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Year Number of Results
2013 1
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2017 64
2018 106
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2020 128
2021 134
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2024 46

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Page 1
Alexander disease: models, mechanisms, and medicine.
Hagemann TL. Hagemann TL. Curr Opin Neurobiol. 2022 Feb;72:140-147. doi: 10.1016/j.conb.2021.10.002. Epub 2021 Nov 23. Curr Opin Neurobiol. 2022. PMID: 34826654 Free PMC article. Review.
Regulation of GFAP Expression.
Brenner M, Messing A. Brenner M, et al. ASN Neuro. 2021 Jan-Dec;13:1759091420981206. doi: 10.1177/1759091420981206. ASN Neuro. 2021. PMID: 33601918 Free PMC article. Review.
Human Adult Neurogenesis: Evidence and Remaining Questions.
Kempermann G, Gage FH, Aigner L, Song H, Curtis MA, Thuret S, Kuhn HG, Jessberger S, Frankland PW, Cameron HA, Gould E, Hen R, Abrous DN, Toni N, Schinder AF, Zhao X, Lucassen PJ, Frisén J. Kempermann G, et al. Cell Stem Cell. 2018 Jul 5;23(1):25-30. doi: 10.1016/j.stem.2018.04.004. Epub 2018 Apr 19. Cell Stem Cell. 2018. PMID: 29681514 Free PMC article. Review.
Human Stem Cell-Derived Neurons Repair Circuits and Restore Neural Function.
Xiong M, Tao Y, Gao Q, Feng B, Yan W, Zhou Y, Kotsonis TA, Yuan T, You Z, Wu Z, Xi J, Haberman A, Graham J, Block J, Zhou W, Chen Y, Zhang SC. Xiong M, et al. Cell Stem Cell. 2021 Jan 7;28(1):112-126.e6. doi: 10.1016/j.stem.2020.08.014. Epub 2020 Sep 22. Cell Stem Cell. 2021. PMID: 32966778 Free PMC article.
3D bioprinting of human neural tissues with functional connectivity.
Yan Y, Li X, Gao Y, Mathivanan S, Kong L, Tao Y, Dong Y, Li X, Bhattacharyya A, Zhao X, Zhang SC. Yan Y, et al. Cell Stem Cell. 2024 Feb 1;31(2):260-274.e7. doi: 10.1016/j.stem.2023.12.009. Cell Stem Cell. 2024. PMID: 38306994 Free article.
Reproducibility and staging of 3D human retinal organoids across multiple pluripotent stem cell lines.
Capowski EE, Samimi K, Mayerl SJ, Phillips MJ, Pinilla I, Howden SE, Saha J, Jansen AD, Edwards KL, Jager LD, Barlow K, Valiauga R, Erlichman Z, Hagstrom A, Sinha D, Sluch VM, Chamling X, Zack DJ, Skala MC, Gamm DM. Capowski EE, et al. Development. 2019 Jan 9;146(1):dev171686. doi: 10.1242/dev.171686. Development. 2019. PMID: 30567931 Free PMC article.
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study; Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Snijders Blok L, et al. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
650 results