| Year |
Citation |
Score |
| 2022 |
He L, Caudill MS, Jing J, Wang W, Sun Y, Tang J, Jiang X, Zoghbi HY. A weakened recurrent circuit in the hippocampus of Rett syndrome mice disrupts long-term memory representations. Neuron. PMID 35290792 DOI: 10.1016/j.neuron.2022.02.014 |
0.425 |
|
| 2021 |
Achilly NP, He LJ, Kim OA, Ohmae S, Wojaczynski GJ, Lin T, Sillitoe RV, Medina JF, Zoghbi HY. Deleting from the cerebellum rather than its neuronal subtypes causes a delay in motor learning in mice. Elife. 10. PMID 33494858 DOI: 10.7554/eLife.64833 |
0.535 |
|
| 2020 |
Yu B, Yuan B, Dai JK, Cheng TL, Xia SN, He LJ, Yuan YT, Zhang YF, Xu HT, Xu FQ, Liang ZF, Qiu ZL. Reversal of Social Recognition Deficit in Adult Mice with MECP2 Duplication via Normalization of MeCP2 in the Medial Prefrontal Cortex. Neuroscience Bulletin. PMID 32144612 DOI: 10.1007/S12264-020-00467-W |
0.448 |
|
| 2019 |
Tong DL, Chen RG, Lu YL, Li WK, Zhang YF, Lin JK, He LJ, Dang T, Shan SF, Xu XH, Zhang Y, Zhang C, Du YS, Zhou WH, Wang X, et al. The critical role of ASD-related gene CNTNAP3 in regulating synaptic development and social behavior in mice. Neurobiology of Disease. 104486. PMID 31150793 DOI: 10.1016/J.Nbd.2019.104486 |
0.449 |
|
| 2019 |
Wang L, Pang K, Han K, Adamski CJ, Wang W, He L, Lai JK, Bondar VV, Duman JG, Richman R, Tolias KF, Barth P, Palzkill T, Liu Z, Holder JL, et al. An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function. Molecular Psychiatry. PMID 30610205 DOI: 10.1038/S41380-018-0324-X |
0.578 |
|
| 2016 |
Lu H, Ash RT, He L, Kee SE, Wang W, Yu D, Hao S, Meng X, Ure K, Ito-Ishida A, Tang B, Sun Y, Ji D, Tang J, Arenkiel BR, et al. Loss and Gain of MeCP2 Cause Similar Hippocampal Circuit Dysfunction that Is Rescued by Deep Brain Stimulation in a Rett Syndrome Mouse Model. Neuron. PMID 27499081 DOI: 10.1016/J.Neuron.2016.07.018 |
0.705 |
|
| 2016 |
Meng X, Wang W, Lu H, He LJ, Chen W, Chao E, Fiorotto ML, Tang B, Herrera JA, Seymour ML, Neul JL, Pereira FA, Tang J, Xue M, Zoghbi HY. Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders. Elife. 5. PMID 27328325 DOI: 10.7554/Elife.14199 |
0.666 |
|
| 2016 |
Ure K, Lu H, Wang W, Ito-Ishida A, Wu Z, He LJ, Sztainberg Y, Chen W, Tang J, Zoghbi HY. Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett Syndrome. Elife. 5. PMID 27328321 DOI: 10.7554/Elife.14198 |
0.678 |
|
| 2016 |
Meng X, Wang W, Lu H, He L, Chen W, Chao ES, Fiorotto ML, Tang B, Herrera JA, Seymour ML, Neul JL, Pereira FA, Tang J, Xue M, Zoghbi HY. Author response: Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders Elife. DOI: 10.7554/Elife.14199.020 |
0.62 |
|
| 2016 |
Ure K, Lu H, Wang W, Ito-Ishida A, Wu Z, He L, Sztainberg Y, Chen W, Tang J, Zoghbi HY. Author response: Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome Elife. DOI: 10.7554/Elife.14198.015 |
0.607 |
|
| 2015 |
Lyu J, Yu X, He L, Cheng T, Zhou J, Cheng C, Chen Z, Cheng G, Qiu Z, Zhou W. The protein phosphatase activity of PTEN is essential for regulating neural stem cell differentiation. Molecular Brain. 8: 26. PMID 25927309 DOI: 10.1186/S13041-015-0114-1 |
0.411 |
|
| 2014 |
He LJ, Liu N, Cheng TL, Chen XJ, Li YD, Shu YS, Qiu ZL, Zhang XH. Conditional deletion of Mecp2 in parvalbumin-expressing GABAergic cells results in the absence of critical period plasticity. Nature Communications. 5: 5036. PMID 25297674 DOI: 10.1038/Ncomms6036 |
0.659 |
|
| 2011 |
Gong LQ, He LJ, Dong ZY, Lu XH, Poo MM, Zhang XH. Postinduction requirement of NMDA receptor activation for late-phase long-term potentiation of developing retinotectal synapses in vivo. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 3328-35. PMID 21368044 DOI: 10.1523/Jneurosci.5936-10.2011 |
0.533 |
|
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