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Summary Anatomy Item Literature (1229) Expression Attributions Wiki
XB-ANAT-736

Papers associated with neural tube (and pax2)

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Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis., Saumweber E., Front Cell Dev Biol. January 1, 2024; 12 1316048.                            

Xenopus Ssbp2 is required for embryonic pronephros morphogenesis and terminal differentiation., Cervino AS., Sci Rep. October 4, 2023; 13 (1): 16671.                                          

lrpap1 as a specific marker of proximal pronephric kidney tubuli in Xenopus laevis embryos., Neuhaus H., Int J Dev Biol. January 1, 2018; 62 (4-5): 319-324.          

Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              

Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.                                        

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

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

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.            

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.                                                                    

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.                

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

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

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

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.                          

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.                            

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

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

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.                          

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

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

FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    

Induction and specification of cranial placodes., Schlosser G., Dev Biol. June 15, 2006; 294 (2): 303-51.                

Negative regulation of Hedgehog signaling by the cholesterogenic enzyme 7-dehydrocholesterol reductase., Koide T., Development. June 1, 2006; 133 (12): 2395-405.                

Regulation of melanoblast and retinal pigment epithelium development by Xenopus laevis Mitf., Kumasaka M., Dev Dyn. November 1, 2005; 234 (3): 523-34.      

Xenopus hairy2b specifies anterior prechordal mesoderm identity within Spemann's organizer., Yamaguti M., Dev Dyn. September 1, 2005; 234 (1): 102-13.          

Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.                  

Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.                          

Systematic screening for genes specifically expressed in the anterior neuroectoderm during early Xenopus development., Takahashi N., Int J Dev Biol. January 1, 2005; 49 (8): 939-51.                                    

Molecular anatomy of placode development in Xenopus laevis., Schlosser G., Dev Biol. July 15, 2004; 271 (2): 439-66.                          

Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.                

PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.            

Xdtx1, a Xenopus Deltex homologue expressed in differentiating neurons and in photoreceptive organs., Andreazzoli M., Mech Dev. December 1, 2002; 119 Suppl 1 S247-51.      

Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney., Saulnier DM., Dev Biol. August 1, 2002; 248 (1): 13-28.                    

Axes establishment during eye morphogenesis in Xenopus by coordinate and antagonistic actions of BMP4, Shh, and RA., Sasagawa S., Genesis. June 1, 2002; 33 (2): 86-96.                      

The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A., Development. April 1, 2002; 129 (7): 1609-21.                  

Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo., Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.          

Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation., Lamar E., Development. April 1, 2001; 128 (8): 1335-46.              

Expanded retina territory by midbrain transformation upon overexpression of Six6 (Optx2) in Xenopus embryos., Bernier G., Mech Dev. May 1, 2000; 93 (1-2): 59-69.            

Role of Xrx1 in Xenopus eye and anterior brain development., Andreazzoli M., Development. June 1, 1999; 126 (11): 2451-60.            

Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development., Heller N., Mech Dev. December 1, 1997; 69 (1-2): 83-104.        

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