Kowalczuk S - Search Results

1

Molecular cloning of the mouse IMINO system: an Na+- and Cl--dependent proline transporter.

Kowalczuk S, Bröer A, Munzinger M, Tietze N, Klingel K, Bröer S. Kowalczuk S, et al. Biochem J. 2005 Mar 15;386(Pt 3):417-22. doi: 10.1042/BJ20050100. Biochem J. 2005. PMID: 15689184 Free PMC article.

2

Molecular cloning of mouse amino acid transport system B0, a neutral amino acid transporter related to Hartnup disorder.

Bröer A, Klingel K, Kowalczuk S, Rasko JE, Cavanaugh J, Bröer S. Bröer A, et al. Among authors: kowalczuk s. J Biol Chem. 2004 Jun 4;279(23):24467-76. doi: 10.1074/jbc.M400904200. Epub 2004 Mar 25. J Biol Chem. 2004. PMID: 15044460 Free article.

3

Characterization of mouse amino acid transporter B0AT1 (slc6a19).

Böhmer C, Bröer A, Munzinger M, Kowalczuk S, Rasko JE, Lang F, Bröer S. Böhmer C, et al. Among authors: kowalczuk s. Biochem J. 2005 Aug 1;389(Pt 3):745-51. doi: 10.1042/BJ20050083. Biochem J. 2005. PMID: 15804236 Free PMC article.

4

The orphan transporter v7-3 (slc6a15) is a Na+-dependent neutral amino acid transporter (B0AT2).

Bröer A, Tietze N, Kowalczuk S, Chubb S, Munzinger M, Bak LK, Bröer S. Bröer A, et al. Among authors: kowalczuk s. Biochem J. 2006 Jan 1;393(Pt 1):421-30. doi: 10.1042/BJ20051273. Biochem J. 2006. PMID: 16185194 Free PMC article.

5

A protein complex in the brush-border membrane explains a Hartnup disorder allele.

Kowalczuk S, Bröer A, Tietze N, Vanslambrouck JM, Rasko JE, Bröer S. Kowalczuk S, et al. FASEB J. 2008 Aug;22(8):2880-7. doi: 10.1096/fj.08-107300. Epub 2008 Apr 18. FASEB J. 2008. PMID: 18424768

6

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.

Bröer S, Bailey CG, Kowalczuk S, Ng C, Vanslambrouck JM, Rodgers H, Auray-Blais C, Cavanaugh JA, Bröer A, Rasko JE. Bröer S, et al. Among authors: kowalczuk s. J Clin Invest. 2008 Dec;118(12):3881-92. doi: 10.1172/JCI36625. Epub 2008 Nov 6. J Clin Invest. 2008. PMID: 19033659 Free PMC article.

7

Further evidence for allelic heterogeneity in Hartnup disorder.

Azmanov DN, Kowalczuk S, Rodgers H, Auray-Blais C, Giguère R, Rasko JE, Bröer S, Cavanaugh JA. Azmanov DN, et al. Among authors: kowalczuk s. Hum Mutat. 2008 Oct;29(10):1217-21. doi: 10.1002/humu.20777. Hum Mutat. 2008. PMID: 18484095

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