| Year |
Citation |
Score |
| 2023 |
Carpenter KA, Thurlow KE, Craig SEL, Grainger S. Wnt regulation of hematopoietic stem cell development and disease. Current Topics in Developmental Biology. 153: 255-279. PMID 36967197 DOI: 10.1016/bs.ctdb.2022.12.001 |
0.403 |
|
| 2020 |
Gumber D, Do M, Suresh Kumar N, Sonavane PR, Wu CCN, Cruz LS, Grainger S, Carson D, Gaasterland T, Willert K. Selective activation of FZD7 promotes mesendodermal differentiation of human pluripotent stem cells. Elife. 9. PMID 33331818 DOI: 10.7554/eLife.63060 |
0.343 |
|
| 2020 |
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, et al. Haematopoietic stem cell-dependent Notch transcription is mediated by p53 through the Histone chaperone Supt16h. Nature Cell Biology. PMID 33230303 DOI: 10.1038/s41556-020-00604-7 |
0.555 |
|
| 2019 |
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. EGFR is required for Wnt9a-Fzd9b signalling specificity in haematopoietic stem cells. Nature Cell Biology. PMID 31110287 DOI: 10.1038/S41556-019-0330-5 |
0.57 |
|
| 2019 |
Grainger S, Traver D. Embryonic Immune Cells Remodel the Heart. Developmental Cell. 48: 595-596. PMID 30861372 DOI: 10.1016/J.Devcel.2019.02.017 |
0.472 |
|
| 2018 |
Bickers C, Española SD, Grainger S, Pouget C, Traver D. Zebrafish snai2 mutants fail to phenocopy morphant phenotypes. Plos One. 13: e0202747. PMID 30208064 DOI: 10.1371/Journal.Pone.0202747 |
0.553 |
|
| 2018 |
Grainger S, Willert K. Mechanisms of Wnt signaling and control. Wiley Interdisciplinary Reviews. Systems Biology and Medicine. e1422. PMID 29600540 DOI: 10.1002/Wsbm.1422 |
0.403 |
|
| 2018 |
Grainger S, Traver D, Willert K. Wnt Signaling in Hematological Malignancies. Progress in Molecular Biology and Translational Science. 153: 321-341. PMID 29389522 DOI: 10.1016/Bs.Pmbts.2017.11.002 |
0.529 |
|
| 2017 |
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, et al. Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing. Nature Genetics. PMID 28092684 DOI: 10.1038/Ng.3762 |
0.498 |
|
| 2016 |
Grainger S, Lonquich B, Oon CH, Nguyen N, Willert K, Traver D. CRISPR Guide RNA Validation In Vitro. Zebrafish. PMID 27829120 DOI: 10.1089/Zeb.2016.1358 |
0.453 |
|
| 2016 |
Grainger S, Richter J, Palazón RE, Pouget C, Lonquich B, Wirth S, Grassme KS, Herzog W, Swift MR, Weinstein BM, Traver D, Willert K. Wnt9a Is Required for the Aortic Amplification of Nascent Hematopoietic Stem Cells. Cell Reports. 17: 1595-1606. PMID 27806298 DOI: 10.1016/J.Celrep.2016.10.027 |
0.586 |
|
| 2012 |
Grainger S, Lam J, Savory JG, Mears AJ, Rijli FM, Lohnes D. Cdx regulates Dll1 in multiple lineages. Developmental Biology. 361: 1-11. PMID 22015720 DOI: 10.1016/J.Ydbio.2011.09.034 |
0.395 |
|
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