Similar articles for PMID: 20123860

Year	Number of Results
2000	1
2001	3
2002	3
2003	6
2004	1
2005	4
2006	3
2007	5
2008	13
2009	7
2010	10
2011	4
2012	6
2013	9
2014	7
2015	1
2016	1
2017	4
2018	3
2019	6
2020	3
2021	6
2022	7
2023	1
2024	0

1

Loss of thymidine kinase 2 alters neuronal bioenergetics and leads to neurodegeneration.

Bartesaghi S, Betts-Henderson J, Cain K, Dinsdale D, Zhou X, Karlsson A, Salomoni P, Nicotera P. Bartesaghi S, et al. Hum Mol Genet. 2010 May 1;19(9):1669-77. doi: 10.1093/hmg/ddq043. Epub 2010 Feb 1. Hum Mol Genet. 2010. PMID: 20123860 Free PMC article.

2

Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene.

Chanprasert S, Wang J, Weng SW, Enns GM, Boué DR, Wong BL, Mendell JR, Perry DA, Sahenk Z, Craigen WJ, Alcala FJ, Pascual JM, Melancon S, Zhang VW, Scaglia F, Wong LJ. Chanprasert S, et al. Mol Genet Metab. 2013 Sep-Oct;110(1-2):153-61. doi: 10.1016/j.ymgme.2013.07.009. Epub 2013 Jul 17. Mol Genet Metab. 2013. PMID: 23932787

3

Thymidine kinase 2 deficiency-induced mtDNA depletion in mouse liver leads to defect β-oxidation.

Zhou X, Kannisto K, Curbo S, von Döbeln U, Hultenby K, Isetun S, Gåfvels M, Karlsson A. Zhou X, et al. PLoS One. 2013;8(3):e58843. doi: 10.1371/journal.pone.0058843. Epub 2013 Mar 7. PLoS One. 2013. PMID: 23505564 Free PMC article.

4

Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance.

Akman HO, Dorado B, López LC, García-Cazorla A, Vilà MR, Tanabe LM, Dauer WT, Bonilla E, Tanji K, Hirano M. Akman HO, et al. Hum Mol Genet. 2008 Aug 15;17(16):2433-40. doi: 10.1093/hmg/ddn143. Epub 2008 May 8. Hum Mol Genet. 2008. PMID: 18467430 Free PMC article.

5

Targeted impairment of thymidine kinase 2 expression in cells induces mitochondrial DNA depletion and reveals molecular mechanisms of compensation of mitochondrial respiratory activity.

Villarroya J, Lara MC, Dorado B, Garrido M, García-Arumí E, Meseguer A, Hirano M, Vilà MR. Villarroya J, et al. Biochem Biophys Res Commun. 2011 Apr 8;407(2):333-8. doi: 10.1016/j.bbrc.2011.03.018. Epub 2011 Mar 5. Biochem Biophys Res Commun. 2011. PMID: 21382338 Free PMC article.

6

Blázquez-Bermejo C, Molina-Granada D, Vila-Julià F, Jiménez-Heis D, Zhou X, Torres-Torronteras J, Karlsson A, Martí R, Cámara Y. Blázquez-Bermejo C, et al. EBioMedicine. 2019 Aug;46:342-355. doi: 10.1016/j.ebiom.2019.07.042. Epub 2019 Jul 24. EBioMedicine. 2019. PMID: 31351931 Free PMC article.

7

Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene.

Papadimas GK, Vargiami E, Dragoumi P, Van Coster R, Smet J, Seneca S, Papadopoulos C, Kararizou E, Zafeiriou D. Papadimas GK, et al. Acta Myol. 2020 Jun 1;39(2):94-97. doi: 10.36185/2532-1900-012. eCollection 2020 Jun. Acta Myol. 2020. PMID: 32904881 Free PMC article.

8

Gene expression deregulation in postnatal skeletal muscle of TK2 deficient mice reveals a lower pool of proliferating myogenic progenitor cells.

Paredes JA, Zhou X, Höglund S, Karlsson A. Paredes JA, et al. PLoS One. 2013;8(1):e53698. doi: 10.1371/journal.pone.0053698. Epub 2013 Jan 14. PLoS One. 2013. PMID: 23341978 Free PMC article.

9

Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.

Mancuso M, Salviati L, Sacconi S, Otaegui D, Camaño P, Marina A, Bacman S, Moraes CT, Carlo JR, Garcia M, Garcia-Alvarez M, Monzon L, Naini AB, Hirano M, Bonilla E, Taratuto AL, DiMauro S, Vu TH. Mancuso M, et al. Neurology. 2002 Oct 22;59(8):1197-202. doi: 10.1212/01.wnl.0000028689.93049.9a. Neurology. 2002. PMID: 12391347

10

Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.

Tyynismaa H, Sun R, Ahola-Erkkilä S, Almusa H, Pöyhönen R, Korpela M, Honkaniemi J, Isohanni P, Paetau A, Wang L, Suomalainen A. Tyynismaa H, et al. Hum Mol Genet. 2012 Jan 1;21(1):66-75. doi: 10.1093/hmg/ddr438. Epub 2011 Sep 21. Hum Mol Genet. 2012. PMID: 21937588

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