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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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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.
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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.
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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
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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
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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
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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
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