المؤلفون: Li, Yongang, Ji, GuiKai, Lian, Mengjia, Liu, Xuan, Xu, Ying, Gui, Yaxing^{Aff3, IDs40120023005420_cor6}

المصدر: Neurology and Therapy. 12(6):2021-2040

المؤلفون: Yongang Li, GuiKai Ji, Mengjia Lian, Xuan Liu, Ying Xu, Yaxing Gui

المصدر: Neurology and Therapy, Vol 12, Iss 6, Pp 2021-2040 (2023)

مصطلحات موضوعية: Parkinson's disease, Exosomes, Lipids, PLA2G6, SMPD1, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2193-8253; https://doaj.org/toc/2193-6536

URL الوصول: https://doaj.org/article/320512bc938943eda5af202a16194ce1

المؤلفون: Bi, Junfeng, Khan, Atif, Tang, Jun, Armando, Aaron M, Wu, Sihan, Zhang, Wei, Gimple, Ryan C, Reed, Alex, Jing, Hui, Koga, Tomoyuki, Wong, Ivy Tsz-Lo, Gu, Yuchao, Miki, Shunichiro, Yang, Huijun, Prager, Briana, Curtis, Ellis J, Wainwright, Derek A, Furnari, Frank B, Rich, Jeremy N, Cloughesy, Timothy F, Kornblum, Harley I, Quehenberger, Oswald, Rzhetsky, Andrey, Cravatt, Benjamin F, Mischel, Paul S

المصدر: Cell Reports. 37(5)

مصطلحات موضوعية: Biological Sciences, Cancer, Brain Cancer, Mental Health, Brain Disorders, Rare Diseases, Neurosciences, Depression, 6.1 Pharmaceuticals, Evaluation of treatments and therapeutic interventions, Animals, Antineoplastic Agents, Antineoplastic Combined Chemotherapy Protocols, Blood-Brain Barrier, Brain Neoplasms, Cell Line, Tumor, Drug Repositioning, Electronic Health Records, Energy Metabolism, ErbB Receptors, Female, Fluoxetine, Glioblastoma, Humans, Mice, Nude, Permeability, Retrospective Studies, Signal Transduction, Sphingomyelin Phosphodiesterase, Sphingomyelins, Temozolomide, Tumor Burden, Tumor Cells, Cultured, Xenograft Model Antitumor Assays, EGFR signaling, Membrane lipids, SMPD1, combination therapy, electronic medical records, fluoxetine, glioblastoma, real-world evidence, sphingolipid metabolism, Biochemistry and Cell Biology, Medical Physiology, Biological sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/32f5f79f

المؤلفون: Ellegaard, Anne-Marie^{Aff12, Aff13}, Bach, Peter^{Aff12, Aff14}, Jäättelä, Marja^Aff15

المساهمون: Pedersen, Stine Helene Falsig, Editor-in-Chief^{Aff1, Aff10}, Barber, Diane L., Series Editor^{Aff2, Aff11}, Cordat, Emmanuelle, Series Editor^Aff3, Kajimura, Mayumi, Series Editor^Aff4, Leipziger, Jens G., Series Editor^Aff5, O'Donnell, Martha E., Series Editor^Aff6, Pardo, Luis A., Series Editor^Aff7, Schmitt, Nicole, Series Editor^Aff8, Stock, Christian, Series Editor^Aff9

المصدر: Organelles in Disease. 185:107-152

المؤلفون: Dursun, Fadime Ersoy^{Aff1, IDs1103302308275x_cor1}, Özen, Filiz

المصدر: Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. 50(4):3355-3363

المؤلفون: Claudio Tirelli, Ornella Rondinone, Marta Italia, Sabrina Mira, Luca Alessandro Belmonte, Mauro De Grassi, Gabriele Guido, Sara Maggioni, Michele Mondoni, Monica Rosa Miozzo, Stefano Centanni

المصدر: Biomolecules, Vol 14, Iss 2, p 211 (2024)

مصطلحات موضوعية: Niemann–Pick Disease, acid sphingomyelinase deficiency, SMPD1, NPC1, NPC2, Olipudase α, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2218-273X/14/2/211; https://doaj.org/toc/2218-273X

URL الوصول: https://doaj.org/article/e836cbb5e22d47f59c450f8d9cde2c8d

المؤلفون: Maria Judit Molnar, Tamas Szlepak, Ildikó Csürke, Szendile Loth, Rita Káposzta, Melinda Erdős, Antal Dezsőfi

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: ASMD, acid sphingomyelinase deficiency type A/B, intermediate-type acid sphingomyelinase deficiency, Niemann-Pick disease type A/B, SMPD1, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1158108/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/4e5af7abff8345f7874df2075855a40b

المؤلفون: Zhe-wen Zhou, Shou-hao Wang, Cheng-an Xu, Wen-hao Wu, Tian-chen Hui, Qiao-qiao Yin, Wei Zheng, Hong-ying Pan

المصدر: BMC Medical Genomics, Vol 15, Iss 1, Pp 1-6 (2022)

مصطلحات موضوعية: Niemann Pick disease type B, Sea-blue histiocytosis, Budd-Chiari syndrome, SMPD1 gene, Case report, Internal medicine, RC31-1245, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1755-8794

URL الوصول: https://doaj.org/article/8d571523027547d08df209e10db93575

المؤلفون: Carsana, Emma Veronica, Lunghi, Giulia, Prioni, Simona, Mauri, Laura, Loberto, Nicoletta, Prinetti, Alessandro, Zucca, Fabio Andrea, Bassi, Rosaria, Sonnino, Sandro, Chiricozzi, Elena, Duga, Stefano^{Aff3, Aff4}, Straniero, Letizia^{Aff3, Aff4}, Asselta, Rosanna^{Aff3, Aff4}, Soldà, Giulia^{Aff3, Aff4}, Samarani, Maura, Aureli, Massimo^{Aff1, IDs12031022020364_cor16}

المصدر: Journal of Molecular Neuroscience. 72(7):1482-1499

المؤلفون: Zhou, Zhe-wen^{Aff1, Aff2}, Wang, Shou-hao, Xu, Cheng-an, Wu, Wen-hao, Hui, Tian-chen, Yin, Qiao-qiao, Zheng, Wei, Pan, Hong-ying^{Aff1, Aff2, IDs12920022013532_cor8}

المصدر: BMC Medical Genomics. 15(1)