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SLC16A2 gene
Known as:
SLC16A2
, XPCT
, X-LINKED PEST-CONTAINING TRANSPORTER
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National Institutes of Health
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Related topics
Related topics
2 relations
SLC16A10 gene
SLC16A6 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis.
Steffen Mayerl
,
Julia Müller
,
+7 authors
H. Heuer
Journal of Clinical Investigation
2014
Corpus ID: 3331840
Allan-Herndon-Dudley syndrome (AHDS), a severe form of psychomotor retardation with abnormal thyroid hormone (TH) parameters, is…
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Highly Cited
2011
Highly Cited
2011
Developmental and cell type‐specific expression of thyroid hormone transporters in the mouse brain and in primary brain cells
Doreen Braun
,
A. Kinne
,
+5 authors
U. Schweizer
Glia
2011
Corpus ID: 30226019
Cellular thyroid hormone uptake and efflux are mediated by transmembrane transport proteins. One of these, monocarboxylate…
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Highly Cited
2010
Highly Cited
2010
Essential Molecular Determinants for Thyroid Hormone Transport and First Structural Implications for Monocarboxylate Transporter 8*
A. Kinne
,
G. Kleinau
,
+4 authors
U. Schweizer
Journal of Biological Chemistry
2010
Corpus ID: 205301324
Monocarboxylate transporter 8 (MCT8, SLC16A2) is a thyroid hormone (TH) transmembrane transport protein mutated in Allan-Herndon…
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Review
2009
Review
2009
Minireview: Pathophysiological importance of thyroid hormone transporters.
H. Heuer
,
T. Visser
Endocrinology
2009
Corpus ID: 20759774
Thyroid hormone metabolism and action are largely intracellular events that require transport of iodothyronines across the plasma…
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Highly Cited
2009
Highly Cited
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
E. Wirth
,
Stephan Roth
,
+14 authors
U. Schweizer
Journal of Neuroscience
2009
Corpus ID: 33337244
Thyroid hormone transport into cells requires plasma membrane transport proteins. Mutations in one of these, monocarboxylate…
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Highly Cited
2008
Highly Cited
2008
Possible mechanisms of thyroid hormone disruption in mice by BDE 47, a major polybrominated diphenyl ether congener.
V. Richardson
,
D. Staskal
,
D. Ross
,
J. Diliberto
,
M. DeVito
,
L. Birnbaum
Toxicology and Applied Pharmacology
2008
Corpus ID: 36431930
Highly Cited
2006
Highly Cited
2006
Thyroid hormone transport by the human monocarboxylate transporter 8 and its rate-limiting role in intracellular metabolism.
E. Friesema
,
G. Kuiper
,
J. Jansen
,
T. Visser
,
M. Kester
Molecular Endocrinology
2006
Corpus ID: 22829630
Cellular entry of thyroid hormone is mediated by plasma membrane transporters. We have identified rat monocarboxylate transporter…
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Highly Cited
2005
Highly Cited
2005
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.
C. Schwartz
,
M. May
,
+12 authors
R. Stevenson
American Journal of Human Genetics
2005
Corpus ID: 41082157
Allan-Herndon-Dudley syndrome was among the first of the X-linked mental retardation syndromes to be described (in 1944) and…
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Highly Cited
2005
Highly Cited
2005
The monocarboxylate transporter 8 linked to human psychomotor retardation is highly expressed in thyroid hormone-sensitive neuron populations.
H. Heuer
,
Michael Maier
,
+4 authors
K. Bauer
Endocrinology
2005
Corpus ID: 36697812
Recent genetic analysis in several patients presenting a severe form of X-linked psychomotor retardation combined with abnormal…
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Highly Cited
2004
Highly Cited
2004
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene.
A. Dumitrescu
,
X. Liao
,
T. B. Best
,
K. Brockmann
,
S. Refetoff
American Journal of Human Genetics
2004
Corpus ID: 12985288
Thyroid hormones are iodothyronines that control growth and development, as well as brain function and metabolism. Although…
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