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Year | Number of Results |
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2014 | 1 |
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Page 1
Cohesin mutations in myeloid malignancies: underlying mechanisms.
Exp Hematol Oncol. 2014 May 8;3:13. doi: 10.1186/2162-3619-3-13. eCollection 2014.
Exp Hematol Oncol. 2014.
PMID: 24904756
Free PMC article.
Review.
Riboceine Rescues Auranofin-Induced Craniofacial Defects in Zebrafish.
Leask M, Carleton C, Leeke B, Newman T, Antoun J, Farella M, Horsfield J.
Leask M, et al. Among authors: leeke b.
Antioxidants (Basel). 2021 Dec 8;10(12):1964. doi: 10.3390/antiox10121964.
Antioxidants (Basel). 2021.
PMID: 34943067
Free PMC article.
Item in Clipboard
Nucleolar-based Dux repression is essential for embryonic two-cell stage exit.
Xie SQ, Leeke BJ, Whilding C, Wagner RT, Garcia-Llagostera F, Low Y, Chammas P, Cheung NT, Dormann D, McManus MT, Percharde M.
Xie SQ, et al. Among authors: leeke bj.
Genes Dev. 2022 Mar 1;36(5-6):331-347. doi: 10.1101/gad.349172.121. Epub 2022 Mar 10.
Genes Dev. 2022.
PMID: 35273077
Free PMC article.
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Dynamic enlargement and mobilization of lipid droplets in pluripotent cells coordinate morphogenesis during mouse peri-implantation development.
Mau KHT, Karimlou D, Barneda D, Brochard V, Royer C, Leeke B, de Souza RA, Pailles M, Percharde M, Srinivas S, Jouneau A, Christian M, Azuara V.
Mau KHT, et al. Among authors: leeke b.
Nat Commun. 2022 Jul 5;13(1):3861. doi: 10.1038/s41467-022-31323-2.
Nat Commun. 2022.
PMID: 35790717
Free PMC article.
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A neural crest origin for cohesinopathy heart defects.
Schuster K, Leeke B, Meier M, Wang Y, Newman T, Burgess S, Horsfield JA.
Schuster K, et al. Among authors: leeke b.
Hum Mol Genet. 2015 Dec 15;24(24):7005-16. doi: 10.1093/hmg/ddv402. Epub 2015 Sep 29.
Hum Mol Genet. 2015.
PMID: 26420840
Free PMC article.
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Embryonic oxidative stress results in reproductive impairment for adult zebrafish.
Newman TAC, Carleton CR, Leeke B, Hampton MB, Horsfield JA.
Newman TAC, et al. Among authors: leeke b.
Redox Biol. 2015 Dec;6:648-655. doi: 10.1016/j.redox.2015.10.010. Epub 2015 Nov 4.
Redox Biol. 2015.
PMID: 26584358
Free PMC article.
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Antioxidant treatment ameliorates phenotypic features of SMC1A-mutated Cornelia de Lange syndrome in vitro and in vivo.
Cukrov D, Newman TAC, Leask M, Leeke B, Sarogni P, Patimo A, Kline AD, Krantz ID, Horsfield JA, Musio A.
Cukrov D, et al. Among authors: leeke b.
Hum Mol Genet. 2018 Sep 1;27(17):3002-3011. doi: 10.1093/hmg/ddy203.
Hum Mol Genet. 2018.
PMID: 29860495
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