Mei D - Search Results

1

Evaluating the relationship between the proportion of X-chromosome deletions and clinical manifestations in children with turner syndrome.

Wang G, Liu X, Wang M, Wang J, Zhang Z, Allegaert K, Mei D, Zhang Y, Luo S, Fang Y, Li D, Chen Y, Wei H. Wang G, et al. Among authors: mei d. Front Endocrinol (Lausanne). 2024 Feb 28;15:1324160. doi: 10.3389/fendo.2024.1324160. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 38481442 Free PMC article.

2

Neuronal Nitric Oxide Synthase Knockdown Within Basolateral Amygdala Induces Autistic-Related Phenotypes and Decreases Excitatory Synaptic Transmission in Mice.

Wang X, Gao C, Zhang Y, Xu J, Fang Q, Gou L, Yang Z, Mei D, Liu L, Li L, Liu J, Zhang H, Song Y. Wang X, et al. Among authors: mei d. Front Neurosci. 2020 Aug 31;14:886. doi: 10.3389/fnins.2020.00886. eCollection 2020. Front Neurosci. 2020. PMID: 32982674 Free PMC article.

3

[Phenotypic and genetic analysis of a case with hypohidrotic ectodermal dysplasia due to Xq13.1 microdeletion].

Mei D, Mei S, Chen G, Wang Y, Wang X, Zhang J, Chen X, Li D, Zhang Y. Mei D, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Mar 10;38(3):219-223. doi: 10.3760/cma.j.cn511374-20200515-00347. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33751528 Chinese.

4

The GluN2B-Trp373 NMDA Receptor Variant is Associated with Autism-, Epilepsy-Related Phenotypes and Reduces NMDA Receptor Currents in Rats.

Wang X, Guo Z, Mei D, Zhang Y, Zhao S, Hu S, Luo S, Wang Q, Gao C. Wang X, et al. Among authors: mei d. Neurochem Res. 2022 Jun;47(6):1588-1597. doi: 10.1007/s11064-022-03554-8. Epub 2022 Feb 18. Neurochem Res. 2022. PMID: 35181828

5

Paternal uniparental disomy of chromosome 16 resulting in homozygosity of a GPT2 mutation causes intellectual and developmental disability.

Liu J, Chen B, Liu Y, Kong J, Zhang B, Han L, Mei D, Ma CY, Shang Q, Xie Z, Xiao M, Mei S, Zhang Y, Gao C, Li D. Liu J, et al. Among authors: mei d, mei s. Eur J Med Genet. 2022 Sep;65(9):104554. doi: 10.1016/j.ejmg.2022.104554. Epub 2022 Jul 3. Eur J Med Genet. 2022. PMID: 35793769

6

Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant.

Gu Y, Mei D, Wang X, Ma A, Kong J, Zhang Y. Gu Y, et al. Among authors: mei d. Front Neurol. 2023 May 9;14:1135044. doi: 10.3389/fneur.2023.1135044. eCollection 2023. Front Neurol. 2023. PMID: 37228410 Free PMC article.

7

Functional Evaluation of a Novel GRIN2B Missense Variant Associated with Epilepsy and Intellectual Disability.

Wang X, Mei D, Gou L, Zhao S, Gao C, Guo J, Luo S, Guo B, Yang Z, Wang Q, Tan T, Zhang Y. Wang X, et al. Among authors: mei d. Neuroscience. 2023 Aug 21;526:107-120. doi: 10.1016/j.neuroscience.2023.06.018. Epub 2023 Jun 28. Neuroscience. 2023. PMID: 37385334 Free article.

8

GABA_B1 receptor knockdown in prefrontal cortex induces behavioral aberrations associated with autism spectrum disorder in mice.

Wang X, Zhao Z, Guo J, Mei D, Duan Y, Zhang Y, Gou L. Wang X, et al. Among authors: mei d. Brain Res Bull. 2023 Oct 1;202:110755. doi: 10.1016/j.brainresbull.2023.110755. Epub 2023 Sep 7. Brain Res Bull. 2023. PMID: 37678443 Free article.

9

Neuroprotective Effects of CXCR2 Antagonist SB332235 on Traumatic Brain Injury Through Suppressing NLRP3 Inflammasome.

Zhao K, Zhou X, Chen M, Gou L, Mei D, Gao C, Zhao S, Luo S, Wang X, Tan T, Zhang Y. Zhao K, et al. Among authors: mei d. Neurochem Res. 2024 Jan;49(1):184-198. doi: 10.1007/s11064-023-04021-8. Epub 2023 Sep 13. Neurochem Res. 2024. PMID: 37702890 Free PMC article.

10

Restoration of nNOS Expression Rescues Autistic-Like Phenotypes Through Normalization of AMPA Receptor-Mediated Neurotransmission.

Wang X, Zhang Y, Luo S, Zhao K, Gao C, Mei D, Duan Y, Hu S. Wang X, et al. Among authors: mei d. Mol Neurobiol. 2024 Sep;61(9):6599-6612. doi: 10.1007/s12035-024-03997-w. Epub 2024 Feb 8. Mol Neurobiol. 2024. PMID: 38329681

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