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

Year Number of Results
1992 2
1993 2
1994 1
1996 2
1997 2
1998 1
1999 4
2000 1
2002 1
2003 2
2004 2
2005 2
2006 3
2007 1
2008 2
2009 1
2010 2
2011 1
2012 1
2013 2
2016 1
2019 3
2020 1
2021 1
2022 3
2024 0

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42 results

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Page 1
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects.
Sanchez-Martin I, Magalhães P, Ranjzad P, Fatmi A, Richard F, Manh TPV, Saurin AJ, Feuillet G, Denis C, Woolf AS, Schanstra JP, Zürbig P, Caubit X, Fasano L. Sanchez-Martin I, et al. Among authors: caubit x. Hum Mol Genet. 2022 Jun 22;31(12):1921-1945. doi: 10.1093/hmg/ddab362. Hum Mol Genet. 2022. PMID: 34919690
Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like Behavior.
Chabbert D, Caubit X, Roubertoux PL, Carlier M, Habermann B, Jacq B, Salin P, Metwaly M, Frahm C, Fatmi A, Garratt AN, Severac D, Dubois E, Kerkerian-Le Goff L, Fasano L, Gubellini P. Chabbert D, et al. Among authors: caubit x. Biol Psychiatry. 2019 Aug 15;86(4):274-285. doi: 10.1016/j.biopsych.2019.03.974. Epub 2019 Mar 28. Biol Psychiatry. 2019. PMID: 31060802 Free article.
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.
Caubit X, Gubellini P, Andrieux J, Roubertoux PL, Metwaly M, Jacq B, Fatmi A, Had-Aissouni L, Kwan KY, Salin P, Carlier M, Liedén A, Rudd E, Shinawi M, Vincent-Delorme C, Cuisset JM, Lemaitre MP, Abderrehamane F, Duban B, Lemaitre JF, Woolf AS, Bockenhauer D, Severac D, Dubois E, Zhu Y, Sestan N, Garratt AN, Lydia Kerkerian-Le Goff, Fasano L. Caubit X, et al. Nat Genet. 2016 Nov;48(11):1359-1369. doi: 10.1038/ng.3681. Epub 2016 Sep 26. Nat Genet. 2016. PMID: 27668656 Free PMC article.
42 results