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Cell type transcriptome atlas for the planarian Schmidtea mediterranea.
Science. 2018 May 25;360(6391):eaaq1736. doi: 10.1126/science.aaq1736. Epub 2018 Apr 19.
Science. 2018.
PMID: 29674431
Free PMC article.
foxF-1 Controls Specification of Non-body Wall Muscle and Phagocytic Cells in Planarians.
Scimone ML, Wurtzel O, Malecek K, Fincher CT, Oderberg IM, Kravarik KM, Reddien PW.
Scimone ML, et al. Among authors: fincher ct.
Curr Biol. 2018 Dec 3;28(23):3787-3801.e6. doi: 10.1016/j.cub.2018.10.030. Epub 2018 Nov 21.
Curr Biol. 2018.
PMID: 30471994
Free PMC article.
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Muscle and neuronal guidepost-like cells facilitate planarian visual system regeneration.
Scimone ML, Atabay KD, Fincher CT, Bonneau AR, Li DJ, Reddien PW.
Scimone ML, et al. Among authors: fincher ct.
Science. 2020 Jun 26;368(6498):eaba3203. doi: 10.1126/science.aba3203.
Science. 2020.
PMID: 32586989
Free PMC article.
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A transcription factor atlas of stem cell fate in planarians.
King HO, Owusu-Boaitey KE, Fincher CT, Reddien PW.
King HO, et al. Among authors: fincher ct.
Cell Rep. 2024 Mar 26;43(3):113843. doi: 10.1016/j.celrep.2024.113843. Epub 2024 Feb 23.
Cell Rep. 2024.
PMID: 38401119
Free article.
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A positional Toll receptor code directs convergent extension in Drosophila.
Paré AC, Vichas A, Fincher CT, Mirman Z, Farrell DL, Mainieri A, Zallen JA.
Paré AC, et al. Among authors: fincher ct.
Nature. 2014 Nov 27;515(7528):523-7. doi: 10.1038/nature13953. Epub 2014 Nov 2.
Nature. 2014.
PMID: 25363762
Free PMC article.
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Erratum: A positional Toll receptor code directs convergent extension in Drosophila.
Paré AC, Vichas A, Fincher CT, Mirman Z, Farrell DL, Mainieri A, Zallen JA.
Paré AC, et al. Among authors: fincher ct.
Nature. 2015 Nov 19;527(7578):398. doi: 10.1038/nature15719. Epub 2015 Oct 7.
Nature. 2015.
PMID: 26444242
No abstract available.
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Kaiser FJ, Ansari M, Braunholz D, Concepción Gil-Rodríguez M, Decroos C, Wilde JJ, Fincher CT, Kaur M, Bando M, Amor DJ, Atwal PS, Bahlo M, Bowman CM, Bradley JJ, Brunner HG, Clark D, Del Campo M, Di Donato N, Diakumis P, Dubbs H, Dyment DA, Eckhold J, Ernst S, Ferreira JC, Francey LJ, Gehlken U, Guillén-Navarro E, Gyftodimou Y, Hall BD, Hennekam R, Hudgins L, Hullings M, Hunter JM, Yntema H, Innes AM, Kline AD, Krumina Z, Lee H, Leppig K, Lynch SA, Mallozzi MB, Mannini L, McKee S, Mehta SG, Micule I; Care4Rare Canada Consortium; Mohammed S, Moran E, Mortier GR, Moser JA, Noon SE, Nozaki N, Nunes L, Pappas JG, Penney LS, Pérez-Aytés A, Petersen MB, Puisac B, Revencu N, Roeder E, Saitta S, Scheuerle AE, Schindeler KL, Siu VM, Stark Z, Strom SP, Thiese H, Vater I, Willems P, Williamson K, Wilson LC; University of Washington Center for Mendelian Genomics; Hakonarson H, Quintero-Rivera F, Wierzba J, Musio A, Gillessen-Kaesbach G, Ramos FJ, Jackson LG, Shirahige K, Pié J, Christianson DW, Krantz ID, Fitzpatrick DR, Deardorff MA.
Kaiser FJ, et al. Among authors: fincher ct.
Hum Mol Genet. 2014 Jun 1;23(11):2888-900. doi: 10.1093/hmg/ddu002. Epub 2014 Jan 8.
Hum Mol Genet. 2014.
PMID: 24403048
Free PMC article.
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Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.
Braunholz D, Hullings M, Gil-Rodríguez MC, Fincher CT, Mallozzi MB, Loy E, Albrecht M, Kaur M, Limon J, Rampuria A, Clark D, Kline A, Dalski A, Eckhold J, Tzschach A, Hennekam R, Gillessen-Kaesbach G, Wierzba J, Krantz ID, Deardorff MA, Kaiser FJ.
Braunholz D, et al. Among authors: fincher ct.
Eur J Hum Genet. 2012 Mar;20(3):271-6. doi: 10.1038/ejhg.2011.175. Epub 2011 Sep 21.
Eur J Hum Genet. 2012.
PMID: 21934712
Free PMC article.
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