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Results by year

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

Year Number of Results
1935 1
1946 2
1947 1
1949 1
1954 1
1955 1
1961 1
1964 1
1965 1
1966 1
1967 3
1968 3
1970 1
1971 1
1972 3
1974 8
1975 2
1976 3
1977 5
1978 6
1979 5
1980 4
1981 12
1982 3
1983 5
1984 5
1985 8
1986 15
1987 18
1988 9
1989 13
1990 19
1991 17
1992 20
1993 16
1994 26
1995 28
1996 42
1997 25
1998 35
1999 37
2000 43
2001 52
2002 47
2003 61
2004 59
2005 63
2006 88
2007 120
2008 113
2009 102
2010 107
2011 148
2012 148
2013 127
2014 137
2015 131
2016 102
2017 136
2018 134
2019 164
2020 203
2021 262
2022 214
2023 61
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Article attribute
Article type
Publication date

Search Results

2,921 results
Results by year
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Page 1
Mitochondrial copper depletion suppresses triple-negative breast cancer in mice.
Cui L, Gouw AM, LaGory EL, Guo S, Attarwala N, Tang Y, Qi J, Chen YS, Gao Z, Casey KM, Bazhin AA, Chen M, Hu L, Xie J, Fang M, Zhang C, Zhu Q, Wang Z, Giaccia AJ, Gambhir SS, Zhu W, Felsher DW, Pegram MD, Goun EA, Le A, Rao J. Cui L, et al. Among authors: rao j. Nat Biotechnol. 2021 Mar;39(3):357-367. doi: 10.1038/s41587-020-0707-9. Epub 2020 Oct 19. Nat Biotechnol. 2021. PMID: 33077961 Free PMC article.
Nogo-B is a key mediator of hepatic ischemia and reperfusion injury.
Rao J, Cheng F, Zhou H, Yang W, Qiu J, Yang C, Ni X, Yang S, Xia Y, Pan X, Zhang F, Lu L, Wang X. Rao J, et al. Redox Biol. 2020 Oct;37:101745. doi: 10.1016/j.redox.2020.101745. Epub 2020 Oct 8. Redox Biol. 2020. PMID: 33099216 Free PMC article.
MiR-206 regulates the Th17/Treg ratio during osteoarthritis.
Ye X, Lu Q, Yang A, Rao J, Xie W, He C, Wang W, Li H, Zhang Z. Ye X, et al. Among authors: rao j. Mol Med. 2021 Jun 19;27(1):64. doi: 10.1186/s10020-021-00315-1. Mol Med. 2021. PMID: 34147072 Free PMC article.
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Klämbt V, Deutsch K, Wu CW, Kolvenbach CM, Kause F, Ottlewski I, Schneider R, Kitzler TM, Majmundar AJ, Buerger F, Onuchic-Whitford AC, Youying M, Kolb A, Salmanullah D, Chen E, van der Ven AT, Rao J, Ityel H, Seltzsam S, Rieke JM, Chen J, Vivante A, Hwang DY, Kohl S, Dworschak GC, Hermle T, Alders M, Bartolomaeus T, Bauer SB, Baum MA, Brilstra EH, Challman TD, Zyskind J, Costin CE, Dipple KM, Duijkers FA, Ferguson M, Fitzpatrick DR, Fick R, Glass IA, Hulick PJ, Kline AD, Krey I, Kumar S, Lu W, Marco EJ, Wentzensen IM, Mefford HC, Platzer K, Povolotskaya IS, Savatt JM, Shcherbakova NV, Senguttuvan P, Squire AE, Stein DR, Thiffault I, Voinova VY, Somers MJG, Ferguson MA, Traum AZ, Daouk GH, Daga A, Rodig NM, Terhal PA, van Binsbergen E, Eid LA, Tasic V, Rasouly HM, Lim TY, Ahram DF, Gharavi AG, Reutter HM, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Lifton RP, Xu H, Mane SM, Sanna-Cherchi S, Sharrocks AD, Raught B, Fisher SE, Bouchard M, Khokha MK, Shril S, Hildebrandt F. Connaughton DM, et al. Among authors: rao j. Am J Hum Genet. 2020 Oct 1;107(4):727-742. doi: 10.1016/j.ajhg.2020.08.013. Epub 2020 Sep 4. Am J Hum Genet. 2020. PMID: 32891193 Free PMC article.
2,921 results