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

Year Number of Results
1970 1
1971 3
1972 1
1973 1
1974 2
1975 4
1976 2
1977 2
1978 1
1979 3
1980 3
1981 2
1982 3
1983 1
1984 2
1985 4
1986 3
1987 6
1988 3
1989 4
1990 6
1991 6
1992 8
1993 3
1994 5
1995 4
1996 9
1997 7
1998 12
1999 5
2000 6
2001 6
2002 6
2003 8
2004 7
2005 10
2006 8
2007 5
2008 7
2009 2
2010 8
2011 2
2012 4
2013 5
2014 6
2015 2
2016 8
2017 6
2018 1
2019 5
2020 3
2021 3
Text availability
Article attribute
Article type
Publication date

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225 results
Results by year
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Page 1
Retraction.
Flavell RA, Kaczmarek LK, Badou A, Boulpaep EL, Desai R, Basavappa S, Matza D, Peng YQ, Mehal WZ. Flavell RA, et al. Among authors: kaczmarek lk. Science. 2005 Dec 23;310(5756):1903. doi: 10.1126/science.310.5756.1903b. Science. 2005. PMID: 16373558 No abstract available.
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Barcia G, Fleming MR, Deligniere A, Gazula VR, Brown MR, Langouet M, Chen H, Kronengold J, Abhyankar A, Cilio R, Nitschke P, Kaminska A, Boddaert N, Casanova JL, Desguerre I, Munnich A, Dulac O, Kaczmarek LK, Colleaux L, Nabbout R. Barcia G, et al. Among authors: kaczmarek lk. Nat Genet. 2012 Nov;44(11):1255-9. doi: 10.1038/ng.2441. Epub 2012 Oct 21. Nat Genet. 2012. PMID: 23086397 Free PMC article.
Zika Virus Disrupts Phospho-TBK1 Localization and Mitosis in Human Neuroepithelial Stem Cells and Radial Glia.
Onorati M, Li Z, Liu F, Sousa AMM, Nakagawa N, Li M, Dell'Anno MT, Gulden FO, Pochareddy S, Tebbenkamp ATN, Han W, Pletikos M, Gao T, Zhu Y, Bichsel C, Varela L, Szigeti-Buck K, Lisgo S, Zhang Y, Testen A, Gao XB, Mlakar J, Popovic M, Flamand M, Strittmatter SM, Kaczmarek LK, Anton ES, Horvath TL, Lindenbach BD, Sestan N. Onorati M, et al. Among authors: kaczmarek lk. Cell Rep. 2016 Sep 6;16(10):2576-2592. doi: 10.1016/j.celrep.2016.08.038. Epub 2016 Aug 24. Cell Rep. 2016. PMID: 27568284 Free PMC article.
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.
Martin HC, Kim GE, Pagnamenta AT, Murakami Y, Carvill GL, Meyer E, Copley RR, Rimmer A, Barcia G, Fleming MR, Kronengold J, Brown MR, Hudspith KA, Broxholme J, Kanapin A, Cazier JB, Kinoshita T, Nabbout R; WGS500 Consortium, Bentley D, McVean G, Heavin S, Zaiwalla Z, McShane T, Mefford HC, Shears D, Stewart H, Kurian MA, Scheffer IE, Blair E, Donnelly P, Kaczmarek LK, Taylor JC. Martin HC, et al. Among authors: kaczmarek lk. Hum Mol Genet. 2014 Jun 15;23(12):3200-11. doi: 10.1093/hmg/ddu030. Epub 2014 Jan 25. Hum Mol Genet. 2014. PMID: 24463883 Free PMC article.
Mechanisms underlying auditory processing deficits in Fragile X syndrome.
McCullagh EA, Rotschafer SE, Auerbach BD, Klug A, Kaczmarek LK, Cramer KS, Kulesza RJ Jr, Razak KA, Lovelace JW, Lu Y, Koch U, Wang Y. McCullagh EA, et al. Among authors: kaczmarek lk. FASEB J. 2020 Mar;34(3):3501-3518. doi: 10.1096/fj.201902435R. Epub 2020 Feb 10. FASEB J. 2020. PMID: 32039504 Free PMC article. Review.
Kv3.3 potassium channels and spinocerebellar ataxia.
Zhang Y, Kaczmarek LK. Zhang Y, et al. Among authors: kaczmarek lk. J Physiol. 2016 Aug 15;594(16):4677-84. doi: 10.1113/JP271343. Epub 2015 Nov 15. J Physiol. 2016. PMID: 26442672 Free PMC article. Review.
225 results
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