Fan C - Search Results

1

Upregulated NMDAR-mediated GABAergic transmission underlies autistic-like deficits in Htr3a knockout mice.

Huang L, Wang J, Liang G, Gao Y, Jin SY, Hu J, Yang X, Lao J, Chen J, Luo ZC, Fan C, Xiong L, Zhu X, Gao TM, Zhong M, Yang X. Huang L, et al. Among authors: fan c. Theranostics. 2021 Sep 7;11(19):9296-9310. doi: 10.7150/thno.60531. eCollection 2021. Theranostics. 2021. PMID: 34646371 Free PMC article.

2

Transcriptomics of Gabra4 knockout mice reveals common NMDAR pathways underlying autism, memory, and epilepsy.

Fan C, Gao Y, Liang G, Huang L, Wang J, Yang X, Shi Y, Dräger UC, Zhong M, Gao TM, Yang X. Fan C, et al. Mol Autism. 2020 Feb 7;11(1):13. doi: 10.1186/s13229-020-0318-9. Mol Autism. 2020. PMID: 32033586 Free PMC article.

3

Cyclophilin A inhibits trophoblast migration and invasion in vitro and vivo through p38/ERK/JNK pathways and causes features of preeclampsia in mice.

Hu H, Jiang J, Chen Q, Wei S, Liu M, Chen X, Fan C, Ma J, Chen W, Wang X, Zhong M. Hu H, et al. Among authors: fan c. Life Sci. 2020 Nov 15;261:118351. doi: 10.1016/j.lfs.2020.118351. Epub 2020 Aug 26. Life Sci. 2020. PMID: 32858039

4

Distinct placental molecular processes associated with early-onset and late-onset preeclampsia.

Ren Z, Gao Y, Gao Y, Liang G, Chen Q, Jiang S, Yang X, Fan C, Wang H, Wang J, Shi YW, Xiao C, Zhong M, Yang X. Ren Z, et al. Among authors: fan c. Theranostics. 2021 Mar 5;11(10):5028-5044. doi: 10.7150/thno.56141. eCollection 2021. Theranostics. 2021. PMID: 33754042 Free PMC article.

5

Heterozygous variants in USP25 cause genetic generalized epilepsy.

Fan CX, Liu XR, Mei DQ, Li BM, Li WB, Xie HC, Wang J, Shen NX, Ye ZL, You QL, Li LY, Qu XC, Chen LZ, Liang JJ, Zhang MR, He N, Li J, Gao JY, Deng WY, Liu WZ, Wang WT, Liao WP, Chen Q, Shi YW. Fan CX, et al. Brain. 2024 Oct 3;147(10):3442-3457. doi: 10.1093/brain/awae191. Brain. 2024. PMID: 38875478

6

NUS1 Variants Cause Lennox-Gastaut Syndrome Related to Unfolded Protein Reaction Activation.

Shen NX, Qu XC, Yu J, Fan CX, Min FL, Li LY, Zhang MR, Li BM, Wang J, He N, Liao WP, Shi YW, Li WB. Shen NX, et al. Mol Neurobiol. 2024 Nov;61(11):8518-8530. doi: 10.1007/s12035-024-04123-6. Epub 2024 Mar 23. Mol Neurobiol. 2024. PMID: 38520610

7

Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A.

Wang JY, Tang B, Sheng WX, Hua LD, Zeng Y, Fan CX, Deng WY, Gao MM, Zhu WW, He N, Su T. Wang JY, et al. Front Mol Neurosci. 2022 Mar 14;15:828846. doi: 10.3389/fnmol.2022.828846. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35359575 Free PMC article.

8

Novel PANK2 Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype Correlation.

Li WB, Shen NX, Zhang C, Xie HC, Li ZY, Cao L, Chen LZ, Zeng YJ, Fan CX, Chen Q, Shi YW, Song XW. Li WB, et al. Among authors: fan cx. Front Aging Neurosci. 2022 Apr 6;14:848919. doi: 10.3389/fnagi.2022.848919. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35462688 Free PMC article.

9

ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus.

Tian Y, Zhai QX, Li XJ, Shi Z, Cheng CF, Fan CX, Tang B, Zhang Y, He YY, Li WB, Luo S, Hou C, Chen WX, Liao WP, Wang J. Tian Y, et al. Among authors: fan cx. Front Mol Neurosci. 2022 May 6;15:889534. doi: 10.3389/fnmol.2022.889534. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35600075 Free PMC article.

10

Corrigendum: ATP6V0C is associated with febrile seizures and epilepsy with febrile seizures plus.

Tian Y, Zhai QX, Li XJ, Shi Z, Cheng CF, Fan CX, Tang B, Zhang Y, He YY, Li WB, Luo S, Hou C, Chen WX, Liao WP, Wang J. Tian Y, et al. Among authors: fan cx. Front Mol Neurosci. 2024 Mar 1;17:1385915. doi: 10.3389/fnmol.2024.1385915. eCollection 2024. Front Mol Neurosci. 2024. PMID: 38495552 Free PMC article.

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