-
1
-
-
33751550166
-
International Union of Pharmacology LIX the pharmacology and classification of the nuclear receptor superfamily: Thyroid hormone receptors
-
Flamant, F. et al. International Union of Pharmacology. LIX. The pharmacology and classification of the nuclear receptor superfamily: thyroid hormone receptors. Pharmacol. Rev. 58, 705-711 (2006
-
(2006)
Pharmacol. Rev
, vol.58
, pp. 705-711
-
-
Flamant, F.1
-
2
-
-
84921019737
-
A temporary compendium of thyroid hormone target genes in brain
-
Chatonnet, F., Flamant, F. & Morte, B. A temporary compendium of thyroid hormone target genes in brain. Biochim. Biophys. Acta 1849, 122-129 (2015
-
(2015)
Biochim. Biophys. Acta
, vol.1849
, pp. 122-129
-
-
Chatonnet, F.1
Flamant, F.2
Morte, B.3
-
3
-
-
84901202692
-
Nongenomic thyroid hormone signaling occurs through a plasma membrane-localized receptor
-
Kalyanaraman, H. et al. Nongenomic thyroid hormone signaling occurs through a plasma membrane-localized receptor. Sci. Signal. 7, ra48 (2014
-
(2014)
Sci. Signal
, vol.7
, pp. ra48
-
-
Kalyanaraman, H.1
-
4
-
-
84907042872
-
A rapid cytoplasmic mechanism for PI3 kinase regulation by the nuclear thyroid hormone receptor TRβ, and genetic evidence for its role in the maturation of mouse hippocampal synapses in vivo
-
Martin, N. P. et al. A rapid cytoplasmic mechanism for PI3 kinase regulation by the nuclear thyroid hormone receptor, TRβ, and genetic evidence for its role in the maturation of mouse hippocampal synapses in vivo. Endocrinology 155, 3713-3724 (2014
-
(2014)
Endocrinology
, vol.155
, pp. 3713-3724
-
-
Martin, N.P.1
-
5
-
-
41549094427
-
Mechanisms of nongenomic actions of thyroid hormone
-
Davis, P. J., Leonard, J. L. & Davis, F. B. Mechanisms of nongenomic actions of thyroid hormone. Front. Neuroendocrinol. 29, 211-218 (2008
-
(2008)
Front. Neuroendocrinol
, vol.29
, pp. 211-218
-
-
Davis, P.J.1
Leonard, J.L.2
Davis, F.B.3
-
6
-
-
77953639982
-
Molecular aspects of thyroid hormone actions
-
Cheng, S. Y., Leonard, J. L. & Davis, P. J. Molecular aspects of thyroid hormone actions. Endocr. Rev. 31, 139-170 (2010
-
(2010)
Endocr. Rev
, vol.31
, pp. 139-170
-
-
Cheng, S.Y.1
Leonard, J.L.2
Davis, P.J.3
-
7
-
-
0002552433
-
-
Thyroid Disease Manager (ed. DeGroot L. J.) [online]
-
Visser, T. J. & Peeters, R. P. Metabolism of Thyroid Hormone. Thyroid Disease Manager (ed. DeGroot, L. J.) [online], http: //www.thyroidmanager.org/chapter/metabolism-of-thyroid-hormone (2012
-
(2012)
Metabolism of Thyroid Hormone
-
-
Visser, T.J.1
Peeters, R.P.2
-
8
-
-
57349119069
-
Cellular and molecular basis of deiodinase-regulated thyroid hormone signaling
-
Gereben, B. et al. Cellular and molecular basis of deiodinase-regulated thyroid hormone signaling. Endocr. Rev. 29, 898-938 (2008
-
(2008)
Endocr. Rev
, vol.29
, pp. 898-938
-
-
Gereben, B.1
-
9
-
-
0000387731
-
-
ed. Wilson, J. D., Foster, D. W., Kronenberg, H. M. & Larsen, P. R. Saunders Co
-
Larsen, P. R., Davies, T. F. & Hay, I. D. in Williams Text Book of Endocrinology (ed. Wilson, J. D., Foster, D. W., Kronenberg, H. M. & Larsen, P. R.) 389-515 (Saunders Co, 1998
-
(1998)
Williams Text Book of Endocrinology
, pp. 389-515
-
-
Larsen, P.R.1
Davies, T.F.2
Hay, I.D.3
-
10
-
-
0034892914
-
Plasma membrane transport of thyroid hormones and its role in thyroid hormone metabolism and bioavailability
-
Hennemann, G. et al. Plasma membrane transport of thyroid hormones and its role in thyroid hormone metabolism and bioavailability. Endocr. Rev. 22, 451-476 (2001
-
(2001)
Endocr. Rev
, vol.22
, pp. 451-476
-
-
Hennemann, G.1
-
12
-
-
0347634343
-
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
-
Dumitrescu, A. M., Liao, X. H., Best, T. B., Brockmann, K. & Refetoff, S. A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene. Am. J. Hum. Genet. 74, 168-175 (2004
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 168-175
-
-
Dumitrescu, A.M.1
Liao, X.H.2
Best, T.B.3
Brockmann, K.4
Refetoff, S.5
-
13
-
-
5644276275
-
Association between mutations in a thyroid hormone transporter and severe X linked psychomotor retardation
-
Friesema, E. C. H. et al. Association between mutations in a thyroid hormone transporter and severe X linked psychomotor retardation. Lancet 364, 1435-1437 (2004
-
(2004)
Lancet
, vol.364
, pp. 1435-1437
-
-
Friesema, E.C.H.1
-
14
-
-
0028332347
-
A novel transmembrane transporter encoded by the XPCT gene in Xq13.2
-
Lafreni're, R. G., Carrel, L. & Willard, H. F. A novel transmembrane transporter encoded by the XPCT gene in Xq13.2. Hum. Mol. Genet. 3, 1133-1139 (1994
-
(1994)
Hum. Mol. Genet
, vol.3
, pp. 1133-1139
-
-
Lafreni're, R.G.1
Carrel, L.2
Willard, H.F.3
-
15
-
-
0141891099
-
Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter
-
Friesema, E. C. H. et al. Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter. J. Biol. Chem. 278, 40128-40135 (2003
-
(2003)
J. Biol. Chem
, vol.278
, pp. 40128-40135
-
-
Friesema, E.C.H.1
-
16
-
-
20444473155
-
Thyroid hormone transporters
-
Friesema, E. C. H., Jansen, J., Milici, C. & Visser, T. J. Thyroid hormone transporters. Vitam. Horm. 70, 137-167 (2005
-
(2005)
Vitam. Horm
, vol.70
, pp. 137-167
-
-
Friesema, E.C.H.1
Jansen, J.2
Milici, C.3
Visser, T.J.4
