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	The Role of RNA-Binding Proteins in Vertebrate Neural Crest and Craniofacial Development., Forman TE., J Dev Biol. August 27, 2021; 9 (3):
	Modeling human congenital disorders with neural crest developmental defects using patient-derived induced pluripotent stem cells., Okuno H., Regen Ther. August 24, 2021; 18 275-280.
	Haploinsufficiency of SF3B2 causes craniofacial microsomia., Timberlake AT., Nat Commun. August 3, 2021; 12 (1): 4680.
	Retinol binding protein 1 affects Xenopus anterior neural development via all-trans retinoic acid signaling., Flach H., Dev Dyn. August 1, 2021; 250 (8): 1096-1112.
	BMP signaling is enhanced intracellularly by FHL3 controlling WNT-dependent spatiotemporal emergence of the neural crest., Alkobtawi M., Cell Rep. June 22, 2021; 35 (12): 109289.
	Fibroblast dedifferentiation as a determinant of successful regeneration., Lin TY., Dev Cell. May 17, 2021; 56 (10): 1541-1551.e6.
	Kindlin2 regulates neural crest specification via integrin-independent regulation of the FGF signaling pathway., Wang H., Development. May 15, 2021; 148 (10):
	4-Octylphenol induces developmental abnormalities and interferes the differentiation of neural crest cells in Xenopus laevis embryos., Xu Y., Environ Pollut. April 1, 2021; 274 116560.
	Characterising open chromatin in chick embryos identifies cis-regulatory elements important for paraxial mesoderm formation and axis extension., Mok GF., Nat Commun. February 19, 2021; 12 (1): 1157.
	Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders., Wyatt BH., Genesis. February 1, 2021; 59 (1-2): e23394.
	Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J., Genesis. February 1, 2021; 59 (1-2): e23404.
	The RNA helicase DDX3 induces neural crest by promoting AKT activity., Perfetto M., Development. January 19, 2021; 148 (2):
	Evolution of Somite Compartmentalization: A View From Xenopus., Della Gaspera B., Front Cell Dev Biol. January 1, 2021; 9 790847.
	Axial Skeletal Malformations in Genetically Modified Xenopus laevis and Xenopus tropicalis., Zlatow AL., Comp Med. December 1, 2020; 70 (6): 532-541.
	Anatomical and histological analyses reveal that tail repair is coupled with regrowth in wild-caught, juvenile American alligators (Alligator mississippiensis)., Xu C., Sci Rep. November 18, 2020; 10 (1): 20122.
	De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome., Ufartes R., Hum Genet. November 1, 2020; 139 (11): 1363-1379.
	Evolutionary repression of chondrogenic genes in the vertebrate osteoblast., Nguyen JKB., FEBS J. October 1, 2020; 287 (20): 4354-4361.
	Paired Box 9 (PAX9), the RNA polymerase II transcription factor, regulates human ribosome biogenesis and craniofacial development., Farley-Barnes KI., PLoS Genet. August 19, 2020; 16 (8): e1008967.
	Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
	The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled., Kratzer MC., Development. May 22, 2020; 147 (10):
	Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. March 3, 2020; 13 (3):
	Disrupted ER membrane protein complex-mediated topogenesis drives congenital neural crest defects., Marquez J., J Clin Invest. February 3, 2020; 130 (2): 813-826.
	M-Channel Activation Contributes to the Anticonvulsant Action of the Ketone Body β-Hydroxybutyrate., Manville RW., J Pharmacol Exp Ther. February 1, 2020; 372 (2): 148-156.
	The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration., Schwenty-Lara J., Hum Mol Genet. January 15, 2020; 29 (2): 305-319.
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	Effect of nano-encapsulation of β-carotene on Xenopus laevis embryos development (FETAX)., Battistoni M., Toxicol Rep. January 1, 2020; 7 510-519.
	Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation., Nasr T., Dev Cell. December 16, 2019; 51 (6): 665-674.e6.
	Skeletal Mineralization in Association with Type X Collagen Expression Is an Ancestral Feature for Jawed Vertebrates., Debiais-Thibaud M., Mol Biol Evol. October 1, 2019; 36 (10): 2265-2276.
	NEIL1 and NEIL2 DNA glycosylases protect neural crest development against mitochondrial oxidative stress., Han D., Elife. September 30, 2019; 8
	Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome., Greenberg RS., Cell. September 5, 2019; 178 (6): 1421-1436.e24.
	Xenopus fraseri: Mr. Fraser, where did your frog come from?, Evans BJ., PLoS One. September 3, 2019; 14 (9): e0220892.
	A new transgenic reporter line reveals Wnt-dependent Snai2 re-expression and cranial neural crest differentiation in Xenopus., Li J., Sci Rep. August 1, 2019; 9 (1): 11191.
	Adaptive correction of craniofacial defects in pre-metamorphic Xenopus laevis tadpoles involves thyroid hormone-independent tissue remodeling., Pinet K., Development. July 22, 2019; 146 (14):
	PDGF-B: The missing piece in the mosaic of PDGF family role in craniofacial development., Corsinovi D., Dev Dyn. July 1, 2019; 248 (7): 603-612.
	Epithelial-Mesenchymal Transition Promotes the Differentiation Potential of Xenopus tropicalis Immature Sertoli Cells., Nguyen TMX., Stem Cells Int. May 5, 2019; 2019 8387478.
	The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals., Kwong-Brown U., Elife. January 8, 2019; 8
	How thyroid hormones and their inhibitors affect cartilage growth and shape in the frog Xenopus laevis., Rose CS., J Anat. January 1, 2019; 234 (1): 89-105.
	Latrophilin2 is involved in neural crest cell migration and placode patterning in Xenopus laevis., Yokote N., Int J Dev Biol. January 1, 2019; 63 (1-2): 29-35.
	Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in Xenopus laevis., Mills A., Front Physiol. January 1, 2019; 10 431.
	Comparative analysis of p4ha1 and p4ha2 expression during Xenopus laevis development., Martini D., Int J Dev Biol. January 1, 2019; 63 (6-7): 311-316.
	The Many Faces of Xenopus: Xenopus laevis as a Model System to Study Wolf-Hirschhorn Syndrome., Lasser M., Front Physiol. January 1, 2019; 10 817.
	Physiological effects of KDM5C on neural crest migration and eye formation during vertebrate development., Kim Y., Epigenetics Chromatin. December 6, 2018; 11 (1): 72.
	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	Bone regeneration after traumatic skull injury in Xenopus tropicalis., Muñoz D., Mech Dev. December 1, 2018; 154 153-161.
	Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb., Herrera-Rincon C., Cell Rep. November 6, 2018; 25 (6): 1593-1609.e7.
	Bapx1 is required for jaw joint development in amphibians., Lukas P., Evol Dev. November 1, 2018; 20 (6): 192-206.
	Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos., Willsey HR., Dev Biol. October 15, 2018; 442 (2): 276-287.
	ITGBL1 modulates integrin activity to promote cartilage formation and protect against arthritis., Song EK., Sci Transl Med. October 10, 2018; 10 (462):
	Cdc42 regulates the cellular localization of Cdc42ep1 in controlling neural crest cell migration., Cohen S., J Mol Cell Biol. October 1, 2018; 10 (5): 376-387.
	Nosip functions during vertebrate eye and cranial cartilage development., Flach H., Dev Dyn. September 1, 2018; 247 (9): 1070-1082.

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