| 1 | SLC9A9
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| Differential expression of SLC9A9 and interacting molecules in the hippocampus of rat models for attention deficit/hyperactivity disorder.
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| Zhang-James Y, Middleton FA, Sagvolden T, Faraone SV.
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| Dev Neurosci 34(2-3):218-27. Epub 2012 Jul 6.
2012
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| 2 | SLC9A9
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| SLC9A9 mutations, gene expression, and protein-protein interactions in rat models of attention-deficit/hyperactivity disorder.
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| Zhang-James Y, DasBanerjee T, Sagvolden T, Middleton FA, Faraone SV.
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| Am J Med Genet B Neuropsychiatr Genet 156B(7):835-43. doi: 10.1002/ajmg.b.31229. Epub 2011 Aug 19.
2011
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| 3 | SLC9A9
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| Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.
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| Markunas CA, Quinn KS, Collins AL, Garrett ME, Lachiewicz AM, Sommer JL, Morrissey-Kane E, Kollins SH, Anastopoulos AD, Ashley-Koch AE.
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| Psychiatr Genet 20(2):73-81.
2010
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| 4 | RACK1, SLC9A9, SLC9A7, SLC9A6
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| Cell surface levels of organellar Na+/H+ exchanger isoform 6 are regulated by interaction with RACK1.
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| Ohgaki R, Fukura N, Matsushita M, Mitsui K, Kanazawa H.
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| J Biol Chem 283(7):4417-29. Epub 2007 Dec 5. 2008
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| 5 | AUTS16, CNTN3, DIPK2A, PCDH10, RNF8, SCN7A, SLC9A9
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| Identifying autism Loci and genes by tracing recent shared ancestry.
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| Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA.
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| Science 321(5886):218-23. 2008
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| 6 | SLC9A9
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| Four Na+/H+ exchanger isoforms are distributed to Golgi and post-Golgi compartments and are involved in organelle pH regulation.
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| Nakamura N, Tanaka S, Teko Y, Mitsui K, Kanazawa H.
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| J Biol Chem 280(2):1561-72. Epub 2004 Nov 2. 2005
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| 7 | DOCK3, MANF, SLC9A9
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| Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.
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| De Silva MG, Elliott K, Dahl HH, Fitzpatrick E, Wilcox S, Delatycki M, Williamson R, Efron D, Lynch M, Forrest S.
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| J Med Genet 40(10):733-740. 2003
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