-
17
-
-
0028861989
-
Replacement therapy for hypothyroidism with thyroxine alone does not ensure euthyroidism in all tissues, as studied in thyroidectomized rats
-
Escobar-Morreale, H. F., Obregon, M. J., Escobar del Rey, F. & Morreale De Escobar, G. Replacement therapy for hypothyroidism with thyroxine alone does not ensure euthyroidism in all tissues, as studied in thyroidectomized rats. J. Clin. Invest. 96, 2828-2838 (1995
-
(1995)
J. Clin. Invest
, vol.96
, pp. 2828-2838
-
-
Escobar-Morreale, H.F.1
Obregon, M.J.2
Escobar Del Rey, F.3
Morreale, D.E.4
Escobar, G.5
-
18
-
-
0021996489
-
Stereospecific transport of triiodothyronine from plasma to cytosol and from cytosol to nucleus in rat liver, kidney, brain, and heart
-
Oppenheimer, J. H. & Schwartz, H. L. Stereospecific transport of triiodothyronine from plasma to cytosol and from cytosol to nucleus in rat liver, kidney, brain, and heart. J. Clin. Invest. 75, 147-154 (1985
-
(1985)
J. Clin. Invest
, vol.75
, pp. 147-154
-
-
Oppenheimer, J.H.1
Schwartz, H.L.2
-
19
-
-
33646355062
-
Thyroid function tests: Assay of thyroid hormones and related substances
-
ed. DeGroot L. J.) [online]
-
Spencer, C. A. Thyroid function tests: Assay of thyroid hormones and related substances. Thyroid Disease Manager (ed. DeGroot, L. J.) [online], http: //www.thyroidmanager.org/chapter/assay-of-thyroid-hormones-And-related-substances/ (2013
-
(2013)
Thyroid Disease Manager
-
-
Spencer, C.A.1
-
20
-
-
79961195158
-
Primary and secondary thyroid hormone transporters
-
Kinne, A., Schülein, R. & Krause, G. Primary and secondary thyroid hormone transporters. Thyroid Res. 4 (Suppl. 1), S7 (2011
-
(2011)
Thyroid Res
, vol.4
, pp. S7
-
-
Kinne, A.1
Schülein, R.2
Krause, G.3
-
21
-
-
84906901689
-
An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex
-
Zhang, Y. et al. An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex. J. Neurosci. 34, 11929-11947 (2014
-
(2014)
J. Neurosci
, vol.34
, pp. 11929-11947
-
-
Zhang, Y.1
-
22
-
-
84855444042
-
The monocarboxylate transporter family--structure and functional characterization
-
Halestrap, A. P. The monocarboxylate transporter family--structure and functional characterization. IUBMB Life 64, 1-9 (2012
-
(2012)
IUBMB Life
, vol.64
, pp. 1-9
-
-
Halestrap, A.P.1
-
23
-
-
44649089035
-
Effective cellular uptake and efflux of thyroid hormone by human monocarboxylate transporter 10
-
Friesema, E. C. H. et al. Effective cellular uptake and efflux of thyroid hormone by human monocarboxylate transporter 10. Mol. Endocrinol. 22, 1357-1369 (2008
-
(2008)
Mol. Endocrinol
, vol.22
, pp. 1357-1369
-
-
Friesema, E.C.H.1
-
24
-
-
15444378008
-
The monocarboxylate transporter 8 linked to human psychomotor retardation is highly expressed in thyroid hormone-sensitive neuron populations
-
Heuer, H. et al. The monocarboxylate transporter 8 linked to human psychomotor retardation is highly expressed in thyroid hormone-sensitive neuron populations. Endocrinology 146, 1701-1706 (2005
-
(2005)
Endocrinology
, vol.146
, pp. 1701-1706
-
-
Heuer, H.1
-
25
-
-
68049138998
-
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
-
Wirth, E. K. et al. 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. J. Neurosci. 29, 9439-9449 (2009
-
(2009)
J. Neurosci
, vol.29
, pp. 9439-9449
-
-
Wirth, E.K.1
-
26
-
-
57349180438
-
Expression of the thyroid hormone transporters monocarboxylate transporter 8 (SLC16A2) and organic ion transporter 14 (SLCO1C1) at the blood-brain barrier
-
Roberts, L. M. et al. Expression of the thyroid hormone transporters monocarboxylate transporter 8 (SLC16A2) and organic ion transporter 14 (SLCO1C1) at the blood-brain barrier. Endocrinology 149, 6251-6261 (2008
-
(2008)
Endocrinology
, vol.149
, pp. 6251-6261
-
-
Roberts, L.M.1
-
27
-
-
78951470785
-
Developmental and cell type-specific expression of thyroid hormone transporters in the mouse brain and in primary brain cells
-
Braun, D. et al. Developmental and cell type-specific expression of thyroid hormone transporters in the mouse brain and in primary brain cells. Glia 59, 463-471 (2011
-
(2011)
Glia
, vol.59
, pp. 463-471
-
-
Braun, D.1
-
28
-
-
84905444529
-
Expression pattern of thyroid hormone transporters in the postnatal mouse brain
-
Müller, J. & Heuer, H. Expression pattern of thyroid hormone transporters in the postnatal mouse brain. Front. Endocrinol. (Lausanne) 5, 92 (2014
-
(2014)
Front. Endocrinol. (Lausanne)
, vol.5
, pp. 92
-
-
Müller, J.1
Heuer, H.2
-
29
-
-
84891854345
-
Sodium-dependent bile salt transporters of the SLC10A transporter family: More than solute transporters
-
Anwer, M. S. & Stieger, B. Sodium-dependent bile salt transporters of the SLC10A transporter family: more than solute transporters. Pflugers Arch. 466, 77-89 (2014
-
(2014)
Pflugers Arch
, vol.466
, pp. 77-89
-
-
Anwer, M.S.1
Stieger, B.2
-
30
-
-
71849113110
-
Study of the transport of thyroid hormone by transporters of the SLC10 family
-
Visser, W. E. et al. Study of the transport of thyroid hormone by transporters of the SLC10 family. Mol. Cell. Endocrinol. 315, 138-145 (2010
-
(2010)
Mol. Cell. Endocrinol
, vol.315
, pp. 138-145
-
-
Visser, W.E.1
-
31
-
-
0032744038
-
