Papers associated with roof of mouth

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	Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes., Lansdon LA., Am J Hum Genet. January 5, 2023; 110 (1): 71-91.
	E-liquids and vanillin flavoring disrupts retinoic acid signaling and causes craniofacial defects in Xenopus embryos., Dickinson AJG., Dev Biol. January 1, 2022; 481 14-29.
	Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer., Levin M., Cell. April 15, 2021;
	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.
	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 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.
	CALHM3 Is Essential for Rapid Ion Channel-Mediated Purinergic Neurotransmission of GPCR-Mediated Tastes., Ma Z., Neuron. May 2, 2018; 98 (3): 547-561.e10.
	Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans., Lansdon LA., Genetics. January 1, 2018; 208 (1): 283-296.
	Mouth development., Chen J., Wiley Interdiscip Rev Dev Biol. September 1, 2017; 6 (5):
	In vitro models of cranial neural crest development toward toxicity tests: frog, mouse, and human., Suga M., Oral Dis. July 1, 2017; 23 (5): 559-565.
	Role of JNK during buccopharyngeal membrane perforation, the last step of embryonic mouth formation., Houssin NS., Dev Dyn. February 1, 2017; 246 (2): 100-115.
	Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome., Devotta A., Dev Biol. July 15, 2016; 415 (2): 371-382.
	The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery., Toriyama M., Nat Genet. June 1, 2016; 48 (6): 648-56.
	Using frogs faces to dissect the mechanisms underlying human orofacial defects., Dickinson AJ., Semin Cell Dev Biol. March 1, 2016; 51 54-63.
	Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy., Zaharieva IT., Brain. March 1, 2016; 139 (Pt 3): 674-91.
	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.
	The role of folate metabolism in orofacial development and clefting., Wahl SE., Dev Biol. September 1, 2015; 405 (1): 108-22.
	Spindle orientation processes in epithelial growth and organisation., Panousopoulou E., Semin Cell Dev Biol. October 1, 2014; 34 124-32.
	Quantitative analysis of orofacial development and median clefts in Xenopus laevis., Kennedy AE., Anat Rec (Hoboken). May 1, 2014; 297 (5): 834-55.
	Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome., Karpinski BA., Dis Model Mech. February 1, 2014; 7 (2): 245-57.
	Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes., Kennedy AE., Dev Biol. May 1, 2012; 365 (1): 229-40.
	Hedgehog signalling in development of the secondary palate., Cobourne MT., Front Oral Biol. January 1, 2012; 16 52-9.
	Combinatorial roles for BMPs and Endothelin 1 in patterning the dorsal-ventral axis of the craniofacial skeleton., Alexander C., Development. December 1, 2011; 138 (23): 5135-46.
	Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice., Rainger J., PLoS Genet. July 1, 2011; 7 (7): e1002114.
	Sox9 function in craniofacial development and disease., Lee YH, Lee YH., Genesis. April 1, 2011; 49 (4): 200-8.
	SPLUNC1 expression reduces surface levels of the epithelial sodium channel (ENaC) in Xenopus laevis oocytes., Rollins BM., Channels (Austin). January 1, 2010; 4 (4): 255-9.
	SPLUNC1 regulates airway surface liquid volume by protecting ENaC from proteolytic cleavage., Garcia-Caballero A., Proc Natl Acad Sci U S A. July 7, 2009; 106 (27): 11412-7.
	Maternal Interferon Regulatory Factor 6 is required for the differentiation of primary superficial epithelia in Danio and Xenopus embryos., Sabel JL., Dev Biol. January 1, 2009; 325 (1): 249-62.
	Tissue engineering in cleft palate and other congenital malformations., Panetta NJ., Pediatr Res. May 1, 2008; 63 (5): 545-51.
	Chemical rescue of cleft palate and midline defects in conditional GSK-3beta mice., Liu KJ, Liu KJ., Nature. March 1, 2007; 446 (7131): 79-82.
	Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase (Xdhcr7) in neural development., Tadjuidje E., Dev Dyn. August 1, 2006; 235 (8): 2095-110.
	Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation., Liu H., Gene Expr Patterns. August 1, 2006; 6 (6): 632-6.
	Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test., Juriloff DM., Birth Defects Res A Clin Mol Teratol. August 1, 2006; 76 (8): 574-9.
	Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality., Parrish M., Mol Cell Biol. August 1, 2004; 24 (16): 7102-12.
	Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features., Roessler E., Proc Natl Acad Sci U S A. November 11, 2003; 100 (23): 13424-9.
	Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate., Jezewski PA., J Med Genet. June 1, 2003; 40 (6): 399-407.
	A new member of the spalt like zinc finger protein family, Msal-3, is expressed in the CNS and sites of epithelial/mesenchymal interaction., Ott T., Mech Dev. March 1, 2001; 101 (1-2): 203-7.
	Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development., Mo R., Development. January 1, 1997; 124 (1): 113-23.
	Multiple defects and perinatal death in mice deficient in follistatin., Matzuk MM., Nature. March 23, 1995; 374 (6520): 360-3.
	Functional analysis of activins during mammalian development., Matzuk MM., Nature. March 23, 1995; 374 (6520): 354-6.
	Endogenous distribution of retinoids during normal development and teratogenesis in the mouse embryo., Horton C., Dev Dyn. March 1, 1995; 202 (3): 312-23.
	Calcium-binding proteins in chemoreceptors of Xenopus laevis., Kerschbaum HH., Tissue Cell. January 1, 1992; 24 (5): 719-24.
	Hyaluronan as a propellant for epithelial movement: the development of semicircular canals in the inner ear of Xenopus., Haddon CM., Development. June 1, 1991; 112 (2): 541-50.
	Development and ciliation of the palate in two frogs, Bombina and Xenopus; a comparative study., LeCluyse EL., Tissue Cell. January 1, 1985; 17 (6): 853-64.

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