{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T03:06:43Z","timestamp":1790046403006,"version":"4.0.1"},"reference-count":77,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Proteomics"],"published-print":{"date-parts":[[2024,7]]},"DOI":"10.1016\/j.jprot.2024.105202","type":"journal-article","created":{"date-parts":[[2024,5,24]],"date-time":"2024-05-24T17:16:40Z","timestamp":1716571000000},"page":"105202","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"special_numbering":"C","title":["Hippocampal proteome comparison of infant and adult Fmr1 deficiency mice reveals adult-related changes associated with postsynaptic density"],"prefix":"10.1016","volume":"303","author":[{"given":"Cui","family":"Yang","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yu-Ting","family":"Huang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yi-Fei","family":"Yao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jun-Yi","family":"Fu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yue-Sheng","family":"Long","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jprot.2024.105202_bb0005","doi-asserted-by":"crossref","DOI":"10.1016\/j.nbd.2020.104740","article-title":"Fragile X syndrome and associated disorders: clinical aspects and pathology","volume":"136","author":"Salcedo-Arellano","year":"2020","journal-title":"Neurobiol. Dis."},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0010","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1186\/s40246-023-00507-2","article-title":"Phenotypic variability to medication management: an update on fragile X syndrome","volume":"17","author":"Elhawary","year":"2023","journal-title":"Hum. Genomics"},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0015","doi-asserted-by":"crossref","first-page":"905","DOI":"10.1016\/0092-8674(91)90397-H","article-title":"Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome","volume":"65","author":"Verkerk","year":"1991","journal-title":"Cell"},{"key":"10.1016\/j.jprot.2024.105202_bb0020","doi-asserted-by":"crossref","first-page":"17065","DOI":"10.1038\/nrdp.2017.65","article-title":"Fragile X syndrome","volume":"3","author":"Hagerman","year":"2017","journal-title":"Nat. Rev. Dis. Primers."},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0025","doi-asserted-by":"crossref","first-page":"591","DOI":"10.1016\/S0092-8674(01)00589-X","article-title":"Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function","volume":"107","author":"Zhang","year":"2001","journal-title":"Cell"},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0030","doi-asserted-by":"crossref","first-page":"2572","DOI":"10.1152\/jn.90558.2008","article-title":"Altered hippocampal synaptic plasticity in the FMR1 gene family knockout mouse models","volume":"101","author":"Zhang","year":"2009","journal-title":"J. Neurophysiol."},{"issue":"21","key":"10.1016\/j.jprot.2024.105202_bb0035","doi-asserted-by":"crossref","first-page":"5977","DOI":"10.1093\/hmg\/ddv299","article-title":"Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXS","volume":"24","author":"Till","year":"2015","journal-title":"Hum. Mol. Genet."},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0040","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1016\/S0092-8674(01)00566-9","article-title":"Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function","volume":"107","author":"Darnell","year":"2001","journal-title":"Cell"},{"issue":"3","key":"10.1016\/j.jprot.2024.105202_bb0045","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1016\/S0092-8674(03)00079-5","article-title":"The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses","volume":"112","author":"Zalfa","year":"2003","journal-title":"Cell"},{"issue":"2","key":"10.1016\/j.jprot.2024.105202_bb0050","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1016\/j.neuron.2008.10.004","article-title":"Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function","volume":"60","author":"Bassell","year":"2008","journal-title":"Neuron"},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0055","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1016\/j.cell.2014.03.040","article-title":"A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response","volume":"157","author":"Alpatov","year":"2014","journal-title":"Cell"},{"issue":"19","key":"10.1016\/j.jprot.2024.105202_bb0060","doi-asserted-by":"crossref","first-page":"14926","DOI":"10.3390\/ijms241914926","article-title":"Transcriptional dysregulation and impaired neuronal activity in FMR1 Knock-out and fragile X Patients\u2019 iPSC-derived models","volume":"24","author":"Maussion","year":"2023","journal-title":"Int. J. Mol. Sci."