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Page 1
Proteomic Analysis of Histone Variants and Their PTMs: Strategies and Pitfalls.
Proteomes. 2018 Jun 21;6(3):29. doi: 10.3390/proteomes6030029.
Proteomes. 2018.
PMID: 29933573
Free PMC article.
Review.
Systematic quantitative analysis of H2A and H2B variants by targeted proteomics.
El Kennani S, Adrait A, Permiakova O, Hesse AM, Ialy-Radio C, Ferro M, Brun V, Cocquet J, Govin J, Pflieger D.
El Kennani S, et al.
Epigenetics Chromatin. 2018 Jan 12;11(1):2. doi: 10.1186/s13072-017-0172-y.
Epigenetics Chromatin. 2018.
PMID: 29329550
Free PMC article.
Item in Clipboard
Multi-omic analysis of gametogenesis reveals a novel signature at the promoters and distal enhancers of active genes.
Crespo M, Damont A, Blanco M, Lastrucci E, Kennani SE, Ialy-Radio C, Khattabi LE, Terrier S, Louwagie M, Kieffer-Jaquinod S, Hesse AM, Bruley C, Chantalat S, Govin J, Fenaille F, Battail C, Cocquet J, Pflieger D.
Crespo M, et al. Among authors: kennani se.
Nucleic Acids Res. 2020 May 7;48(8):4115-4138. doi: 10.1093/nar/gkaa163.
Nucleic Acids Res. 2020.
PMID: 32182340
Free PMC article.
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MS_HistoneDB, a manually curated resource for proteomic analysis of human and mouse histones.
El Kennani S, Adrait A, Shaytan AK, Khochbin S, Bruley C, Panchenko AR, Landsman D, Pflieger D, Govin J.
El Kennani S, et al.
Epigenetics Chromatin. 2017 Jan 10;10:2. doi: 10.1186/s13072-016-0109-x. eCollection 2017.
Epigenetics Chromatin. 2017.
PMID: 28096900
Free PMC article.
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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome.
Cappuccio G, Sayou C, Tanno PL, Tisserant E, Bruel AL, Kennani SE, Sá J, Low KJ, Dias C, Havlovicová M, Hančárová M, Eichler EE, Devillard F, Moutton S, Van-Gils J, Dubourg C, Odent S, Gerard B, Piton A, Yamamoto T, Okamoto N, Firth H, Metcalfe K, Moh A, Chapman KA, Aref-Eshghi E, Kerkhof J, Torella A, Nigro V, Perrin L, Piard J, Le Guyader G, Jouan T, Thauvin-Robinet C, Duffourd Y, George-Abraham JK, Buchanan CA, Williams D, Kini U, Wilson K; Telethon Undiagnosed Diseases Program; Sousa SB, Hennekam RCM, Sadikovic B, Thevenon J, Govin J, Vitobello A, Brunetti-Pierri N.
Cappuccio G, et al. Among authors: kennani se.
Genet Med. 2020 Nov;22(11):1838-1850. doi: 10.1038/s41436-020-0898-y. Epub 2020 Jul 22.
Genet Med. 2020.
PMID: 32694869
Free article.
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