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。Genetics and phenomics of thyroid hormone transport by MCT8
Edith C. H. Friesema et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2010)
Pelizaeus-Merzbacher-Like Disease Presentation of MCT8 Mutated Male Subjects
Catherine Vaurs-Barriere et al.
ANNALS OF NEUROLOGY (2009)
Evidence for a Homodimeric Structure of Human Monocarboxylate Transporter 8
W. Edward Visser et al.
ENDOCRINOLOGY (2009)
Identification and Characterization of 3-Iodothyronamine Intracellular Transport
Alexandra G. Ianculescu et al.
ENDOCRINOLOGY (2009)
Minireview: 3-Iodothyronamine (T(1)AM): A New Player on the Thyroid Endocrine Team?
Thomas S. Scanlan
ENDOCRINOLOGY (2009)
A Thyroid Hormone Analog with Reduced Dependence on the Monocarboxylate Transporter 8 for Tissue Transport
Caterina Di Cosmo et al.
ENDOCRINOLOGY (2009)
Novel Pathogenic Mechanism Suggested by Ex Vivo Analysis of MCT8 (SLC16A2) Mutations
W. Edward Visser et al.
HUMAN MUTATION (2009)
Studies on the DIDS-binding Site of Monocarboxylate Transporter 1 Suggest a Homology Model of the Open Conformation and a Plausible Translocation Cycle
Marieangela C. Wilson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Surface translocation and tri-iodothyronine uptake of mutant MCT8 proteins are cell type-dependent
Anita Kinne et al.
JOURNAL OF MOLECULAR ENDOCRINOLOGY (2009)
Neuronal 3′,3,5-Triiodothyronine (T3) Uptake and Behavioral Phenotype of Mice Deficient in Mct8, the Neuronal T3 Transporter Mutated in Allan-Herndon-Dudley Syndrome
Eva K. Wirth et al.
JOURNAL OF NEUROSCIENCE (2009)
Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8
Jurgen Jansen et al.
ENDOCRINOLOGY (2008)
Thyronamines are isozyme-specific substrates of deiodinases
S. Piehl et al.
ENDOCRINOLOGY (2008)
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Think globally: Act locally New insights into the local regulation of thyroid hormone availability challenge long accepted dogmas
Ulrich Schweizer et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2008)
Effective cellular uptake and efflux of thyroid hormone by human monocarboxylate transporter 10
Edith C. H. Friesema et al.
MOLECULAR ENDOCRINOLOGY (2008)
A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay
Anastasios Papadimitriou et al.
PEDIATRICS (2008)
Development of a validated liquid chromatography/tandem mass spectrometry method for the distinction of thyronine and thyronamine constitutional isomers and for the identification of new deiodinase substrates
Susanne Piehl et al.
RAPID COMMUNICATIONS IN MASS SPECTROMETRY (2008)
Clustal W and clustal X version 2.0
M. A. Larkin et al.
BIOINFORMATICS (2007)
Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
Marija Trajkovic et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
The role of charged residues in the transmembrane helices of monocarboxylate transporter 1 and its ancillary protein basigin in determining plasma membrane expression and catalytic activity
Christine Manoharan et al.
MOLECULAR MEMBRANE BIOLOGY (2006)
Structural rearrangements in the thyroid hormone receptor hinge domain and their putative role in the receptor function
Alessandro S. Nascimento et al.
JOURNAL OF MOLECULAR BIOLOGY (2006)
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (Mct) 8-deficient mice
Alexandra M. Dumitrescu et al.
ENDOCRINOLOGY (2006)
Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8
H Biebermann et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2005)
Alternate pathways of thyroid hormone metabolism
SY Wu et al.
THYROID (2005)
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
CE Schwartz et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
The monocarboxylate transporter 8 linked to human psychomotor retardation is highly expressed in thyroid hormone-sensitive neuron populations
H Heuer et al.
ENDOCRINOLOGY (2005)
Molecular packing and packing defects in helical membrane proteins
PW Hildebrand et al.
BIOPHYSICAL JOURNAL (2005)
The SLC16 gene family -: from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond
AP Halestrap et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2004)
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
AM Dumitrescu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Predicting the three-dimensional structure of the human facilitative glucose transporter Glut1 by a novel evolutionary homology strategy: Insights on the molecular mechanism of substrate migration, and binding sites for glucose and inhibitory molecules
A Salas-Burgos et al.
BIOPHYSICAL JOURNAL (2004)
3-iodothyronamine is an endogenous and rapid-acting derivative of thyroid hormone
TS Scanlan et al.
NATURE MEDICINE (2004)
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
ECH Friesema et al.
LANCET (2004)
Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter
ECH Friesema et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Structure and mechanism of the glycerol-3-phosphate transporter from Escherichia coli
YF Huang et al.
SCIENCE (2003)
Thyroid hormone transport by the heterodimeric human system L amino acid transporter
ECH Friesema et al.
ENDOCRINOLOGY (2001)
Plasma membrane transport of thyroid hormones and its role in thyroid hormone metabolism and bioavailability
G Hennemann et al.
ENDOCRINE REVIEWS (2001)
Hormone selectivity in thyroid hormone receptors
RL Wagner et al.
MOLECULAR ENDOCRINOLOGY (2001)