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Year | Number of Results |
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2013 | 2 |
2014 | 2 |
2015 | 1 |
2024 | 0 |
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Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.
Am J Hum Genet. 2014 Jan 2;94(1):62-72. doi: 10.1016/j.ajhg.2013.11.019. Epub 2013 Dec 19.
Am J Hum Genet. 2014.
PMID: 24360808
Free PMC article.
Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: A dissociation of hippocampal Fos from seizure activity.
Kadiyala SB, Papandrea D, Tuz K, Anderson TM, Jayakumar S, Herron BJ, Ferland RJ.
Kadiyala SB, et al.
Epilepsy Res. 2015 Jan;109:183-96. doi: 10.1016/j.eplepsyres.2014.11.009. Epub 2014 Nov 22.
Epilepsy Res. 2015.
PMID: 25524858
Free PMC article.
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The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactions.
Tuz K, Hsiao YC, Juárez O, Shi B, Harmon EY, Phelps IG, Lennartz MR, Glass IA, Doherty D, Ferland RJ.
Tuz K, et al.
J Biol Chem. 2013 May 10;288(19):13676-94. doi: 10.1074/jbc.M112.420786. Epub 2013 Mar 26.
J Biol Chem. 2013.
PMID: 23532844
Free PMC article.
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