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

Year Number of Results
1951 1
1953 1
1965 1
1969 2
1973 1
1974 2
1975 1
1976 3
1977 1
1978 2
1980 1
1981 3
1982 3
1983 1
1984 3
1985 4
1986 6
1987 12
1988 2
1989 5
1990 8
1991 5
1992 8
1993 8
1994 5
1995 6
1996 4
1997 8
1998 11
1999 10
2000 14
2001 21
2002 21
2003 19
2004 14
2005 34
2006 46
2007 53
2008 42
2009 67
2010 47
2011 56
2012 71
2013 64
2014 79
2015 83
2016 81
2017 74
2018 84
2019 104
2020 123
2021 128
2022 118
2023 124
2024 37

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The following term was not found in PubMed: Rosaliya
Page 1
Reply.
Lois N; of the EMERALD Study Group. Lois N, et al. Ophthalmology. 2021 Sep;128(9):e46-e47. doi: 10.1016/j.ophtha.2021.05.014. Epub 2021 Jun 25. Ophthalmology. 2021. PMID: 34183173 No abstract available.
Mechano-bactericidal actions of nanostructured surfaces.
Linklater DP, Baulin VA, Juodkazis S, Crawford RJ, Stoodley P, Ivanova EP. Linklater DP, et al. Nat Rev Microbiol. 2021 Jan;19(1):8-22. doi: 10.1038/s41579-020-0414-z. Epub 2020 Aug 17. Nat Rev Microbiol. 2021. PMID: 32807981 Review.
Three-Dimensional Pyrene-Fused N-Heteroacenes.
Hu BL, An C, Wagner M, Ivanova G, Ivanova A, Baumgarten M. Hu BL, et al. J Am Chem Soc. 2019 Apr 3;141(13):5130-5134. doi: 10.1021/jacs.9b01082. Epub 2019 Mar 18. J Am Chem Soc. 2019. PMID: 30860825 Free PMC article.
Compared to their two-dimensional counterparts, the solubility of these 3D pyrene-fused N-heteroacenes is improved by this 3D covalent linkage with two-dimensional units. The diameters of P1-P4 are 3.66, 6.06, 8.48 and 10.88 nm, respectively, and these 3D molecules are cha …
Compared to their two-dimensional counterparts, the solubility of these 3D pyrene-fused N-heteroacenes is improved by this 3D covalen …
Synthetic Thymidine Analog Labeling without Misconceptions.
Ivanova A, Gruzova O, Ermolaeva E, Astakhova O, Itaman S, Enikolopov G, Lazutkin A. Ivanova A, et al. Cells. 2022 Jun 10;11(12):1888. doi: 10.3390/cells11121888. Cells. 2022. PMID: 35741018 Free PMC article.
Donor-Acceptor Cyclopropanes in the Synthesis of Carbocycles.
Ivanova OA, Trushkov IV. Ivanova OA, et al. Chem Rec. 2019 Nov;19(11):2189-2208. doi: 10.1002/tcr.201800166. Epub 2019 Feb 1. Chem Rec. 2019. PMID: 30707497 Review.
Donor-acceptor cyclopropanes not only participate in a broad range of ring openings with nucleophiles, electrophiles, radical and red-ox agents, but also are excellent substrates for various (3+n)-cycloaddition and (3+n)-annulation processes. Moreover, under treatme …
Donor-acceptor cyclopropanes not only participate in a broad range of ring openings with nucleophiles, electrophiles, radical and red-ox age …
1,578 results