},{"key":"10.1016\/j.jprot.2024.105202_bb0065","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1016\/j.neuroscience.2017.02.044","article-title":"A novel role of fragile X mental retardation protein in pre-mRNA alternative splicing through RNA-binding protein 14","volume":"349","author":"Zhou","year":"2017","journal-title":"Neuroscience"},{"issue":"13","key":"10.1016\/j.jprot.2024.105202_bb0070","doi-asserted-by":"crossref","first-page":"4459","DOI":"10.1016\/j.celrep.2020.02.076","article-title":"FMRP control of ribosome translocation promotes chromatin modifications and alternative splicing of neuronal genes linked to autism","volume":"30","author":"Shah","year":"2020","journal-title":"Cell Rep."},{"issue":"12","key":"10.1016\/j.jprot.2024.105202_bb0075","doi-asserted-by":"crossref","first-page":"1517","DOI":"10.1038\/nn.2950","article-title":"Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein","volume":"14","author":"Bhogal","year":"2011","journal-title":"Nat. Neurosci."},{"issue":"11","key":"10.1016\/j.jprot.2024.105202_bb0080","doi-asserted-by":"crossref","first-page":"1580","DOI":"10.1080\/15476286.2017.1338232","article-title":"Absence of the fragile X mental retardation protein results in defects of RNA editing of neuronal mRNAs in mouse","volume":"14","author":"Filippini","year":"2017","journal-title":"RNA Biol."},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0085","doi-asserted-by":"crossref","first-page":"845","DOI":"10.1016\/j.celrep.2019.06.072","article-title":"FMRP modulates neural differentiation through m(6)A-dependent mRNA nuclear export","volume":"28","author":"Edens","year":"2019","journal-title":"Cell Rep."},{"key":"10.1016\/j.jprot.2024.105202_bb0090","doi-asserted-by":"crossref","DOI":"10.1016\/j.jprot.2022.104720","article-title":"Lysine acetylome profiling in mouse hippocampus and its alterations upon FMRP deficiency linked to abnormal energy metabolism","volume":"269","author":"Wu","year":"2022","journal-title":"J. Proteome"},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0095","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1038\/s41583-021-00432-0","article-title":"The molecular biology of FMRP: new insights into fragile X syndrome","volume":"22","author":"Richter","year":"2021","journal-title":"Nat. Rev. Neurosci."},{"issue":"3","key":"10.1016\/j.jprot.2024.105202_bb0100","doi-asserted-by":"crossref","first-page":"1053","DOI":"10.1007\/s12035-014-8770-1","article-title":"A MicroRNA profile in Fmr1 knockout mice reveals MicroRNA expression alterations with possible roles in fragile X syndrome","volume":"51","author":"Liu","year":"2015","journal-title":"Mol. Neurobiol."},{"issue":"10","key":"10.1016\/j.jprot.2024.105202_bb0105","doi-asserted-by":"crossref","first-page":"1516","DOI":"10.3390\/genes12101516","article-title":"Development of a quantitative FMRP assay for mouse tissue applications","volume":"12","author":"Adayev","year":"2021","journal-title":"Genes (Basel)"},{"key":"10.1016\/j.jprot.2024.105202_bb0110","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1016\/j.brainres.2014.11.023","article-title":"Expression of fragile X mental retardation protein in neurons and glia of the developing and adult mouse brain","volume":"1596","author":"Gholizadeh","year":"2015","journal-title":"Brain Res."},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0115","doi-asserted-by":"crossref","first-page":"818","DOI":"10.1002\/cne.24100","article-title":"Cellular distribution of the fragile X mental retardation protein in the mouse brain","volume":"525","author":"Zorio","year":"2017","journal-title":"J. Comp. Neurol."},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0120","first-page":"433","article-title":"An \u201cOmic\u201d overview of fragile X syndrome","volume":"10","author":"Dionne","year":"2021","journal-title":"Biology (Basel)"},{"key":"10.1016\/j.jprot.2024.105202_bb0125","doi-asserted-by":"crossref","DOI":"10.1016\/j.jprot.2023.104822","article-title":"Proteome profiling of the prefrontal cortex of Fmr1 knockout mouse reveals enhancement of complement and coagulation cascades","volume":"274","author":"Gao","year":"2023","journal-title":"J. Proteome"},{"issue":"9","key":"10.1016\/j.jprot.2024.105202_bb0130","doi-asserted-by":"crossref","first-page":"3054","DOI":"10.1021\/acs.jproteome.3c00363","article-title":"Mouse model of fragile X syndrome analyzed by quantitative proteomics: a comparison of methods","volume":"22","author":"Filandrova","year":"2023","journal-title":"J. Proteome Res."