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Summary Anatomy Item Literature (14672) Expression Attributions Wiki
XB-ANAT-213

Papers associated with central nervous system (and pax2)

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Expression patterns of chick Musashi-1 in the developing nervous system., Wilson JM., Gene Expr Patterns. August 1, 2007; 7 (7): 817-25.            


Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.          


Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.                                


Upstream stimulatory factors, USF1 and USF2 are differentially expressed during Xenopus embryonic development., Fujimi TJ., Gene Expr Patterns. July 1, 2008; 8 (6): 376-381.                          


Enhancement of axonal regeneration by in vitro conditioning and its inhibition by cyclopentenone prostaglandins., Tonge D., J Cell Sci. August 1, 2008; 121 (Pt 15): 2565-77.                        


Fli1 acts at the top of the transcriptional network driving blood and endothelial development., Liu F., Curr Biol. August 26, 2008; 18 (16): 1234-40.                              


Fibroblast growth factor receptor-induced phosphorylation of ephrinB1 modulates its interaction with Dishevelled., Lee HS., Mol Biol Cell. January 1, 2009; 20 (1): 124-33.                    


xArx2: an aristaless homolog that regulates brain regionalization during development in Xenopus laevis., Wolanski M., Genesis. January 1, 2009; 47 (1): 19-31.              


Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.          


Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.              


The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.                


In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      


The role of miR-124a in early development of the Xenopus eye., Qiu R., Mech Dev. October 1, 2009; 126 (10): 804-16.          


Zebrafish CiA interneurons are late-born primary neurons., Yeo SY., Neurosci Lett. December 11, 2009; 466 (3): 131-4.


Sonic hedgehog is involved in formation of the ventral optic cup by limiting Bmp4 expression to the dorsal domain., Zhao L., Mech Dev. January 1, 2010; 127 (1-2): 62-72.                


XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.                  


Competition for ligands between FGFR1 and FGFR4 regulates Xenopus neural development., Yamagishi M., Int J Dev Biol. January 1, 2010; 54 (1): 93-104.          


Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.          


En2, Pax2/5 and Tcf-4 transcription factors cooperate in patterning the Xenopus brain., Koenig SF., Dev Biol. April 15, 2010; 340 (2): 318-28.                  


Polypyrimidine tract-binding protein is required for the repression of gene expression by all-trans retinoic acid., Tamanoue Y., Dev Growth Differ. June 1, 2010; 52 (5): 469-79.                    


Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns., Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.              


Nkx6 genes pattern the frog neural plate and Nkx6.1 is necessary for motoneuron axon projection., Dichmann DS., Dev Biol. January 15, 2011; 349 (2): 378-86.                            


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.                            


A conserved function of the chromatin ATPase Kismet in the regulation of hedgehog expression., Terriente-Félix A., Dev Biol. February 15, 2011; 350 (2): 382-92.                  


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.                          


Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.                        


Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney., Sauert K., PLoS One. January 1, 2012; 7 (3): e33522.                  


Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis., Barnett C., Mech Dev. January 1, 2012; 129 (9-12): 324-38.              


Xenopus as a model system for the study of GOLPH2/GP73 function: Xenopus GOLPH2 is required for pronephros development., Li L., PLoS One. January 1, 2012; 7 (6): e38939.                                              


Evolution of a tissue-specific silencer underlies divergence in the expression of pax2 and pax8 paralogues., Ochi H., Nat Commun. May 22, 2012; 3 848.      


Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning., Steventon B., Dev Biol. July 1, 2012; 367 (1): 55-65.                


Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing., del Viso F., BMC Genomics. November 21, 2012; 13 649.                  


Hes4 controls proliferative properties of neural stem cells during retinal ontogenesis., El Yakoubi W., Stem Cells. December 1, 2012; 30 (12): 2784-95.              


HNF1B controls proximal-intermediate nephron segment identity in vertebrates by regulating Notch signalling components and Irx1/2., Heliot C., Development. February 1, 2013; 140 (4): 873-85.  


Developmental mechanisms directing early anterior forebrain specification in vertebrates., Andoniadou CL., Cell Mol Life Sci. October 1, 2013; 70 (20): 3739-52.        


Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein., Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.                              


Stabilization of speckle-type POZ protein (Spop) by Daz interacting protein 1 (Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling., Schwend T., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.                


The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube., Hanotel J., Dev Biol. February 15, 2014; 386 (2): 340-57.                                                                    


Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.                                                                


Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.                                                    


The evolutionary history of vertebrate cranial placodes--I: cell type evolution., Patthey C., Dev Biol. May 1, 2014; 389 (1): 82-97.        


The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.            


Custos controls β-catenin to regulate head development during vertebrate embryogenesis., Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.                                


Identification of distal enhancers for Six2 expression in pronephros., Suzuki N., Int J Dev Biol. January 1, 2015; 59 (4-6): 241-6.      


Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.                        


Understanding early organogenesis using a simplified in situ hybridization protocol in Xenopus., Deimling SJ., J Vis Exp. January 12, 2015; (95): e51526.            


Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.                            


Opportunities and limits of the one gene approach: the ability of Atoh1 to differentiate and maintain hair cells depends on the molecular context., Jahan I., Front Cell Neurosci. February 5, 2015; 9 26.  


The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.                              


Dorsoventral patterning of the Xenopus eye involves differential temporal changes in the response of optic stalk and retinal progenitors to Hh signalling., Wang X., Neural Dev. March 20, 2015; 10 7.              

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