| Year |
Citation |
Score |
| 2023 |
Zhou J, Cattoglio C, Shao Y, Tirumala HP, Vetralla C, Bajikar SS, Li Y, Chen H, Wang Q, Wu Z, Tang B, Zahabiyon M, Bajic A, Meng X, Ferrie JJ, et al. A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels. Genes & Development. PMID 37890975 DOI: 10.1101/gad.350733.123 |
0.51 |
|
| 2020 |
Ward CS, Huang TW, Herrera JA, Samaco RC, McGraw CM, Parra DE, Arvide EM, Ito-Ishida A, Meng X, Ure K, Zoghbi HY, Neul JL. Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia. Frontiers in Neurology. 11: 593554. PMID 33193060 DOI: 10.3389/fneur.2020.593554 |
0.573 |
|
| 2019 |
Meng X, McGraw CM, Wang W, Jing J, Yeh SY, Wang L, Lopez J, Brown AM, Lin T, Chen W, Xue M, Sillitoe RV, Jiang X, Zoghbi HY. Neurexophilin4 is a selectively expressed α-neurexin ligand that modulates specific cerebellar synapses and motor functions. Elife. 8. PMID 31524598 DOI: 10.7554/Elife.46773 |
0.623 |
|
| 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 |
0.704 |
|
| 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 |
0.647 |
|
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