Thyroid hormone transport by 4F2hc-IU12 heterodimers expressed in Xenopus oocytes
-
Ritchie, J. W., Peter, G. J., Shi, Y. B. & Taylor, P. M. Thyroid hormone transport by 4F2hc-IU12 heterodimers expressed in Xenopus oocytes. J. Endocrinol. 163, R5-R9 (1999
-
(1999)
J. Endocrinol
, vol.163
, pp. R5-R9
-
-
Ritchie, J.W.1
Peter, G.J.2
Shi, Y.B.3
Taylor, P.M.4
-
32
-
-
0034801886
-
Thyroid hormone transport by the heterodimeric human system L amino acid transporter
-
Friesema, E. C. et al. Thyroid hormone transport by the heterodimeric human system L amino acid transporter. Endocrinology 142, 4339-4348 (2001
-
(2001)
Endocrinology
, vol.142
, pp. 4339-4348
-
-
Friesema, E.C.1
-
33
-
-
58149158070
-
Establishment and characterization of mammalian cell lines stably expressing human L type amino acid transporters
-
Morimoto, E. et al. Establishment and characterization of mammalian cell lines stably expressing human L type amino acid transporters. J. Pharmacol. Sci. 108, 505-516 (2008
-
(2008)
J. Pharmacol. Sci
, vol.108
, pp. 505-516
-
-
Morimoto, E.1
-
34
-
-
13044258426
-
Selective expression of the large neutral amino acid transporter at the blood-brain barrier
-
Boado, R. J., Li, J. Y., Nagaya, M., Zhang, C. & Pardridge, W. M. Selective expression of the large neutral amino acid transporter at the blood-brain barrier. Proc. Natl Acad. Sci. USA 96, 12079-12084 (1999
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 12079-12084
-
-
Boado, R.J.1
Li, J.Y.2
Nagaya, M.3
Zhang, C.4
Pardridge, W.M.5
-
35
-
-
84901283686
-
Cerebral cortex hyperthyroidism of newborn Mct8-deficient mice transiently suppressed by Lat2 inactivation
-
Núñez, B. et al. Cerebral cortex hyperthyroidism of newborn Mct8-deficient mice transiently suppressed by Lat2 inactivation. PLoS ONE 9, e96915 (2014
-
(2014)
PLoS ONE
, vol.9
, pp. e96915
-
-
Núñez, B.1
-
36
-
-
0037427972
-
The superfamily of organic anion transporting polypeptides
-
Hagenbuch, B. & Meier, P. J. The superfamily of organic anion transporting polypeptides. Biochim. Biophys. Acta 1609, 1-18 (2003
-
(2003)
Biochim. Biophys. Acta
, vol.1609
, pp. 1-18
-
-
Hagenbuch, B.1
Meier, P.J.2
-
37
-
-
1242272736
-
Organic anion transporting polypeptides of the OATP/ SLC21 family: Phylogenetic classification as OATP/ SLCO superfamily, new nomenclature and molecular/functional properties
-
Hagenbuch, B. & Meier, P. J. Organic anion transporting polypeptides of the OATP/ SLC21 family: phylogenetic classification as OATP/ SLCO superfamily, new nomenclature and molecular/functional properties. Pflugers Arch. 447, 653-665 (2004
-
(2004)
Pflugers Arch
, vol.447
, pp. 653-665
-
-
Hagenbuch, B.1
Meier, P.J.2
-
38
-
-
84855869661
-
The expression and function of organic anion transporting polypeptides in normal tissues and in cancer
-
Obaidat, A., Roth, M. & Hagenbuch, B. The expression and function of organic anion transporting polypeptides in normal tissues and in cancer. Annu. Rev. Pharmacol. Toxicol. 52, 135-151 (2012
-
(2012)
Annu. Rev. Pharmacol. Toxicol
, vol.52
, pp. 135-151
-
-
Obaidat, A.1
Roth, M.2
Hagenbuch, B.3
-
39
-
-
34249981138
-
Cellular entry of thyroid hormones by organic anion transporting polypeptides
-
Hagenbuch, B. Cellular entry of thyroid hormones by organic anion transporting polypeptides. Best Pract. Res. Clin. Endocrinol. Metab. 21, 209-221 (2007
-
(2007)
Best Pract. Res. Clin. Endocrinol. Metab
, vol.21
, pp. 209-221
-
-
Hagenbuch, B.1
-
40
-
-
78650916392
-
Minireview: Thyroid hormone transporters: The knowns and the unknowns
-
Visser, W. E., Friesema, E. C. H. & Visser, T. J. Minireview: thyroid hormone transporters: the knowns and the unknowns. Mol. Endocrinol. 25, 1-14 (2011
-
(2011)
Mol. Endocrinol
, vol.25
, pp. 1-14
-
-
Visser, W.E.1
Friesema, E.C.H.2
Visser, T.J.3
-
41
-
-
15444342300
-
Molecular characterization and tissue distribution of a new organic anion transporter subtype (Oatp3) that transports thyroid hormones and taurocholate and comparison with Oatp2
-
Abe, T. et al. Molecular characterization and tissue distribution of a new organic anion transporter subtype (Oatp3) that transports thyroid hormones and taurocholate and comparison with Oatp2. J. Biol. Chem. 273, 22395-22401 (1998
-
(1998)
J. Biol. Chem
, vol.273
, pp. 22395-22401
-
-
Abe, T.1
-
42
-
-
0036793106
-
Identification of a novel human organic anion transporting polypeptide as a high affinity thyroxine transporter
-
Pizzagalli, F. et al. Identification of a novel human organic anion transporting polypeptide as a high affinity thyroxine transporter. Mol. Endocrinol. 16, 2283-2296 (2002
-
(2002)
Mol. Endocrinol
, vol.16
, pp. 2283-2296
-
-
Pizzagalli, F.1
-
43
-
-
0242384851
-
Functional characterization of rat brain-specific organic anion transporter (Oatp14) at the blood-brain barrier: High affinity transporter for thyroxine
-
Sugiyama, D. et al. Functional characterization of rat brain-specific organic anion transporter (Oatp14) at the blood-brain barrier: high affinity transporter for thyroxine. J. Biol. Chem. 278, 43489-43495 (2003
-
(2003)
J. Biol. Chem
, vol.278
, pp. 43489-43495
-
-
Sugiyama, D.1
-
44
-
-
33847069574
-
Characterization of two splice variants of human organic anion transporting polypeptide 3A1 isolated from human brain
