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

Year Number of Results
2002 2
2004 7
2005 2
2006 3
2008 3
2009 5
2010 7
2011 5
2012 3
2013 11
2014 3
2015 4
2016 2
2017 2
2018 2
2019 1
2020 5
2021 2
2022 3
2023 3
2024 0

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67 results

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Page 1
Triglyceride Lowering with Pemafibrate to Reduce Cardiovascular Risk.
Das Pradhan A, Glynn RJ, Fruchart JC, MacFadyen JG, Zaharris ES, Everett BM, Campbell SE, Oshima R, Amarenco P, Blom DJ, Brinton EA, Eckel RH, Elam MB, Felicio JS, Ginsberg HN, Goudev A, Ishibashi S, Joseph J, Kodama T, Koenig W, Leiter LA, Lorenzatti AJ, Mankovsky B, Marx N, Nordestgaard BG, Páll D, Ray KK, Santos RD, Soran H, Susekov A, Tendera M, Yokote K, Paynter NP, Buring JE, Libby P, Ridker PM; PROMINENT Investigators. Das Pradhan A, et al. N Engl J Med. 2022 Nov 24;387(21):1923-1934. doi: 10.1056/NEJMoa2210645. Epub 2022 Nov 5. N Engl J Med. 2022. PMID: 36342113 Clinical Trial.
Relevance of CYP2C9 Function in Valproate Therapy.
Monostory K, Nagy A, Tóth K, Bűdi T, Kiss Á, Déri M, Csukly G. Monostory K, et al. Among authors: nagy a. Curr Neuropharmacol. 2019;17(1):99-106. doi: 10.2174/1570159X15666171109143654. Curr Neuropharmacol. 2019. PMID: 29119932 Free PMC article. Review.
Prolonged activity of the transposase helper may raise safety concerns during DNA transposon-based gene therapy.
Imre G, Takács B, Czipa E, Drubi AB, Jaksa G, Latinovics D, Nagy A, Karkas R, Hudoba L, Vásárhelyi BM, Pankotai-Bodó G, Blastyák A, Hegedűs Z, Germán P, Bálint B, Ahmed Abdullah KS, Kopasz AG, Kovács A, Nagy LG, Sükösd F, Pintér L, Rülicke T, Barta E, Nagy I, Haracska L, Mátés L. Imre G, et al. Among authors: nagy a. Mol Ther Methods Clin Dev. 2023 Mar 14;29:145-159. doi: 10.1016/j.omtm.2023.03.003. eCollection 2023 Jun 8. Mol Ther Methods Clin Dev. 2023. PMID: 37025950 Free PMC article.
PRIM1 deficiency causes a distinctive primordial dwarfism syndrome.
Parry DA, Tamayo-Orrego L, Carroll P, Marsh JA, Greene P, Murina O, Uggenti C, Leitch A; Scottish Genomes Partnership; Káposzta R, Merő G, Nagy A, Orlik B, Kovács-Pászthy B, Quigley AJ, Riszter M, Rankin J, Reijns MAM, Szakszon K, Jackson AP; Members of the Scottish Genome Partnership include. Parry DA, et al. Among authors: nagy a. Genes Dev. 2020 Nov 1;34(21-22):1520-1533. doi: 10.1101/gad.340190.120. Epub 2020 Oct 15. Genes Dev. 2020. PMID: 33060134 Free PMC article.
A versatile transposon-based technology to generate loss- and gain-of-function phenotypes in the mouse liver.
Kopasz AG, Pusztai DZ, Karkas R, Hudoba L, Abdullah KSA, Imre G, Pankotai-Bodó G, Migh E, Nagy A, Kriston A, Germán P, Drubi AB, Molnár A, Fekete I, Dani VÉ, Ocsovszki I, Puskás LG, Horváth P, Sükösd F, Mátés L. Kopasz AG, et al. Among authors: nagy a. BMC Biol. 2022 Apr 1;20(1):74. doi: 10.1186/s12915-022-01262-x. BMC Biol. 2022. PMID: 35361222 Free PMC article.
Clinical and genetic characteristics of craniosynostosis in Hungary.
Bessenyei B, Nagy A, Szakszon K, Mokánszki A, Balogh E, Ujfalusi A, Tihanyi M, Novák L, Bognár L, Oláh É. Bessenyei B, et al. Among authors: nagy a. Am J Med Genet A. 2015 Dec;167A(12):2985-91. doi: 10.1002/ajmg.a.37298. Epub 2015 Aug 20. Am J Med Genet A. 2015. PMID: 26289989
67 results