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

Year Number of Results
1980 1
1984 1
1985 1
1987 1
1989 4
1990 6
1991 3
1992 6
1993 6
1994 8
1995 11
1996 11
1997 7
1998 23
1999 20
2000 34
2001 41
2002 45
2003 65
2004 70
2005 75
2006 104
2007 108
2008 123
2009 157
2010 172
2011 257
2012 246
2013 274
2014 326
2015 439
2016 412
2017 471
2018 525
2019 639
2020 812
2021 871
2022 970
2023 1088
2024 1318
2025 1467
2026 481

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10,496 results

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Page 1
Antifibrotic drug finerenone restores fertility in premature ovarian insufficiency.
Lin Z, Li Y, Zhao Y, Liu D, Deng S, Gu J, Li Y, Zhao X, Wu P, Xiao Y, Su J, Sun Y, Zhang Y, Lee YL, Sato Y, Zeng H, Lu H, Zhang J, Ko JKY, Zhao J, Kawamura K, Ng EHY, Jiang S, Li Y, Xia X, Chan KKL, Yeung WSB, Wang TR, Liu K. Lin Z, et al. Among authors: zeng h. Science. 2026 Feb 5;391(6785):eadz4075. doi: 10.1126/science.adz4075. Epub 2026 Feb 5. Science. 2026. PMID: 41643022
Brain neuron-derived WDFY1 induces bone loss.
Chen CY, Wang Z, Hong CG, Tan YJ, Duan YX, Luo Y, Wang X, Zeng HJ, Luo JY, Wan TF, Yin H, Liu XX, Zhu H, Zhou Y, Wang ZG, He ZH, Hu XY, Hu GW, Lang HL, Wang ZX, Cao J, Rao SS, Xie H. Chen CY, et al. Among authors: zeng hj. Nat Aging. 2026 Feb;6(2):329-348. doi: 10.1038/s43587-025-01032-8. Epub 2026 Jan 5. Nat Aging. 2026. PMID: 41491871
Enantioselective protein affinity selection mass spectrometry (E-ASMS).
Wang X, Sun J, Ahmad S, Yang D, Li F, Chan UH, Zeng H, Simoben CV, Green SR, Silva M, Houliston S, Dong A, Bolotokova A, Gibson E, Kutera M, Ghiabi P, Kondratov I, Matviyuk T, Chuprina A, Mavridi D, Lenz C, Joerger AC, Brown BD, Heath RB, Yue WW, Robbie LK, Beyett TS, Müller S, Knapp S, Owen DR, Harding R, Schapira M, Brown PJ, Santhakumar V, Ackloo S, Arrowsmith CH, Edwards AM, Peng H, Halabelian L. Wang X, et al. Among authors: zeng h. Nat Commun. 2025 Dec 17;17(1):651. doi: 10.1038/s41467-025-67403-2. Nat Commun. 2025. PMID: 41407727 Free PMC article.
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Kröll-Hermi A, Stoetzel C, Etard C, Halabelian L, Schaefer E, Scheidecker S, Kahrizi K, Payman J, Geoffroy V, Prasad M, Obringer C, Ruch L, Girard A, Zeng H, Li F, Plassard D, Keime C, Mattioli F, Feger C, Piton A, Fujita A, Matsumoto N, Castro MAA, Ae KC, Ruaud L, Levy J, Dozières B, Tabet AC, Wentzensen IM, Santiago-Sim T, Yusupov R, Tveten K, Smeland MF, Alkhunaizi E, Cowing G, Li C, Wortmann SB, Feichtinger RG, Mayr JA, Gonorazky H, Jing G, Wang X, Wang J, Bierhals T, Grinstein L, Herget T, Ruiz A, Gabau E, Kampmeier A, Kassel O, Kuechler A, Platzer K, Jamra RA, Woerner A, Idleburg M, Kircher SG, Laccone F, Golob B, Peterlin B, Čuturilo G, Tasic V, Kolvenbach CM, Hildebrandt F, Ramos LLP, Kok F, Buck CB, van de Laar IMBH, de Man SA, Taşdelen E, Sezer A, Büke A, Yavuz Z, Çomoğlu SS, Costin C, Tran Mau Them F, Lacaze E, Courtin T, Héron D, Keren B, Whalen S, Roume J, Yang Y, Hoffer MJV, van Haeringen A, Najmabadi H, Arrowsmith CH, Strähle U, Dollfus H, Muller J. Kröll-Hermi A, et al. Among authors: zeng h. Am J Hum Genet. 2025 Dec 4;112(12):2943-2960. doi: 10.1016/j.ajhg.2025.10.014. Epub 2025 Nov 18. Am J Hum Genet. 2025. PMID: 41260215 Free PMC article.
10,496 results
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