},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0135","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0121464","article-title":"Quantitative profiling of brain lipid raft proteome in a mouse model of fragile X syndrome","volume":"10","author":"Kalinowska","year":"2015","journal-title":"PLoS One"},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0140","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1186\/s13041-021-00783-w","article-title":"FMRP attenuates activity dependent modifications in the mitochondrial proteome","volume":"14","author":"B\u00fclow","year":"2021","journal-title":"Mol. Brain"},{"issue":"34","key":"10.1016\/j.jprot.2024.105202_bb0145","doi-asserted-by":"crossref","first-page":"E4697","DOI":"10.1073\/pnas.1502258112","article-title":"Fmr1 deficiency promotes age-dependent alterations in the cortical synaptic proteome","volume":"112","author":"Tang","year":"2015","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.jprot.2024.105202_bb0150","doi-asserted-by":"crossref","first-page":"1258615","DOI":"10.3389\/fnmol.2023.1258615","article-title":"Impaired synaptic incorporation of AMPA receptors in a mouse model of fragile X syndrome","volume":"16","author":"Chojnacka","year":"2023","journal-title":"Front. Mol. Neurosci."},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0155","doi-asserted-by":"crossref","first-page":"3236","DOI":"10.1038\/s41467-022-30979-0","article-title":"Excess ribosomal protein production unbalances translation in a model of fragile X syndrome","volume":"13","author":"Seo","year":"2022","journal-title":"Nat. Commun."},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0160","doi-asserted-by":"crossref","first-page":"1335","DOI":"10.1017\/S0954579420000942","article-title":"Emergence and rate of autism in fragile X syndrome across the first years of life","volume":"32","author":"Roberts","year":"2020","journal-title":"Dev. Psychopathol."},{"issue":"2","key":"10.1016\/j.jprot.2024.105202_bb0165","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1016\/j.cell.2011.06.013","article-title":"FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism","volume":"146","author":"Darnell","year":"2011","journal-title":"Cell"},{"issue":"40","key":"10.1016\/j.jprot.2024.105202_bb0170","doi-asserted-by":"crossref","first-page":"15281","DOI":"10.1073\/pnas.0804678105","article-title":"3rd Yates, quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice","volume":"105","author":"Liao","year":"2008","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.jprot.2024.105202_bb0175","first-page":"17","article-title":"Synaptic vesicle dynamic changes in a model of fragile X. Mol","volume":"7","author":"Broek","year":"2016","journal-title":"Autism"},{"key":"10.1016\/j.jprot.2024.105202_bb0180","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1016\/B978-0-444-52002-9.00023-1","article-title":"Autism and related disorders","volume":"106","author":"McPartland","year":"2012","journal-title":"Handb. Clin. Neurol."},{"key":"10.1016\/j.jprot.2024.105202_bb0185","doi-asserted-by":"crossref","first-page":"1213410","DOI":"10.3389\/fnins.2023.1213410","article-title":"Neurodevelopment and early pharmacological interventions in fragile X syndrome","volume":"17","author":"Milla","year":"2023","journal-title":"Front. Neurosci."},{"key":"10.1016\/j.jprot.2024.105202_bb0190","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.pneurobio.2013.04.001","article-title":"Brain development in rodents and humans: identifying benchmarks of maturation and vulnerability to injury across species","volume":"106-107","author":"Semple","year":"2013","journal-title":"Prog. Neurobiol."},{"issue":"2","key":"10.1016\/j.jprot.2024.105202_bb0195","doi-asserted-by":"crossref","first-page":"507","DOI":"10.1042\/BST0380507","article-title":"The developmental roles of FMRP","volume":"38","author":"Till","year":"2010","journal-title":"Biochem. Soc. Trans."