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Summary Expression Phenotypes Gene Literature (227) GO Terms (47) Nucleotides (208) Proteins (86) Interactants (1798) Wiki
XB--482739

Papers associated with pax3 (and Disease Ontology)



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referenced by:

The contribution of de novo coding mutations to meningomyelocele., Ha YJ, Nisal A, Tang I, Lee C, Jhamb I, Wallace C, Howarth R, Schroeder S, Vong KI, Meave N, Jiwani F, Barrows C, Lee S, Jiang N, Patel A, Bagga K, Banka N, Friedman L, Blanco FA, Yu S, Rhee S, Jeong HS, Plutzer I, Major MB, Benoit B, Poüs C, Heffner C, Kibar Z, Bot GM, Northrup H, Au KS, Strain M, Ashley-Koch AE, Finnell RH, Le JT, Meltzer HS, Araujo C, Machado HR, Stevenson RE, Yurrita A, Mumtaz S, Ahmed A, Khara MH, Mutchinick OM, Medina-Bereciartu JR, Hildebrandt F, Melikishvili G, Marwan AI, Capra V, Noureldeen MM, Salem AMS, Issa MY, Zaki MS, Xu L, Lee JE, Shin D, Alkelai A, Shuldiner AR, Kingsmore SF, Murray SA, Gee HY, Miller WT, Tolias KF, Wallingford JB, Spina Bifida Sequencing Consortium, Kim S, Gleeson JG., Nature. May 26, 2025; 641 (8062): 419-426.

Cutaneous Pigment Cell Distributions and Skin Structure of Xenopus., Liang W, Hou C, Zhu Z, Wang P, Wang X, Li Z, Xue J, Ran R., Pigment Cell Melanoma Res. May 1, 2025; 38 (3): e70022.

Dyrk1a is required for craniofacial development in Xenopus laevis., Johnson HK, Wahl SE, Sesay F, Litovchick L, Dickinson AJ., Dev Biol. July 15, 2024; 511 63-75.

Popeye domain containing proteins modulate the voltage-gated cardiac sodium channel Nav1.5., Rinné S, Kiper AK, Jacob R, Ortiz-Bonnin B, Schindler RFR, Fischer S, Komadowski M, De Martino E, Schäfer MK, Cornelius T, Fabritz L, Helker CSM, Brand T, Decher N., iScience. May 17, 2024; 27 (5): 109696.   


Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ, Rajasekaran A, Jusić N, Taylor L, Read M, Alfandari D, Alfandari D, Pignoni F, Moody SA., J Exp Zool B Mol Dev Evol. May 1, 2024; 342 (3): 212-240.   


Xenopus as a model system for studying pigmentation and pigmentary disorders., El Mir J, Nasrallah A, Thézé N, Cario M, Fayyad-Kazan H, Thiébaud P, Rezvani HR., Pigment Cell Melanoma Res. January 7, 2024; 38 (1): e13178.   


Small molecule-mediated reprogramming of Xenopus blastula stem cells to a neural crest state., Huber PB, LaBonne C., Dev Biol. January 25, 2023; 505 34-41.   


Zmym4 is required for early cranial gene expression and craniofacial cartilage formation., Jourdeuil K, Neilson KM, Cousin H, Tavares ALP, Majumdar HD, Alfandari D, Alfandari D, Moody SA., Front Cell Dev Biol. January 1, 2023; 11 1274788.   


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


Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J, Pauli S, Borchers A., Genesis. February 1, 2021; 59 (1-2): e23404.   


The RNA helicase DDX3 induces neural crest by promoting AKT activity., Perfetto M, Xu X, Lu C, Shi Y, Yousaf N, Li J, Yien YY, Wei S., Development. January 19, 2021; 148 (2):   


Mcrs1 interacts with Six1 to influence early craniofacial and otic development., Neilson KM, Keer S, Bousquet N, Macrorie O, Majumdar HD, Kenyon KL, Alfandari D, Alfandari D, Moody SA., Dev Biol. November 1, 2020; 467 (1-2): 39-50.   


The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration., Schwenty-Lara J, Nehl D, Borchers A., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.   


Prdm12 Directs Nociceptive Sensory Neuron Development by Regulating the Expression of the NGF Receptor TrkA., Desiderio S, Vermeiren S, Van Campenhout C, Kricha S, Malki E, Richts S, Fletcher EV, Vanwelden T, Schmidt BZ, Henningfeld KA, Pieler T, Woods CG, Nagy V, Verfaillie C, Bellefroid EJ., Cell Rep. March 26, 2019; 26 (13): 3522-3536.e5.   


Ketamine Modulates Zic5 Expression via the Notch Signaling Pathway in Neural Crest Induction., Shi Y, Shi Y, Li J, Chen C, Xia Y, Li Y, Zhang P, Xu Y, Xu Y, Li T, Zhou W, Song W., Front Mol Neurosci. February 7, 2018; 11 9.   


Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus., Bae CJ, Hong CS, Saint-Jeannet JP., Biochem Biophys Res Commun. January 15, 2018; 495 (3): 2257-2263.   


A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates., Plouhinec JL, Medina-Ruiz S, Borday C, Bernard E, Vert JP, Eisen MB, Harland RM, Monsoro-Burq AH., PLoS Biol. October 19, 2017; 15 (10): e2004045.   


Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM, Abbruzzesse G, Kenyon K, Bartolo V, Krohn P, Alfandari D, Alfandari D, Moody SA., Dev Biol. January 15, 2017; 421 (2): 171-182.   


Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome., Devotta A, Juraver-Geslin H, Gonzalez JA, Hong CS, Saint-Jeannet JP., Dev Biol. July 15, 2016; 415 (2): 371-382.   


Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectin., Gouignard N, Maccarana M, Strate I, von Stedingk K, Malmström A, Pera EM., Dis Model Mech. June 1, 2016; 9 (6): 607-20.   


5-Mehtyltetrahydrofolate rescues alcohol-induced neural crest cell migration abnormalities., Shi Y, Shi Y, Li J, Chen C, Gong M, Chen Y, Liu Y, Chen J, Li T, Song W., Mol Brain. September 16, 2014; 7 67.   


Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C, Maczkowiak F, Roche DD, Monsoro-Burq AH., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.   


The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS, Saint-Jeannet JP., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.   


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


Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome., Pizzuti A, Novelli G, Mari A, Ratti A, Colosimo A, Amati F, Penso D, Sangiuolo F, Calabrese G, Palka G, Silani V, Gennarelli M, Mingarelli R, Scarlato G, Scambler P, Dallapiccola B., Am J Hum Genet. April 1, 1996; 58 (4): 722-9.   

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