Kersseboom S - Search Results

1

In Vitro Characterization of Human, Mouse, and Zebrafish MCT8 Orthologues.

Groeneweg S, Kersseboom S, van den Berge A, Dolcetta-Capuzzo A, van Geest FS, van Heerebeek REA, Arjona FJ, Meima ME, Peeters RP, Visser WE, Visser TJ. Groeneweg S, et al. Among authors: kersseboom s. Thyroid. 2019 Oct;29(10):1499-1510. doi: 10.1089/thy.2019.0009. Epub 2019 Oct 7. Thyroid. 2019. PMID: 31436139

2

MCT8: from gene to disease and therapeutic approach.

Kersseboom S, Visser TJ. Kersseboom S, et al. Ann Endocrinol (Paris). 2011 Apr;72(2):77-81. doi: 10.1016/j.ando.2011.03.003. Epub 2011 Apr 20. Ann Endocrinol (Paris). 2011. PMID: 21511238

3

Mutations in MCT8 in patients with Allan-Herndon-Dudley-syndrome affecting its cellular distribution.

Kersseboom S, Kremers GJ, Friesema EC, Visser WE, Klootwijk W, Peeters RP, Visser TJ. Kersseboom S, et al. Mol Endocrinol. 2013 May;27(5):801-13. doi: 10.1210/me.2012-1356. Epub 2013 Apr 2. Mol Endocrinol. 2013. PMID: 23550058 Free PMC article.

4

The role of Arg445 and Asp498 in the human thyroid hormone transporter MCT8.

Groeneweg S, Friesema EC, Kersseboom S, Klootwijk W, Visser WE, Peeters RP, Visser TJ. Groeneweg S, et al. Among authors: kersseboom s. Endocrinology. 2014 Feb;155(2):618-26. doi: 10.1210/en.2013-1521. Epub 2013 Nov 21. Endocrinology. 2014. PMID: 24265446

5

In vitro and mouse studies supporting therapeutic utility of triiodothyroacetic acid in MCT8 deficiency.

Kersseboom S, Horn S, Visser WE, Chen J, Friesema EC, Vaurs-Barrière C, Peeters RP, Heuer H, Visser TJ. Kersseboom S, et al. Mol Endocrinol. 2014 Dec;28(12):1961-70. doi: 10.1210/me.2014-1135. Mol Endocrinol. 2014. PMID: 25389909 Free PMC article.

6

Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 Mutation.

Armour CM, Kersseboom S, Yoon G, Visser TJ. Armour CM, et al. Among authors: kersseboom s. PLoS One. 2015 Oct 1;10(10):e0139343. doi: 10.1371/journal.pone.0139343. eCollection 2015. PLoS One. 2015. PMID: 26426690 Free PMC article.

7

Tissue-specific effects of mutations in the thyroid hormone transporter MCT8.

Kersseboom S, Visser TJ. Kersseboom S, et al. Arq Bras Endocrinol Metabol. 2011 Feb;55(1):1-5. doi: 10.1590/s0004-27302011000100001. Arq Bras Endocrinol Metabol. 2011. PMID: 21468514 No abstract available.

8

Role of the Bile Acid Transporter SLC10A1 in Liver Targeting of the Lipid-Lowering Thyroid Hormone Analog Eprotirome.

Kersseboom S, van Gucht ALM, van Mullem A, Brigante G, Farina S, Carlsson B, Donkers JM, van de Graaf SFJ, Peeters RP, Visser TJ. Kersseboom S, et al. Endocrinology. 2017 Oct 1;158(10):3307-3318. doi: 10.1210/en.2017-00433. Endocrinology. 2017. PMID: 28938430

9

Characterization of Chicken Thyroid Hormone Transporters.

Bourgeois NM, Van Herck SL, Vancamp P, Delbaere J, Zevenbergen C, Kersseboom S, Darras VM, Visser TJ. Bourgeois NM, et al. Among authors: kersseboom s. Endocrinology. 2016 Jun;157(6):2560-74. doi: 10.1210/en.2015-2025. Epub 2016 Apr 12. Endocrinology. 2016. PMID: 27070099

10

Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutations.

Anık A, Kersseboom S, Demir K, Catlı G, Yiş U, Böber E, van Mullem A, van Herebeek RE, Hız S, Abacı A, Visser TJ. Anık A, et al. Among authors: kersseboom s. Horm Res Paediatr. 2014;82(4):261-71. doi: 10.1159/000365191. Epub 2014 Sep 18. Horm Res Paediatr. 2014. PMID: 25247785

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