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  1. Article

    Open Access

    From wings to whiskers to stem cells: why every model matters in fragile X syndrome research

    Fragile X syndrome (FXS) is caused by epigenetic silencing of the X-linked fragile X messenger ribonucleoprotein 1 (FMR1) gene located on chromosome Xq27.3, which leads to the loss of its protein product, fragile...

    Soraya O. Sandoval, Natasha M. Méndez-Albelo in Journal of Neurodevelopmental Disorders (2024)

  2. No Access

    Article

    CCL2 Potentiates Inflammation Pain and Related Anxiety-Like Behavior Through NMDA Signaling in Anterior Cingulate Cortex

    Previous studies have shown that the C-C motif chemokine ligand 2 (CCL2) is widely expressed in the nervous system and involved in regulating the development of chronic pain and related anxiety-like behaviors,...

    Huan Guo, Wen-chao Hu, Hang **an, Yun-xin Shi, Yuan-ying Liu in Molecular Neurobiology (2023)

  3. No Access

    Article

    Shared and Distinct Topographic Alterations of Alpha-Range Resting EEG Activity in Schizophrenia, Bipolar Disorder, and Depression

    Rui Xue, **ao**g Li, Jianning Chen, Sugai Liang, Hua Yu in Neuroscience Bulletin (2023)

  4. No Access

    Article

    Imbalance of multiple neurotransmitter pathways leading to depression-like behavior and cognitive dysfunction in the triple transgenic mouse model of Alzheimer disease

    Depression is among the most frequent psychiatric comorbid conditions in Alzheimer disease (AD). However, pharmacotherapy for depressive disorders in AD is still a big challenge, and the data on the efffcacy o...

    Meng Zhang, Li-yuan Liu, Yong Xu, Wen-zhi Wang, Nian-zhuang Qiu in Metabolic Brain Disease (2023)

  5. Article

    Open Access

    Alzheimer’s pathology is associated with altered cognition, brain volume, and plasma biomarker patterns in traumatic encephalopathy syndrome

    Traumatic encephalopathy syndrome (TES) is a clinical phenotype sensitive but non-specific to underlying chronic traumatic encephalopathy (CTE) neuropathology. However, cognitive symptoms of TES overlap with A...

    Breton M. Asken, Jeremy A. Tanner, Leslie S. Gaynor in Alzheimer's Research & Therapy (2023)

  6. No Access

    Article

    Longitudinal study of multi-parameter quantitative magnetic resonance imaging in Duchenne muscular dystrophy: hyperresponsiveness of gluteus maximus and detection of subclinical disease progression in functionally stable patients

    To describe the disease progression of Duchenne muscular dystrophy (DMD) in the pelvic and thigh muscles over 1-year using multiple-parameter quantitative magnetic resonance imaging (qMRI), and to determine th...

    Fei Peng, Huayan Xu, Yu Song, Ke Xu, Shuhao Li, **aotang Cai in Journal of Neurology (2023)

  7. No Access

    Article

    Isobavachalcone’s Alleviation of Pyroptosis Contributes to Enhanced Apoptosis in Glioblastoma: Possible Involvement of NLRP3

    Glioblastoma multiforme (GBM) is the most malignant intracranial tumor with high mortality rates and invariably poor prognosis due to its limited clinical treatments. There is an urgent need to develop new the...

    Yueshan Wu, **g Chang, Juanjuan Ge, Kangyan Xu, Quan Zhou in Molecular Neurobiology (2022)

  8. Article

    Open Access

    Real-world outcomes of teriflunomide in relapsing–remitting multiple sclerosis: a prospective cohort study

    To explore efficacy, risk factors, safety, and persistence of teriflunomide in relapsing–remitting multiple sclerosis (RRMS) cohort.

    Yao Zhang, Hexiang Yin, Dingding Zhang, Yan Xu, Bin Peng in Journal of Neurology (2022)

  9. Article

    Correction to: 3-Hz Postural Tremor in MSA-C and SCA: Revisiting an Old but Underestimated Cerebellar Sign by Posturography

    **aodi Li, **ao Lv, Churong Liu, **long Ye, Yan Xu, Gengmao Ma, Zhong Li in The Cerebellum (2022)

  10. No Access

    Article

    Combined influence of ABCB1 genetic polymorphism and DNA methylation on aspirin resistance in Chinese ischemic stroke patients

    Genetic variants of ABCB1 may affect intestinal absorption of aspirin (ASA). However, it is unclear whether ABCB1 polymorphisms and DNA methylation are associated with ASA efficacy for ischemic stroke. Our aim...

    Liyan Xu, Yan Wang in Acta Neurologica Belgica (2022)

  11. Article

    Open Access

    Astrocyte reactivation in medial prefrontal cortex contributes to obesity-promoted depressive-like behaviors

    Little is known about how the obesogenic environment influences emotional states associated with glial responses and neuronal function. Here, we investigated glial reactivation and neuronal electrophysiologica...

