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Journal Abstract Search

326 related items for PubMed ID: 21264952

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  • 2. 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 EK, Roth S, Blechschmidt C, Hölter SM, Becker L, Racz I, Zimmer A, Klopstock T, Gailus-Durner V, Fuchs H, Wurst W, Naumann T, Bräuer A, de Angelis MH, Köhrle J, Grüters A, Schweizer U.
    J Neurosci; 2009 Jul 29; 29(30):9439-49. PubMed ID: 19641107
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  • 3. The monocarboxylate transporter 8 and L-type amino acid transporters 1 and 2 are expressed in mouse skeletons and in osteoblastic MC3T3-E1 cells.
    Capelo LP, Beber EH, Fonseca TL, Gouveia CH.
    Thyroid; 2009 Feb 29; 19(2):171-80. PubMed ID: 19133747
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  • 7. Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivation.
    Núñez B, Martínez de Mena R, Obregon MJ, Font-Llitjós M, Nunes V, Palacín M, Dumitrescu AM, Morte B, Bernal J.
    PLoS One; 2014 Feb 29; 9(5):e96915. PubMed ID: 24819605
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  • 9. Thyroid hormone transport in developing brain.
    Bernal J.
    Curr Opin Endocrinol Diabetes Obes; 2011 Oct 29; 18(5):295-9. PubMed ID: 21825978
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  • 10. Monocarboxylate transporter 10 functions as a thyroid hormone transporter in chondrocytes.
    Abe S, Namba N, Abe M, Fujiwara M, Aikawa T, Kogo M, Ozono K.
    Endocrinology; 2012 Aug 29; 153(8):4049-58. PubMed ID: 22719050
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  • 12. Changes in thyroid status during perinatal development of MCT8-deficient male mice.
    Ferrara AM, Liao XH, Gil-Ibáñez P, Marcinkowski T, Bernal J, Weiss RE, Dumitrescu AM, Refetoff S.
    Endocrinology; 2013 Jul 29; 154(7):2533-41. PubMed ID: 23696569
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  • 13. Consequences of monocarboxylate transporter 8 deficiency for renal transport and metabolism of thyroid hormones in mice.
    Trajkovic-Arsic M, Visser TJ, Darras VM, Friesema EC, Schlott B, Mittag J, Bauer K, Heuer H.
    Endocrinology; 2010 Feb 29; 151(2):802-9. PubMed ID: 19996182
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  • 14. Tissue-specific alterations in thyroid hormone homeostasis in combined Mct10 and Mct8 deficiency.
    Müller J, Mayerl S, Visser TJ, Darras VM, Boelen A, Frappart L, Mariotta L, Verrey F, Heuer H.
    Endocrinology; 2014 Jan 29; 155(1):315-25. PubMed ID: 24248460
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  • 17. Mechanisms of disease: psychomotor retardation and high T3 levels caused by mutations in monocarboxylate transporter 8.
    Friesema EC, Jansen J, Heuer H, Trajkovic M, Bauer K, Visser TJ.
    Nat Clin Pract Endocrinol Metab; 2006 Sep 29; 2(9):512-23. PubMed ID: 16957765
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  • 19. Thyroid hormone transport by monocarboxylate transporters.
    Visser WE, Friesema EC, Jansen J, Visser TJ.
    Best Pract Res Clin Endocrinol Metab; 2007 Jun 29; 21(2):223-36. PubMed ID: 17574005
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  • 20. The importance of thyroid hormone transporters for brain development and function.
    Heuer H.
    Best Pract Res Clin Endocrinol Metab; 2007 Jun 29; 21(2):265-76. PubMed ID: 17574008
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