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

Year Number of Results
2009 1
2010 1
2011 1
2012 1
2013 1
2015 2
2016 3
2017 3
2018 2
2019 2
2020 1
2021 5
2022 1
2023 3
2024 2

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24 results

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Page 1
Blood biomarkers for assessment of mitochondrial dysfunction: An expert review.
Hubens WHG, Vallbona-Garcia A, de Coo IFM, van Tienen FHJ, Webers CAB, Smeets HJM, Gorgels TGMF. Hubens WHG, et al. Among authors: van tienen fhj. Mitochondrion. 2022 Jan;62:187-204. doi: 10.1016/j.mito.2021.10.008. Epub 2021 Nov 2. Mitochondrion. 2022. PMID: 34740866 Free article. Review.
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle.
Boyer O, Butler-Browne G, Chinoy H, Cossu G, Galli F, Lilleker JB, Magli A, Mouly V, Perlingeiro RCR, Previtali SC, Sampaolesi M, Smeets H, Schoewel-Wolf V, Spuler S, Torrente Y, Van Tienen F; Study Group. Boyer O, et al. Among authors: van tienen f. Front Genet. 2021 Aug 2;12:702547. doi: 10.3389/fgene.2021.702547. eCollection 2021. Front Genet. 2021. PMID: 34408774 Free PMC article. Review.
Human embryonic stem cell-derived cardiomyocytes as an in vitro model to study cardiac insulin resistance.
Geraets IME, Chanda D, van Tienen FHJ, van den Wijngaard A, Kamps R, Neumann D, Liu Y, Glatz JFC, Luiken JJFP, Nabben M. Geraets IME, et al. Among authors: van tienen fhj. Biochim Biophys Acta Mol Basis Dis. 2018 May;1864(5 Pt B):1960-1967. doi: 10.1016/j.bbadis.2017.12.025. Epub 2017 Dec 20. Biochim Biophys Acta Mol Basis Dis. 2018. PMID: 29277329 Free article. Review.
European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17-19, 2023, Barcelona, Spain.
Smeets H, Verbrugge B, Bulbena X, Hristova L, Vogt J, van Beckhoven I; all participants; Patient organizations/patient representatives: LAMA2-Europe, Voor Sara-the Netherlands, ImpulsaT-Spain, LAMA2-France, CMD-Turkey, LAMA2-Bulgaria, Cure-CMD. Smeets H, et al. Neuromuscul Disord. 2024 Mar;36:16-22. doi: 10.1016/j.nmd.2024.01.001. Epub 2024 Jan 9. Neuromuscul Disord. 2024. PMID: 38306718
Low mitochondrial DNA copy number in buffy coat DNA of primary open-angle glaucoma patients.
Vallbona-Garcia A, Hamers IHJ, van Tienen FHJ, Ochoteco-Asensio J, Berendschot TTJM, de Coo IFM, Benedikter BJ, Webers CAB, Smeets HJM, Gorgels TGMF. Vallbona-Garcia A, et al. Among authors: van tienen fhj. Exp Eye Res. 2023 Jul;232:109500. doi: 10.1016/j.exer.2023.109500. Epub 2023 May 11. Exp Eye Res. 2023. PMID: 37178956 Free article.
Smad1/5/8 are myogenic regulators of murine and human mesoangioblasts.
Costamagna D, Quattrocelli M, van Tienen F, Umans L, de Coo IF, Zwijsen A, Huylebroeck D, Sampaolesi M. Costamagna D, et al. Among authors: van tienen f. J Mol Cell Biol. 2016 Feb;8(1):73-87. doi: 10.1093/jmcb/mjv059. Epub 2015 Oct 8. J Mol Cell Biol. 2016. PMID: 26450990 Free PMC article.
Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
Paulussen AD, Steyls A, Vanoevelen J, van Tienen FH, Krapels IP, Claes GR, Chocron S, Velter C, Tan-Sindhunata GM, Lundin C, Valenzuela I, Nagy B, Bache I, Maroun LL, Avela K, Brunner HG, Smeets HJ, Bakkers J, van den Wijngaard A. Paulussen AD, et al. Among authors: van tienen fh. Eur J Hum Genet. 2016 Dec;24(12):1783-1791. doi: 10.1038/ejhg.2016.91. Epub 2016 Jul 13. Eur J Hum Genet. 2016. PMID: 27406248 Free PMC article.
24 results