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Summary Anatomy Item Literature (5836) Expression Attributions Wiki
XB-ANAT-2

Papers associated with ectoderm∨derBy=4 (and cyp26a1)

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Thyroid hormone receptor knockout prevents the loss of Xenopus tail regeneration capacity at metamorphic climax., Wang S., Cell Biosci. February 23, 2023; 13 (1): 40.              


Alcohol induces neural tube defects by reducing retinoic acid signaling and promoting neural plate expansion., Edri T., Front Cell Dev Biol. January 1, 2023; 11 1282273.                    


Retinoic Acid is Required for Normal Morphogenetic Movements During Gastrulation., Gur M., Front Cell Dev Biol. January 1, 2022; 10 857230.                  


Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis., Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.                      


Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis., Gere-Becker MB., Development. June 8, 2018; 145 (12):                                   


Acetaldehyde inhibits retinoic acid biosynthesis to mediate alcohol teratogenicity., Shabtai Y., Sci Rep. January 10, 2018; 8 (1): 347.                  


Xenopus Limb bud morphogenesis., Keenan SR., Dev Dyn. March 1, 2016; 245 (3): 233-43.            


G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.                                          


Development of the vertebrate tailbud., Beck CW., Wiley Interdiscip Rev Dev Biol. January 1, 2015; 4 (1): 33-44.        


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.        


Retinoic acid regulation by CYP26 in vertebrate lens regeneration., Thomas AG., Dev Biol. February 15, 2014; 386 (2): 291-301.            


Dhrs3 protein attenuates retinoic acid signaling and is required for early embryonic patterning., Kam RK., J Biol Chem. November 1, 2013; 288 (44): 31477-87.                    


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.                                                              


Expression of Ski can act as a negative feedback mechanism on retinoic acid signaling., Melling MA., Dev Dyn. June 1, 2013; 242 (6): 604-13.                      


A hindbrain-repressive Wnt3a/Meis3/Tsh1 circuit promotes neuronal differentiation and coordinates tissue maturation., Elkouby YM., Development. April 1, 2012; 139 (8): 1487-97.                    


xCOUP-TF-B regulates xCyp26 transcription and modulates retinoic acid signaling for anterior neural patterning in Xenopus., Tanibe M., Int J Dev Biol. January 1, 2012; 56 (4): 239-44.            


Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration., Love NR., BMC Dev Biol. November 15, 2011; 11 70.              


Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.                                


B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.                


Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.                


Retinoic acid regulates anterior-posterior patterning within the lateral plate mesoderm of Xenopus., Deimling SJ., Mech Dev. October 1, 2009; 126 (10): 913-23.                        


Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.                


The efficiency of Xenopus primordial germ cell migration depends on the germplasm mRNA encoding the PDZ domain protein Grip2., Kirilenko P., Differentiation. April 1, 2008; 76 (4): 392-403.                    


Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis., Davey JC., Environ Health Perspect. February 1, 2008; 116 (2): 165-72.                


Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis., Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.                        


Control of kidney, eye and limb expression of Bmp7 by an enhancer element highly conserved between species., Adams D., Dev Biol. November 15, 2007; 311 (2): 679-90.  


Gene expression in Xenopus laevis embryos after Triadimefon exposure., Papis E., Gene Expr Patterns. January 1, 2007; 7 (1-2): 137-42.          


Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.                  


Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation., Van Campenhout C., Dev Biol. June 1, 2006; 294 (1): 203-19.                


Microarray-based identification of VegT targets in Xenopus., Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.                                          


Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction., Monsoro-Burq AH., Dev Cell. February 1, 2005; 8 (2): 167-78.            


Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.                          


The Meis3 protein and retinoid signaling interact to pattern the Xenopus hindbrain., Dibner C., Dev Biol. July 1, 2004; 271 (1): 75-86.              


The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development., Barreto G., Mech Dev. April 1, 2003; 120 (4): 415-28.            


PKCgamma regulates syndecan-2 inside-out signaling during xenopus left-right development., Kramer KL., Cell. December 27, 2002; 111 (7): 981-90.                


Two myogenin-related genes are differentially expressed in Xenopus laevis myogenesis and differ in their ability to transactivate muscle structural genes., Charbonnier F., J Biol Chem. January 11, 2002; 277 (2): 1139-47.              


Isolation and characterization of a Xenopus gene (XMLP) encoding a MARCKS-like protein., Zhao H., Int J Dev Biol. October 1, 2001; 45 (7): 817-26.                        


Increased XRALDH2 activity has a posteriorizing effect on the central nervous system of Xenopus embryos., Chen Y., Mech Dev. March 1, 2001; 101 (1-2): 91-103.        


A gene trap approach in Xenopus., Bronchain OJ., Curr Biol. October 21, 1999; 9 (20): 1195-8.        


Immediate upstream sequence of arrestin directs rod-specific expression in Xenopus., Mani SS., J Biol Chem. May 28, 1999; 274 (22): 15590-7.              


Regionalized metabolic activity establishes boundaries of retinoic acid signalling., Hollemann T., EMBO J. December 15, 1998; 17 (24): 7361-72.


Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.                                                            


Cloning and functional expression of a ClC Cl- channel from the renal cell line A6., Lindenthal S., Am J Physiol. October 1, 1997; 273 (4 Pt 1): C1176-85.  


[An analysis of the expression of the genes containing the LeR-1 and VeR-1 sequences in the embryogenesis, regeneration and in the intact tissues of newts]., Markitantova IuV., Ontogenez. January 1, 1997; 28 (4): 262-70.

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