Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria

The position of an arginine residue influences substrate affinity and K+ coupling in the human glutamate transporter, EAAT1

(2010) Renae M. Ryan et al.   JOURNAL OF NEUROCHEMISTRY

A family-based association study of the glutamate transporter geneSLC1A1in obsessive-compulsive disorder in 378 families

(2009) Y.Y. Shugart et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Association of the Glutamate Transporter Gene SLC1A1 With Atypical Antipsychotics–Induced Obsessive-compulsive Symptoms

(2009) Jun Soo Kwon et al.   ARCHIVES OF GENERAL PSYCHIATRY

A Haplotype Containing Quantitative Trait Loci for SLC1A1 Gene Expression and Its Association With Obsessive-Compulsive Disorder

(2009) Jens R. Wendland et al.   ARCHIVES OF GENERAL PSYCHIATRY

Neuronal Transporters Regulate Glutamate Clearance, NMDA Receptor Activation, and Synaptic Plasticity in the Hippocampus

(2009) A. Scimemi et al.   JOURNAL OF NEUROSCIENCE

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

(2008) Sonja Kowalczuk et al.   FASEB JOURNAL

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

(2008) Stefan Bröer et al.   JOURNAL OF CLINICAL INVESTIGATION

Aminoacidurias: Clinical and molecular aspects

(2008) S.M.R. Camargo et al.   KIDNEY INTERNATIONAL

Amino Acid Transport Across Mammalian Intestinal and Renal Epithelia

(2008) Stefan Bröer   PHYSIOLOGICAL REVIEWS