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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 7
2003 2
2004 7
2005 7
2006 9
2007 6
2008 7
2009 6
2010 8
2011 7
2012 11
2013 8
2014 7
2015 7
2016 4
2017 9
2018 9
2019 16
2020 11
2021 7
2022 9
2023 10
2024 3

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162 results

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Page 1
Retinal pathological features and proteome signatures of Alzheimer's disease.
Koronyo Y, Rentsendorj A, Mirzaei N, Regis GC, Sheyn J, Shi H, Barron E, Cook-Wiens G, Rodriguez AR, Medeiros R, Paulo JA, Gupta VB, Kramerov AA, Ljubimov AV, Van Eyk JE, Graham SL, Gupta VK, Ringman JM, Hinton DR, Miller CA, Black KL, Cattaneo A, Meli G, Mirzaei M, Fuchs DT, Koronyo-Hamaoui M. Koronyo Y, et al. Among authors: cattaneo a. Acta Neuropathol. 2023 Apr;145(4):409-438. doi: 10.1007/s00401-023-02548-2. Epub 2023 Feb 11. Acta Neuropathol. 2023. PMID: 36773106 Free PMC article.
Tuning GABAergic Inhibition: Gephyrin Molecular Organization and Functions.
Pizzarelli R, Griguoli M, Zacchi P, Petrini EM, Barberis A, Cattaneo A, Cherubini E. Pizzarelli R, et al. Among authors: cattaneo a. Neuroscience. 2020 Jul 15;439:125-136. doi: 10.1016/j.neuroscience.2019.07.036. Epub 2019 Jul 26. Neuroscience. 2020. PMID: 31356900 Free PMC article. Review.
Tau Modulates VGluT1 Expression.
Siano G, Varisco M, Caiazza MC, Quercioli V, Mainardi M, Ippolito C, Cattaneo A, Di Primio C. Siano G, et al. Among authors: cattaneo a. J Mol Biol. 2019 Feb 15;431(4):873-884. doi: 10.1016/j.jmb.2019.01.023. Epub 2019 Jan 18. J Mol Biol. 2019. PMID: 30664870 Free article.
Reduced levels of NGF shift astrocytes toward a neurotoxic phenotype.
Tiberi A, Carucci NM, Testa G, Rizzi C, Pacifico P, Borgonovo G, Arisi I, D'Onofrio M, Brandi R, Gan WB, Capsoni S, Cattaneo A. Tiberi A, et al. Among authors: cattaneo a. Front Cell Dev Biol. 2023 Apr 18;11:1165125. doi: 10.3389/fcell.2023.1165125. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37143894 Free PMC article.
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Salpietro V, Maroofian R, Zaki MS, Wangen J, Ciolfi A, Barresi S, Efthymiou S, Lamaze A, Aughey GN, Al Mutairi F, Rad A, Rocca C, Calì E, Accogli A, Zara F, Striano P, Mojarrad M, Tariq H, Giacopuzzi E, Taylor JC, Oprea G, Skrahina V, Rehman KU, Abd Elmaksoud M, Bassiony M, El Said HG, Abdel-Hamid MS, Al Shalan M, Seo G, Kim S, Lee H, Khang R, Issa MY, Elbendary HM, Rafat K, Marinakis NM, Traeger-Synodinos J, Ververi A, Sourmpi M, Eslahi A, Khadivi Zand F, Beiraghi Toosi M, Babaei M, Jackson A; SYNAPS Study Group; Bertoli-Avella A, Pagnamenta AT, Niceta M, Battini R, Corsello A, Leoni C, Chiarelli F, Dallapiccola B, Faqeih EA, Tallur KK, Alfadhel M, Alobeid E, Maddirevula S, Mankad K, Banka S, Ghayoor-Karimiani E, Tartaglia M, Chung WK, Green R, Alkuraya FS, Jepson JEC, Houlden H. Salpietro V, et al. Am J Hum Genet. 2024 Jan 4;111(1):200-210. doi: 10.1016/j.ajhg.2023.11.012. Epub 2023 Dec 20. Am J Hum Genet. 2024. PMID: 38118446 Free PMC article.
162 results