4.5 Article

The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter

Related references

Note: Only part of the references are listed.
Review Biochemistry & Molecular Biology

The monocarboxylate transporter familyuStructure and functional characterization

Andrew P. Halestrap

IUBMB LIFE (2012)

Review Biochemistry & Molecular Biology

The monocarboxylate transporter familyuRole and regulation

Andrew P. Halestrap et al.

IUBMB LIFE (2012)

Article Endocrinology & Metabolism

Detection of variants in SLC6A8 and functional analysis of unclassified missense variants

Ofir T. Betsalel et al.

MOLECULAR GENETICS AND METABOLISM (2012)

Article Biochemistry & Molecular Biology

Creatine as an antioxidant

Piero Sestili et al.

AMINO ACIDS (2011)

Article Biochemistry & Molecular Biology

The creatine kinase system and pleiotropic effects of creatine

Theo Wallimann et al.

AMINO ACIDS (2011)

Article Biochemistry & Molecular Biology

ER stress modulates cellular metabolism

Xiaoli Wang et al.

BIOCHEMICAL JOURNAL (2011)

Article Urology & Nephrology

SGLT2 Mediates Glucose Reabsorption in the Early Proximal Tubule

Volker Vallon et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2011)

Article Endocrinology & Metabolism

Glutathione in the blood and cerebrospinal fluid: A study in healthy male volunteers

M. Samuelsson et al.

NEUROPEPTIDES (2011)

Review Biology

Homeostasis in the vertebrate lens: mechanisms of solute exchange

Ralf Dahm et al.

PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2011)

Article Ophthalmology

Juvenile Cataract-Associated Mutation of Solute Carrier SLC16A12 Impairs Trafficking of the Protein to the Plasma Membrane

John J. Castorino et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)

Review Clinical Neurology

Creatine and Creatine Deficiency Syndromes: Biochemical and Clinical Aspects

Fahmi Nasrallah et al.

PEDIATRIC NEUROLOGY (2010)

Article Physiology

Regulation of the creatine transporter by AMP-activated protein kinase in kidney epithelial cells

Hui Li et al.

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2010)

Article Ophthalmology

Alterations of the 5′Untranslated Region of SLC16A12 Lead to Age-Related Cataract

Jurian Zuercher et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)

Review Ophthalmology

On the mechanism of organelle degradation in the vertebrate lens

Steven Bassnett

EXPERIMENTAL EYE RESEARCH (2009)

Article Genetics & Heredity

Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria

Barbara Kloeckener-Gruissem et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Article Biochemistry & Molecular Biology

The solute carrier (SLC) complement of the human genome: Phylogenetic classification reveals four major families

Robert Fredriksson et al.

FEBS LETTERS (2008)

Review Pharmacology & Pharmacy

The SLC16 monocaboxylate transporter family

D. Meredith et al.

XENOBIOTICA (2008)

Article Ophthalmology

Juvenile cataract associated with microcornea and glucosuria: A new syndrome

K. Vandekerckhove et al.

KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE (2007)

Review Biochemistry & Molecular Biology

The lens circulation

Richard T. Mathias et al.

JOURNAL OF MEMBRANE BIOLOGY (2007)

Article Cell Biology

Basolateral aromatic amino acid transporter TAT1 (Slc16A10) functions as an efflux pathway

T Ramadan et al.

JOURNAL OF CELLULAR PHYSIOLOGY (2006)

Article Biochemistry & Molecular Biology

Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter

ECH Friesema et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Article Biochemistry & Molecular Biology

Inhibition of the mitochondrial permeability transition by creatine kinase substrates - Requirement for microcompartmentation

M Dolder et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Article Biochemistry & Molecular Biology

Functional cooperation of epithelial heteromeric amino acid transporters expressed in madin-darby canine kidney cells

C Bauch et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2003)

Article Endocrinology & Metabolism

X-linked creatine transporter defect: An overview

GS Salomons et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2003)

Article Biochemical Research Methods

Between-group analysis of microarray data

AC Culhane et al.

BIOINFORMATICS (2002)

Article Genetics & Heredity

X-linked creatine-transporter gene (SLC6A8) defect:: A new creatine-deficiency syndrome

GS Salomons et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2001)