Papers associated with mouth primordium

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	Jak2 and Jaw Muscles Are Required for Buccopharyngeal Membrane Perforation during Mouth Development., Dickinson AJG., J Dev Biol. May 31, 2023; 11 (2):
	Noggin is required for first pharyngeal arch differentiation in the frog Xenopus tropicalis., Young JJ., Dev Biol. June 15, 2017; 426 (2): 245-254.
	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.
	Using frogs faces to dissect the mechanisms underlying human orofacial defects., Dickinson AJ., Semin Cell Dev Biol. March 1, 2016; 51 54-63.
	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.
	G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.
	Budgett's frog (Lepidobatrachus laevis): A new amphibian embryo for developmental biology., Amin NM., Dev Biol. September 15, 2015; 405 (2): 291-303.
	The role of folate metabolism in orofacial development and clefting., Wahl SE., Dev Biol. September 1, 2015; 405 (1): 108-22.
	The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. May 19, 2015; 7 62.
	A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements., Square T., Dev Biol. January 15, 2015; 397 (2): 293-304.
	Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy., Simons C., Nat Genet. January 1, 2015; 47 (1): 73-7.
	Hedgehog activity controls opening of the primary mouth., Tabler JM., Dev Biol. December 1, 2014; 396 (1): 1-7.
	Quantification of orofacial phenotypes in Xenopus., Kennedy AE., J Vis Exp. November 6, 2014; (93): e52062.
	Retinoic acid induced-1 (Rai1) regulates craniofacial and brain development in Xenopus., Tahir R., Mech Dev. August 1, 2014; 133 91-104.
	The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.
	A hydrophobic barrier deep within the inner pore of the TWIK-1 K2P potassium channel., Aryal P., Nat Commun. July 8, 2014; 5 4377.
	Quantitative analysis of orofacial development and median clefts in Xenopus laevis., Kennedy AE., Anat Rec (Hoboken). May 1, 2014; 297 (5): 834-55.
	The evolutionary history of vertebrate cranial placodes II. Evolution of ectodermal patterning., Schlosser G., Dev Biol. May 1, 2014; 389 (1): 98-119.
	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.
	The morphology and attachment of Protopolystoma xenopodis (Monogenea: Polystomatidae) infecting the African clawed frog Xenopus laevis., Theunissen M., Parasite. January 1, 2014; 21 20.
	Lack of negatively charged residues at the external mouth of Kir2.2 channels enable the voltage-dependent block by external Mg2+., Li J., PLoS One. January 1, 2014; 9 (10): e111372.
	Osmotic water transport in aquaporins: evidence for a stochastic mechanism., Zeuthen T., J Physiol. October 15, 2013; 591 (20): 5017-29.
	Voltage-dependent inhibition of outward Kir2.1 currents by extracellular spermine., Chang HK., Biochim Biophys Acta. February 1, 2013; 1828 (2): 765-75.
	Cranial muscles in amphibians: development, novelties and the role of cranial neural crest cells., Schmidt J., J Anat. January 1, 2013; 222 (1): 134-46.
	A leucine zipper motif essential for gating of hyperpolarization-activated channels., Wemhöner K., J Biol Chem. November 23, 2012; 287 (48): 40150-60.
	High Ca(2+) permeability of a peptide-gated DEG/ENaC from Hydra., Dürrnagel S., J Gen Physiol. October 1, 2012; 140 (4): 391-402.
	Marine algal toxin azaspiracid is an open-state blocker of hERG potassium channels., Twiner MJ., Chem Res Toxicol. September 17, 2012; 25 (9): 1975-84.
	Characterization of a novel somatic KCNJ5 mutation delI157 in an aldosterone-producing adenoma., Murthy M., J Hypertens. September 1, 2012; 30 (9): 1827-33.
	Extracellular finger domain modulates the response of the epithelial sodium channel to shear stress., Shi S., J Biol Chem. May 4, 2012; 287 (19): 15439-44.
	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.
	Ion selectivity and current saturation in inward-rectifier K+ channels., Yang L., J Gen Physiol. February 1, 2012; 139 (2): 145-57.
	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.
	A maternally established SoxB1/SoxF axis is a conserved feature of chordate germ layer patterning., Cattell MV., Evol Dev. January 1, 2012; 14 (1): 104-15.
	Low frequency vibrations induce malformations in two aquatic species in a frequency-, waveform-, and direction-specific manner., Vandenberg LN., PLoS One. January 1, 2012; 7 (12): e51473.
	5-HT3 receptor ion size selectivity is a property of the transmembrane channel, not the cytoplasmic vestibule portals., McKinnon NK., J Gen Physiol. October 1, 2011; 138 (4): 453-66.
	The origins and evolution of vertebrate metamorphosis., Laudet V., Curr Biol. September 27, 2011; 21 (18): R726-37.
	Development of the venous pole of the heart in the frog Xenopus laevis: a morphological study with special focus on the development of the venoatrial connections., Jahr M., Dev Dyn. June 1, 2011; 240 (6): 1518-27.
	Microvascularization of the interhyoid muscle in larval Xenopus laevis (Daudin): Scanning electron microscopy of vascular corrosion casts and correlative light microscopy., Rattey J., J Morphol. March 1, 2011; 272 (3): 342-53.
	Recombinant expression of the toxic peptide ErgTx1 and role of Met35 on its stability and function., Jimenez-Vargas JM., Peptides. March 1, 2011; 32 (3): 560-7.
	A K+ channel from salt-tolerant melon inhibited by Na+., Zhang YD, Zhang YD., New Phytol. February 1, 2011; 189 (3): 856-868.
	Functional analysis of novel aquaporins from Fasciola gigantica., Geadkaew A., Mol Biochem Parasitol. February 1, 2011; 175 (2): 144-53.
	The ascidian mouth opening is derived from the anterior neuropore: reassessing the mouth/neural tube relationship in chordate evolution., Veeman MT., Dev Biol. August 1, 2010; 344 (1): 138-49.
	Aquatic feeding in pipid frogs: the use of suction for prey capture., Carreño CA., J Exp Biol. June 15, 2010; 213 (Pt 12): 2001-8.
	The 5'-untranslated region of the mouse mammary tumor virus mRNA exhibits cap-independent translation initiation., Vallejos M., Nucleic Acids Res. January 1, 2010; 38 (2): 618-32.
	Insights into the molecular determinants of proton inhibition in an acid-inactivated degenerins and mammalian epithelial Na(+) channel., Wang Y., Biochemistry. October 27, 2009; 48 (42): 10005-13.
	Bactrian camel (Camelus bactrianus) integrins alphavbeta3 and alphavbeta6 as FMDV receptors: molecular cloning, sequence analysis and comparison with other species., Du J., Vet Immunol Immunopathol. October 15, 2009; 131 (3-4): 190-9.
	An intersubunit salt bridge near the selectivity filter stabilizes the active state of Kir1.1., Sackin H., Biophys J. August 19, 2009; 97 (4): 1058-66.
	Concerted action of two cation filters in the aquaporin water channel., Wu B., EMBO J. August 5, 2009; 28 (15): 2188-94.
	Multisensory integration in mesencephalic trigeminal neurons in Xenopus tadpoles., Pratt KG., J Neurophysiol. July 1, 2009; 102 (1): 399-412.
	Molecular features of thyroid hormone-regulated skin remodeling in Xenopus laevis during metamorphosis., Suzuki K., Dev Growth Differ. May 1, 2009; 51 (4): 411-27.

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