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

Year Number of Results
1983 8
1984 7
1985 3
1986 6
1988 3
1990 2
1991 3
1992 5
1993 8
1994 8
1995 7
1996 11
1997 5
1998 4
1999 13
2000 13
2001 12
2002 15
2003 14
2004 19
2005 26
2006 17
2007 24
2008 33
2009 27
2010 35
2011 30
2012 47
2013 41
2014 54
2015 48
2016 46
2017 52
2018 33
2019 44
2020 46
2021 37
2022 31
2023 37
2024 28

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803 results

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Page 1
Spatially coordinated heterochromatinization of long synaptic genes in fragile X syndrome.
Malachowski T, Chandradoss KR, Boya R, Zhou L, Cook AL, Su C, Pham K, Haws SA, Kim JH, Ryu HS, Ge C, Luppino JM, Nguyen SC, Titus KR, Gong W, Wallace O, Joyce EF, Wu H, Rojas LA, Phillips-Cremins JE. Malachowski T, et al. Cell. 2023 Dec 21;186(26):5840-5858.e36. doi: 10.1016/j.cell.2023.11.019. Cell. 2023. PMID: 38134876 Free article.
The fragile X syndrome.
Hoogeveen AT, Oostra BA. Hoogeveen AT, et al. J Inherit Metab Dis. 1997 Jun;20(2):139-51. doi: 10.1023/a:1005392319533. J Inherit Metab Dis. 1997. PMID: 9211186 Review.
BDNF in fragile X syndrome.
Castrén ML, Castrén E. Castrén ML, et al. Neuropharmacology. 2014 Jan;76 Pt C:729-36. doi: 10.1016/j.neuropharm.2013.05.018. Epub 2013 May 29. Neuropharmacology. 2014. PMID: 23727436 Review.
Targeted Treatments for Fragile X Syndrome.
Johnson D, Clark C, Hagerman R. Johnson D, et al. Adv Neurobiol. 2023;30:225-253. doi: 10.1007/978-3-031-21054-9_10. Adv Neurobiol. 2023. PMID: 36928853
GABAergic abnormalities in the fragile X syndrome.
Van der Aa N, Kooy RF. Van der Aa N, et al. Eur J Paediatr Neurol. 2020 Jan;24:100-104. doi: 10.1016/j.ejpn.2019.12.022. Epub 2019 Dec 24. Eur J Paediatr Neurol. 2020. PMID: 31926845 Review.
Translational endpoints in fragile X syndrome.
de Esch CE, Zeidler S, Willemsen R. de Esch CE, et al. Neurosci Biobehav Rev. 2014 Oct;46 Pt 2:256-69. doi: 10.1016/j.neubiorev.2013.10.012. Epub 2013 Oct 30. Neurosci Biobehav Rev. 2014. PMID: 24184744 Review.
803 results