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Summary Anatomy Item Literature (994) Expression Attributions Wiki
XB-ANAT-95

Papers associated with pharyngeal arch (and pax2)

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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.        

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.            

Expression of the Xvax2 gene demarcates presumptive ventral telencephalon and specific visual structures in Xenopus laevis., Liu Y., Mech Dev. January 1, 2001; 100 (1): 115-8.                

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

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

Tsukushi functions as an organizer inducer by inhibition of BMP activity in cooperation with chordin., Ohta K., Dev Cell. September 1, 2004; 7 (3): 347-358.        

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.                          

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

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.                    

Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination., Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.          

Alterations of rx1 and pax6 expression levels at neural plate stages differentially affect the production of retinal cell types and maintenance of retinal stem cell qualities., Zaghloul NA., Dev Biol. June 1, 2007; 306 (1): 222-40.                      

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.                          

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.                          

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.              

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.      

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.                  

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.                              

Rdh10a Provides a Conserved Critical Step in the Synthesis of Retinoic Acid during Zebrafish Embryogenesis., D'Aniello E., PLoS One. September 1, 2015; 10 (9): e0138588.                  

Hspa9 is required for pronephros specification and formation in Xenopus laevis., Gassié L., Dev Dyn. December 1, 2015; 244 (12): 1538-49.                      

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

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.                              

Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM., Dev Biol. January 15, 2017; 421 (2): 171-182.                    

Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development., Tavares ALP., Development. September 1, 2021; 148 (17):                       

Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.        

Systematic mapping of rRNA 2'-O methylation during frog development and involvement of the methyltransferase Fibrillarin in eye and craniofacial development in Xenopus laevis., Delhermite J., PLoS Genet. January 18, 2022; 18 (1): e1010012.                                                              

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

Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;             

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

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