368 related articles for article (PubMed ID: 21825978)
1. Thyroid hormone transport in developing brain.
Bernal J
Curr Opin Endocrinol Diabetes Obes; 2011 Oct; 18(5):295-9. PubMed ID: 21825978
[TBL] [Abstract][Full Text] [Related]
2. Thyroid hormone transporters and resistance.
Visser TJ
Endocr Dev; 2013; 24():1-10. PubMed ID: 23392090
[TBL] [Abstract][Full Text] [Related]
3. Thyroid hormone transporters--functions and clinical implications.
Bernal J; Guadaño-Ferraz A; Morte B
Nat Rev Endocrinol; 2015 Jul; 11(7):406-17. PubMed ID: 25942657
[TBL] [Abstract][Full Text] [Related]
4. Thyroid hormone cell membrane transport defect.
Ramos HE
Endocr Dev; 2014; 26():108-17. PubMed ID: 25231447
[TBL] [Abstract][Full Text] [Related]
5. Brain Gene Expression in Systemic Hypothyroidism and Mouse Models of MCT8 Deficiency: The Mct8-Oatp1c1-Dio2 Triad.
Morte B; Gil-Ibañez P; Heuer H; Bernal J
Thyroid; 2021 Jun; 31(6):985-993. PubMed ID: 33307956
[No Abstract] [Full Text] [Related]
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
PLoS One; 2015; 10(10):e0139343. PubMed ID: 26426690
[TBL] [Abstract][Full Text] [Related]
7. 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
Horm Res Paediatr; 2014; 82(4):261-71. PubMed ID: 25247785
[TBL] [Abstract][Full Text] [Related]
8. Genetics and phenomics of thyroid hormone transport by MCT8.
Friesema EC; Visser WE; Visser TJ
Mol Cell Endocrinol; 2010 Jun; 322(1-2):107-13. PubMed ID: 20083155
[TBL] [Abstract][Full Text] [Related]
9. 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
Mol Endocrinol; 2014 Dec; 28(12):1961-70. PubMed ID: 25389909
[TBL] [Abstract][Full Text] [Related]
10. Developmental and cell type-specific expression of thyroid hormone transporters in the mouse brain and in primary brain cells.
Braun D; Kinne A; Bräuer AU; Sapin R; Klein MO; Köhrle J; Wirth EK; Schweizer U
Glia; 2011 Mar; 59(3):463-71. PubMed ID: 21264952
[TBL] [Abstract][Full Text] [Related]
11. Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis.
Mayerl S; Müller J; Bauer R; Richert S; Kassmann CM; Darras VM; Buder K; Boelen A; Visser TJ; Heuer H
J Clin Invest; 2014 May; 124(5):1987-99. PubMed ID: 24691440
[TBL] [Abstract][Full Text] [Related]
12. Disorder of thyroid hormone transport into the tissues.
Groeneweg S; Visser WE; Visser TJ
Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):241-253. PubMed ID: 28648511
[TBL] [Abstract][Full Text] [Related]
13. 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; Mariotti S; Dessì V; Pruna D; Meloni A; Loudianos G
Eur J Med Genet; 2010; 53(6):392-5. PubMed ID: 20713192
[TBL] [Abstract][Full Text] [Related]
14. Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by
Refetoff S; Pappa T; Williams MK; Matheus MG; Liao XH; Hansen K; Nicol L; Pierce M; Blasco PA; Wiebers Jensen M; Bernal J; Weiss RE; Dumitrescu AM; LaFranchi S
Thyroid; 2021 May; 31(5):713-720. PubMed ID: 32746752
[No Abstract] [Full Text] [Related]
15. Functional analysis of monocarboxylate transporter 8 mutations in Japanese Allan-Herndon-Dudley syndrome patients.
Islam MS; Namba N; Ohata Y; Fujiwara M; Nakano C; Takeyari S; Miyata K; Nakano Y; Yamamoto K; Nakayama H; Kitaoka T; Kubota T; Ozono K
Endocr J; 2019 Jan; 66(1):19-29. PubMed ID: 30369548
[TBL] [Abstract][Full Text] [Related]
16. From zebrafish to human: A comparative approach to elucidate the role of the thyroid hormone transporter MCT8 during brain development.
Vancamp P; Darras VM
Gen Comp Endocrinol; 2018 Sep; 265():219-229. PubMed ID: 29183795
[TBL] [Abstract][Full Text] [Related]
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; 2(9):512-23. PubMed ID: 16957765
[TBL] [Abstract][Full Text] [Related]
18. Impaired T3 uptake and action in MCT8-deficient cerebral organoids underlie Allan-Herndon-Dudley syndrome.
Salas-Lucia F; Escamilla S; Bianco AC; Dumitrescu A; Refetoff S
JCI Insight; 2024 Feb; 9(7):. PubMed ID: 38376950
[TBL] [Abstract][Full Text] [Related]
19. 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; Dessì V; Meloni A; Loudianos G
Eur J Med Genet; 2013 Apr; 56(4):207-10. PubMed ID: 23419639
[TBL] [Abstract][Full Text] [Related]
20.
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
Thyroid; 2019 Oct; 29(10):1499-1510. PubMed ID: 31436139
[No Abstract] [Full Text] [Related]
[Next] [New Search]