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25 hasil untuk "Linlin Wan"

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  1. Artikel Jurnal

    Research on CORE Paper Association Discovery and Semantic Services Based on Semantic Similarity

    Bai Linlin, Wan Ni

    Zhishi guanli luntan, Vol. 6 No. 5 · 2021 · Tionghoa · DOAJ

    [Purpose/significance] This paper dissects the process and services of article association discovery in Connecting Repositories, and hopes to provide powerful reference for the recommendation and semantic linking of the content of articles in Chinese open access repositories. [Method/process] This…

  2. Artikel Jurnal

    Third-generation versus first-generation EGFR tyrosine kinase inhibitors in Asian patients with advanced EGFR mutant non-small cell lung cancer: a meta-analysis of randomized controlled trials

    Manzhen Xu; Wei Ding; Linlin Wan dkk.

    Discover Oncology, Vol. 16 No. 1 · 2025 · Inggris · DOAJ Scopus

    Abstract Background Third-generation EGFR-TKIs (TGETs) have demonstrated improved clinical outcomes compared to first-generation EGFR-TKIs (FGETs) in patients with EGFR-mutant non-small-cell lung cancer (NSCLC). Nonetheless, the comparative safety and efficacy of TGETs as a first-line option for…

  3. Artikel Jurnal

    Analysis of the Brain Protective Effect of Flow Percentage Cerebral Perfusion Combined With Unilateral Antegrade Selective Cerebral Perfusion in Acute Aortic Dissection Arch Reconstruction Surgery

    YiHui Yu; JunCheng Shi; Lei Wang dkk.

    The Heart Surgery Forum, Vol. 28 No. 11 · 2025 · Inggris · DOAJ

    Background: To evaluate the neuroprotective efficacy of combining unilateral antegrade selective cerebral perfusion with percentage-controlled flow regulation during aortic arch reconstruction surgery for aortic dissection. Methods: A retrospective analysis was conducted using clinical data from…

  4. Artikel Jurnal

    Serum vitamin levels in multiple system atrophy: A case-control study

    Daji Chen; Linlin Wan; Zhao Chen dkk.

    Frontiers in Aging Neuroscience, Vol. 14 · 2023 · Inggris · DOAJ Scopus

    AimThere is increasing evidence suggesting that vitamins may play important roles in the pathogenesis of multiple system atrophy (MSA). The purpose of this study was to detect the changes of serum vitamin levels and investigate their correlation with disease severity in MSA patients.MethodsIn this…

  5. Artikel Jurnal

    Multidimensional biomarkers for multiple system atrophy: an update and future directions

    Linlin Wan; Sudan Zhu; Zhao Chen dkk.

    Translational Neurodegeneration, Vol. 12 No. 1 · 2023 · Inggris · DOAJ Scopus

    Abstract Multiple system atrophy (MSA) is a fatal progressive neurodegenerative disease. Biomarkers are urgently required for MSA to improve the diagnostic and prognostic accuracy in clinic and facilitate the development and monitoring of disease-modifying therapies. In recent years, significant…

  6. Artikel Jurnal

    Comparison of outcomes between axillary and femoral artery cannulation for type A aortic dissection surgery

    ZhenHong Wang; YiHui Yu; XinYi Xie dkk.

    Journal of Cardiothoracic Surgery, Vol. 20 No. 1 · 2025 · Inggris · DOAJ Scopus

    Abstract Objective To compare the application and outcomes of femoral versus axillary arterial cannulation in adult patients undergoing surgery for type A aortic dissection. Methods We conducted a retrospective review of 108 patients who underwent surgery for type A aortic dissection, dividing them…

  7. Artikel Jurnal

    Hypolipidemic effect of Fragarianilgerrensis Schlecht. medicine compound on hyperlipidemic rats

    Liangcai Gao; Zejie Lin; Yilian Liu dkk.

    Lipids in Health and Disease, Vol. 17 No. 1 · 2018 · Inggris · DOAJ Scopus

    Abstract Background Fragarianilgerrensis Schlecht. medicine compound (FN-MC) is a kind of Chinese herbs’ compound consisted of Fragarianilgerrensis Schlecht. and Centella asiatica (L.) Urban. The study was to investigate the hypolipidemia effect of FN-MC in a hypolipidemic rat model. Methods Male…

  8. Artikel Jurnal

    Attention-enhanced dilated convolution for Parkinson’s disease detection using transcranial sonography

    Shuang Chen; Yuting Shi; Linlin Wan dkk.

    BioMedical Engineering OnLine, Vol. 23 No. 1 · 2024 · Inggris · DOAJ Scopus

    Abstract Background Transcranial sonography (TCS) plays a crucial role in diagnosing Parkinson's disease. However, the intricate nature of TCS pathological features, the lack of consistent diagnostic criteria, and the dependence on physicians' expertise can hinder accurate diagnosis. Current…

  9. Artikel Jurnal

    Lactylation and human disease

    Linlin Wan; HuiJuan Zhang; Jialing Liu dkk.

    Expert Reviews in Molecular Medicine, Vol. 27 · 2025 · Inggris · DOAJ Scopus

    Abstract Background Lactylation, a new epigenetic modification, is an important way in which lactate exerts physiological functions. There is a close relationship between increased lactylations caused by lactate and glycolysis, which can interact and play a role in disease through lactate as an…

  10. Artikel Jurnal

    MR Imaging of SCA3/MJD

    Na Wan; Zhao Chen; Linlin Wan dkk.

