4.5 Article

Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Gastroenterology & Hepatology

Tissue-Specific Amino Acid Transporter Partners ACE2 and Collectrin Differentially Interact With Hartnup Mutations

Simone M. R. Camargo et al.

GASTROENTEROLOGY (2009)

Article Biochemistry & Molecular Biology

Orphan Transporter SLC6A18 Is Renal Neutral Amino Acid Transporter B0AT3

Dustin Singer et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2009)

Article Biochemistry & Molecular Biology

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

Sonja Kowalczuk et al.

FASEB JOURNAL (2008)

Article Medicine, Research & Experimental

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

Stefan Broeer et al.

JOURNAL OF CLINICAL INVESTIGATION (2008)

Review Physiology

Amino acid transport across mammalian intestinal and renal epithelia

Stefan Broer

PHYSIOLOGICAL REVIEWS (2008)

Article Medicine, General & Internal

Prevalence of chronic kidney disease in the United States

Josef Coresh et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2007)

Article Biochemical Research Methods

Isolation of renal proximal tubular brush-border membranes

Juerg Biber et al.

NATURE PROTOCOLS (2007)

Article Multidisciplinary Sciences

Essential role for collectrin in renal amino acid transport

Ursula Danilczyk et al.

NATURE (2006)

Article Biochemistry & Molecular Biology

Characterization of a branched-chain amino-acid transporter SBAT1 (SLC6A15) that is expressed in human brain

H Takanaga et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)

Article Biochemistry & Molecular Biology

Molecular cloning of the mouse IMINO system:: an Na+- and Cl--dependent proline transporter

S Kowalczuk et al.

BIOCHEMICAL JOURNAL (2005)

Article Biochemistry & Molecular Biology

Identification of mammalian proline transporter SIT1 ( SLC6A20) with characteristics of classical system imino

H Takanaga et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2005)

Article Genetics & Heredity

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

R Kleta et al.

NATURE GENETICS (2004)

Article Biochemistry & Molecular Biology

Substrate specificity and transport mode of the proton-dependent amino acid transporter mPAT2

M Foltz et al.

EUROPEAN JOURNAL OF BIOCHEMISTRY (2004)

Article Biochemistry & Molecular Biology

Molecular cloning of mouse amino acid transport system B0, a neutral amino acid transporter related to Hartnup disorder

A Bröer et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2004)

Article Biotechnology & Applied Microbiology

A cluster of proton/amino acid transporter genes in the human and mouse genomes

M Boll et al.

GENOMICS (2003)

Article Biochemistry & Molecular Biology

Comparative human/murine sequence analysis of the common eliminated region 1 from human 3p21.3

H Kiss et al.

MAMMALIAN GENOME (2002)