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Results by year

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

Year Number of Results
1956 1
1958 1
1959 4
1960 3
1961 1
1962 1
1963 2
1964 4
1965 1
1967 1
1969 3
1972 1
1974 2
1977 1
1978 1
1979 1
1980 2
1981 3
1982 5
1983 10
1984 5
1985 6
1986 2
1987 5
1988 3
1989 4
1990 3
1991 8
1992 7
1993 10
1994 11
1995 11
1996 6
1997 18
1998 15
1999 17
2000 13
2001 12
2002 11
2003 11
2004 11
2005 10
2006 5
2007 9
2008 9
2009 10
2010 6
2011 10
2012 14
2013 16
2014 15
2015 15
2016 16
2017 8
2018 7
2019 6
2020 18
2021 10
2022 12
2023 15
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

431 results

Results by year

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Page 1
Exercise for dysmenorrhoea.
Armour M, Ee CC, Naidoo D, Ayati Z, Chalmers KJ, Steel KA, de Manincor MJ, Delshad E. Armour M, et al. Among authors: steel ka. Cochrane Database Syst Rev. 2019 Sep 20;9(9):CD004142. doi: 10.1002/14651858.CD004142.pub4. Cochrane Database Syst Rev. 2019. PMID: 31538328 Free PMC article.
IL-17 in the immunopathogenesis of spondyloarthritis.
Taams LS, Steel KJA, Srenathan U, Burns LA, Kirkham BW. Taams LS, et al. Among authors: steel kja. Nat Rev Rheumatol. 2018 Aug;14(8):453-466. doi: 10.1038/s41584-018-0044-2. Nat Rev Rheumatol. 2018. PMID: 30006601 Review.
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.
Alzheimer's disease.
Steel K. Steel K. N Engl J Med. 2010 May 13;362(19):1844; author reply 1844-5. N Engl J Med. 2010. PMID: 20468086 Free article. No abstract available.
Getting to the core of ADAR2 activity in AML.
Steel K, Jamieson C. Steel K, et al. Blood. 2023 Jun 22;141(25):3014-3015. doi: 10.1182/blood.2023019923. Blood. 2023. PMID: 37347500 No abstract available.
431 results