},{"key":"10.1016\/j.jprot.2024.105202_bb0200","article-title":"Autism symptoms in children and young adults with fragile X syndrome, Angelman syndrome, tuberous sclerosis complex, and Neurofibromatosis type 1: a cross-syndrome comparison","volume":"13","author":"Lubbers","year":"2022","journal-title":"Front. Psychol."},{"issue":"3","key":"10.1016\/j.jprot.2024.105202_bb0205","doi-asserted-by":"crossref","first-page":"385","DOI":"10.3390\/brainsci12030385","article-title":"Pragmatic profiles of adults with fragile X syndrome and Williams syndrome","volume":"12","author":"Diez-Itza","year":"2022","journal-title":"Brain Sci."},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0210","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1002\/ddrr.1129","article-title":"Fragile X syndrome: an aging perspective","volume":"18","author":"Schneider","year":"2013","journal-title":"Dev. Disabil. Res. Rev."},{"issue":"2","key":"10.1016\/j.jprot.2024.105202_bb0215","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1007\/s00401-019-02099-5","article-title":"Loss of fragile X mental retardation protein precedes Lewy pathology in Parkinson\u2019s disease","volume":"139","author":"Tan","year":"2020","journal-title":"Acta Neuropathol."},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0220","doi-asserted-by":"crossref","first-page":"758","DOI":"10.3390\/cells12050758","article-title":"Age-dependent dysregulation of APP in neuronal and skin cells from fragile X individuals","volume":"12","author":"Cencelli","year":"2023","journal-title":"Cells"},{"key":"10.1016\/j.jprot.2024.105202_bb0225","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1016\/j.brainres.2009.01.059","article-title":"Whole-brain expression analysis of FMRP in adult monkey and its relationship to cognitive deficits in fragile X syndrome","volume":"1264","author":"Zangenehpour","year":"2009","journal-title":"Brain Res."},{"issue":"2","key":"10.1016\/j.jprot.2024.105202_bb0230","doi-asserted-by":"crossref","DOI":"10.1016\/j.celrep.2021.108991","article-title":"Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis","volume":"35","author":"Raj","year":"2021","journal-title":"Cell Rep."},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0235","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1038\/s41593-018-0287-x","article-title":"Widespread RNA editing dysregulation in brains from autistic individuals","volume":"22","author":"Tran","year":"2019","journal-title":"Nat. Neurosci."},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0240","doi-asserted-by":"crossref","first-page":"ar36","DOI":"10.1091\/mbc.E22-05-0157","article-title":"The nuclear isoforms of the fragile X mental retardation RNA-binding protein associate with genomic DNA bridges","volume":"34","author":"Ledoux","year":"2023","journal-title":"Mol. Biol. Cell"},{"issue":"10","key":"10.1016\/j.jprot.2024.105202_bb0245","doi-asserted-by":"crossref","first-page":"1795","DOI":"10.3390\/genes13101795","article-title":"Profiling genome-wide DNA methylation in children with autism Spectrum disorder and in children with fragile X syndrome","volume":"13","author":"Jasoliya","year":"2022","journal-title":"Genes (Basel)"},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0250","doi-asserted-by":"crossref","first-page":"859","DOI":"10.1038\/s41467-022-28547-7","article-title":"Dynamic FMR1 granule phase switch instructed by m6A modification contributes to maternal RNA decay","volume":"13","author":"Zhang","year":"2022","journal-title":"Nat. Commun."},{"issue":"48","key":"10.1016\/j.jprot.2024.105202_bb0255","doi-asserted-by":"crossref","first-page":"30400","DOI":"10.1073\/pnas.2009161117","article-title":"FMRP links optimal codons to mRNA stability in neurons","volume":"117","author":"Shu","year":"2020","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"issue":"8","key":"10.1016\/j.jprot.2024.105202_bb0260","doi-asserted-by":"crossref","first-page":"1093","DOI":"10.1038\/nn.4337","article-title":"Dynamic regulation of RNA editing in human brain development and disease","volume":"19","author":"Hwang","year":"2016","journal-title":"Nat. Neurosci."},{"issue":"9","key":"10.1016\/j.jprot.2024.105202_bb0265","doi-asserted-by":"crossref","first-page":"1521","DOI":"10.1038\/s41593-019-0461-9","article-title":"Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage","volume":"22","author":"Lee","year":"2019","journal-title":"Nat. Neurosci."