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

Year Number of Results
1991 1
1992 2
1993 3
1997 2
1998 1
1999 1
2000 2
2001 1
2002 2
2003 3
2004 4
2005 3
2006 1
2007 3
2008 7
2009 10
2010 7
2011 7
2012 6
2013 6
2014 7
2015 4
2016 5
2017 1
2018 2
2019 2
2020 3
2021 2
2022 1
2023 2
2024 0

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PubMed (RefSeq) for id: 1677499743

89 results

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Page 1
Bearing variant alleles at uridine glucuronosyltransferase polymorphisms UGT2B7 -161C > T (rs7668258) or UGT1A4*3 c.142 T > G (rs2011425) has no relevant consequences for lamotrigine troughs in adults with epilepsy.
Božina N, Sporiš IŠ, Domjanović IK, Ganoci L, Šimičević L, Lovrić M, Romić ZČ, Gadže ŽP, Trkulja V. Božina N, et al. Eur J Clin Pharmacol. 2023 Aug;79(8):1117-1129. doi: 10.1007/s00228-023-03526-z. Epub 2023 Jun 20. Eur J Clin Pharmacol. 2023. PMID: 37340142
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, Szpyt J, Gassaway BM, Panov A, Parzen H, Fu S, Golbazi A, Maenpaa E, Stricker K, Guha Thakurta S, Zhang T, Rad R, Pan J, Nusinow DP, Paulo JA, Schweppe DK, Vaites LP, Harper JW, Gygi SP. Huttlin EL, et al. Cell. 2021 May 27;184(11):3022-3040.e28. doi: 10.1016/j.cell.2021.04.011. Epub 2021 May 6. Cell. 2021. PMID: 33961781 Free PMC article.
UGT polymorphisms and lamotrigine clearance during pregnancy.
Petrenaite V, Öhman I, Ekström L, Sæbye D, Hansen TF, Tomson T, Sabers A. Petrenaite V, et al. Epilepsy Res. 2018 Feb;140:199-208. doi: 10.1016/j.eplepsyres.2018.01.011. Epub 2018 Jan 31. Epilepsy Res. 2018. PMID: 29395496
89 results