Li J - Search Results

1

GSN gene frameshift mutations in Alzheimer's disease.

Jiang Y, Wan M, Xiao X, Lin Z, Liu X, Zhou Y, Liao X, Lin J, Zhou H, Zhou L, Weng L, Wang J, Guo J, Jiang H, Zhang Z, Xia K, Li J, Tang B, Jiao B, Shen L. Jiang Y, et al. Among authors: li j. J Neurol Neurosurg Psychiatry. 2023 Jun;94(6):436-447. doi: 10.1136/jnnp-2022-330465. Epub 2023 Jan 17. J Neurol Neurosurg Psychiatry. 2023. PMID: 36650038 Free PMC article.

2

Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease.

Liu Q, Zhang K, Kang Y, Li Y, Deng P, Li Y, Tian Y, Sun Q, Tang Y, Xu K, Zhou Y, Wang JL, Guo J, Li JD, Xia K, Meng Q, Allen EG, Wen Z, Li Z, Jiang H, Shen L, Duan R, Yao B, Tang B, Jin P, Pan Y. Liu Q, et al. Among authors: li y, li z, li jd. Sci Adv. 2022 Nov 25;8(47):eadd6391. doi: 10.1126/sciadv.add6391. Epub 2022 Nov 23. Sci Adv. 2022. PMID: 36417528 Free PMC article.

3

KCTD10 regulates brain development by destabilizing brain disorder-associated protein KCTD13.

Cheng J, Wang Z, Tang M, Zhang W, Li G, Tan S, Mu C, Hu M, Zhang D, Jia X, Wen Y, Guo H, Xu D, Liu L, Li J, Xia K, Li F, Duan R, Xu Z, Yuan L. Cheng J, et al. Among authors: li f, li j, li g. Proc Natl Acad Sci U S A. 2024 Mar 19;121(12):e2315707121. doi: 10.1073/pnas.2315707121. Epub 2024 Mar 15. Proc Natl Acad Sci U S A. 2024. PMID: 38489388 Free PMC article.

4

A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.

Wang X, Chen D, Zhao Y, Men M, Chen Z, Jiang F, Zheng R, Stamou MI, Plummer L, Balasubramanian R, Li JD. Wang X, et al. Hum Mol Genet. 2023 May 5;32(10):1722-1729. doi: 10.1093/hmg/ddad014. Hum Mol Genet. 2023. PMID: 36694982 Free PMC article.

5

Recurrent de novo single point variant on the gene encoding Na⁺/K⁺ pump results in epilepsy.

Duan R, Li HM, Hu WB, Hong CG, Chen ML, Cao J, Wang ZX, Chen CY, Yin F, Hu ZH, Li JD, Xie H, Liu ZZ. Duan R, et al. Among authors: li hm, li jd. Prog Neurobiol. 2022 Sep;216:102310. doi: 10.1016/j.pneurobio.2022.102310. Epub 2022 Jun 18. Prog Neurobiol. 2022. PMID: 35724808

6

Contactin-associated protein-like 2 (CNTNAP2) mutations impair the essential α-secretase cleavages, leading to autism-like phenotypes.

Zhang Q, Xing M, Bao Z, Xu L, Bai Y, Chen W, Pan W, Cai F, Wang Q, Guo S, Zhang J, Wang Z, Wu Y, Zhang Y, Li JD, Song W. Zhang Q, et al. Among authors: li jd. Signal Transduct Target Ther. 2024 Mar 1;9(1):51. doi: 10.1038/s41392-024-01768-6. Signal Transduct Target Ther. 2024. PMID: 38424048 Free PMC article.

7

A glucose-blue light AND gate-controlled chemi-optogenetic cell-implanted therapy for treating type-1 diabetes in mice.

Li CY, Wu T, Zhao XJ, Yu CP, Wang ZX, Zhou XF, Li SN, Li JD. Li CY, et al. Front Bioeng Biotechnol. 2023 Feb 10;11:1052607. doi: 10.3389/fbioe.2023.1052607. eCollection 2023. Front Bioeng Biotechnol. 2023. PMID: 36845170 Free PMC article.

8

Targeting BMAL1 reverses drug resistance of acute myeloid leukemia cells and promotes ferroptosis through HMGB1-GPX4 signaling pathway.

Zheng H, Wu T, Lin Z, Wang D, Zhang J, Zeng T, Liu L, Shen J, Zhao M, Li JD, Yang M. Zheng H, et al. Among authors: li jd. J Cancer Res Clin Oncol. 2024 May 4;150(5):231. doi: 10.1007/s00432-024-05753-y. J Cancer Res Clin Oncol. 2024. PMID: 38703241 Free PMC article.

9

FMRP binds Per1 mRNA and downregulates its protein expression in mice.

Tang X, Zhang J, Li X, Hu Y, Liu D, Li JD, Lu R. Tang X, et al. Among authors: li x, li jd. Mol Brain. 2023 Apr 5;16(1):33. doi: 10.1186/s13041-023-01023-z. Mol Brain. 2023. PMID: 37020302 Free PMC article.

10

A genome-wide CRISPR screen identifies USP1 as a novel regulator of the mammalian circadian clock.

Hu Y, Li X, Zhang J, Liu D, Lu R, Li JD. Hu Y, et al. Among authors: li x, li jd. FEBS J. 2024 Feb;291(3):445-457. doi: 10.1111/febs.16990. Epub 2023 Nov 10. FEBS J. 2024. PMID: 37909373

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