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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1990 1
1991 1
1996 1
1997 1
1998 4
1999 2
2000 5
2001 1
2003 1
2004 4
2005 6
2006 3
2007 4
2008 3
2009 4
2010 4
2011 1
2012 3
2014 2
2015 1
2016 2
2017 1
2018 1
2020 1
2021 4
2022 3
2023 3
2024 0

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Publication date

PubMed for id: 1372805

61 results

Results by year

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Page 1
Lack of L-type amino acid transporter 2 in murine thyroid tissue induces autophagy.
Venugopalan V, Rehders M, Weber J, Rodermund L, Al-Hashimi A, Bargmann T, Golchert J, Reinecke V, Homuth G, Völker U, Verrey F, Kirstein J, Heuer H, Schweizer U, Braun D, Wirth EK, Brix K. Venugopalan V, et al. J Mol Endocrinol. 2022 Dec 7;70(1):e220060. doi: 10.1530/JME-22-0060. Print 2023 Jan 1. J Mol Endocrinol. 2022. PMID: 36129170
Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect.
Bernal Barquero CE, Geysels RC, Jacques V, Carro GH, Martín M, Peyret V, Abregú MC, Papendieck P, Masini-Repiso AM, Savagner F, Chiesa AE, Citterio CE, Nicola JP. Bernal Barquero CE, et al. Int J Mol Sci. 2022 Aug 17;23(16):9251. doi: 10.3390/ijms23169251. Int J Mol Sci. 2022. PMID: 36012511 Free PMC article.
Genetics of primary congenital hypothyroidism-a review.
Kostopoulou E, Miliordos K, Spiliotis B. Kostopoulou E, et al. Hormones (Athens). 2021 Jun;20(2):225-236. doi: 10.1007/s42000-020-00267-x. Epub 2021 Jan 5. Hormones (Athens). 2021. PMID: 33400193 Review.
Iodide handling disorders (NIS, TPO, TG, IYD).
Targovnik HM, Citterio CE, Rivolta CM. Targovnik HM, et al. Best Pract Res Clin Endocrinol Metab. 2017 Mar;31(2):195-212. doi: 10.1016/j.beem.2017.03.006. Epub 2017 Apr 4. Best Pract Res Clin Endocrinol Metab. 2017. PMID: 28648508 Review.
61 results