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

Year Number of Results
1971 1
1974 2
1979 1
1987 1
1990 3
1991 5
1992 3
1994 1
1995 4
1996 1
1997 2
1998 3
1999 4
2000 2
2001 3
2002 5
2003 3
2004 7
2005 14
2006 8
2007 12
2008 7
2009 7
2010 7
2011 11
2012 11
2013 8
2014 9
2015 10
2016 17
2017 18
2018 15
2019 8
2020 9
2021 10
2022 15
2023 14
2024 12

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238 results

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Page 1
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus.
Galosi S, Edani BH, Martinelli S, Hansikova H, Eklund EA, Caputi C, Masuelli L, Corsten-Janssen N, Srour M, Oegema R, Bosch DGM, Ellis CA, Amlie-Wolf L, Accogli A, Atallah I, Averdunk L, Barañano KW, Bei R, Bagnasco I, Brusco A, Demarest S, Alaix AS, Di Bonaventura C, Distelmaier F, Elmslie F, Gan-Or Z, Good JM, Gripp K, Kamsteeg EJ, Macnamara E, Marcelis C, Mercier N, Peeden J, Pizzi S, Pannone L, Shinawi M, Toro C, Verbeek NE, Venkateswaran S, Wheeler PG, Zdrazilova L, Zhang R, Zorzi G, Guerrini R, Sessa WC, Lefeber DJ, Tartaglia M, Hamdan FF, Grabińska KA, Leuzzi V. Galosi S, et al. Among authors: eklund ea. Brain. 2022 Mar 29;145(1):208-223. doi: 10.1093/brain/awab299. Brain. 2022. PMID: 34382076 Free PMC article.
Excessive copper impairs intrahepatocyte trafficking and secretion of selenoprotein P.
Schwarz M, Meyer CE, Löser A, Lossow K, Hackler J, Ott C, Jäger S, Mohr I, Eklund EA, Patel AAH, Gul N, Alvarez S, Altinonder I, Wiel C, Maares M, Haase H, Härtlova A, Grune T, Schulze MB, Schwerdtle T, Merle U, Zischka H, Sayin VI, Schomburg L, Kipp AP. Schwarz M, et al. Among authors: eklund ea. Nat Commun. 2023 Jun 13;14(1):3479. doi: 10.1038/s41467-023-39245-3. Nat Commun. 2023. PMID: 37311819 Free PMC article.
Essentials of glycosylation.
Eklund EA, Freeze HH. Eklund EA, et al. Semin Pediatr Neurol. 2005 Sep;12(3):134-43. doi: 10.1016/j.spen.2005.11.001. Semin Pediatr Neurol. 2005. PMID: 16584072 Review. No abstract available.
Regulation of HOX gene expression in AML.
Khan I, Amin MA, Eklund EA, Gartel AL. Khan I, et al. Among authors: eklund ea. Blood Cancer J. 2024 Mar 7;14(1):42. doi: 10.1038/s41408-024-01004-y. Blood Cancer J. 2024. PMID: 38453907 Free PMC article. Review.
Therapeutic Vulnerabilities of Transcription Factors in AML.
Khan I, Eklund EE, Gartel AL. Khan I, et al. Among authors: eklund ee. Mol Cancer Ther. 2021 Feb;20(2):229-237. doi: 10.1158/1535-7163.MCT-20-0115. Epub 2020 Nov 6. Mol Cancer Ther. 2021. PMID: 33158995 Free PMC article. Review.
Neurological aspects of human glycosylation disorders.
Freeze HH, Eklund EA, Ng BG, Patterson MC. Freeze HH, et al. Among authors: eklund ea. Annu Rev Neurosci. 2015 Jul 8;38:105-25. doi: 10.1146/annurev-neuro-071714-034019. Epub 2015 Apr 2. Annu Rev Neurosci. 2015. PMID: 25840006 Free PMC article. Review.
Thrombocytopenia and cancer.
Eklund EA. Eklund EA. Cancer Treat Res. 2009;148:279-93. doi: 10.1007/978-0-387-79962-9_16. Cancer Treat Res. 2009. PMID: 19377930 Review. No abstract available.
Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants.
Vogel GF, Mozer-Glassberg Y, Landau YE, Schlieben LD, Prokisch H, Feichtinger RG, Mayr JA, Brennenstuhl H, Schröter J, Pechlaner A, Alkuraya FS, Baker JJ, Barcia G, Baric I, Braverman N, Burnyte B, Christodoulou J, Ciara E, Coman D, Das AM, Darin N, Della Marina A, Distelmaier F, Eklund EA, Ersoy M, Fang W, Gaignard P, Ganetzky RD, Gonzales E, Howard C, Hughes J, Konstantopoulou V, Kose M, Kerr M, Khan A, Lenz D, McFarland R, Margolis MG, Morrison K, Müller T, Murayama K, Nicastro E, Pennisi A, Peters H, Piekutowska-Abramczuk D, Rötig A, Santer R, Scaglia F, Schiff M, Shagrani M, Sharrard M, Soler-Alfonso C, Staufner C, Storey I, Stormon M, Taylor RW, Thorburn DR, Teles EL, Wang JS, Weghuber D, Wortmannd S. Vogel GF, et al. Among authors: eklund ea. Genet Med. 2023 Jun;25(6):100828. doi: 10.1016/j.gim.2023.100828. Epub 2023 Apr 13. Genet Med. 2023. PMID: 37272928 Free article. No abstract available.
Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants.
Vogel GF, Mozer-Glassberg Y, Landau YE, Schlieben LD, Prokisch H, Feichtinger RG, Mayr JA, Brennenstuhl H, Schröter J, Pechlaner A, Alkuraya FS, Baker JJ, Barcia G, Baric I, Braverman N, Burnyte B, Christodoulou J, Ciara E, Coman D, Das AM, Darin N, Della Marina A, Distelmaier F, Eklund EA, Ersoy M, Fang W, Gaignard P, Ganetzky RD, Gonzales E, Howard C, Hughes J, Konstantopoulou V, Kose M, Kerr M, Khan A, Lenz D, McFarland R, Margolis MG, Morrison K, Müller T, Murayama K, Nicastro E, Pennisi A, Peters H, Piekutowska-Abramczuk D, Rötig A, Santer R, Scaglia F, Schiff M, Shagrani M, Sharrard M, Soler-Alfonso C, Staufner C, Storey I, Stormon M, Taylor RW, Thorburn DR, Teles EL, Wang JS, Weghuber D, Wortmann S. Vogel GF, et al. Among authors: eklund ea. Genet Med. 2023 Jun;25(6):100314. doi: 10.1016/j.gim.2022.09.015. Epub 2022 Oct 29. Genet Med. 2023. PMID: 36305855 Free article.
238 results