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

Year Number of Results
2005 1
2006 4
2007 1
2008 2
2009 5
2010 1
2011 4
2012 1
2014 2
2015 2
2016 4
2017 1
2018 2
2019 2
2020 4
2021 1
2022 1
2023 1
2024 0

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32 results

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Page 1
Hereditary Disorders of Cardiovascular Calcification.
Rutsch F, Buers I, Nitschke Y. Rutsch F, et al. Among authors: buers i. Arterioscler Thromb Vasc Biol. 2021 Jan;41(1):35-47. doi: 10.1161/ATVBAHA.120.315577. Epub 2020 Nov 12. Arterioscler Thromb Vasc Biol. 2021. PMID: 33176451 Free article. Review.
CRLF1 and CLCF1 in Development, Health and Disease.
Crisponi L, Buers I, Rutsch F. Crisponi L, et al. Among authors: buers i. Int J Mol Sci. 2022 Jan 17;23(2):992. doi: 10.3390/ijms23020992. Int J Mol Sci. 2022. PMID: 35055176 Free PMC article. Review.
Compartmentalization of proteins in lipid droplet biogenesis.
Robenek H, Buers I, Hofnagel O, Robenek MJ, Troyer D, Severs NJ. Robenek H, et al. Among authors: buers i. Biochim Biophys Acta. 2009 Jun;1791(6):408-18. doi: 10.1016/j.bbalip.2008.12.001. Epub 2008 Dec 11. Biochim Biophys Acta. 2009. PMID: 19118639 Review.
Efficient non-viral transfection of THP-1 cells.
Schnoor M, Buers I, Sietmann A, Brodde MF, Hofnagel O, Robenek H, Lorkowski S. Schnoor M, et al. Among authors: buers i. J Immunol Methods. 2009 May 31;344(2):109-15. doi: 10.1016/j.jim.2009.03.014. Epub 2009 Apr 5. J Immunol Methods. 2009. PMID: 19345690
A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome.
Rutsch F, MacDougall M, Lu C, Buers I, Mamaeva O, Nitschke Y, Rice GI, Erlandsen H, Kehl HG, Thiele H, Nürnberg P, Höhne W, Crow YJ, Feigenbaum A, Hennekam RC. Rutsch F, et al. Among authors: buers i. Am J Hum Genet. 2015 Feb 5;96(2):275-82. doi: 10.1016/j.ajhg.2014.12.014. Epub 2015 Jan 22. Am J Hum Genet. 2015. PMID: 25620204 Free PMC article.
32 results