Papers associated with midbrain (and dkk1)

Limit to papers also referencing gene:
Show all midbrain papers

???pagination.result.count???

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

Sort Newest To Oldest

Sort Oldest To Newest

	Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):
	The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer., Chang LS., Elife. January 14, 2020; 9
	Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;
	Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
	Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis., Ding Y., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.
	The phosphatase Pgam5 antagonizes Wnt/β-Catenin signaling in embryonic anterior-posterior axis patterning., Rauschenberger V., Development. June 15, 2017; 144 (12): 2234-2247.
	Kruppel-like factor family genes are expressed during Xenopus embryogenesis and involved in germ layer formation and body axis patterning., Gao Y., Dev Dyn. October 1, 2015; 244 (10): 1328-46.
	JmjC Domain-containing Protein 6 (Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 (Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis., Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.
	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.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification., Yasuoka Y., Nat Commun. July 9, 2014; 5 4322.
	Developmental mechanisms directing early anterior forebrain specification in vertebrates., Andoniadou CL., Cell Mol Life Sci. October 1, 2013; 70 (20): 3739-52.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Plasma membrane cholesterol depletion disrupts prechordal plate and affects early forebrain patterning., Reis AH., Dev Biol. May 15, 2012; 365 (2): 350-62.
	A hindbrain-repressive Wnt3a/Meis3/Tsh1 circuit promotes neuronal differentiation and coordinates tissue maturation., Elkouby YM., Development. April 1, 2012; 139 (8): 1487-97.
	Evolution of vertebrate central nervous system is accompanied by novel expression changes of duplicate genes., Chen Y, Chen Y., J Genet Genomics. December 20, 2011; 38 (12): 577-84.
	Waif1/5T4 inhibits Wnt/β-catenin signaling and activates noncanonical Wnt pathways by modifying LRP6 subcellular localization., Kagermeier-Schenk B., Dev Cell. December 13, 2011; 21 (6): 1129-43.
	Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart., Puskaric S., Hum Mol Genet. December 1, 2010; 19 (23): 4625-33.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.
	Differential requirements of BMP and Wnt signalling during gastrulation and neurulation define two steps in neural crest induction., Steventon B., Development. March 1, 2009; 136 (5): 771-9.
	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.
	Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm., Carmona-Fontaine C., Dev Biol. September 15, 2007; 309 (2): 208-21.
	Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.
	PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.
	Kremen proteins interact with Dickkopf1 to regulate anteroposterior CNS patterning., Davidson G., Development. December 1, 2002; 129 (24): 5587-96.
	Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse., Mukhopadhyay M., Dev Cell. September 1, 2001; 1 (3): 423-34.
	Zebrafish Dkk1, induced by the pre-MBT Wnt signaling, is secreted from the prechordal plate and patterns the anterior neural plate., Shinya M., Mech Dev. November 1, 2000; 98 (1-2): 3-17.
	The role of Xenopus dickkopf1 in prechordal plate specification and neural patterning., Kazanskaya O., Development. November 1, 2000; 127 (22): 4981-92.
	Dickkopf genes are co-ordinately expressed in mesodermal lineages., Monaghan AP., Mech Dev. September 1, 1999; 87 (1-2): 45-56.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.

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