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

Year Number of Results
1980 1
1982 1
1983 8
1984 2
1985 2
1987 4
1989 2
1991 4
1992 6
1993 3
1994 6
1995 6
1996 2
1997 10
1998 10
1999 12
2000 8
2001 8
2002 9
2003 10
2004 7
2005 5
2006 2
2007 4
2008 5
2009 8
2010 4
2011 7
2012 12
2013 11
2014 8
2015 7
2016 6
2017 3
2018 4
2019 1
2020 4
2021 3
2022 7
2023 7
2024 0

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219 results

Results by year

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Page 1
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.
Simon MM, Greenaway S, White JK, Fuchs H, Gailus-Durner V, Wells S, Sorg T, Wong K, Bedu E, Cartwright EJ, Dacquin R, Djebali S, Estabel J, Graw J, Ingham NJ, Jackson IJ, Lengeling A, Mandillo S, Marvel J, Meziane H, Preitner F, Puk O, Roux M, Adams DJ, Atkins S, Ayadi A, Becker L, Blake A, Brooker D, Cater H, Champy MF, Combe R, Danecek P, di Fenza A, Gates H, Gerdin AK, Golini E, Hancock JM, Hans W, Hölter SM, Hough T, Jurdic P, Keane TM, Morgan H, Müller W, Neff F, Nicholson G, Pasche B, Roberson LA, Rozman J, Sanderson M, Santos L, Selloum M, Shannon C, Southwell A, Tocchini-Valentini GP, Vancollie VE, Westerberg H, Wurst W, Zi M, Yalcin B, Ramirez-Solis R, Steel KP, Mallon AM, de Angelis MH, Herault Y, Brown SD. Simon MM, et al. Among authors: steel kp. Genome Biol. 2013 Jul 31;14(7):R82. doi: 10.1186/gb-2013-14-7-r82. Genome Biol. 2013. PMID: 23902802 Free PMC article.
Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study.
Le Quesne Stabej P, Saihan Z, Rangesh N, Steele-Stallard HB, Ambrose J, Coffey A, Emmerson J, Haralambous E, Hughes Y, Steel KP, Luxon LM, Webster AR, Bitner-Glindzicz M. Le Quesne Stabej P, et al. Among authors: steel kp. J Med Genet. 2012 Jan;49(1):27-36. doi: 10.1136/jmedgenet-2011-100468. Epub 2011 Dec 1. J Med Genet. 2012. PMID: 22135276 Free PMC article.
A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.
Lenassi E, Vincent A, Li Z, Saihan Z, Coffey AJ, Steele-Stallard HB, Moore AT, Steel KP, Luxon LM, Héon E, Bitner-Glindzicz M, Webster AR. Lenassi E, et al. Among authors: steel kp. Eur J Hum Genet. 2015 Oct;23(10):1318-27. doi: 10.1038/ejhg.2014.283. Epub 2015 Feb 4. Eur J Hum Genet. 2015. PMID: 25649381 Free PMC article.
Genetics of deafness.
Steel KP, Brown SD. Steel KP, et al. Curr Opin Neurobiol. 1996 Aug;6(4):520-5. doi: 10.1016/s0959-4388(96)80059-6. Curr Opin Neurobiol. 1996. PMID: 8794099 Review.
Genes and deafness.
Steel KP, Brown SD. Steel KP, et al. Trends Genet. 1994 Dec;10(12):428-35. doi: 10.1016/0168-9525(94)90113-9. Trends Genet. 1994. PMID: 7871592 Review.
MicroRNAs in mouse development and disease.
Lewis MA, Steel KP. Lewis MA, et al. Among authors: steel kp. Semin Cell Dev Biol. 2010 Sep;21(7):774-80. doi: 10.1016/j.semcdb.2010.02.004. Epub 2010 Feb 10. Semin Cell Dev Biol. 2010. PMID: 20152923 Free PMC article. Review.
More deafness genes.
Steel KP, Brown SD. Steel KP, et al. Science. 1998 May 29;280(5368):1403. doi: 10.1126/science.280.5368.1403. Science. 1998. PMID: 9634418 No abstract available.
219 results