-
Huber, R. D. et al. Characterization of two splice variants of human organic anion transporting polypeptide 3A1 isolated from human brain. Am. J. Physiol. Cell Physiol. 292, C795-C806 (2007
-
(2007)
Am. J. Physiol. Cell Physiol
, vol.292
, pp. C795-C806
-
-
Huber, R.D.1
-
45
-
-
65249143403
-
Mechanisms of pH-gradient driven transport mediated by organic anion polypeptide transporters
-
Leuthold, S. et al. Mechanisms of pH-gradient driven transport mediated by organic anion polypeptide transporters. Am. J. Physiol. Cell Physiol. 296, C570-C582 (2009
-
(2009)
Am. J. Physiol. Cell Physiol
, vol.296
, pp. C570-C582
-
-
Leuthold, S.1
-
46
-
-
0000033737
-
Some examples of the inheritance of mental deficiency: Apparently sex-linked iodicy and microcephaly
-
Allan, W., Herndon, C. N. & Dudley, F. L. Some examples of the inheritance of mental deficiency: apparently sex-linked iodicy and microcephaly. Am. J. Ment. Defic. 48, 325-334 (1944
-
(1944)
Am. J. Ment. Defic
, vol.48
, pp. 325-334
-
-
Allan, W.1
Herndon, C.N.2
Dudley, F.L.3
-
47
-
-
28044454499
-
X linked MCT8 gene mutations: Characterization of the pediatric neurologic phenotype
-
Holden, K R. et al. X linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J. Child Neurol. 20, 852-857 (2005
-
(2005)
J. Child Neurol
, vol.20
, pp. 852-857
-
-
Holden, K.R.1
-
48
-
-
20544454120
-
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
-
Schwartz, C. E. et al. Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene. Am. J. Hum. Genet. 77, 41-53 (2005
-
(2005)
Am. J. Hum. Genet
, vol.77
, pp. 41-53
-
-
Schwartz, C.E.1
-
50
-
-
38049038812
-
A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay
-
Papadimitriou, A. et al. A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay. Pediatrics 121, e199-e202 (2008
-
(2008)
Pediatrics
, vol.121
, pp. e199-e202
-
-
Papadimitriou, A.1
-
51
-
-
26244446806
-
Extended clinical phenotype, endocrine investigations and functional studies of a loss of function mutation A150V in the thyroid hormone specific transporter MCT8
-
Biebermann, H. et al. Extended clinical phenotype, endocrine investigations and functional studies of a loss of function mutation A150V in the thyroid hormone specific transporter MCT8. Eur. J. Endocrinol. 153, 359-366 (2005
-
(2005)
Eur. J. Endocrinol
, vol.153
, pp. 359-366
-
-
Biebermann, H.1
-
52
-
-
84875910280
-
Allan-Herndon-Dudley syndrome (AHDS) in two consecutive generations caused by a missense MCT8 gene mutation Phenotypic variability with the presence of normal serum T3 levels
-
Boccone, L., Dess', V., Meloni, A. & Loudianos, G. Allan-Herndon-Dudley syndrome (AHDS) in two consecutive generations caused by a missense MCT8 gene mutation. Phenotypic variability with the presence of normal serum T3 levels. Eur. J. Med. Genet. 56, 207-210 (2013
-
(2013)
Eur. J. Med. Genet
, vol.56
, pp. 207-210
-
-
Boccone, L.1
Dess, V.2
Meloni, A.3
Loudianos, G.4
-
53
-
-
33845237318
-
Unexpected peripheral markers of thyroid function in a patient with a novel mutation of the MCT8 thyroid hormone transporter gene
-
Herzovich, V. et al. Unexpected peripheral markers of thyroid function in a patient with a novel mutation of the MCT8 thyroid hormone transporter gene. Horm. Res. 67, 1-6 (2007
-
(2007)
Horm. Res
, vol.67
, pp. 1-6
-
-
Herzovich, V.1
-
54
-
-
26844513342
-
A novel mutation in the monocarboxylate transporter 8 gene in a boy with putamen lesions and low free T4 levels in cerebrospinal fluid
-
Kakinuma, H., Itoh, M. & Takahashi, H. A novel mutation in the monocarboxylate transporter 8 gene in a boy with putamen lesions and low free T4 levels in cerebrospinal fluid. J. Pediatr. 147, 552-554 (2005
-
(2005)
J. Pediatr
, vol.147
, pp. 552-554
-
-
Kakinuma, H.1
Itoh, M.2
Takahashi, H.3
-
55
-
-
44349154242
-
Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter
-
Namba, N. et al. Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter. Eur. J. Pediatr. 167, 785-791 (2008
-
(2008)
Eur. J. Pediatr
, vol.167
, pp. 785-791
-
-
Namba, N.1
-
56
-
-
33747590148
-
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (Mct) 8 deficient mice
-
Dumitrescu, A. M., Liao, X. H., Weiss, R. E., Millen, K. & Refetoff, S. Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (Mct) 8 deficient mice. Endocrinology 147, 4036-4043 (2006
-
(2006)
Endocrinology
, vol.147
, pp. 4036-4043
-
-
Dumitrescu, A.M.1
Liao, X.H.2
Weiss, R.E.3
Millen, K.4
Refetoff, S.5
-
57
-
-
33847400151
-
Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
-
Trajkovic-Arsic, M. et al. Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8. J. Clin. Invest. 117, 627-635 (2007
-
(2007)
J. Clin. Invest
, vol.117
, pp. 627-635
-
-
Trajkovic-Arsic, M.1
-
58
-
-
79951883954
-
Distinct roles of deiodinases on the phenotype of Mct8 defect: A comparison of eight different mouse genotypes
-
Liao, X. H. et al. Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes. Endocrinology 152, 1180-1191 (2011
-
(2011)
Endocrinology
, vol.152
, pp. 1180-1191
-
-
Liao, X.H.1
-
59
-
-
77956379884
-
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion
-
Di Cosmo, C. et al. Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion. J. Clin. Invest. 120, 3377-3388 (2010