    Frontiers in Neuroscience, Vol. 14 · 2020 · Inggris · DOAJ Scopus

    Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a progressive autosomal dominantly inherited cerebellar ataxia characterized by the aggregation of polyglutamine-expanded protein within neuronal nuclei in the brain, which can lead to brain damage that precedes the onset of…

  11. Artikel Jurnal

    The characteristic and biomarker value of transcranial sonography in cerebellar ataxia

    Sudan Zhu; Yuting Shi; Zhao Chen dkk.

    Annals of Clinical and Translational Neurology, Vol. 11 No. 8 · 2024 · Inggris · DOAJ Scopus

    Abstract Objective Transcranial sonography (TCS) is a noninvasive neuroimaging technique, visualizing deep brain structures and the ventricular system. Although widely employed in diagnosing various movement disorders, such as Parkinson's disease and dystonia, by detecting disease‐specific…

  12. Artikel Jurnal

    Roles of Post-translational Modifications in Spinocerebellar Ataxias

    Linlin Wan; Keqin Xu; Zhao Chen dkk.

    Frontiers in Cellular Neuroscience, Vol. 12 · 2018 · Inggris · DOAJ Scopus

    Post-translational modifications (PTMs), including phosphorylation, acetylation, ubiquitination, SUMOylation, etc., of proteins can modulate protein properties such as intracellular distribution, activity, stability, aggregation, and interactions. Therefore, PTMs are vital regulatory mechanisms for…

  13. Artikel Jurnal

    VR-based quantitative oculomotor analysis and association with regional brain atrophy in MSA

    You Fu; Linlin Wan; Zhao Chen dkk.

    Journal of Parkinson’s Disease, Vol. 16 · 2026 · Inggris · DOAJ Scopus

    Background The quantitative assessment of the oculomotor system has emerged as a promising biomarker for neurodegenerative disorders. Although oculomotor impairments are commonly observed in multiple system atrophy (MSA) patients, the specific abnormalities and underlying neural structural changes…

  14. Artikel Jurnal

    Alterations of the skin microbiome in multiple system atrophy: a pilot study

    Daji Chen; Lang Sun; Linlin Wan dkk.

    npj Parkinson's Disease, Vol. 11 No. 1 · 2025 · Inggris · DOAJ Scopus

    Abstract Multiple system atrophy (MSA) alters skin physiology, potentially impacting skin microbiota. This pilot study investigated whether skin microbiota differs in MSA and whether these differences relate to disease severity. Using 16S rRNA sequencing of cervical and axillary sites in MSA…

  15. Artikel Jurnal

    Tri-modal assessment reveals early visual pathway degeneration in patients with MSA-C

    Chunrong Wang; Feiyan Deng; Zhao Chen dkk.

    Neurobiology of Disease, Vol. 218 · 2026 · Inggris · DOAJ Scopus

    Background and objectives: Post-mortem evidence suggests neurodegeneration in the visual pathway in multiple system atrophy-cerebellar type (MSA-C), yet robust in vivo evidence remains scarce. This study aimed to characterize these visual pathway changes in MSA-C patients by integrating optical…

  16. Artikel Jurnal

    Erythropoiesis–inosine metabolic axis failure underlying retinal neurodegeneration in glaucoma: novel diagnoses and therapies

    Yuyu Chou; Wuping Liu; Yanxiu Li dkk.

    Experimental and Molecular Medicine, Vol. 58 No. 2 · 2026 · Inggris · DOAJ Scopus

    Abstract Glaucoma, long considered an ocular-limited, age-dependent and hypoxia-driven neurodegeneration, is here reframed as a systemic erythroid–inosine axis failure that originates in the bone marrow yet culminates in retinal ganglion cell (RGC) death. By mining UK Biobank datasets (n = 127,028)…

  17. Artikel Jurnal

    Inosine promotes erythrocyte metabolic reprogramming and restores oxygen release for rejuvenation via 2,3-BPG-PNP axis

    Wuping Liu; Zhaoyu Yang; Changhan Chen dkk.

    Cell Discovery, Vol. 12 No. 1 · 2026 · Inggris · DOAJ Scopus

    Abstract Aging-related diseases are aggravated by tissue hypoxia; however, the underlying mechanism remains unknown. Here, we report that the oxygen (O2) release capacity of red blood cells (RBCs) gradually decreases with age and is closely associated with aging-related tissue dysfunction…

  18. Artikel Jurnal

    The genetic landscape and phenotypic spectrum of GAA-FGF14 ataxia in China: a large cohort studyResearch in context

    Riwei Ouyang; Linlin Wan; David Pellerin dkk.

    EBioMedicine, Vol. 102 · 2024 · Inggris · DOAJ Scopus

    Summary: Background: An intronic GAA repeat expansion in FGF14 was recently identified as a cause of GAA-FGF14 ataxia. We aimed to characterise the frequency and phenotypic profile of GAA-FGF14 ataxia in a large Chinese ataxia cohort. Methods: A total of 1216 patients that included 399 typical…

  19. Artikel Jurnal

    CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells

    Lang He; Shang Wang; Linliu Peng dkk.

    Translational Psychiatry, Vol. 11 No. 1 · 2021 · Inggris · DOAJ Scopus

    Abstract Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a progressive autosomal dominant neurodegenerative disease caused by abnormal CAG repeats in the exon 10 of ATXN3. The accumulation of the mutant ataxin-3 proteins carrying expanded polyglutamine (polyQ) leads to selective…