pCSDest Citations (16)
Originally described in: Gateway compatible vectors for analysis of gene function in the zebrafish.Villefranc JA, Amigo J, Lawson ND Dev Dyn. 2007 Nov . 236(11):3077-87. PubMed Journal
Articles Citing pCSDest
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| EFCAB7 and IQCE regulate hedgehog signaling by tethering the EVC-EVC2 complex to the base of primary cilia. Pusapati GV, Hughes CE, Dorn KV, Zhang D, Sugianto P, Aravind L, Rohatgi R. Dev Cell. 2014 Mar 10;28(5):483-96. doi: 10.1016/j.devcel.2014.01.021. Epub 2014 Feb 27. PubMed |
| LKB1 loss at transcriptional level promotes tumor malignancy and poor patient outcomes in colorectal cancer. He TY, Tsai LH, Huang CC, Chou MC, Lee H. Ann Surg Oncol. 2014 Dec;21 Suppl 4:S703-10. doi: 10.1245/s10434-014-3824-1. Epub 2014 May 31. PubMed |
| ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease. Hayes M, Gao X, Yu LX, Paria N, Henkelman RM, Wise CA, Ciruna B. Nat Commun. 2014 Sep 3;5:4777. doi: 10.1038/ncomms5777. PubMed |
Dynamic visualization of transcription and RNA subcellular localization in zebrafish.
Campbell PD, Chao JA, Singer RH, Marlow FL.
Development. 2015 Apr 1;142(7):1368-74. doi: 10.1242/dev.118968. Epub 2015 Mar 10.
PubMed
Associated Plasmids |
In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes.
Schmidt HB, Rohatgi R.
Cell Rep. 2016 Aug 2;16(5):1228-36. doi: 10.1016/j.celrep.2016.06.088. Epub 2016 Jul 21.
PubMed
Associated Plasmids |
| Comparative genetic screens in human cells reveal new regulatory mechanisms in WNT signaling. Lebensohn AM, Dubey R, Neitzel LR, Tacchelly-Benites O, Yang E, Marceau CD, Davis EM, Patel BB, Bahrami-Nejad Z, Travaglini KJ, Ahmed Y, Lee E, Carette JE, Rohatgi R. Elife. 2016 Dec 20;5. doi: 10.7554/eLife.21459. PubMed |
| Dynamic regulation of VEGF-inducible genes by an ERK/ERG/p300 transcriptional network. Fish JE, Cantu Gutierrez M, Dang LT, Khyzha N, Chen Z, Veitch S, Cheng HS, Khor M, Antounians L, Njock MS, Boudreau E, Herman AM, Rhyner AM, Ruiz OE, Eisenhoffer GT, Medina-Rivera A, Wilson MD, Wythe JD. Development. 2017 Jul 1;144(13):2428-2444. doi: 10.1242/dev.146050. Epub 2017 May 23. PubMed |
| A chemical screen in zebrafish embryonic cells establishes that Akt activation is required for neural crest development. Ciarlo C, Kaufman CK, Kinikoglu B, Michael J, Yang S, D Amato C, Blokzijl-Franke S, den Hertog J, Schlaeger TM, Zhou Y, Liao E, Zon LI. Elife. 2017 Aug 23;6. pii: 29145. doi: 10.7554/eLife.29145. PubMed |
A single N-terminal phosphomimic disrupts TDP-43 polymerization, phase separation, and RNA splicing.
Wang A, Conicella AE, Schmidt HB, Martin EW, Rhoads SN, Reeb AN, Nourse A, Ramirez Montero D, Ryan VH, Rohatgi R, Shewmaker F, Naik MT, Mittag T, Ayala YM, Fawzi NL.
EMBO J. 2018 Mar 1;37(5). pii: embj.201797452. doi: 10.15252/embj.201797452. Epub 2018 Feb 9.
PubMed
Associated Plasmids |
| Spatiotemporal expression profile of embryonic and adult ankyrin repeat and EF-hand domain containing protein 1-encoding genes ankef1a and ankef1b in zebrafish. Daniel JG, Panizzi JR. Gene Expr Patterns. 2019 Dec;34:119069. doi: 10.1016/j.gep.2019.119069. Epub 2019 Sep 12. PubMed |
| Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians. Pellerin D, Aykanat A, Ellezam B, Troiano EC, Karamchandani J, Dicaire MJ, Petitclerc M, Robertson R, Allard-Chamard X, Brunet D, Konersman CG, Mathieu J, Warman Chardon J, Gupta VA, Beggs AH, Brais B, Chrestian N. Ann Neurol. 2020 Apr;87(4):568-583. doi: 10.1002/ana.25685. Epub 2020 Feb 8. PubMed |
| SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype. Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cave H, Zenker M, Tartaglia M. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. PubMed |
| TNNT1 myopathy with novel compound heterozygous mutations. Lee S, Eum J, Park S, Ki S, Hwang BJ, Kee Y, Chae JH. Neuromuscul Disord. 2022 Feb;32(2):176-184. doi: 10.1016/j.nmd.2021.12.003. Epub 2021 Dec 16. PubMed |
| Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish. Fasano G, Muto V, Radio FC, Venditti M, Mosaddeghzadeh N, Coppola S, Paradisi G, Zara E, Bazgir F, Ziegler A, Chillemi G, Bertuccini L, Tinari A, Vetro A, Pantaleoni F, Pizzi S, Conti LA, Petrini S, Bruselles A, Prandi IG, Mancini C, Chandramouli B, Barth M, Bris C, Milani D, Selicorni A, Macchiaiolo M, Gonfiantini MV, Bartuli A, Mariani R, Curry CJ, Guerrini R, Slavotinek A, Iascone M, Dallapiccola B, Ahmadian MR, Lauri A, Tartaglia M. Nat Commun. 2022 Nov 11;13(1):6841. doi: 10.1038/s41467-022-34354-x. PubMed |
| A minimally invasive fin scratching protocol for fast genotyping and early selection of zebrafish embryos. Venditti M, Pedalino C, Rosello M, Fasano G, Serafini M, Revenu C, Del Bene F, Tartaglia M, Lauri A. Sci Rep. 2022 Dec 30;12(1):22597. doi: 10.1038/s41598-022-26822-7. PubMed |
| SARS-CoV-2 activates the TLR4/MyD88 pathway in human macrophages: A possible correlation with strong pro-inflammatory responses in severe COVID-19. Sahanic S, Hilbe R, Dunser C, Tymoszuk P, Loffler-Ragg J, Rieder D, Trajanoski Z, Krogsdam A, Demetz E, Yurchenko M, Fischer C, Schirmer M, Theurl M, Lener D, Hirsch J, Holfeld J, Gollmann-Tepekoylu C, Zinner CP, Tzankov A, Zhang SY, Casanova JL, Posch W, Wilflingseder D, Weiss G, Tancevski I. Heliyon. 2023 Nov 17;9(11):e21893. doi: 10.1016/j.heliyon.2023.e21893. eCollection 2023 Nov. PubMed |
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