-
(2010)
J. Clin. Invest
, vol.120
, pp. 3377-3388
-
-
Di Cosmo, C.1
-
60
-
-
77957284457
-
Impact of monocarboxylate transporter 8 deficiency on the hypothalamus pituitary thyroid axis in mice
-
Trajkovic-Arsic, M. et al. Impact of monocarboxylate transporter 8 deficiency on the hypothalamus pituitary thyroid axis in mice. Endocrinology 151, 5053-5062 (2010
-
(2010)
Endocrinology
, vol.151
, pp. 5053-5062
-
-
Trajkovic-Arsic, M.1
-
61
-
-
80053482206
-
Monocarboxylate transporter 8 deficiency: Altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomy
-
Wirth, E. K. et al. Monocarboxylate transporter 8 deficiency: altered thyroid morphology and persistent high triiodothyronine/thyroxine ratio after thyroidectomy. Eur. J. Endocrinol. 165, 555-561 (2011
-
(2011)
Eur. J. Endocrinol
, vol.165
, pp. 555-561
-
-
Wirth, E.K.1
-
62
-
-
84871675603
-
Deiodinase activities in thyroids and tissues of iodine-deficient female rats
-
Lavado-Autric, R., Calvo, R. M., De Mena, R. M., De Escobar, G. M. & Obregón, M. J. Deiodinase activities in thyroids and tissues of iodine-deficient female rats. Endocrinology 154, 529-536 (2013
-
(2013)
Endocrinology
, vol.154
, pp. 529-536
-
-
Lavado-Autric, R.1
Calvo, R.M.2
De Mena, R.M.3
De Escobar, G.M.4
Obregón, M.J.5
-
63
-
-
84891418244
-
Tissue-specific alterations in thyroid hormone homeostasis in combined Mct10 and Mct8 deficiency
-
Müller, J. et al. Tissue-specific alterations in thyroid hormone homeostasis in combined Mct10 and Mct8 deficiency. Endocrinology 155, 315-325 (2014
-
(2014)
Endocrinology
, vol.155
, pp. 315-325
-
-
Müller, J.1
-
64
-
-
0033602853
-
Regulation of thyroid hormone metabolism during fetal development
-
Darras, V. M., Hume, R. & Visser, T. J. Regulation of thyroid hormone metabolism during fetal development. Mol. Cell. Endocrinol. 151, 37-47 (1999
-
(1999)
Mol. Cell. Endocrinol
, vol.151
, pp. 37-47
-
-
Darras, V.M.1
Hume, R.2
Visser, T.J.3
-
65
-
-
74949127411
-
Consequences of monocarboxylate transporter 8 deficiency for renal transport and metabolism of thyroid hormones in mice
-
Trajkovic-Arsic, M. et al. Consequences of monocarboxylate transporter 8 deficiency for renal transport and metabolism of thyroid hormones in mice. Endocrinology 151, 802-809 (2010
-
(2010)
Endocrinology
, vol.151
, pp. 802-809
-
-
Trajkovic-Arsic, M.1
-
66
-
-
84888216297
-
Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels
-
Di Cosmo, C. et al. Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels. Endocrinology 154, 4885-4895 (2013
-
(2013)
Endocrinology
, vol.154
, pp. 4885-4895
-
-
Di Cosmo, C.1
-
67
-
-
84864381327
-
Monocarboxylate transporter 10 functions as a thyroid hormone transporter in chondrocytes
-
Abe, S., Abe, M., Fujiwara, M., Aikawa, T. & Kogo, M. Monocarboxylate transporter 10 functions as a thyroid hormone transporter in chondrocytes. Endocrinology 153, 4049-4058 (2012
-
(2012)
Endocrinology
, vol.153
, pp. 4049-4058
-
-
Abe, S.1
Abe, M.2
Fujiwara, M.3
Aikawa, T.4
Kogo, M.5
-
68
-
-
84879310018
-
Changes in thyroid status during perinatal development of Mct8-deficient male mice
-
Ferrara, A. M. et al. Changes in thyroid status during perinatal development of Mct8-deficient male mice. Endocrinology 154, 2533-2541 (2013
-
(2013)
Endocrinology
, vol.154
, pp. 2533-2541
-
-
Ferrara, A.M.1
-
69
-
-
32444438623
-
Type 3 deiodinase is critical for the maturation and function of the thyroid axis
-
Hernandez, A., Martinez, M. E., Fiering, S., Galton, V. A. & St Germain, D. Type 3 deiodinase is critical for the maturation and function of the thyroid axis. J. Clin. Invest. 116, 476-484 (2006
-
(2006)
J. Clin. Invest
, vol.116
, pp. 476-484
-
-
Hernandez, A.1
Martinez, M.E.2
Fiering, S.3
Galton, V.A.4
St Germain, D.5
-
70
-
-
34249984656
-
Syndromes of reduced sensitivity to thyroid hormone: Genetic defects in hormone receptors, cell transporters and deiodination
-
Refetoff, S. & Dumitrescu, A. M. Syndromes of reduced sensitivity to thyroid hormone: genetic defects in hormone receptors, cell transporters and deiodination. Best Pract. Res. Clin. Endocrinol. Metab. 21, 277-305 (2007
-
(2007)
Best Pract. Res. Clin. Endocrinol. Metab
, vol.21
, pp. 277-305
-
-
Refetoff, S.1
Dumitrescu, A.M.2
-
71
-
-
78349304919
-
Allan-Herndon-Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH
-
Boccone, L. et al. Allan-Herndon-Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH. Eur. J. Med. Genet. 53, 392-395 (2010
-
(2010)
Eur. J. Med. Genet
, vol.53
, pp. 392-395
-
-
Boccone, L.1
-
72
-
-
69249115321
-
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport
-
Di Cosmo, C., Liao, X. H., Dumitrescu, A. M., Weiss, R. E. & Refetoff, S. A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport. Endocrinology 150, 4450-4458 (2009
-
(2009)
Endocrinology
, vol.150
, pp. 4450-4458
-
-
Di Cosmo, C.1
Liao, X.H.2
Dumitrescu, A.M.3
Weiss, R.E.4
Refetoff, S.5
-
73
-
-
84897395869
-
Central regulation of hypothalamic pituitary thyroid axis under physiological and pathophysiological conditions
-
Fekete, C. & Lechan, R. M. Central regulation of hypothalamic pituitary thyroid axis under physiological and pathophysiological conditions. Endocr. Rev. 35, 159-194 (2014
-
(2014)
Endocr. Rev.
