Cystinuria: Defective Intestinal Transport of Dibasic Amino Acids and Cystine

Gelijkaardige items

• Transport of Neutral and Dibasic Amino Acids by Human Leukocytes: Absence of Defect in Cystinuria
  door: Rosenberg, Leon E., et al.
  Gepubliceerd in: (1965)
• Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease
  door: Groth, Ulrich, et al.
  Gepubliceerd in: (1972)
• Defective Uptake of Basic Amino Acids and l-Cystine by Intestinal Mucosa of Patients with Cystinuria
  door: McCarthy, C. F., et al.
  Gepubliceerd in: (1964)
• Dibasic amino acid transport: lessons from human disease.
  door: Thier, S. O.
  Gepubliceerd in: (1984)
• Luminal Heterodimeric Amino Acid Transporter Defective in Cystinuria
  door: Pfeiffer, Rahel, et al.
  Gepubliceerd in: (1999)