Carsten A. Wagner

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

Robert Kleta, Elisa Romeo, Zorica Ristic et al. · Nature Genetics · 2004 · 308 citations · Full text

Mendelian Disorder, Genetic Disorder, Cause Hartnup Disorder +7

Tissue-Specific Amino Acid Transporter Partners ACE2 and Collectrin Differentially Interact With Hartnup Mutations

Simone M. R. Camargo, Dustin Singer, Victoria Makrides et al. · Gastroenterology · 2008 · 292 citations · Full text

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia

Karl P. Schlingmann, Justyna Ruminska, Martin Kaufmann et al. · Journal of the American Society of Nephrology · 2015 · 270 citations · Full text

Autosomal-recessive Mutations, Metabolic Disorder, Genetics +19

Essential role for collectrin in renal amino acid transport

Ursula Danilczyk, Renu Sarao, Christine Remy et al. · Nature · 2006 · 245 citations · Full text

Renal Function, Molecular Physiology, Essential Role +7

The Astroglial ASCT2 Amino Acid Transporter as a Mediator of Glutamine Efflux

Angelika Bröer, Neville Brookes, V. Ganapathy et al. · Journal of Neurochemistry · 1999 · 237 citations · Full text

Glutamine Efflux, Neurotransmitter, Cellular Neurobiology +19