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Items: 1 to 20 of 31

1.

Apical transporters for neutral amino acids: physiology and pathophysiology.

Bröer S.

Physiology (Bethesda). 2008 Apr;23:95-103. doi: 10.1152/physiol.00045.2007. Review.

2.
3.

Amino acid transport across mammalian intestinal and renal epithelia.

Bröer S.

Physiol Rev. 2008 Jan;88(1):249-86. doi: 10.1152/physrev.00018.2006. Review.

4.
5.

[Hartnup disorder: Pathogenesis, pathophysiology, and therapy].

Ohura T.

Nihon Rinsho. 2006 Feb;64 Suppl 2:541-4. Review. Japanese. No abstract available.

PMID:
16523951
6.

The molecular basis of neutral aminoacidurias.

Bröer A, Cavanaugh JA, Rasko JE, Bröer S.

Pflugers Arch. 2006 Jan;451(4):511-7. Epub 2005 Jul 29. Review.

PMID:
16052352
7.

The genetics of heteromeric amino acid transporters.

Palacín M, Nunes V, Font-Llitjós M, Jiménez-Vidal M, Fort J, Gasol E, Pineda M, Feliubadaló L, Chillarón J, Zorzano A.

Physiology (Bethesda). 2005 Apr;20:112-24. Review.

8.

The SLC6 orphans are forming a family of amino acid transporters.

Bröer S.

Neurochem Int. 2006 May-Jun;48(6-7):559-67. Epub 2006 Mar 15. Review.

PMID:
16540203
9.

Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder.

Bröer S, Cavanaugh JA, Rasko JE.

Biochem Soc Trans. 2005 Feb;33(Pt 1):233-6. Review.

PMID:
15667315
10.

Structure, function and regulation of glycine neurotransporters.

Aragón C, López-Corcuera B.

Eur J Pharmacol. 2003 Oct 31;479(1-3):249-62. Review.

PMID:
14612155
11.

Molecular characteristics of mammalian and insect amino acid transporters: implications for amino acid homeostasis.

Castagna M, Shayakul C, Trotti D, Sacchi VF, Harvey WR, Hediger MA.

J Exp Biol. 1997 Jan;200(Pt 2):269-86. Review.

12.

Novel mutation in SLC6A19 causing late-onset seizures in Hartnup disorder.

Cheon CK, Lee BH, Ko JM, Kim HJ, Yoo HW.

Pediatr Neurol. 2010 May;42(5):369-71. doi: 10.1016/j.pediatrneurol.2010.01.009. Review.

PMID:
20399395
13.

Lysinuric protein intolerance: mechanisms of pathophysiology.

Palacín M, Bertran J, Chillarón J, Estévez R, Zorzano A.

Mol Genet Metab. 2004 Apr;81 Suppl 1:S27-37. Review.

PMID:
15050971
14.

The SLC3 and SLC7 families of amino acid transporters.

Fotiadis D, Kanai Y, Palacín M.

Mol Aspects Med. 2013 Apr-Jun;34(2-3):139-58. doi: 10.1016/j.mam.2012.10.007. Review.

PMID:
23506863
15.

Aminoacidurias: Clinical and molecular aspects.

Camargo SM, Bockenhauer D, Kleta R.

Kidney Int. 2008 Apr;73(8):918-25. doi: 10.1038/sj.ki.5002790. Epub 2008 Jan 16. Review.

16.

Heteromeric amino acid transporters explain inherited aminoacidurias.

Palacín M, Bertran J, Zorzano A.

Curr Opin Nephrol Hypertens. 2000 Sep;9(5):547-53. Review.

PMID:
10990376
17.

Collectrin and ACE2 in renal and intestinal amino acid transport.

Singer D, Camargo SM.

Channels (Austin). 2011 Sep-Oct;5(5):410-23. doi: 10.4161/chan.5.5.16470. Epub 2011 Sep 1. Review.

PMID:
21814048
18.

The glutamate and neutral amino acid transporter family: physiological and pharmacological implications.

Kanai Y, Hediger MA.

Eur J Pharmacol. 2003 Oct 31;479(1-3):237-47. Review.

PMID:
14612154
19.

Recent advances in amino acid transporters and excitatory amino acid receptors.

Matthews JC, Anderson KJ.

Curr Opin Clin Nutr Metab Care. 2002 Jan;5(1):77-84. Review.

PMID:
11790954
20.

Inherited disorders of amino acid transport in relation to the kidney.

Buehler BA.

Ann Clin Lab Sci. 1981 May-Jun;11(3):274-8. Review.

PMID:
7018372

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