Wu Z - Search Results

1

Gating of hippocampal rhythms and memory by synaptic plasticity in inhibitory interneurons.

He X, Li J, Zhou G, Yang J, McKenzie S, Li Y, Li W, Yu J, Wang Y, Qu J, Wu Z, Hu H, Duan S, Ma H. He X, et al. Among authors: wu z. Neuron. 2021 Mar 17;109(6):1013-1028.e9. doi: 10.1016/j.neuron.2021.01.014. Epub 2021 Feb 5. Neuron. 2021. PMID: 33548174 Free PMC article.

2

Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease.

Chen CX, Dong HL, Wei Q, Li LX, Yu H, Li JQ, Liu GL, Li HF, Bai G, Ma H, Wu ZY. Chen CX, et al. Clin Genet. 2019 Nov;96(5):439-448. doi: 10.1111/cge.13616. Epub 2019 Aug 8. Clin Genet. 2019. PMID: 31372974

3

New clinical characteristics and novel pathogenic variants of patients with hereditary leukodystrophies.

Xie JJ, Ni W, Wei Q, Ma H, Bai G, Shen Y, Wu ZY. Xie JJ, et al. CNS Neurosci Ther. 2020 May;26(5):567-575. doi: 10.1111/cns.13284. Epub 2019 Dec 29. CNS Neurosci Ther. 2020. PMID: 31885218 Free PMC article.

4

Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot-Marie-Tooth disease.

Dong HL, Wei Q, Li JQ, Li HF, Bai G, Ma H, Wu ZY. Dong HL, et al. J Peripher Nerv Syst. 2020 Jun;25(2):107-111. doi: 10.1111/jns.12377. Epub 2020 May 7. J Peripher Nerv Syst. 2020. PMID: 32319184

5

Cell type-differential modulation of prefrontal cortical GABAergic interneurons on low gamma rhythm and social interaction.

Liu L, Xu H, Wang J, Li J, Tian Y, Zheng J, He M, Xu TL, Wu ZY, Li XM, Duan SM, Xu H. Liu L, et al. Sci Adv. 2020 Jul 22;6(30):eaay4073. doi: 10.1126/sciadv.aay4073. eCollection 2020 Jul. Sci Adv. 2020. PMID: 32832654 Free PMC article.

6

Basal forebrain mediates prosocial behavior via disinhibition of midbrain dopamine neurons.

Wang J, Li J, Yang Q, Xie YK, Wen YL, Xu ZZ, Li Y, Xu T, Wu ZY, Duan S, Xu H. Wang J, et al. Proc Natl Acad Sci U S A. 2021 Feb 16;118(7):e2019295118. doi: 10.1073/pnas.2019295118. Proc Natl Acad Sci U S A. 2021. PMID: 33563763 Free PMC article.

7

Dual roles of hexokinase 2 in shaping microglial function by gating glycolytic flux and mitochondrial activity.

Hu Y, Cao K, Wang F, Wu W, Mai W, Qiu L, Luo Y, Ge WP, Sun B, Shi L, Zhu J, Zhang J, Wu Z, Xie Y, Duan S, Gao Z. Hu Y, et al. Among authors: wu w, wu z. Nat Metab. 2022 Dec;4(12):1756-1774. doi: 10.1038/s42255-022-00707-5. Epub 2022 Dec 19. Nat Metab. 2022. PMID: 36536134

8

Cerebellar spreading depolarization mediates paroxysmal movement disorder.

Lu B, Lou SS, Xu RS, Kong DL, Wu RJ, Zhang J, Zhuang L, Wu XM, He JY, Wu ZY, Xiong ZQ. Lu B, et al. Cell Rep. 2021 Sep 21;36(12):109743. doi: 10.1016/j.celrep.2021.109743. Cell Rep. 2021. PMID: 34551285 Free article.

9

A novel de novo SPTAN1 nonsense variant causes hereditary motor neuropathy in a Chinese family.

Dong HL, Chen L, Wu ZY. Dong HL, et al. Brain. 2021 Feb 12;144(1):e11. doi: 10.1093/brain/awaa357. Brain. 2021. PMID: 33578420 No abstract available.

10

Identification of pathogenic C9orf72 hexanucleotide repeat expansion in a Chinese patient with frontotemporal dementia: A case report.

Xue YY, Wu ZY, Li HF. Xue YY, et al. CNS Neurosci Ther. 2021 Jun;27(6):725-727. doi: 10.1111/cns.13639. Epub 2021 Mar 31. CNS Neurosci Ther. 2021. PMID: 33788382 Free PMC article. No abstract available.

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