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Haematopoietic stem cell-dependent Notch transcription is mediated by p53 through the Histone chaperone Supt16h.
Espanola SG, Song H, Ryu E, Saxena A, Kim ES, Manegold JE, Nasamran CA, Sahoo D, Oh CK, Bickers C, Shin U, Grainger S, Park YH, Pandolfo L, Kang MS, Kang S, Myung K, Cooper KL, Yelon D, Traver D, Lee Y. Espanola SG, et al. Among authors: grainger s. Nat Cell Biol. 2020 Dec;22(12):1411-1422. doi: 10.1038/s41556-020-00604-7. Epub 2020 Nov 23. Nat Cell Biol. 2020. PMID: 33230303 Free PMC article.
CRISPR Guide RNA Validation In Vitro.
Grainger S, Lonquich B, Oon CH, Nguyen N, Willert K, Traver D. Grainger S, et al. Zebrafish. 2017 Aug;14(4):383-386. doi: 10.1089/zeb.2016.1358. Epub 2016 Nov 9. Zebrafish. 2017. PMID: 27829120 Free PMC article.
Wnt Signaling in Hematological Malignancies.
Grainger S, Traver D, Willert K. Grainger S, et al. Prog Mol Biol Transl Sci. 2018 Jan;153:321-341. doi: 10.1016/bs.pmbts.2017.11.002. Epub 2017 Dec 29. Prog Mol Biol Transl Sci. 2018. PMID: 29389522 Free PMC article. Review.
Zebrafish snai2 mutants fail to phenocopy morphant phenotypes.
Bickers C, Española SD, Grainger S, Pouget C, Traver D. Bickers C, et al. Among authors: grainger s. PLoS One. 2018 Sep 12;13(9):e0202747. doi: 10.1371/journal.pone.0202747. eCollection 2018. PLoS One. 2018. PMID: 30208064 Free PMC article.
Embryonic Immune Cells Remodel the Heart.
Grainger S, Traver D. Grainger S, et al. Dev Cell. 2019 Mar 11;48(5):595-596. doi: 10.1016/j.devcel.2019.02.017. Dev Cell. 2019. PMID: 30861372 Free article.
EGFR is required for Wnt9a-Fzd9b signalling specificity in haematopoietic stem cells.
Grainger S, Nguyen N, Richter J, Setayesh J, Lonquich B, Oon CH, Wozniak JM, Barahona R, Kamei CN, Houston J, Carrillo-Terrazas M, Drummond IA, Gonzalez D, Willert K, Traver D. Grainger S, et al. Nat Cell Biol. 2019 Jun;21(6):721-730. doi: 10.1038/s41556-019-0330-5. Epub 2019 May 20. Nat Cell Biol. 2019. PMID: 31110287 Free PMC article.
Generation of vascular endothelial and smooth muscle cells from human pluripotent stem cells.
Patsch C, Challet-Meylan L, Thoma EC, Urich E, Heckel T, O'Sullivan JF, Grainger SJ, Kapp FG, Sun L, Christensen K, Xia Y, Florido MH, He W, Pan W, Prummer M, Warren CR, Jakob-Roetne R, Certa U, Jagasia R, Freskgård PO, Adatto I, Kling D, Huang P, Zon LI, Chaikof EL, Gerszten RE, Graf M, Iacone R, Cowan CA. Patsch C, et al. Nat Cell Biol. 2015 Aug;17(8):994-1003. doi: 10.1038/ncb3205. Epub 2015 Jul 27. Nat Cell Biol. 2015. PMID: 26214132 Free PMC article.
Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing.
Lardelli RM, Schaffer AE, Eggens VR, Zaki MS, Grainger S, Sathe S, Van Nostrand EL, Schlachetzki Z, Rosti B, Akizu N, Scott E, Silhavy JL, Heckman LD, Rosti RO, Dikoglu E, Gregor A, Guemez-Gamboa A, Musaev D, Mande R, Widjaja A, Shaw TL, Markmiller S, Marin-Valencia I, Davies JH, de Meirleir L, Kayserili H, Altunoglu U, Freckmann ML, Warwick L, Chitayat D, Blaser S, Çağlayan AO, Bilguvar K, Per H, Fagerberg C, Christesen HT, Kibaek M, Aldinger KA, Manchester D, Matsumoto N, Muramatsu K, Saitsu H, Shiina M, Ogata K, Foulds N, Dobyns WB, Chi NC, Traver D, Spaccini L, Bova SM, Gabriel SB, Gunel M, Valente EM, Nassogne MC, Bennett EJ, Yeo GW, Baas F, Lykke-Andersen J, Gleeson JG. Lardelli RM, et al. Among authors: grainger s. Nat Genet. 2017 Mar;49(3):457-464. doi: 10.1038/ng.3762. Epub 2017 Jan 16. Nat Genet. 2017. PMID: 28092684 Free PMC article.
126 results