Cystinuria: Defective Intestinal Transport of Dibasic Amino Acids and Cystine*
AUTOR(ES)
Thier, S. O.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=292494Documentos Relacionados
- Defective Uptake of Basic Amino Acids and l-Cystine by Intestinal Mucosa of Patients with Cystinuria *
- Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease
- Transport of Neutral and Dibasic Amino Acids by Human Leukocytes: Absence of Defect in Cystinuria*
- Expression cloning of a cDNA from rabbit kidney cortex that induces a single transport system for cystine and dibasic and neutral amino acids.
- INULIN AND ENDOGENOUS AMINO ACID RENAL CLEARANCES IN CYSTINURIA: EVIDENCE FOR TUBULAR SECRETION*