Amino Acid Transport Across Mammalian Intestinal and Renal Epithelia (original) (raw)
Apical Transporters for Neutral Amino Acids: Physiology and Pathophysiology
S. Bröer
Physiology, 2008
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Kidney amino acid transport
Tamara Ramadan
Pflugers Archiv-european Journal of Physiology, 2009
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Molecular Cloning of Mouse Amino Acid Transport System B0, a Neutral Amino Acid Transporter Related to Hartnup Disorder
Angelika Bröer
Journal of Biological Chemistry, 2004
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L-type amino acid transporters in two intestinal epithelial cell lines function as exchangers with neutral amino acids
Patricio Soares-da-Silva
The Journal of nutrition, 2002
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The genetics of heteromeric amino acid transporters
Joana Fort, Mariona Font-llitjós
Physiology (Bethesda, Md.), 2005
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Heteromeric amino acid transporters: biochemistry, genetics, and physiology
Alfonso Valencia
American Journal of Physiology-Renal Physiology, 2001
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The amino acid transport system bo,+ and cystinuria
M. Palacin
Molecular Membrane Biology, 2001
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Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder
Stefan Broer
Biochemical Society Transactions, 2005
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The role of amino acid transporters in inherited and acquired diseases
S. Bröer
Biochemical Journal, 2011
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Amino acid transport by small intestinal, hepatic, and pancreatic epithelia
Giovanni Mann
Gastroenterology, 1995
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Cellular transport in the regulation of amino acid metabolism
Mark Shotwell
Biochemical Society Transactions, 1986
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The regulation of neutral amino acid transport in mammalian cells
Mark Shotwell
Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1983
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Enzymatic influences on amino acid transport across the small intestine
Camille Nassar
Comparative biochemistry and physiology. A, Comparative physiology, 1989
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Regulation and Genetics of Amino Acid Transport
Mark Shotwell
Annals of the New York Academy of Sciences, 1985
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Expression cloning of a cDNA from rabbit kidney cortex that induces a single transport system for cystine and dibasic and neutral amino acids
Heini Murer
Proceedings of the National Academy of Sciences, 1992
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Solubilization and reconstitution of high-and low-affinity Na+-dependent neutral l-α-amino acid transporters from rabbit small intestine
Akihiko Moriyama
Biochimica et Biophysica Acta (BBA) - Biomembranes, 1993
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Complex subcellular distribution of sodium-dependent amino acid transport systems in kidney cortex and LLC-PK1/Cl4 cells
Austin Mircheff
Kidney International, 1994
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Characterization of the rat neutral and basic amino acid transporter utilizing anti-peptide antibodies
Ning Yan
Proceedings of the National Academy of Sciences, 1993
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Evidence for the transport of neutral as well as cationic amino acids by ATA3, a novel and liver-specific subtype of amino acid transport system A
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Biochimica et Biophysica Acta (BBA) - Biomembranes, 2001
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The molecular basis of neutral aminoacidurias
Angelika Bröer
Pflügers Archiv - European Journal of Physiology, 2005
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Obligatory Amino Acid Exchange via Systems bo,+-like and y+L-like. A TERTIARY ACTIVE TRANSPORT MECHANISM FOR RENAL REABSORPTION OF CYSTINE AND DIBASIC AMINO ACIDS
Raúl Estévez
Journal of Biological Chemistry, 1996
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Aminoaciduria and altered renal expression of luminal amino acid transporters in mice lacking novel gene collectrin
th le
AJP: Renal Physiology, 2006
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Multiple Pathways for Cationic Amino Acid Transport in Rat Seminiferous Tubule Cells
stefania de micheli
Biology of Reproduction, 2007
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Functional characterization, localization, and molecular identification of rabbit intestinal N-amino acid transporter
Prosenjit Saha
AJP: Gastrointestinal and Liver Physiology, 2008
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Identification and characterization of an amino acid transporter expressed differentially in liver
Llewelyn Roderick
Proceedings of the …, 2000
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Adaptation of plasma membrane amino acid transport mechanisms to physiological demands
Stefan Bröer
Pfl�gers Archiv European Journal of Physiology, 2002
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Differential cystine and dibasic amino acid handling after loss of function of the amino acid transporter b0,+AT (Slc7a9) in mice
virginia Nunes
American Journal of Physiology-Renal Physiology, 2013
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Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19
Heng Fong Seow
Nature Genetics, 2004
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