Feng W - Search Results

1

Risk stratification by long non-coding RNAs profiling in COVID-19 patients.

Cheng J, Zhou X, Feng W, Jia M, Zhang X, An T, Luan M, Pan Y, Zhang S, Zhou Z, Wen L, Sun Y, Zhou C. Cheng J, et al. Among authors: feng w. J Cell Mol Med. 2021 May;25(10):4753-4764. doi: 10.1111/jcmm.16444. Epub 2021 Mar 23. J Cell Mol Med. 2021. PMID: 33759345 Free PMC article.

2

CHD7 in oocytes is essential for female fertility.

Cheng J, Dong Q, Lu Y, Shi L, Yao G, Wang C, Zhou C, Zhou Z, Huang Z, Han Z, Zhu M, Feng W. Cheng J, et al. Among authors: feng w. Ann Transl Med. 2022 Mar;10(5):260. doi: 10.21037/atm-22-609. Ann Transl Med. 2022. PMID: 35402599 Free PMC article.

3

A single-cell atlas reveals the heterogeneity of meningeal immunity in a mouse model of Methyl CpG binding protein 2 deficiency.

Li H, Hu M, Huang Z, Wang Y, Xu Y, Deng J, Zhu M, Feng W, Xu X. Li H, et al. Among authors: feng w. Front Immunol. 2023 Jan 10;13:1056447. doi: 10.3389/fimmu.2022.1056447. eCollection 2022. Front Immunol. 2023. PMID: 36703978 Free PMC article.

4

Generation and characterization of Chd7-iCreERT2-tdTomato mice.

Han Z, Wang Z, Huang Z, Feng W. Han Z, et al. Among authors: feng w. Genesis. 2024 Feb;62(1):e23575. doi: 10.1002/dvg.23575. Epub 2023 Nov 22. Genesis. 2024. PMID: 37991218

5

AAV-mediated Stambp gene replacement therapy rescues neurological defects in a mouse model of microcephaly-capillary malformation syndrome.

Hu M, Li J, Deng J, Liu C, Liu Y, Li H, Feng W, Xu X. Hu M, et al. Among authors: feng w. Mol Ther. 2024 Nov 6;32(11):4095-4107. doi: 10.1016/j.ymthe.2024.08.017. Epub 2024 Aug 22. Mol Ther. 2024. PMID: 39169623

6

Novel compound heterozygous mutation in STAMBP causes a neurodevelopmental disorder by disrupting cortical proliferation.

Hu M, Li H, Huang Z, Li D, Xu Y, Xu Q, Chen B, Wang Y, Deng J, Zhu M, Feng W, Xu X. Hu M, et al. Among authors: feng w. Front Neurosci. 2022 Aug 10;16:963813. doi: 10.3389/fnins.2022.963813. eCollection 2022. Front Neurosci. 2022. PMID: 36033615 Free PMC article.

7

Editorial: Molecular characteristics and personalized treatment for pediatric brain tumors.

Feng W, Kawauchi D, Wan F. Feng W, et al. Front Oncol. 2022 Dec 29;12:1114280. doi: 10.3389/fonc.2022.1114280. eCollection 2022. Front Oncol. 2022. PMID: 36644632 Free PMC article. No abstract available.

8

Lead exposure leads to premature neural differentiation via inhibiting Wnt signaling.

Li J, Hu M, Liu Y, Lu R, Feng W. Li J, et al. Among authors: feng w. Environ Pollut. 2024 Nov 1;363(Pt 2):125232. doi: 10.1016/j.envpol.2024.125232. Online ahead of print. Environ Pollut. 2024. PMID: 39489322

9

A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids.

Xu Y, Lu R, Li H, Feng W, Zhao R. Xu Y, et al. Among authors: feng w. Biochim Biophys Acta Mol Basis Dis. 2024 Aug;1870(6):167232. doi: 10.1016/j.bbadis.2024.167232. Epub 2024 May 15. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 38759814

10

Combined carbapenem resulted in a 4.48-fold increase in valproic acid clearance: a population pharmacokinetic model in Chinese children and adults with epilepsy or after neurosurgery.

Zhang L, Wu R, Li X, Feng W, Zhao Z, Mei S. Zhang L, et al. Among authors: feng w. Front Pharmacol. 2024 Nov 8;15:1423411. doi: 10.3389/fphar.2024.1423411. eCollection 2024. Front Pharmacol. 2024. PMID: 39584136 Free PMC article.

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