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

Year Number of Results
1964 2
1972 1
1974 4
1975 1
1976 2
1978 5
1980 2
1981 1
1983 2
1984 1
1985 2
1987 2
1988 2
1993 2
1995 2
1996 1
1997 1
1999 2
2000 1
2001 1
2002 1
2003 2
2004 1
2005 1
2006 3
2007 2
2008 2
2010 1
2011 6
2012 3
2013 3
2014 2
2015 2
2016 3
2017 6
2020 2
2021 0
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Publication date

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72 results
Results by year
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Page 1
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
Tillotson R, Selfridge J, Koerner MV, Gadalla KKE, Guy J, De Sousa D, Hector RD, Cobb SR, Bird A. Tillotson R, et al. Among authors: cobb sr. Nature. 2017 Oct 19;550(7676):398-401. doi: 10.1038/nature24058. Epub 2017 Oct 11. Nature. 2017. PMID: 29019980 Free PMC article.
A kinome-wide screen identifies a CDKL5-SOX9 regulatory axis in epithelial cell death and kidney injury.
Kim JY, Bai Y, Jayne LA, Hector RD, Persaud AK, Ong SS, Rojesh S, Raj R, Feng MJHH, Chung S, Cianciolo RE, Christman JW, Campbell MJ, Gardner DS, Baker SD, Sparreboom A, Govindarajan R, Singh H, Chen T, Poi M, Susztak K, Cobb SR, Pabla NS. Kim JY, et al. Among authors: cobb sr. Nat Commun. 2020 Apr 21;11(1):1924. doi: 10.1038/s41467-020-15638-6. Nat Commun. 2020. PMID: 32317630 Free PMC article.
Neurodevelopmental disorders.
Cobb SR, Davies CH. Cobb SR, et al. Neuropharmacology. 2013 May;68:1. doi: 10.1016/j.neuropharm.2013.02.001. Epub 2013 Feb 8. Neuropharmacology. 2013. PMID: 23402709 No abstract available.
Rett syndrome: from bed to bench.
Weng SM, Bailey ME, Cobb SR. Weng SM, et al. Among authors: cobb sr. Pediatr Neonatol. 2011 Dec;52(6):309-16. doi: 10.1016/j.pedneo.2011.08.002. Epub 2011 Nov 6. Pediatr Neonatol. 2011. PMID: 22192257 Free article. Review.
Characterisation of Cdkl5 transcript isoforms in rat.
Hector RD, Dando O, Ritakari TE, Kind PC, Bailey ME, Cobb SR. Hector RD, et al. Among authors: cobb sr. Gene. 2017 Mar 1;603:21-26. doi: 10.1016/j.gene.2016.12.001. Epub 2016 Dec 7. Gene. 2017. PMID: 27940108 Free article.
CDKL5 variants: Improving our understanding of a rare neurologic disorder.
Hector RD, Kalscheuer VM, Hennig F, Leonard H, Downs J, Clarke A, Benke TA, Armstrong J, Pineda M, Bailey MES, Cobb SR. Hector RD, et al. Among authors: cobb sr. Neurol Genet. 2017 Dec 15;3(6):e200. doi: 10.1212/NXG.0000000000000200. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264392 Free PMC article.
72 results
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