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Browsing by Author Rasko, John Edward

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Showing results 1 to 9 of 9

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

Author(s)Kowalczuk, Sonja; Broer, Angelika; Tietze, Nadine, et al
TypeJournal article
Date Published2008
Date Created-

Characterization of mouse amino acid transporter Boat1(slc6a19)

Author(s)Bohmer, Christoph; Broer, Angelika; Kingsland (previously Munzinger), Michael, et al
TypeJournal article
Date Published2005
Date Created-

Further Evidence for Allelic Heterogeneity in Hartnup Disorder

Author(s)Azmanov, Dimitar; Kowalczuk, Sonja; Rodgers, Helen, et al
TypeJournal article
Date Published2008
Date Created-

Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

Author(s)Seow, Heng; Broer, Stefan; Broer, Angelika, et al
TypeJournal article
Date Published2004
Date Created-

Molecular Cloning of Mouse Amino Acid Transport System B 0 , a Neutral Amino Acid Transporter Related to Hartnup Disorder

Author(s)Broer, Angelika; Klingel, Karen; Kowalczuk, Sonja, et al
TypeJournal article
Date Published2004
Date Created-

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

Author(s)Broer, Stefan; Cavanaugh, Juleen; Rasko, John Edward
TypeJournal article
Date Published2005
Date Created-

Persistence of the Common Hartnup disease D173N Allele in populations of European origin

Author(s)Azmanov, Dimitar; Rodgers, Helen; Auray-Blais, Christiane, et al
TypeJournal article
Date Published2007
Date Created-

Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria

Author(s)Vanslambrouck, Jessica M.; Broer, Angelika; Thavyogarajah, Thuvaraka, et al
TypeJournal article
Date Published2010
Date Created-

The molecular basis of neutral aminoacidurias

Author(s)Broer, Angelika; Cavanaugh, Juleen; Rasko, John Edward, et al
TypeJournal article
Date Published2006
Date Created-
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