},{"issue":"7","key":"10.1016\/j.jprot.2024.105202_bb0270","doi-asserted-by":"crossref","first-page":"1092","DOI":"10.1038\/s41588-019-0433-8","article-title":"Recessive gene disruptions in autism spectrum disorder","volume":"51","author":"Doan","year":"2019","journal-title":"Nat. Genet."},{"issue":"3","key":"10.1016\/j.jprot.2024.105202_bb0275","doi-asserted-by":"crossref","first-page":"606","DOI":"10.1046\/j.1471-4159.2001.00598.x","article-title":"Neuronal differentiation is triggered by oleic acid synthesized and released by astrocytes","volume":"79","author":"Tabernero","year":"2001","journal-title":"J. Neurochem."},{"issue":"7085","key":"10.1016\/j.jprot.2024.105202_bb0280","doi-asserted-by":"crossref","first-page":"813","DOI":"10.1038\/nature04598","article-title":"Omega-3 and omega-6 fatty acids stimulate cell membrane expansion by acting on syntaxin 3","volume":"440","author":"Darios","year":"2006","journal-title":"Nature"},{"issue":"18","key":"10.1016\/j.jprot.2024.105202_bb0285","doi-asserted-by":"crossref","first-page":"1603","DOI":"10.1089\/ars.2017.7284","article-title":"Redox signaling mechanisms in nervous system development","volume":"28","author":"Olgu\u00edn-Albuerne","year":"2018","journal-title":"Antioxid. Redox Signal."},{"key":"10.1016\/j.jprot.2024.105202_bb0290","doi-asserted-by":"crossref","DOI":"10.7554\/eLife.51063","article-title":"Sensing of nutrients by CPT1C regulates late endosome\/lysosome anterograde transport and axon growth","volume":"8","author":"Palomo-Guerrero","year":"2019","journal-title":"Elife"},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0295","doi-asserted-by":"crossref","first-page":"1077","DOI":"10.3390\/nu15051077","article-title":"Stimulation of GHRH neuron axon growth by leptin and impact of nutrition during suckling in mice","volume":"15","author":"Decourtye-Espiard","year":"2023","journal-title":"Nutrients"},{"issue":"1","key":"10.1016\/j.jprot.2024.105202_bb0300","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1186\/s12944-023-01817-z","article-title":"HDL and LDL have distinct, opposing effects on LPS-induced brain inflammation","volume":"22","author":"Radford-Smith","year":"2023","journal-title":"Lipids Health Dis."},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0305","doi-asserted-by":"crossref","first-page":"725","DOI":"10.1002\/biof.1541","article-title":"Emerging roles for high-density lipoproteins in neurodegenerative disorders","volume":"45","author":"Bahrami","year":"2019","journal-title":"Biofactors"},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0310","doi-asserted-by":"crossref","first-page":"1172","DOI":"10.1016\/j.cell.2018.06.047","article-title":"Reconstituted postsynaptic density as a molecular platform for understanding synapse formation and plasticity","volume":"174","author":"Zeng","year":"2018","journal-title":"Cell"},{"issue":"11","key":"10.1016\/j.jprot.2024.105202_bb0315","doi-asserted-by":"crossref","first-page":"1760","DOI":"10.1016\/j.neuron.2023.03.008","article-title":"Altered striatal actin dynamics drives behavioral inflexibility in a mouse model of fragile X syndrome","volume":"111","author":"Mercaldo","year":"2023","journal-title":"Neuron"},{"issue":"8","key":"10.1016\/j.jprot.2024.105202_bb0320","doi-asserted-by":"crossref","first-page":"4390","DOI":"10.3390\/ijms23084390","article-title":"Neurodevelopmental disorders associated with PSD-95 and its interaction partners","volume":"23","author":"Levy","year":"2022","journal-title":"Int. J. Mol. Sci."},{"issue":"7","key":"10.1016\/j.jprot.2024.105202_bb0325","doi-asserted-by":"crossref","first-page":"547","DOI":"10.1177\/1533317510382893","article-title":"Review: disruption of the postsynaptic density in Alzheimer\u2019s disease and other neurodegenerative dementias","volume":"25","author":"Gong","year":"2010","journal-title":"Am. J. Alzheimers Dis. Other Dement."},{"issue":"4","key":"10.1016\/j.jprot.2024.105202_bb0330","doi-asserted-by":"crossref","first-page":"789","DOI":"10.1002\/glia.23284","article-title":"Alterations in CA1 hippocampal synapses in a mouse model of fragile X syndrome","volume":"66","author":"Jawaid","year":"2018","journal-title":"Glia"},{"key":"10.1016\/j.jprot.2024.105202_bb0335","doi-asserted-by":"crossref","DOI":"10.1016\/j.nbd.2023.106240","article-title":"Prolonged and specific spatial training during adolescence reverses adult hippocampal network impairments in a mouse model of fragile X syndrome","volume":"185","author":"Zeitouny","year":"2023","journal-title":"Neurobiol. Dis."