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Results by year

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

Year Number of Results
1968 4
1969 1
1970 1
1971 2
1975 4
1976 5
1977 6
1978 3
1979 5
1980 2
1981 1
1982 2
1984 1
1985 5
1986 1
1987 4
1988 3
1989 2
1990 2
1991 4
1992 3
1993 4
1994 2
1995 3
1996 1
1997 7
1998 1
2000 1
2001 1
2002 4
2003 1
2005 1
2006 3
2007 1
2009 1
2010 1
2011 1
2013 3
2016 2
2018 1
2019 2
2020 2
2022 1
2023 2
2024 0

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102 results

Results by year

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Page 1
Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation.
Radford EJ, Tan HK, Andersson MHL, Stephenson JD, Gardner EJ, Ironfield H, Waters AJ, Gitterman D, Lindsay S, Abascal F, Martincorena I, Kolesnik-Taylor A, Ng-Cordell E, Firth HV, Baker K, Perry JRB, Adams DJ, Gerety SS, Hurles ME. Radford EJ, et al. Among authors: stephenson jd. Nat Commun. 2023 Dec 6;14(1):7702. doi: 10.1038/s41467-023-43041-4. Nat Commun. 2023. PMID: 38057330 Free PMC article.
Characterizing 3D RNA structure by single molecule FRET.
Stephenson JD, Kenyon JC, Symmons MF, Lever AM. Stephenson JD, et al. Methods. 2016 Jul 1;103:57-67. doi: 10.1016/j.ymeth.2016.02.004. Epub 2016 Feb 4. Methods. 2016. PMID: 26853327 Review.
VarSite: Disease variants and protein structure.
Laskowski RA, Stephenson JD, Sillitoe I, Orengo CA, Thornton JM. Laskowski RA, et al. Among authors: stephenson jd. Protein Sci. 2020 Jan;29(1):111-119. doi: 10.1002/pro.3746. Epub 2019 Oct 27. Protein Sci. 2020. PMID: 31606900 Free PMC article.
Boron enrichment in martian clay.
Stephenson JD, Hallis LJ, Nagashima K, Freeland SJ. Stephenson JD, et al. PLoS One. 2013 Jun 6;8(6):e64624. doi: 10.1371/journal.pone.0064624. Print 2013. PLoS One. 2013. PMID: 23762242 Free PMC article.
Quantifying the contribution of recessive coding variation to developmental disorders.
Martin HC, Jones WD, McIntyre R, Sanchez-Andrade G, Sanderson M, Stephenson JD, Jones CP, Handsaker J, Gallone G, Bruntraeger M, McRae JF, Prigmore E, Short P, Niemi M, Kaplanis J, Radford EJ, Akawi N, Balasubramanian M, Dean J, Horton R, Hulbert A, Johnson DS, Johnson K, Kumar D, Lynch SA, Mehta SG, Morton J, Parker MJ, Splitt M, Turnpenny PD, Vasudevan PC, Wright M, Bassett A, Gerety SS, Wright CF, FitzPatrick DR, Firth HV, Hurles ME, Barrett JC; Deciphering Developmental Disorders Study. Martin HC, et al. Among authors: stephenson jd. Science. 2018 Dec 7;362(6419):1161-1164. doi: 10.1126/science.aar6731. Epub 2018 Nov 8. Science. 2018. PMID: 30409806 Free PMC article.
Unearthing the root of amino acid similarity.
Stephenson JD, Freeland SJ. Stephenson JD, et al. J Mol Evol. 2013 Oct;77(4):159-69. doi: 10.1007/s00239-013-9565-0. Epub 2013 Jun 7. J Mol Evol. 2013. PMID: 23743923 Free PMC article.
Translational derepression of Elavl4 isoforms at their alternative 5' UTRs determines neuronal development.
Popovitchenko T, Park Y, Page NF, Luo X, Krsnik Z, Liu Y, Salamon I, Stephenson JD, Kraushar ML, Volk NL, Patel SM, Wijeratne HRS, Li D, Suthar KS, Wach A, Sun M, Arnold SJ, Akamatsu W, Okano H, Paillard L, Zhang H, Buyske S, Kostovic I, De Rubeis S, Hart RP, Rasin MR. Popovitchenko T, et al. Among authors: stephenson jd. Nat Commun. 2020 Apr 3;11(1):1674. doi: 10.1038/s41467-020-15412-8. Nat Commun. 2020. PMID: 32245946 Free PMC article.
102 results