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

Year Number of Results
1964 1
2001 1
2002 1
2004 1
2005 4
2006 2
2008 2
2009 1
2010 3
2011 2
2013 2
2014 1
2015 2
2017 2
2019 1
2020 2
2022 3
2023 1
2024 0

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30 results

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Page 1
On the causes of outliers in Affymetrix GeneChip data.
Upton GJ, Sanchez-Graillet O, Rowsell J, Arteaga-Salas JM, Graham NS, Stalteri MA, Memon FN, May ST, Harrison AP. Upton GJ, et al. Among authors: rowsell j. Brief Funct Genomic Proteomic. 2009 May;8(3):199-212. doi: 10.1093/bfgp/elp027. Brief Funct Genomic Proteomic. 2009. PMID: 19734302 Review.
Combining refutations and social norms increases belief change.
Ecker UK, Sanderson JA, McIlhiney P, Rowsell JJ, Quekett HL, Brown GD, Lewandowsky S. Ecker UK, et al. Among authors: rowsell jj. Q J Exp Psychol (Hove). 2023 Jun;76(6):1275-1297. doi: 10.1177/17470218221111750. Epub 2022 Jul 15. Q J Exp Psychol (Hove). 2023. PMID: 35748514 Free PMC article.
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism.
Tavasoli M, Lahire S, Sokolenko S, Novorolsky R, Reid SA, Lefsay A, Otley MOC, Uaesoontrachoon K, Rowsell J, Srinivassane S, Praest M, MacKinnon A, Mammoliti MS, Maloney AA, Moraca M, Pedro Fernandez-Murray J, McKenna M, Sinal CJ, Nagaraju K, Robertson GS, Hoffman EP, McMaster CR. Tavasoli M, et al. Among authors: rowsell j. Nat Commun. 2022 Mar 23;13(1):1559. doi: 10.1038/s41467-022-29270-z. Nat Commun. 2022. PMID: 35322809 Free PMC article.
Hirschsprung's disease in the UK and Ireland: incidence and anomalies.
Bradnock TJ, Knight M, Kenny S, Nair M, Walker GM; British Association of Paediatric Surgeons Congenital Anomalies Surveillance System. Bradnock TJ, et al. Arch Dis Child. 2017 Aug;102(8):722-727. doi: 10.1136/archdischild-2016-311872. Epub 2017 Mar 9. Arch Dis Child. 2017. PMID: 28280094 Free PMC article.
Orthogonal analysis of dystrophin protein and mRNA as a surrogate outcome for drug development.
Uaesoontrachoon K, Srinivassane S, Warford J, Mekhssian K, Montpetit H, Beauvois R, Keyhani A, Hathout Y, Yamashita T, Satou Y, Osaki H, Praest M, Moraca M, Malbasic M, Ross W, MacKinnon A, Rowsell J, Mullen A, Matyas M, Mummidivarpu S, Nagaraju K, Hoffman EP. Uaesoontrachoon K, et al. Among authors: rowsell j. Biomark Med. 2019 Oct;13(14):1209-1225. doi: 10.2217/bmm-2019-0242. Epub 2019 Aug 5. Biomark Med. 2019. PMID: 31379197 Free article.
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia.
Tavasoli M, Feridooni T, Feridooni H, Sokolenko S, Mishra A, Lefsay A, Srinivassane S, Reid SA, Rowsell J, Praest M, MacKinnon A, Mammoliti M, Maloney AA, Moraca M, Uaesoontrachoon K, Nagaraju K, Hoffman EP, Pasumarthi KBS, McMaster CR. Tavasoli M, et al. Among authors: rowsell j. J Biol Chem. 2022 Mar;298(3):101716. doi: 10.1016/j.jbc.2022.101716. Epub 2022 Feb 11. J Biol Chem. 2022. PMID: 35151687 Free PMC article.
30 results