Papers associated with anterior (and wnt5a)

Limit to papers also referencing gene:
Show all anterior papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	RNA localization during early development of the axolotl., Šimková K., Front Cell Dev Biol. January 1, 2023; 11 1260795.
	Hif1α and Wnt are required for posterior gene expression during Xenopus tropicalis tail regeneration., Patel JH., Dev Biol. March 1, 2022; 483 157-168.
	Xenopus laevis il11ra.L is an experimentally proven interleukin-11 receptor component that is required for tadpole tail regeneration., Suzuki S., Sci Rep. February 3, 2022; 12 (1): 1903.
	Rspo2 inhibits TCF3 phosphorylation to antagonize Wnt signaling during vertebrate anteroposterior axis specification., Reis AH., Sci Rep. June 28, 2021; 11 (1): 13433.
	Xenopus gpx3 Mediates Posterior Development by Regulating Cell Death during Embryogenesis., Lee H, Lee H., Antioxidants (Basel). December 12, 2020; 9 (12):
	Bioinformatics Screening of Genes Specific for Well-Regenerating Vertebrates Reveals c-answer, a Regulator of Brain Development and Regeneration., Korotkova DD., Cell Rep. October 22, 2019; 29 (4): 1027-1040.e6.
	Non-acylated Wnts Can Promote Signaling., Speer KF., Cell Rep. January 22, 2019; 26 (4): 875-883.e5.
	Vestigial-like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration., Simon E., Biol Open. October 15, 2017; 6 (10): 1528-1540.
	Genomic integration of Wnt/β-catenin and BMP/Smad1 signaling coordinates foregut and hindgut transcriptional programs., Stevens ML., Development. April 1, 2017; 144 (7): 1283-1295.
	Cholesterol-rich membrane microdomains modulate Wnt/β-catenin morphogen gradient during Xenopus development., Reis AH., Mech Dev. November 1, 2016; 142 30-39.
	Wnt proteins can direct planar cell polarity in vertebrate ectoderm., Chu CW., Elife. September 23, 2016; 5
	Identification of p62/SQSTM1 as a component of non-canonical Wnt VANGL2-JNK signalling in breast cancer., Puvirajesinghe TM., Nat Commun. January 12, 2016; 7 10318.
	GATA2 regulates Wnt signaling to promote primitive red blood cell fate., Mimoto MS., Dev Biol. November 1, 2015; 407 (1): 1-11.
	Cooperative and independent functions of FGF and Wnt signaling during early inner ear development., Wright KD., BMC Dev Biol. October 6, 2015; 15 33.
	Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
	Planar polarization of Vangl2 in the vertebrate neural plate is controlled by Wnt and Myosin II signaling., Ossipova O., Biol Open. April 24, 2015; 4 (6): 722-30.
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.
	Calpain2 protease: A new member of the Wnt/Ca(2+) pathway modulating convergent extension movements in Xenopus., Zanardelli S., Dev Biol. December 1, 2013; 384 (1): 83-100.
	Mutually exclusive signaling signatures define the hepatic and pancreatic progenitor cell lineage divergence., Rodríguez-Seguel E., Genes Dev. September 1, 2013; 27 (17): 1932-46.
	Expression of pluripotency factors in larval epithelia of the frog Xenopus: evidence for the presence of cornea epithelial stem cells., Perry KJ., Dev Biol. February 15, 2013; 374 (2): 281-94.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Functional conservation of Nematostella Wnts in canonical and noncanonical Wnt-signaling., Rigo-Watermeier T., Biol Open. January 15, 2012; 1 (1): 43-51.
	PAPC and the Wnt5a/Ror2 pathway control the invagination of the otic placode in Xenopus., Jung B., BMC Dev Biol. June 10, 2011; 11 36.
	Rab3d is required for Xenopus anterior neurulation by regulating Noggin secretion., Kim H., Dev Dyn. June 1, 2011; 240 (6): 1430-9.
	Retinoic acid is a key regulatory switch determining the difference between lung and thyroid fates in Xenopus laevis., Wang JH., BMC Dev Biol. January 26, 2011; 11 75.
	Expression of Wnt signaling components during Xenopus pronephros development., Zhang B., PLoS One. January 1, 2011; 6 (10): e26533.
	Oriented cell motility and division underlie early limb bud morphogenesis., Wyngaarden LA., Development. August 1, 2010; 137 (15): 2551-8.
	Expression of components of Wnt and Hedgehog pathways in different tissue layers during lung development in Xenopus laevis., Yin A., Gene Expr Patterns. January 1, 2010; 10 (7-8): 338-44.
	XsFRP5 modulates endodermal organogenesis in Xenopus laevis., Damianitsch K., Dev Biol. May 15, 2009; 329 (2): 327-37.
	Overlapping functions of Cdx1, Cdx2, and Cdx4 in the development of the amphibian Xenopus tropicalis., Faas L., Dev Dyn. April 1, 2009; 238 (4): 835-52.
	Xenopus Wnt-5a induces an ectopic larval tail at injured site, suggesting a crucial role for noncanonical Wnt signal in tail regeneration., Sugiura T., Mech Dev. January 1, 2009; 126 (1-2): 56-67.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	The functions and possible significance of Kremen as the gatekeeper of Wnt signalling in development and pathology., Nakamura T., J Cell Mol Med. April 1, 2008; 12 (2): 391-408.
	The mother superior mutation ablates foxd3 activity in neural crest progenitor cells and depletes neural crest derivatives in zebrafish., Montero-Balaguer M., Dev Dyn. December 1, 2006; 235 (12): 3199-212.
	The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
	Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis., Shibata M., Mech Dev. December 1, 2005; 122 (12): 1322-39.
	Wnt5 signaling in vertebrate pancreas development., Kim HJ., BMC Biol. October 24, 2005; 3 23.
	Reorganization of actin cytoskeleton by FRIED, a Frizzled-8 associated protein tyrosine phosphatase., Itoh K., Dev Dyn. September 1, 2005; 234 (1): 90-101.
	Regulation of Msx genes by a Bmp gradient is essential for neural crest specification., Tribulo C., Development. December 1, 2003; 130 (26): 6441-52.
	Role of glypican 4 in the regulation of convergent extension movements during gastrulation in Xenopus laevis., Ohkawara B., Development. May 1, 2003; 130 (10): 2129-38.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	The putative wnt receptor Xenopus frizzled-7 functions upstream of beta-catenin in vertebrate dorsoventral mesoderm patterning., Sumanas S., Development. May 1, 2000; 127 (9): 1981-90.
	Evolutionary relationships between the amphibian, avian, and mammalian stomachs., Smith DM., Evol Dev. January 1, 2000; 2 (6): 348-59.
	Frizzled-8 is expressed in the Spemann organizer and plays a role in early morphogenesis., Deardorff MA., Development. July 1, 1998; 125 (14): 2687-700.
	Activities of the Wnt-1 class of secreted signaling factors are antagonized by the Wnt-5A class and by a dominant negative cadherin in early Xenopus development., Torres MA., J Cell Biol. June 1, 1996; 133 (5): 1123-37.
	Analysis of Wnt/Engrailed signaling in Xenopus embryos using biolistics., Koster JG., Dev Biol. January 10, 1996; 173 (1): 348-52.
	Xwnt-5A: a maternal Wnt that affects morphogenetic movements after overexpression in embryos of Xenopus laevis., Moon RT., Development. September 1, 1993; 119 (1): 97-111.

???pagination.result.page??? 1