Min-Xin Guan[Author] - Search Results

Year	Number of Results
2002	2
2003	3
2004	7
2005	15
2006	14
2007	11
2008	11
2009	12
2010	16
2011	13
2012	13
2013	10
2014	8
2015	9
2016	12
2017	12
2018	10
2019	13
2020	7
2021	9
2022	10
2023	6
2024	6
2025	5
2026	3

1

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

Yu J, Liang X, Ji Y, Ai C, Liu J, Zhu L, Nie Z, Jin X, Wang C, Zhang J, Zhao F, Mei S, Zhao X, Zhou X, Zhang M, Wang M, Huang T, Jiang P, Guan MX. Yu J, et al. Among authors: guan mx. J Clin Invest. 2020 Sep 1;130(9):4935-4946. doi: 10.1172/JCI134965. J Clin Invest. 2020. PMID: 32516135 Free PMC article.

2

Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutation.

Ai C, Li H, Wang C, Ji Y, Wallace DC, Qian J, Zhu Y, Guan MX. Ai C, et al. Among authors: guan mx. JCI Insight. 2025 Mar 4;10(8):e188962. doi: 10.1172/jci.insight.188962. eCollection 2025 Apr 22. JCI Insight. 2025. PMID: 40036074 Free PMC article.

3

Exportin 4 depletion leads to nuclear accumulation of a subset of circular RNAs.

Chen L, Wang Y, Lin J, Song Z, Wang Q, Zhao W, Wang Y, Xiu X, Deng Y, Li X, Li Q, Wang X, Li J, Liu X, Liu K, Zhou J, Li K, Liu Y, Liao S, Deng Q, Xu C, Sun Q, Wu S, Zhang K, Guan MX, Zhou T, Sun F, Cai X, Huang C, Shan G. Chen L, et al. Among authors: guan mx. Nat Commun. 2022 Oct 1;13(1):5769. doi: 10.1038/s41467-022-33356-z. Nat Commun. 2022. PMID: 36182935 Free PMC article.

4

SpliceTransformer predicts tissue-specific splicing linked to human diseases.

You N, Liu C, Gu Y, Wang R, Jia H, Zhang T, Jiang S, Shi J, Chen M, Guan MX, Sun S, Pei S, Liu Z, Shen N. You N, et al. Among authors: guan mx. Nat Commun. 2024 Oct 23;15(1):9129. doi: 10.1038/s41467-024-53088-6. Nat Commun. 2024. PMID: 39443442 Free PMC article.

5

Emerging functions of mitochondria-encoded noncoding RNAs.

Ren B, Guan MX, Zhou T, Cai X, Shan G. Ren B, et al. Among authors: guan mx. Trends Genet. 2023 Feb;39(2):125-139. doi: 10.1016/j.tig.2022.08.004. Epub 2022 Sep 19. Trends Genet. 2023. PMID: 36137834 Free article. Review.

6

A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism.

Meng F, Jia Z, Zheng J, Ji Y, Wang J, Xiao Y, Fu Y, Wang M, Ling F, Guan MX. Meng F, et al. Among authors: guan mx. Nucleic Acids Res. 2022 Sep 9;50(16):9453-9469. doi: 10.1093/nar/gkac720. Nucleic Acids Res. 2022. PMID: 36039763 Free PMC article.

7

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

Chen JR, Chen C, Chen J, Ji Y, Lian Y, Zhang J, Yu J, Li XY, Qu J, Guan MX. Chen JR, et al. Among authors: guan mx. Hum Mol Genet. 2023 Apr 20;32(9):1539-1551. doi: 10.1093/hmg/ddad001. Hum Mol Genet. 2023. PMID: 36611011

8

Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy.

Wang C, Zhang L, Nie Z, Liang M, Liu H, Yi Q, Wang C, Ai C, Zhang J, Gao Y, Ji Y, Guan MX. Wang C, et al. Among authors: guan mx. JCI Insight. 2024 Nov 19;10(1):e182209. doi: 10.1172/jci.insight.182209. JCI Insight. 2024. PMID: 39561005 Free PMC article.

9

Deafness-associated tRNA^Phe mutation impaired mitochondrial and cellular integrity.

Chen X, Meng F, Chen C, Li S, Chou Z, Xu B, Mo JQ, Guo Y, Guan MX. Chen X, et al. Among authors: guan mx. J Biol Chem. 2024 May;300(5):107235. doi: 10.1016/j.jbc.2024.107235. Epub 2024 Mar 27. J Biol Chem. 2024. PMID: 38552739 Free PMC article.

10

Mitochondrial tRNA processing defects reprogram mitochondrial and cellular homeostasis.

Zhu G, He Y, Li X, Xiao Y, Zhan H, Duan M, Guan MX. Zhu G, et al. Among authors: guan mx. J Biol Chem. 2025 Jul;301(7):110334. doi: 10.1016/j.jbc.2025.110334. Epub 2025 Jun 3. J Biol Chem. 2025. PMID: 40473214 Free PMC article.

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