanne). 2021 Dec 16;8:796778. doi: 10.3389/fmed.2021.796778. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34977098 Free PMC article.

4

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.

5

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.

6

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.

7

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.

8

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.

9

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.

10

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

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