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	Common features of cartilage maturation are not conserved in an amphibian model., Nguyen JKB., Dev Dyn. November 1, 2023; 252 (11): 1375-1390.
	FGFR1 variants contributed to families with tooth agenesis., Yao S., Hum Genomics. October 13, 2023; 17 (1): 93.
	The phenotypic spectrum of pathogenic ATP1A1 variants expands: the novel p.P600R substitution causes demyelinating Charcot-Marie-Tooth disease., Cinarli Yuksel F., J Neurol. May 1, 2023; 270 (5): 2576-2590.
	Structural basis for PRC2 decoding of active histone methylation marks H3K36me2/3., Finogenova K., Elife. November 19, 2020; 9
	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.
	Endoparasites infecting exotic captive amphibian pet and zoo animals (Anura, Caudata) in Germany., Hallinger MJ., Parasitol Res. November 1, 2020; 119 (11): 3659-3673.
	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.
	De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy., Park J., J Med Genet. April 1, 2020; 57 (4): 283-288.
	Odontomas in Frogs., LaDouceur EEB., Vet Pathol. January 1, 2020; 57 (1): 147-150.
	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.
	Nervous NDRGs: the N-myc downstream-regulated gene family in the central and peripheral nervous system., Schonkeren SL., Neurogenetics. October 1, 2019; 20 (4): 173-186.
	Xenopus fraseri: Mr. Fraser, where did your frog come from?, Evans BJ., PLoS One. September 3, 2019; 14 (9): e0220892.
	Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons., Cioni JM., Cell. January 10, 2019; 176 (1-2): 56-72.e15.
	The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1., Ott T., Front Physiol. January 1, 2019; 10 134.
	Evolution of dental tissue mineralization: an analysis of the jawed vertebrate SPARC and SPARC-L families., Enault S., BMC Evol Biol. August 30, 2018; 18 (1): 127.
	Tooth germ initiation patterns in a developing dentition: An in vivo study of Xenopus laevis tadpoles., Lamoureux DO., J Morphol. May 1, 2018; 279 (5): 616-625.
	Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2., Lassuthova P., Am J Hum Genet. March 1, 2018; 102 (3): 505-514.
	SHH signaling directed by two oral epithelium-specific enhancers controls tooth and oral development., Sagai T., Sci Rep. October 11, 2017; 7 (1): 13004.
	Mouth development., Chen J., Wiley Interdiscip Rev Dev Biol. September 1, 2017; 6 (5):
	Caspase-9 has a nonapoptotic function in Xenopus embryonic primitive blood formation., Tran HT., J Cell Sci. July 15, 2017; 130 (14): 2371-2381.
	Compound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndrome., Johnston JJ., Cold Spring Harb Mol Case Stud. July 1, 2017; 3 (4):
	Xenopus as a model for studies in mechanical stress and cell division., Stooke-Vaughan GA., Genesis. January 1, 2017; 55 (1-2):
	Targeted Pth4-expressing cell ablation impairs skeletal mineralization in zebrafish., Suarez-Bregua P., PLoS One. January 1, 2017; 12 (10): e0186444.
	PTH1R Mutants Found in Patients with Primary Failure of Tooth Eruption Disrupt G-Protein Signaling., Subramanian H., PLoS One. November 1, 2016; 11 (11): e0167033.
	Structural studies of N-terminal mutants of Connexin 26 and Connexin 32 using (1)H NMR spectroscopy., Batir Y., Arch Biochem Biophys. October 15, 2016; 608 8-19.
	Insight from Frogs: Sonic Hedgehog Gene Expression and a Re-evaluation of the Vertebrate Odontogenic Band., Grieco TM., Anat Rec (Hoboken). August 1, 2016; 299 (8): 1099-109.
	Genetics, Morphology, Advertisement Calls, and Historical Records Distinguish Six New Polyploid Species of African Clawed Frog (Xenopus, Pipidae) from West and Central Africa., Evans BJ., PLoS One. December 16, 2015; 10 (12): e0142823.
	Evolutionary innovation and conservation in the embryonic derivation of the vertebrate skull., Piekarski N., Nat Commun. December 1, 2014; 5 5661.
	A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle., Sartelet A., Dis Model Mech. January 1, 2014; 7 (1): 119-28.
	Identification, characterization, and expression of dentin matrix protein 1 gene in Xenopus laevis., Yonekura T., J Exp Zool B Mol Dev Evol. December 1, 2013; 320 (8): 525-37.
	Role of connexin 32 hemichannels in the release of ATP from peripheral nerves., Nualart-Marti A., Glia. December 1, 2013; 61 (12): 1976-89.
	Venomous secretions from marine snails of the Terebridae family target acetylcholine receptors., Kendel Y., Toxins (Basel). May 21, 2013; 5 (5): 1043-50.
	Expression of the amelogenin gene in the skin of Xenopus tropicalis., Okada M., Zoolog Sci. March 1, 2013; 30 (3): 154-9.
	Metamorphosis in a frog that does not have a tadpole., Elinson RP., Curr Top Dev Biol. January 1, 2013; 103 259-76.
	Genetic basis for tooth malformations: from mice to men and back again., Mitsiadis TA., Clin Genet. October 1, 2011; 80 (4): 319-29.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	Integrating phenotype ontologies across multiple species., Mungall CJ., Genome Biol. January 8, 2010; 11 (1): R2.
	Skeletal advance and arrest in giant non-metamorphosing African clawed frog tadpoles (Xenopus laevis: Daudin)., Kerney R., J Anat. January 1, 2010; 216 (1): 132-43.
	The SCPP gene repertoire in bony vertebrates and graded differences in mineralized tissues., Kawasaki K., Dev Genes Evol. March 1, 2009; 219 (3): 147-57.
	Comparison of molecular and cellular events during lower jaw regeneration of newt (Cynops pyrrhogaster) and West African clawed frog (Xenopus tropicalis)., Kurosaka H., Dev Dyn. February 1, 2008; 237 (2): 354-65.
	Small heat shock protein Hsp27 is required for proper heart tube formation., Brown DD., Genesis. November 1, 2007; 45 (11): 667-78.
	Identification and characterization of matrix metalloproteinase-20 (MMP20; enamelysin) genes in reptile and amphibian., Shintani S., Gene. May 1, 2007; 392 (1-2): 89-97.
	Severe neuropathy with leaky connexin32 hemichannels., Liang GS., Ann Neurol. May 1, 2005; 57 (5): 749-54.
	Induction of tooth and eye by transplantation of activin A-treated, undifferentiated presumptive ectodermal Xenopus cells into the abdomen., Myoishi Y., Int J Dev Biol. December 1, 2004; 48 (10): 1105-12.
	USAG-1: a bone morphogenetic protein antagonist abundantly expressed in the kidney., Yanagita M., Biochem Biophys Res Commun. April 2, 2004; 316 (2): 490-500.
	Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32., Abrams CK., J Neurosci. November 19, 2003; 23 (33): 10548-58.
	Identification and characterization of ameloblastin gene in an amphibian, Xenopus laevis., Shintani S., Gene. October 30, 2003; 318 125-36.
	Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease., Abrams CK., Proc Natl Acad Sci U S A. March 19, 2002; 99 (6): 3980-4.
	The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectrics., Dickinson P., Hum Mol Genet. February 1, 2002; 11 (3): 243-51.

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