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Substrate recognition by the mammalian proton-dependent amino acid transporter PAT1.
Mol Membr Biol. 2003 Jul-Sep;20(3):261-9. doi: 10.1080/0968768031000100759.
Mol Membr Biol. 2003.
PMID: 12893527
Substrate specificity and transport mode of the proton-dependent amino acid transporter mPAT2.
Foltz M, Oechsler C, Boll M, Kottra G, Daniel H.
Foltz M, et al. Among authors: oechsler c.
Eur J Biochem. 2004 Aug;271(16):3340-7. doi: 10.1111/j.1432-1033.2004.04268.x.
Eur J Biochem. 2004.
PMID: 15291811
Free article.
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De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Tiziano FD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E; European Alternating Hemiplegia of Childhood (AHC) Genetics Consortium; Biobanca e Registro Clinico per l'Emiplegia Alternante (I.B.AHC) Consortium; European Network for Research on Alternating Hemiplegia (ENRAH) for Small and Medium-sized Enterpriese (SMEs) Consortium; Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L, Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Haan J, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, Neri G, Arzimanoglou A, van den Maagdenberg AM, Sisodiya SM, Mikati MA, Goldstein DB.
Heinzen EL, et al.
Nat Genet. 2012 Sep;44(9):1030-4. doi: 10.1038/ng.2358. Epub 2012 Jul 29.
Nat Genet. 2012.
PMID: 22842232
Free PMC article.
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Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults.
Panagiotakaki E, Gobbi G, Neville B, Ebinger F, Campistol J, Nevsímalová S, Laan L, Casaer P, Spiel G, Giannotta M, Fons C, Ninan M, Sange G, Schyns T, Vavassori R, Poncelin D; ENRAH Consortium; Arzimanoglou A.
Panagiotakaki E, et al.
Brain. 2010 Dec;133(Pt 12):3598-610. doi: 10.1093/brain/awq295. Epub 2010 Oct 24.
Brain. 2010.
PMID: 20974617
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