, vol.35
, pp. 159-194
-
-
Fekete, C.1
Lechan, R.M.2
-
74
-
-
33645217485
-
Novel neuroanatomical pathways for thyroid hormone action in the human anterior pituitary
-
Alkemade, A. et al. Novel neuroanatomical pathways for thyroid hormone action in the human anterior pituitary. Eur. J. Endocrinol. 154, 491-500 (2006
-
(2006)
Eur. J. Endocrinol
, vol.154
, pp. 491-500
-
-
Alkemade, A.1
-
75
-
-
0018650290
-
Carrier-mediated transport of thyroid hormones through the rat blood-brain barrier: Primary role of albumin-bound hormone
-
Pardridge, W. M. Carrier-mediated transport of thyroid hormones through the rat blood-brain barrier: primary role of albumin-bound hormone. Endocrinology 105, 605-612 (1979
-
(1979)
Endocrinology
, vol.105
, pp. 605-612
-
-
Pardridge, W.M.1
-
76
-
-
66449128624
-
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3, 5, 3' triiodo L-thyronine
-
Ceballos, A. et al. Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3, 5, 3' triiodo L-thyronine. Endocrinology 150, 2491-2496 (2009
-
(2009)
Endocrinology
, vol.150
, pp. 2491-2496
-
-
Ceballos, A.1
-
77
-
-
19944426059
-
Thyroxine-thyroid hormone receptor interactions
-
Sandler, B. et al. Thyroxine-thyroid hormone receptor interactions. J. Biol. Chem. 279, 55801-55808 (2004
-
(2004)
J. Biol. Chem
, vol.279
, pp. 55801-55808
-
-
Sandler, B.1
-
78
-
-
0030928654
-
The type 2 iodothyronine deiodinase is expressed primarily in glial cells in the neonatal rat brain
-
Guadaño-Ferraz, A., Obregon, M. J., St Germain, D. L. & Bernal, J. The type 2 iodothyronine deiodinase is expressed primarily in glial cells in the neonatal rat brain. Proc. Natl Acad. Sci. USA 94, 10391-10396 (1997
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 10391-10396
-
-
Guadaño-Ferraz, A.1
Obregon, M.J.2
St Germain, D.L.3
Bernal, J.4
-
79
-
-
77953158522
-
Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: A study in monocarboxylate transporter 8 and deiodinase 2 deficient mice
-
Morte, B. et al. Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter 8 and deiodinase 2 deficient mice. Endocrinology 151, 2381-2387 (2010
-
(2010)
Endocrinology
, vol.151
, pp. 2381-2387
-
-
Morte, B.1
-
80
-
-
84899760743
-
Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis 1987-2014
-
Mayerl, S. et al. Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis. J. Clin. Invest. 124, 1987-1999 (2014
-
(1999)
J. Clin. Invest
, vol.124
-
-
Mayerl, S.1
-
81
-
-
84857433358
-
Impact of Oatp1c1 deficiency on thyroid hormone metabolism and action in the mouse brain
-
Mayerl, S., Visser, T. J., Darras, V. M., Horn, S. & Heuer, H. Impact of Oatp1c1 deficiency on thyroid hormone metabolism and action in the mouse brain. Endocrinology 153, 1528-1537 (2012).
-
(2012)
Endocrinology
, vol.153
, pp. 1528-1537
-
-
Mayerl, S.1
Visser, T.J.2
Darras, V.M.3
Horn, S.4
Heuer, H.5
-
82
-
-
79953718797
-
Quantitative membrane protein expression at the blood-brain barrier of adult and younger cynomolgus monkeys
-
Ito, K. et al. Quantitative membrane protein expression at the blood-brain barrier of adult and younger cynomolgus monkeys. J. Pharm. Sci. 100, 3939-3950 (2011
-
(2011)
J. Pharm. Sci
, vol.100
, pp. 3939-3950
-
-
Ito, K.1
-
83
-
-
49349102757
-
Subcellular localization of transporters along the rat blood-brain barrier and blood cerebral spinal fluid barrier by in vivo biotinylation
-
Roberts, L. M. et al. Subcellular localization of transporters along the rat blood-brain barrier and blood cerebral spinal fluid barrier by in vivo biotinylation. Neuroscience 155, 423-438 (2008
-
(2008)
Neuroscience
, vol.155
, pp. 423-438
-
-
Roberts, L.M.1
-
84
-
-
80053274858
-
Aminoaciduria, but normal thyroid hormone levels and signalling, in mice lacking the amino acid and thyroid hormone transporter Slc7a8
-
Braun, D., Wohlgemuth, F., Reix, N., Köhrle, J. & Schweizer, U. Aminoaciduria, but normal thyroid hormone levels and signalling, in mice lacking the amino acid and thyroid hormone transporter Slc7a8. Biochem. J. 439, 249-255 (2011
-
(2011)
Biochem. J.
, vol.439
, pp. 249-255
-
-
Braun, D.1
Wohlgemuth, F.2
Reix, N.3
Köhrle, J.4
Schweizer, U.5
-
85
-
-
79953169842
-
Lack of action of exogenously administered T3 on the fetal rat brain despite expression of the monocarboxylate transporter 8
-
Grijota-Martínez, C., Díez, D., Morreale De Escobar, G., Bernal, J. & Morte, B. Lack of action of exogenously administered T3 on the fetal rat brain despite expression of the monocarboxylate transporter 8. Endocrinology 152, 1713-1721 (2011
-
(2011)
Endocrinology
, vol.152
, pp. 1713-1721
-
-
Grijota-Martínez, C.1
Díez, D.2
Morreale De Escobar, G.3
Bernal, J.4
Morte, B.5
-
86
-
-
84862633650
-
Expression profile and thyroid hormone responsiveness of transporters and deiodinases in early embryonic chicken brain development
-
Van Herck, S. L. J., Geysens, S., Delbaere, J., Tylzanowski, P. & Darras, V. M. Expression profile and thyroid hormone responsiveness of transporters and deiodinases in early embryonic chicken brain development. Mol. Cell. Endocrinol. 349, 289-297 (2012
-
(2012)
Mol. Cell. Endocrinol.
