Papers associated with notSearch for not morpholinos using Textpresso
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|Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover.
Kirsch N, Chang LS, Koch S, Glinka A, Dolde C, Colozza G, Benitez MDJ, De Robertis EM, Niehrs C.
Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
|A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo.
Blitz IL, Paraiso KD, Patrushev I, Chiu WTY, Cho KWY, Gilchrist MJ.
Dev Biol. June 15, 2017; 426 (2): 409-417.
|sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis.
Exner CRT, Kim AY, Mardjuki SM, Harland RM.
Dev Biol. May 1, 2017; 425 (1): 33-43.
|FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue.
Polevoy H, Malyarova A, Fonar Y, Elias S, Frank D.
Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
|Activation of a T-box-Otx2-Gsc gene network independent of TBP and TBP-related factors.
Gazdag E, Jacobi UG, van Kruijsbergen I, Weeks DL, Veenstra GJ.
Development. April 15, 2016; 143 (8): 1340-50.
|Specification of anteroposterior axis by combinatorial signaling during Xenopus development.
Carron C, Shi DL.
Wiley Interdiscip Rev Dev Biol. March 1, 2016; 5 (2): 150-68.
|Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1.
Liu C, Lou CH, Shah V, Ritter R, Talley J, Soibam B, Benham A, Zhu H, Perez E, Shieh YE, Gunaratne PH, Sater AK.
Dev Biol. January 1, 2016; 409 (1): 26-38.
|Xenopus CAF1 requires NOT1-mediated interaction with 4E-T to repress translation in vivo.
Waghray S, Williams C, Coon JJ, Wickens M.
RNA. July 1, 2015; 21 (7): 1335-45.
|Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation.
Zhang X, Cheong SM, Amado NG, Reis AH, MacDonald BT, Zebisch M, Jones EY, Abreu JG, He X.
Dev Cell. March 23, 2015; 32 (6): 719-30.
|The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus.
Griffin JN, Sondalle SB, Del Viso F, Baserga SJ, Khokha MK.
PLoS Genet. March 1, 2015; 11 (3): e1005018.
|Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression.
Nelson AC, Cutty SJ, Niini M, Stemple DL, Flicek P, Houart C, Bruce AE, Wardle FC.
BMC Biol. October 3, 2014; 12 81.
|Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification.
Yasuoka Y, Suzuki Y, Takahashi S, Someya H, Sudou N, Haramoto Y, Cho KW, Asashima M, Sugano S, Taira M.
Nat Commun. July 8, 2014; 5 4322.
|Active repression by RARγ signaling is required for vertebrate axial elongation.
Janesick A, Nguyen TT, Aisaki K, Igarashi K, Kitajima S, Chandraratna RA, Kanno J, Blumberg B.
Development. June 1, 2014; 141 (11): 2260-70.
|High-resolution analysis of gene activity during the Xenopus mid-blastula transition.
Collart C, Owens ND, Bhaw-Rosun L, Cooper B, De Domenico E, Patrushev I, Sesay AK, Smith JN, Smith JC, Gilchrist MJ.
Development. May 1, 2014; 141 (9): 1927-39.
|Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus.
Shieh YE, Wells DE, Sater AK.
Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
|Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions.
Vandenberg LN, Blackiston DJ, Rea AC, Dore TM, Levin M.
Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.
|A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance.
Livigni A, Peradziryi H, Sharov AA, Chia G, Hammachi F, Migueles RP, Sukparangsi W, Pernagallo S, Bradley M, Nichols J, Ko MS, Brickman JM.
Curr Biol. November 18, 2013; 23 (22): 2233-44.
|Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning.
Kam RK, Shi W, Chan SO, Chen Y, Xu G, Lau CB, Fung KP, Chan WY, Zhao H.
J Biol Chem. November 1, 2013; 288 (44): 31477-87.
|Directional migration of leading-edge mesoderm generates physical forces: Implication in Xenopus notochord formation during gastrulation.
Hara Y, Nagayama K, Yamamoto TS, Matsumoto T, Suzuki M, Suzuki M, Ueno N.
Dev Biol. October 15, 2013; 382 (2): 482-95.
|The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling.
Wang F, Hu W, Xian J, Ohnuma S, Brenton JD.
Dev Biol. July 1, 2013; 379 (1): 16-27.