    Gang Yu, Feng Cao, Tingting Hou, Yunsheng Cheng, Benli Jia in Journal of Neuroinflammation (2022)

  12. Article

    Correction to: Association Study Between Genetic Variation in Whole Mitochondrial Genome and Ischemic Stroke

    A correction to this paper has been published: https://doi.org/10.1007/s12031-021-01833-7

    Yingying Luan, Dongzhi Yang, Zhao**g Zhang in Journal of Molecular Neuroscience (2021)

  13. No Access

    Article

    Association Study Between Genetic Variation in Whole Mitochondrial Genome and Ischemic Stroke

    Mitochondrial DNA (mtDNA) affects the mitochondrial function, which is potentially related to susceptibility to ischemic stroke (IS). However, study on IS genetics by whole mitochondrial genome sequencing has ...

    Yingying Luan, Dongzhi Yang, Zhao**g Zhang in Journal of Molecular Neuroscience (2021)

  14. No Access

    Article

    Nucleoprotein (P40) Binding to 5HT2C Receptors (5HT2CR) is the Key Point in the Pathogenesis of BoDV-1-Infected Hosts

    Nucleoprotein (P40) is one of the most important proteins of Borna disease virus 1 (BoDV-1), but which proteins it would bind to in the pathogenesis of BoDV-1-infected hosts is unknown. We used lentivirus LV5-...

    Yuanxin Li, Lixin Wang, Xueni Liu, Ying Huang, **aomei Li in Neurochemical Research (2021)

  15. No Access

    Article

    Down-Regulation of ID2-AS1 Alleviates the Neuronal Injury Induced by 1-Methy1-4-Phenylpyridinium in Human Neuroblastoma Cell Line SH-SY5Y Cells Through Regulating miR-199a-5p/IFNAR1/JAK2/STAT1 Axis

    We aimed to illustrate the roles and molecular mechanisms of ID2-AS1 in parkinson’s disease (PD). Methods: qRT-PCR detected the expression of ID2-AS1. CCK-8, LDH release assays the effect of ID2-AS1 knockdown ...

    Furong Xu, Hui Wang, Ju Tian, Haiyan Xu in Neurochemical Research (2021)

  16. No Access

    Article

    Circ_0132817 facilitates cell proliferation, migration, invasion and glycolysis by regulating the miR-432-5p/NOL4L axis in neuroblastoma

    Neuroblastoma (NB) is one of the most common extracranial solid tumors in children. Circular RNAs (circRNAs) have been shown to be involved in the development of NB. However, the function of circ_0132817 in NB...

    Yafei Fang, Yuqian Yao, Kangwei Mao, Yanyan Zhong, Yan Xu in Experimental Brain Research (2021)

  17. No Access

    Article

    3-Hz Postural Tremor in MSA-C and SCA: Revisiting an Old but Underestimated Cerebellar Sign by Posturography

    The aim of this study is to evaluate the prevalence and electrophysiological features of 3-Hz postural tremor in multiple system atrophy-cerebellar type and spinocerebellar ataxia. A static posturography exami...

    **aodi Li, **ao Lv, Churong Liu, **long Ye, Yan Xu, Gengmao Ma, Zhong Li in The Cerebellum (2021)

  18. Article

    Open Access

    Characteristic of Parkinson’s disease with severe COVID-19: a study of 10 cases from Wuhan

    Information about Parkinson’s disease (PD) patients with severe COVID-19 is scarce. We aimed to analyze the clinical characteristics, outcomes, and risk factors affecting the prognosis of PD patients with seve...

    Heng Zhai, Yinzhang Lv, Yu Xu, Yi Wu, Weiqi Zeng in Journal of Neural Transmission (2021)

  19. No Access

    Article

    Adjuvant therapy with Astragalus membranaceus for post-stroke fatigue: a systematic review

    Post-stroke fatigue (PSF) is a common symptom after stroke and interferes with the rehabilitation. There are limited pharmacological therapies for managing PSF. Astragalus membranaceus (Huangqi) is a frequently u...

    Li Xu, **ao-Yan Xu, Xue-Qin Hou, Fu-Gang Wang, Shan Gao in Metabolic Brain Disease (2020)

  20. No Access

    Article

    Biallelic INTS1 Mutations Cause a Rare Neurodevelopmental Disorder in Two Chinese Siblings

    This study presents two Chinese siblings with a rare neurodevelopmental disorder (NDD) caused by biallelic INTS1 mutations and investigates the clinical features of this disease by means of in silico analysis. Tw...

    Xuemin Zhang, Yajian Wang, Fang Yang, Jiulai Tang in Journal of Molecular Neuroscience (2020)

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