Zhang W - Search Results

1

Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.

Mok RSF, Zhang W, Sheikh TI, Pradeepan K, Fernandes IR, DeJong LC, Benigno G, Hildebrandt MR, Mufteev M, Rodrigues DC, Wei W, Piekna A, Liu J, Muotri AR, Vincent JB, Muller L, Martinez-Trujillo J, Salter MW, Ellis J. Mok RSF, et al. Among authors: zhang w. Transl Psychiatry. 2022 Oct 18;12(1):450. doi: 10.1038/s41398-022-02216-1. Transl Psychiatry. 2022. PMID: 36253345 Free PMC article.

2

Deletion of the ubiquitin ligase Nedd4L in lung epithelia causes cystic fibrosis-like disease.

Kimura T, Kawabe H, Jiang C, Zhang W, Xiang YY, Lu C, Salter MW, Brose N, Lu WY, Rotin D. Kimura T, et al. Among authors: zhang w. Proc Natl Acad Sci U S A. 2011 Feb 22;108(8):3216-21. doi: 10.1073/pnas.1010334108. Epub 2011 Feb 7. Proc Natl Acad Sci U S A. 2011. PMID: 21300902 Free PMC article.

3

MECP2e1 isoform mutation affects the form and function of neurons derived from Rett syndrome patient iPS cells.

Djuric U, Cheung AYL, Zhang W, Mok RS, Lai W, Piekna A, Hendry JA, Ross PJ, Pasceri P, Kim DS, Salter MW, Ellis J. Djuric U, et al. Among authors: zhang w. Neurobiol Dis. 2015 Apr;76:37-45. doi: 10.1016/j.nbd.2015.01.001. Epub 2015 Jan 30. Neurobiol Dis. 2015. PMID: 25644311 Free PMC article.

4

Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome.

Khattak S, Brimble E, Zhang W, Zaslavsky K, Strong E, Ross PJ, Hendry J, Mital S, Salter MW, Osborne LR, Ellis J. Khattak S, et al. Among authors: zhang w. Mol Brain. 2015 Nov 24;8(1):77. doi: 10.1186/s13041-015-0168-0. Mol Brain. 2015. PMID: 26603386 Free PMC article.

5

Fyn Kinase regulates GluN2B subunit-dominant NMDA receptors in human induced pluripotent stem cell-derived neurons.

Zhang WB, Ross PJ, Tu Y, Wang Y, Beggs S, Sengar AS, Ellis J, Salter MW. Zhang WB, et al. Sci Rep. 2016 Apr 4;6:23837. doi: 10.1038/srep23837. Sci Rep. 2016. PMID: 27040756 Free PMC article.

6

An evolutionary switch in ND2 enables Src kinase regulation of NMDA receptors.

Scanlon DP, Bah A, Krzeminski M, Zhang W, Leduc-Pessah HL, Dong YN, Forman-Kay JD, Salter MW. Scanlon DP, et al. Among authors: zhang w. Nat Commun. 2017 May 16;8:15220. doi: 10.1038/ncomms15220. Nat Commun. 2017. PMID: 28508887 Free PMC article.

7

SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons.

Zaslavsky K, Zhang WB, McCready FP, Rodrigues DC, Deneault E, Loo C, Zhao M, Ross PJ, El Hajjar J, Romm A, Thompson T, Piekna A, Wei W, Wang Z, Khattak S, Mufteev M, Pasceri P, Scherer SW, Salter MW, Ellis J. Zaslavsky K, et al. Among authors: zhang wb. Nat Neurosci. 2019 Apr;22(4):556-564. doi: 10.1038/s41593-019-0365-8. Epub 2019 Mar 25. Nat Neurosci. 2019. PMID: 30911184 Free PMC article.

8

Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS.

Ross PJ, Zhang WB, Mok RSF, Zaslavsky K, Deneault E, D'Abate L, Rodrigues DC, Yuen RKC, Faheem M, Mufteev M, Piekna A, Wei W, Pasceri P, Landa RJ, Nagy A, Varga B, Salter MW, Scherer SW, Ellis J. Ross PJ, et al. Among authors: zhang wb. Biol Psychiatry. 2020 Jan 15;87(2):139-149. doi: 10.1016/j.biopsych.2019.07.014. Epub 2019 Jul 29. Biol Psychiatry. 2020. PMID: 31540669 Free PMC article.

9

Control of Long-Term Synaptic Potentiation and Learning by Alternative Splicing of the NMDA Receptor Subunit GluN1.

Sengar AS, Li H, Zhang W, Leung C, Ramani AK, Saw NM, Wang Y, Tu Y, Ross PJ, Scherer SW, Ellis J, Brudno M, Jia Z, Salter MW. Sengar AS, et al. Among authors: zhang w. Cell Rep. 2019 Dec 24;29(13):4285-4294.e5. doi: 10.1016/j.celrep.2019.11.087. Cell Rep. 2019. PMID: 31875540 Free article.

10

Targeting NMDA receptors in neuropsychiatric disorders by drug screening on human neurons derived from pluripotent stem cells.

Zhang W, Ross PJ, Ellis J, Salter MW. Zhang W, et al. Transl Psychiatry. 2022 Jun 9;12(1):243. doi: 10.1038/s41398-022-02010-z. Transl Psychiatry. 2022. PMID: 35680847 Free PMC article. Review.

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