Citations for
1ACE2, JAK2, SLC6A19, TMEM27
Stimulation of the amino acid transporter SLC6A19 by JAK2.
Bhavsar SK, Hosseinzadeh Z, Merches K, Gu S, Bröer S, Lang F.
Biochem Biophys Res Commun 414(3):456-61. Epub 2011 Sep 19. 2011
2SLC6A19
Impaired nutrient signaling and body weight control in a Na+ neutral amino acid cotransporter (Slc6a19)-deficient mouse.
Bröer A, Juelich T, Vanslambrouck JM, Tietze N, Solomon PS, Holst J, Bailey CG, Rasko JE, Bröer S.
J Biol Chem 286(30):26638-51. Epub 2011 Jun 2. 2011
3ACE2, SLC6A18, SLC6A19, TMEM27
Collectrin and ACE2 in renal and intestinal amino acid transport.
Singer D, Camargo SM.
Channels (Austin) 5(5):410-23. Epub 2011 Sep 1. Review. 2011
4HND, SLC6A19
Novel mutation in SLC6A19 causing late-onset seizures in Hartnup disorder.
Cheon CK, Lee BH, Ko JM, Kim HJ, Yoo HW.
Pediatr Neurol 42(5):369-71. Review. 2010
5SGK1, SGK2, SGK3, SLC6A19
The serum and glucocorticoid inducible kinases SGK1-3 stimulate the neutral amino acid transporter SLC6A19.
Böhmer C, Sopjani M, Klaus F, Lindner R, Laufer J, Jeyaraj S, Lang F, Palmada M.
Cell Physiol Biochem 25(6):723-32. doi: 10.1159/000315092. Epub 2010 May 18. 2010
6SLC6A19, SLC7A9
Transport characteristics of L-citrulline in renal apical membrane of proximal tubular cells.
Mitsuoka K, Shirasaka Y, Fukushi A, Sato M, Nakamura T, Nakanishi T, Tamai I.
Biopharm Drug Dispos 30(3):126-37.PMID: 19322909 2009
7ACE2, SLC6A19
Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations.
Camargo SM, Singer D, Makrides V, Huggel K, Pos KM, Wagner CA, Kuba K, Danilczyk U, Skovby F, Kleta R, Penninger JM, Verrey F.
Gastroenterology 136(3):872-82. Epub 2008 Oct 29. 2009
8SLC6A19
Minisatellite polymorphisms of the SLC6A19: susceptibility in hypertension.
Seol SY, Lee SY, Kim YD, Do EJ, Kwon JA, Kim SI, Chu IS, Leem SH.
Biochem Biophys Res Commun 374(4):714-9. Epub 2008 Jul 29. 2008
9SLC6A19
Steady-state kinetic characterization of the mouse B(0)AT1 sodium-dependent neutral amino acid transporter.
Camargo SM, Makrides V, Virkki LV, Forster IC, Verrey F.
Pflugers Arch 451(2):338-48. Epub 2005 Aug 26. 2005
10HND, SLC6A19
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
Kleta R, Romeo E, Ristic Z, Ohura T, Stuart C, Arcos-Burgos M, Dave MH, Wagner CA, Camargo SR, Inoue S, Matsuura N, Helip-Wooley A, Bockenhauer D, Warth R, Bernardini I, Visser G, Eggermann T, Lee P, Chairoungdua A, Jutabha P, Babu E, Nilwarangkoon S, Anzai N, Kanai Y, Verrey F, Gahl WA, Koizumi A.
Nat Genet 36(9):999-1002. Epub 2004 Aug 01. 2004
11SLC6A19, HND
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19.
Seow HF, Broer S, Broer A, Bailey CG, Potter SJ, Cavanaugh JA, Rasko JE.
Nat Genet 36(9):1003-7. Epub 2004 Aug 01. 2004