},{"key":"10.1016\/j.jprot.2024.105202_bb0340","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1007\/978-3-7091-0932-8_2","article-title":"Scaffold proteins at the postsynaptic density","volume":"970","author":"Verpelli","year":"2012","journal-title":"Adv. Exp. Med. Biol."},{"key":"10.1016\/j.jprot.2024.105202_bb0345","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1016\/bs.ircmb.2015.09.004","article-title":"Microtubule dynamics in neuronal development, plasticity, and neurodegeneration","volume":"321","author":"Penazzi","year":"2016","journal-title":"Int. Rev. Cell Mol. Biol."},{"issue":"17","key":"10.1016\/j.jprot.2024.105202_bb0350","doi-asserted-by":"crossref","first-page":"4076","DOI":"10.1523\/JNEUROSCI.2684-17.2018","article-title":"Cell-type-specific Shank2 deletion in mice leads to differential synaptic and behavioral phenotypes","volume":"38","author":"Kim","year":"2018","journal-title":"J. Neurosci."},{"issue":"7","key":"10.1016\/j.jprot.2024.105202_bb0355","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1101\/lm.026351.112","article-title":"Molecular and behavioral changes associated with adult hippocampus-specific SynGAP1 knockout","volume":"19","author":"Muhia","year":"2012","journal-title":"Learn. Mem."},{"key":"10.1016\/j.jprot.2024.105202_bb0360","doi-asserted-by":"crossref","first-page":"1174738","DOI":"10.3389\/fnmol.2023.1174738","article-title":"N-methyl-D-aspartate receptor hypofunction as a potential contributor to the progression and manifestation of many neurological disorders","volume":"16","author":"Dong","year":"2023","journal-title":"Front. Mol. Neurosci."},{"key":"10.1016\/j.jprot.2024.105202_bb0365","doi-asserted-by":"crossref","DOI":"10.1016\/j.nbd.2019.104527","article-title":"Progressive neuroanatomical changes caused by Grin1 loss-of-function mutation","volume":"132","author":"Intson","year":"2019","journal-title":"Neurobiol. Dis."},{"issue":"7","key":"10.1016\/j.jprot.2024.105202_bb0370","doi-asserted-by":"crossref","first-page":"2929","DOI":"10.1038\/s41380-020-00859-4","article-title":"Consequences of NMDA receptor deficiency can be rescued in the adult brain","volume":"26","author":"Mielnik","year":"2021","journal-title":"Mol. Psychiatry"},{"issue":"12","key":"10.1016\/j.jprot.2024.105202_bb0375","doi-asserted-by":"crossref","DOI":"10.1016\/j.gim.2023.100971","article-title":"ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizures","volume":"25","author":"Poggio","year":"2023","journal-title":"Genet. Med."},{"issue":"3","key":"10.1016\/j.jprot.2024.105202_bb0380","doi-asserted-by":"crossref","DOI":"10.1101\/mcs.a006233","article-title":"Clinical case report: mosaic ANK3 pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay","volume":"9","author":"Fang","year":"2023","journal-title":"Cold Spring Harb Mol Case Stud"},{"issue":"5","key":"10.1016\/j.jprot.2024.105202_bb0385","doi-asserted-by":"crossref","first-page":"dmm041608","DOI":"10.1242\/dmm.041608","article-title":"Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in dystonia musculorum mice","volume":"13","author":"Yoshioka","year":"2020","journal-title":"Dis. Model. Mech."}],"container-title":["Journal of Proteomics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1874391924001349?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1874391924001349?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,6,30]],"date-time":"2024-06-30T15:00:14Z","timestamp":1719759614000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1874391924001349"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,7]]},"references-count":77,"alternative-id":["S1874391924001349"],"URL":"https:\/\/doi.org\/10.1016\/j.jprot.2024.105202","relation":{},"ISSN":["1874-3919"],"issn-type":[{"value":"1874-3919","type":"print"}],"subject":[],"published":{"date-parts":[[2024,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Hippocampal proteome comparison of infant and adult Fmr1 deficiency mice reveals adult-related changes associated with postsynaptic density","name":"articletitle","label":"Article Title"},{"value":"Journal of Proteomics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jprot.2024.105202","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.","name":"copyright","label":"Copyright"}],"article-number":"105202"}}