Apical reabsorption of dibasic amino acids and cystine in kidney is mediated by the heteromeric amino acid antiporter rBAT/b0,+AT (system b0,+). Mutations in rBAT cause cystinuria type A, whereas mutations in b0,+AT cause cystinuria type B. b0,+AT is th
Durch Gen-Analysen und funktionelle Untersuchungen wurde für die Cystinurie Typ I das hrBAT-Protein ...
Cystinuria is an autosomal recessive disorder of the tubular and intestinal resorption of cystine, o...
Cystinuria is an autosomal recessive disease caused by mutations in SLC3A1 (rBAT) and SLC7A9 (b0,+AT...
The currently identified cDNA clones of mammalian amino acid transporters can be grouped into five d...
Mutations of the glycoprotein rBAT cause cystinuria type I, an autosomal recessive failure of dibasi...
The human rBAT protein elicits sodium-independent, high affinity obligatory exchange of cystine, dib...
Human cystinuria-related transporter: Localization and functional characterization.BackgroundCystinu...
Cystinuria is a genetic disorder characterized by overexcretion of dibasic amino acids and cystine, ...
Abstract Background Cystinuria is caused by the defective renal reabsorption of cystine and dibasic ...
Cystinuria type I: Identification of eight new mutations inSLC3A1.BackgroundCystinuria is a heritabl...
BACKGROUND: Cystinuria is a heritable disorder of amino acid transport characterized by the defectiv...
Cystinuria (OMIM 220100) is a common recessive disorder of renal reabsorption of cystine and dibasic...
BACKGROUND: The human amino acid transporter asc-1 (SLC7A10) exhibits substrate selectivity for smal...
Identification of five novel SLC3A1 (rBAT) gene mutations in Japanese cystinuria.BackgroundCystinuri...
The amino acid transporter asc-1 is not involved in cystinuria.BackgroundThe human amino acid transp...
Durch Gen-Analysen und funktionelle Untersuchungen wurde für die Cystinurie Typ I das hrBAT-Protein ...
Cystinuria is an autosomal recessive disorder of the tubular and intestinal resorption of cystine, o...
Cystinuria is an autosomal recessive disease caused by mutations in SLC3A1 (rBAT) and SLC7A9 (b0,+AT...
The currently identified cDNA clones of mammalian amino acid transporters can be grouped into five d...
Mutations of the glycoprotein rBAT cause cystinuria type I, an autosomal recessive failure of dibasi...
The human rBAT protein elicits sodium-independent, high affinity obligatory exchange of cystine, dib...
Human cystinuria-related transporter: Localization and functional characterization.BackgroundCystinu...
Cystinuria is a genetic disorder characterized by overexcretion of dibasic amino acids and cystine, ...
Abstract Background Cystinuria is caused by the defective renal reabsorption of cystine and dibasic ...
Cystinuria type I: Identification of eight new mutations inSLC3A1.BackgroundCystinuria is a heritabl...
BACKGROUND: Cystinuria is a heritable disorder of amino acid transport characterized by the defectiv...
Cystinuria (OMIM 220100) is a common recessive disorder of renal reabsorption of cystine and dibasic...
BACKGROUND: The human amino acid transporter asc-1 (SLC7A10) exhibits substrate selectivity for smal...
Identification of five novel SLC3A1 (rBAT) gene mutations in Japanese cystinuria.BackgroundCystinuri...
The amino acid transporter asc-1 is not involved in cystinuria.BackgroundThe human amino acid transp...
Durch Gen-Analysen und funktionelle Untersuchungen wurde für die Cystinurie Typ I das hrBAT-Protein ...
Cystinuria is an autosomal recessive disorder of the tubular and intestinal resorption of cystine, o...
Cystinuria is an autosomal recessive disease caused by mutations in SLC3A1 (rBAT) and SLC7A9 (b0,+AT...