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

Year Number of Results
1970 1
1977 2
1979 1
1980 2
1981 2
1982 2
1983 5
1984 8
1985 2
1986 10
1987 5
1988 4
1989 10
1990 12
1991 17
1992 21
1993 16
1994 23
1995 22
1996 29
1997 29
1998 32
1999 41
2000 53
2001 61
2002 54
2003 42
2004 81
2005 67
2006 74
2007 92
2008 85
2009 101
2010 136
2011 125
2012 175
2013 175
2014 199
2015 212
2016 241
2017 251
2018 349
2019 361
2020 471
2021 568
2022 519
2023 510
2024 525
2025 582
2026 244

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5,950 results

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Page 1
Multi-omic analysis reveals transkingdom gut dysbiosis in metabolic dysfunction-associated steatotic liver disease.
Kim H, Nelson P, Nzabarushimana E, Shen J, Jensen J, Bhosle A, Li C, Lee N, Everett C, Berdy B, Frongillo G, Livny J, Hu FB, Simon TG, McIver L, Franzosa EA, Chan AT, Hayete B, Thompson KN, Huttenhower C, Nguyen LH. Kim H, et al. Among authors: nguyen lh. Nat Metab. 2025 Jul;7(7):1476-1492. doi: 10.1038/s42255-025-01318-6. Epub 2025 Jul 2. Nat Metab. 2025. PMID: 40604156 Free PMC article.
Persistent T cell activation and cytotoxicity against glioblastoma following single oncolytic virus treatment in a clinical trial.
Meylan M, Tian Y, Wu L, Ling AL, Kovarsky D, Barlow GL, Nguyen LD, Pyrdol J, Marx S, Westphal L, Michel J, Gonzalez Castro LN, Dumont S, Santos A, Tirosh I, Suvà ML, Chiocca EA, Wucherpfennig KW. Meylan M, et al. Among authors: nguyen ld. Cell. 2026 Mar 5;189(5):1287-1304.e18. doi: 10.1016/j.cell.2025.12.055. Epub 2026 Feb 11. Cell. 2026. PMID: 41679299 Free article. Clinical Trial.
Human Hearts Intrinsically Increase Cardiomyocyte Mitosis After Myocardial Infarction.
Hume RD, Warwick J, Shim WJ, Malecki C, Li M, Seth L, Harney D, Dagher J, Lum T, Tierney G, Cooper W, Slaughter E, Wang X, Nguyen L, Cole L, Edelman J, Rashid FN, Houlahan C, Gao A, Ferguson AL, Chong JJH, Larance M, O'Sullivan JF, Palpant NJ, Bannon P, Lal S. Hume RD, et al. Among authors: nguyen l. Circ Res. 2026 Jan 16;138(2):e327486. doi: 10.1161/CIRCRESAHA.125.327486. Epub 2025 Dec 4. Circ Res. 2026. PMID: 41342124 Free PMC article.
Recessive TMEM167A variants cause neonatal diabetes, microcephaly, and epilepsy syndrome.
Virgilio E, Tielens S, Bonfield G, Nian FS, Sawatani T, Vinci C, Govier M, Montaser H, Lartigue R, Arunagiri A, Liboz A, Da Silva FN, Lytrivi M, Papadopoulou T, Wakeling MN, Russ-Silsby J, Bowman P, Johnson MB, Laver TW, Piron A, Yi X, Fantuzzi F, Hendrickx S, Igoillo-Esteve M, Santacreu BJ, Suntharesan J, Ghildiyal R, Hegde D, Shah N, Acar S, Dönmez BÖ, Özkan B, Mohsin F, Talaat IM, Abbas MT, Abbas OT, Alghamdi HA, Kandemir N, Flanagan SE, Scharfmann R, Arvan P, Raoux M, Nguyen L, Hattersley AT, Cnop M, De Franco E. Virgilio E, et al. Among authors: nguyen l. J Clin Invest. 2025 Sep 9;135(22):e195756. doi: 10.1172/JCI195756. eCollection 2025 Nov 17. J Clin Invest. 2025. PMID: 40924476 Free PMC article.
Cytoskeletal control in adult microglia is essential to restore neurodevelopmental synaptic and cognitive deficits.
Kessels S, Trippaers C, Mertens M, Hamad I, Rombaut B, Janssen A, Ramanathan K, Duwé S, Gharghani AM, Theuwis R, Delbroek A, Vangansewinkel T, Berden L, Beeken J, Vandormael P, Poovathingal S, Voets T, Kleinewietfeld M, Nguyen L, Antel JP, Healy LM, Cowley SA, Ishizuka K, Rigo JM, Hendrix J, Vanmierlo T, Dewachter I, Alpizar YA, Sawa A, Brône B. Kessels S, et al. Among authors: nguyen l. Sci Adv. 2025 Aug 29;11(35):eadw0128. doi: 10.1126/sciadv.adw0128. Epub 2025 Aug 29. Sci Adv. 2025. PMID: 40880479 Free PMC article.
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Leitão E, Santini A, Cogne B, Essid M, Athanasiadou M, LaFlamme CW, Marijon P, Bernard V, Chatron N, Barcia G, Keren B, Mignot C, Charles P, Besnard T, de Sainte Agathe JM, Fuerte EPA, Sengupta S, Milh M, Ramond F, Allan T, An I, Araujo C, Arpin S, Austin-Tse C, Auvin S, Baer S, Bahi-Buisson N, Bak M, Barth M, Baulac S, Weirauch NB, Begemann M, Bennett MF, Bensabath U, Bézieau S, Bhouri R, Biehler M, Hammer TB, Bogoin J, Bonanno E, Boussion S, Bramswig NC, Bris C, Brosseau-Beauvir A, Bruel AL, Buratti J, Chambon P, Chemaly N, Chesneau B, Colin E, Colmard M, Conrad S, Courtin T, Dang LT, de Saint Martin A, de Vanssay de Blavous Legendre C, Denommé-Pichon AS, DiTroia S, Doco-Fenzy M, Dubourg C, Dubucs C, Ducreux S, Dufour L, Duquet R, Durand B, Chehadeh SE, Elbracht M, Faivre L, Faoucher M, Faudet A, Forlani S, Fradin M, Gaignard P, Ganne B, Garde A, Géraud J, Gill D, Goldenberg A, Grabli D, Grisel C, Gueden S, Gueguen P, Guerrot AM, Guichet A, Härting N, Häusler MG, Heide S, Héron B, Héron D, Heulin M, Houdayer C, Isidor B, Jacquette A, Januel L, Jean-Marçais N, Jousselin K, Kaiser FJ, Kaya S, King C, Konyukh M, Kraft F, Krause J, Kirstetter R, Kuechler A, Kurth I, Labalme A, Laloy… See abstract for full author list ➔ Leitão E, et al. Among authors: nguyen l. medRxiv [Preprint]. 2025 Sep 4:2025.09.02.25334923. doi: 10.1101/2025.09.02.25334923. medRxiv. 2025. Update in: Nat Genet. 2026 Apr;58(4):782-797. doi: 10.1038/s41588-026-02547-5. PMID: 40950445 Free PMC article. Updated. Preprint.
5,950 results