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2022 | 1 |
2023 | 5 |
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Page 1
Reliable multiplex generation of pooled induced pluripotent stem cells.
Cell Rep Methods. 2023 Sep 25;3(9):100570. doi: 10.1016/j.crmeth.2023.100570. Epub 2023 Aug 31.
Cell Rep Methods. 2023.
PMID: 37751688
Free PMC article.
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia.
Funes S, Gadd DH, Mosqueda M, Zhong J, Jung J, Shankaracharya, Unger M, Cameron D, Dawes P, Keagle PJ, McDonough JA, Boopathy S, Sena-Esteves M, Lutz C, Skarnes WC, Lim ET, Schafer DP, Massi F, Landers JE, Bosco DA.
Funes S, et al. Among authors: dawes p.
bioRxiv [Preprint]. 2023 Jun 1:2023.06.01.541136. doi: 10.1101/2023.06.01.541136.
bioRxiv. 2023.
PMID: 37398081
Free PMC article.
Updated.
Preprint.
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FACS-Based Sequencing Approach to Evaluate Cell Type to Genotype Associations Using Cerebral Organoids.
Murray L, Olson MN, Barton N, Dawes P, Chan Y, Lim ET.
Murray L, et al. Among authors: dawes p.
Methods Mol Biol. 2023;2683:193-199. doi: 10.1007/978-1-0716-3287-1_15.
Methods Mol Biol. 2023.
PMID: 37300776
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Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia.
Funes S, Jung J, Gadd DH, Mosqueda M, Zhong J, Shankaracharya, Unger M, Stallworth K, Cameron D, Rotunno MS, Dawes P, Fowler-Magaw M, Keagle PJ, McDonough JA, Boopathy S, Sena-Esteves M, Nickerson JA, Lutz C, Skarnes WC, Lim ET, Schafer DP, Massi F, Landers JE, Bosco DA.
Funes S, et al. Among authors: dawes p.
Nat Commun. 2024 Mar 20;15(1):2497. doi: 10.1038/s41467-024-46695-w.
Nat Commun. 2024.
PMID: 38509062
Free PMC article.
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Modeling of mitochondrial genetic polymorphisms reveals induction of heteroplasmy by pleiotropic disease locus 10398A>G.
Smullen M, Olson MN, Murray LF, Suresh M, Yan G, Dawes P, Barton NJ, Mason JN, Zhang Y, Fernandez-Fontaine AA, Church GM, Mastroeni D, Wang Q, Lim ET, Chan Y, Readhead B.
Smullen M, et al. Among authors: dawes p.
Sci Rep. 2023 Jun 27;13(1):10405. doi: 10.1038/s41598-023-37541-y.
Sci Rep. 2023.
PMID: 37369829
Free PMC article.
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Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder.
Lim ET, Chan Y, Dawes P, Guo X, Erdin S, Tai DJC, Liu S, Reichert JM, Burns MJ, Chan YK, Chiang JJ, Meyer K, Zhang X, Walsh CA, Yankner BA, Raychaudhuri S, Hirschhorn JN, Gusella JF, Talkowski ME, Church GM.
Lim ET, et al. Among authors: dawes p.
Nat Commun. 2022 Jun 10;13(1):3243. doi: 10.1038/s41467-022-30968-3.
Nat Commun. 2022.
PMID: 35688811
Free PMC article.
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oFlowSeq: a quantitative approach to identify protein coding mutations affecting cell type enrichment using mosaic CRISPR-Cas9 edited cerebral organoids.
Dawes P, Murray LF, Olson MN, Barton NJ, Smullen M, Suresh M, Yan G, Zhang Y, Fernandez-Fontaine A, English J, Uddin M, Pak C, Church GM, Chan Y, Lim ET.
Dawes P, et al.
Hum Genet. 2023 Aug;142(8):1281-1291. doi: 10.1007/s00439-023-02534-4. Epub 2023 Mar 6.
Hum Genet. 2023.
PMID: 36877372
Free PMC article.
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