, vol.349
, pp. 289-297
-
-
Van Herck, S.L.J.1
Geysens, S.2
Delbaere, J.3
Tylzanowski, P.4
Darras, V.M.5
-
87
-
-
0025885336
-
Transport of iodothyronines from bloodstream to brain: Contributions by blood: Brain and choroid plexus: Cerebrospinal fluid barriers
-
Dratman, M. B., Crutchfield, F. L. & Schoenhoff, M. B. Transport of iodothyronines from bloodstream to brain: contributions by blood: brain and choroid plexus: cerebrospinal fluid barriers. Brain Res. 554, 229-236 (1991
-
(1991)
Brain Res
, vol.554
, pp. 229-236
-
-
Dratman, M.B.1
Crutchfield, F.L.2
Schoenhoff, M.B.3
-
88
-
-
0035157074
-
Development of the choroid plexus
-
Dziegielewska, K. M., Ek, J., Habgood, M. D. & Saunders, N. R. Development of the choroid plexus. Microsc. Res. Tech. 52, 5-20 (2001
-
(2001)
Microsc. Res. Tech
, vol.52
, pp. 5-20
-
-
Dziegielewska, K.M.1
Ek, J.2
Habgood, M.D.3
Saunders, N.R.4
-
89
-
-
0019736173
-
3, 3'5'-triiodothyronine (reverse T3) in human cerebrospinal fluid
-
Nishikawa, M. et al. 3, 3'5'-triiodothyronine (reverse T3) in human cerebrospinal fluid. J. Clin. Endocrinol. Metab. 53, 1030-1035 (1981
-
(1981)
J. Clin. Endocrinol. Metab
, vol.53
, pp. 1030-1035
-
-
Nishikawa, M.1
-
90
-
-
77953168373
-
White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene
-
Gika, A. D. et al. White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene. Dev. Med. Child. Neurol. 52, 475-482 (2010
-
(2010)
Dev. Med. Child. Neurol
, vol.52
, pp. 475-482
-
-
Gika, A.D.1
-
91
-
-
20844451900
-
X linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene
-
Brockmann, K., Dumitrescu, A. M., Best, T. T., Hanefeld, F. & Refetoff, S. X linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene. J. Neurol. 252, 663-666 (2005
-
(2005)
J. Neurol
, vol.252
, pp. 663-666
-
-
Brockmann, K.1
Dumitrescu, A.M.2
Best, T.T.3
Hanefeld, F.4
Refetoff, S.5
-
92
-
-
84885046434
-
Increased oxidative metabolism and neurotransmitter cycling in the brain of mice lacking the thyroid hormone transporter SLC16A2 (MCT8
-
Rodrigues, T. B. et al. Increased oxidative metabolism and neurotransmitter cycling in the brain of mice lacking the thyroid hormone transporter SLC16A2 (MCT8). PLoS ONE 8, e74621 (2013
-
(2013)
PLoS ONE
, vol.8
, pp. e74621
-
-
Rodrigues, T.B.1
-
93
-
-
38849207560
-
The involvement of thyroid hormones and cortisol in the osmotic acclimation of Solea senegalensis
-
Arjona, F. J. et al. The involvement of thyroid hormones and cortisol in the osmotic acclimation of Solea senegalensis. Gen. Comp. Endocrinol. 155, 796-803 (2008
-
(2008)
Gen. Comp. Endocrinol
, vol.155
, pp. 796-803
-
-
Arjona, F.J.1
-
94
-
-
84872072548
-
Zebrafish as a model for monocarboxyl transporter 8 deficiency
-
Vatine, G. D. et al. Zebrafish as a model for monocarboxyl transporter 8 deficiency. J. Biol. Chem. 288, 169-180 (2013
-
(2013)
J. Biol. Chem
, vol.288
, pp. 169-180
-
-
Vatine, G.D.1
-
95
-
-
84907587761
-
Altered behavioral performance and live imaging of circuit-specific neural deficiencies in a zebrafish model for psychomotor retardation
-
Zada, D., Tovin, A., Lerer-Goldshtein, T., Vatine, G. D. & Appelbaum, L. Altered behavioral performance and live imaging of circuit-specific neural deficiencies in a zebrafish model for psychomotor retardation. PLoS Genet. 10, e1004615 (2014
-
(2014)
PLoS Genet
, vol.10
, pp. e1004615
-
-
Zada, D.1
Tovin, A.2
Lerer-Goldshtein, T.3
Vatine, G.D.4
Appelbaum, L.5
-
96
-
-
84901400541
-
Knockdown of monocarboxylate transporter 8 (mct8) disturbs brain development and locomotion in zebrafish
-
De Vrieze, E. et al. Knockdown of monocarboxylate transporter 8 (mct8) disturbs brain development and locomotion in zebrafish. Endocrinology 155, 2320-2330 (2014
-
(2014)
Endocrinology
, vol.155
, pp. 2320-2330
-
-
De Vrieze, E.1
-
97
-
-
84916637399
-
Mutations of the thyroid hormone transporter MCT8 cause prenatal brain damage and persistent hypomyelination
-
López-Espíndola, D. et al. Mutations of the thyroid hormone transporter MCT8 cause prenatal brain damage and persistent hypomyelination. J. Clin. Endocrinol. Metab. 99, E2799-E2804 (2014
-
(2014)
J. Clin. Endocrinol. Metab
, vol.99
, pp. E2799-E2804
-
-
López-Espíndola, D.1
-
98
-
-
0030064165
-
Distribution of parvalbumin immunoreactivity in the neocortex of hypothyroid adult rats
-
Berbel, P., Marco, P., Cerezo, J. R. & DeFelipe, J. Distribution of parvalbumin immunoreactivity in the neocortex of hypothyroid adult rats. Neurosci. Lett. 204, 65-68 (1996
-
(1996)
Neurosci. Lett
, vol.204
, pp. 65-68
-
-
Berbel, P.1
Marco, P.2
Cerezo, J.R.3
Defelipe, J.4
-
99
-
-
0027935617
-
The development of the anterior commissure in normal and hypothyroid rats
-
Guadaño-Ferraz, A., Escobar del Rey, F., Morreale De Escobar, G., Innocenti, G. M. & Berbel, P. The development of the anterior commissure in normal and hypothyroid rats. Brain. Res. Dev. Brain. Res. 81, 293-308 (1994
-
(1994)
Brain. Res. Dev. Brain. Res
, vol.81
, pp. 293-308
-
-
Guadaño-Ferraz, A.1
Escobar Del Rey, F.2
Morreale De Escobar, G.3
Innocenti, G.M.4
Berbel, P.5
-
100
-
-
0036047147
-
Analysis of thyroid hormone-dependent genes in the brain by in situ hybridization
-
Bernal, J. & Guadaño-Ferraz, A. Analysis of thyroid hormone-dependent genes in the brain by in situ hybridization. Methods Mol. Biol. 202, 71-90 (2002
-
(2002)
Methods Mol. Biol
, vol.202
, pp. 71-90
-
-
Bernal, J.1
Guadaño-Ferraz, A.2
-
101
-
-
43249104125
-
1H magnetic resonance spectroscopy in monocarboxylate transporter 8 gene deficiency
-
Sijens, P. E., Rödiger, L. A., Meiners, L. C. & Lunsing, R. J. 1H magnetic resonance spectroscopy in monocarboxylate transporter 8 gene deficiency. J. Clin. Endocrinol. Metab. 93, 1854-1859 (2008
-
(2008)
J. Clin. Endocrinol. Metab
, vol.93
, pp. 1854-1859
-
-
Sijens, P.E.1
Rödiger, L.A.2
Meiners, L.C.3
Lunsing, R.J.4
-
102
-
-
60749137633
-
