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

Year Number of Results
1955 1
1968 4
1969 2
1972 4
1973 2
1976 2
1978 1
1980 4
1981 3
1982 6
1983 2
1985 1
1986 2
1988 2
1991 1
1992 2
1993 1
1994 1
1995 7
1996 4
1997 1
1998 2
1999 1
2000 3
2001 2
2002 9
2003 15
2004 5
2005 9
2006 11
2007 12
2008 9
2009 10
2010 10
2011 13
2012 20
2013 20
2014 25
2015 24
2016 35
2017 34
2018 34
2019 49
2020 66
2021 77
2022 64
2023 77
2024 75

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704 results

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Page 1
Asifa Akhtar.
Akhtar A. Akhtar A. Curr Biol. 2023 Apr 24;33(8):R286-R287. doi: 10.1016/j.cub.2023.03.040. Curr Biol. 2023. PMID: 37098326 Free article.
RNA damage compartmentalization by DHX9 stress granules.
Zhou Y, Panhale A, Shvedunova M, Balan M, Gomez-Auli A, Holz H, Seyfferth J, Helmstädter M, Kayser S, Zhao Y, Erdogdu NU, Grzadzielewska I, Mittler G, Manke T, Akhtar A. Zhou Y, et al. Among authors: akhtar a. Cell. 2024 Mar 28;187(7):1701-1718.e28. doi: 10.1016/j.cell.2024.02.028. Epub 2024 Mar 18. Cell. 2024. PMID: 38503283 Free article.
Hyaluronidases: A Therapeutic Enzyme.
Khan N, Niazi ZR, Rehman FU, Akhtar A, Khan MM, Khan S, Baloch N, Khan S. Khan N, et al. Among authors: akhtar a. Protein Pept Lett. 2018;25(7):663-676. doi: 10.2174/0929866525666180629121823. Protein Pept Lett. 2018. PMID: 29956608 Review.
MSL2 ensures biallelic gene expression in mammals.
Sun Y, Wiese M, Hmadi R, Karayol R, Seyfferth J, Martinez Greene JA, Erdogdu NU, Deboutte W, Arrigoni L, Holz H, Renschler G, Hirsch N, Foertsch A, Basilicata MF, Stehle T, Shvedunova M, Bella C, Pessoa Rodrigues C, Schwalb B, Cramer P, Manke T, Akhtar A. Sun Y, et al. Among authors: akhtar a. Nature. 2023 Dec;624(7990):173-181. doi: 10.1038/s41586-023-06781-3. Epub 2023 Nov 29. Nature. 2023. PMID: 38030723 Free PMC article.
COX17 acetylation via MOF-KANSL complex promotes mitochondrial integrity and function.
Guhathakurta S, Erdogdu NU, Hoffmann JJ, Grzadzielewska I, Schendzielorz A, Seyfferth J, Mårtensson CU, Corrado M, Karoutas A, Warscheid B, Pfanner N, Becker T, Akhtar A. Guhathakurta S, et al. Among authors: akhtar a. Nat Metab. 2023 Nov;5(11):1931-1952. doi: 10.1038/s42255-023-00904-w. Epub 2023 Oct 9. Nat Metab. 2023. PMID: 37813994 Free PMC article.
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.
Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, Kerkhof J, McConkey H, Shvedunova M, Petersen AK, Magnussen K, Zweier C, Vasileiou G, Reis A, Savatt JM, Mulligan MR, Bicknell LS, Poke G, Abu-El-Haija A, Duis J, Hannig V, Srivastava S, Barkoudah E, Hauser NS, van den Born M, Hamiel U, Henig N, Baris Feldman H, McKee S, Krapels IPC, Lei Y, Todorova A, Yordanova R, Atemin S, Rogac M, McConnell V, Chassevent A, Barañano KW, Shashi V, Sullivan JA, Peron A, Iascone M, Canevini MP, Friedman J, Reyes IA, Kierstein J, Shen JJ, Ahmed FN, Mao X, Almoguera B, Blanco-Kelly F, Platzer K, Treu AB, Quilichini J, Bourgois A, Chatron N, Januel L, Rougeot C, Carere DA, Monaghan KG, Rousseau J, Myers KA, Sadikovic B, Akhtar A, Campeau PM. Karayol R, et al. Among authors: akhtar a. Am J Hum Genet. 2024 Jul 11;111(7):1330-1351. doi: 10.1016/j.ajhg.2024.05.001. Epub 2024 May 29. Am J Hum Genet. 2024. PMID: 38815585 Free PMC article.
704 results