Pelizaeus Merzbacher Like disease presentation of MCT8 mutated male subjects
-
Vaurs-Barriere, C. et al. Pelizaeus Merzbacher Like disease presentation of MCT8 mutated male subjects. Ann. Neurol. 65, 114-118 (2009
-
(2009)
Ann. Neurol
, vol.65
, pp. 114-118
-
-
Vaurs-Barriere, C.1
-
103
-
-
84904473773
-
Delayed myelination is not a constant feature of Allan Herndon Dudley syndrome: Report of a new case and review of the literature
-
Azzolini, S. et al. Delayed myelination is not a constant feature of Allan Herndon Dudley syndrome: report of a new case and review of the literature. Brain Dev. 36, 716-720 (2014
-
(2014)
Brain Dev
, vol.36
, pp. 716-720
-
-
Azzolini, S.1
-
104
-
-
33751536051
-
Thyroid hormone transport by the human monocarboxylate transporter 8 and its rate-limiting role in intracellular metabolism
-
Friesema, E. C, Kuiper, G. G., Jansen, J., Visser, T. J. & Kester, M. H. Thyroid hormone transport by the human monocarboxylate transporter 8 and its rate-limiting role in intracellular metabolism. Mol. Endocrinol. 20, 2761-2772 (2006
-
(2006)
Mol. Endocrinol
, vol.20
, pp. 2761-2772
-
-
Friesema, E.C.1
Kuiper, G.G.2
Jansen, J.3
Visser, T.J.4
Kester, M.H.5
-
105
-
-
42449161045
-
Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8
-
Jansen, J., Kester, M. H., Schwartz, C. E. & Visser, T. J. Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8. Endocrinology 149, 2184-2190 (2008
-
(2008)
Endocrinology
, vol.149
, pp. 2184-2190
-
-
Jansen, J.1
Kester, M.H.2
Schwartz, C.E.3
Visser, T.J.4
-
106
-
-
58349086340
-
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
-
Visser, W. E. et al. Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations. Hum. Mutat. 30, 29-38 (2009
-
(2009)
Hum. Mutat
, vol.30
, pp. 29-38
-
-
Visser, W.E.1
-
107
-
-
84870750730
-
Identification, functional analysis, prevalence and treatment of monocarboxylate transporter 8 (MCT8) mutations in a cohort of adult patients with mental retardation
-
Visser, W. E. et al. Identification, functional analysis, prevalence and treatment of monocarboxylate transporter 8 (MCT8) mutations in a cohort of adult patients with mental retardation. Clin. Endocrinol. (Oxf) 78, 310-315 (2013
-
(2013)
Clin. Endocrinol. (Oxf)
, vol.78
, pp. 310-315
-
-
Visser, W.E.1
-
108
-
-
84876880669
-
Mutations in MCT8 in patients with Allan-Herndon-Dudley-syndrome affecting its cellular distribution
-
Kersseboom, S. et al. Mutations in MCT8 in patients with Allan-Herndon-Dudley-syndrome affecting its cellular distribution. Mol. Endocrinol. 27, 801-813 (2013
-
(2013)
Mol. Endocrinol
, vol.27
, pp. 801-813
-
-
Kersseboom, S.1
-
109
-
-
71649109028
-
Surface translocation and tri-iodothyronine uptake of mutant MCT8 proteins are cell type-dependent
-
Kinne, A. et al. Surface translocation and tri-iodothyronine uptake of mutant MCT8 proteins are cell type-dependent. J. Mol. Endocrinol. 43, 263-271 (2009
-
(2009)
J. Mol. Endocrinol
, vol.43
, pp. 263-271
-
-
Kinne, A.1
-
110
-
-
84862751648
-
PTTG-binding factor (PBF) is a novel regulator of the thyroid hormone transporter MCT8
-
Smith, V. E. et al. PTTG-binding factor (PBF) is a novel regulator of the thyroid hormone transporter MCT8. Endocrinology 153, 3526-3536 (2012
-
(2012)
Endocrinology
, vol.153
, pp. 3526-3536
-
-
Smith, V.E.1
-
111
-
-
0021970929
-
Neurological signs in congenital iodine-deficiency disorder (endemic cretinism)
-
DeLong, G. R., Stanbury, J. B. & Fierro-Benitez, R. Neurological signs in congenital iodine-deficiency disorder (endemic cretinism). Dev. Med. Child. Neurol. 27, 317-324 (1985
-
(1985)
Dev. Med. Child. Neurol
, vol.27
, pp. 317-324
-
-
Delong, G.R.1
Stanbury, J.B.2
Fierro-Benitez, R.3
-
112
-
-
0027298828
-
Magnetic resonance imaging of brain and the neuromotor disorder in endemic cretinism
-
Ma, T., Lian, Z. C., Qi, S. P., Heinz, E. R. & DeLong, G. R. Magnetic resonance imaging of brain and the neuromotor disorder in endemic cretinism. Ann. Neurol. 34, 91-94 (1993
-
(1993)
Ann. Neurol
, vol.34
, pp. 91-94
-
-
Ma, T.1
Lian, Z.C.2
Qi, S.P.3
Heinz, E.R.4
Delong, G.R.5
-
113
-
-
0025891519
-
The neurology of endemic cretinism A study of two endemias
-
Halpern, J. P. et al. The neurology of endemic cretinism. A study of two endemias. Brain 114, 825-841 (1991
-
(1991)
Brain
, vol.114
, pp. 825-841
-
-
Halpern, J.P.1
-
114
-
-
0021330905
-
Ontogenesis of the nuclear 3, 5, 3'-triiodothyronine receptor in the human fetal brain
-
Bernal, J. & Pekonen, F. Ontogenesis of the nuclear 3, 5, 3'-triiodothyronine receptor in the human fetal brain. Endocrinology 114, 677-679 (1984
-
(1984)
Endocrinology
, vol.114
, pp. 677-679
-
-
Bernal, J.1
Pekonen, F.2
-
115
-
-
4344581457
-
Involvement of multispecific organic anion transporter, Oatp14 (Slc21a14), in the transport of thyroxine across the blood-brain barrier
-
Tohyama, K., Kusuhara, H. & Sugiyama, Y. Involvement of multispecific organic anion transporter, Oatp14 (Slc21a14), in the transport of thyroxine across the blood-brain barrier. Endocrinology 145, 4384-4391 (2004
-
(2004)
Endocrinology
, vol.145
, pp. 4384-4391
-
-
Tohyama, K.1
Kusuhara, H.2
Sugiyama, Y.3
-
116
-
-
17744376593
-
Identification of thyroid hormone transporters in humans: Different molecules are involved in a tissue-specific manner
-
Fujiwara, K. et al. Identification of thyroid hormone transporters in humans: different molecules are involved in a tissue-specific manner. Endocrinology 142, 2005-2012 (2001
-
(2001)
Endocrinology
, vol.142
, pp. 2005-2012
-
-
Fujiwara, K.1
-
117
-
-
0035875174
-
Role of the System L permease LAT1 in amino acid and iodothyronine transport in placenta
-
Ritchie, J. W. & Taylor, P. M. Role of the System L permease LAT1 in amino acid and iodothyronine transport in placenta. Biochem. J. 356, 719-725 (2001
-
(2001)
Biochem. J.
, vol.356
, pp. 719-725
-
-
Ritchie, J.W.1
Taylor, P.M.2
|