Papers associated with auditory apparatus

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	Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. October 13, 2023;
	Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
	Normal development in Xenopus laevis: A complementary staging table for the skull based on cartilage and bone., MacKenzie EM., Dev Dyn. August 1, 2022; 251 (8): 1340-1356.
	Morphometric study of the vestibuloauditory organ of the African clawed frog, Xenopus laevis., Homma T., Anat Histol Embryol. July 1, 2022; 51 (4): 514-523.
	Vestibular Influence on Vertebrate Skeletal Symmetry and Body Shape., Gordy C., Front Syst Neurosci. October 6, 2021; 15 753207.
	Using Xenopus to analyze neurocristopathies like Kabuki syndrome., Schwenty-Lara J., Genesis. February 1, 2021; 59 (1-2): e23404.
	Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.
	Acute consequences of a unilateral VIIIth nerve transection on vestibulo-ocular and optokinetic reflexes in Xenopus laevis tadpoles., Soupiadou P., J Neurol. December 1, 2020; 267 (Suppl 1): 62-75.
	An In Vitro Study on Prestin Analog Gene in the Bullfrog Hearing Organs., Wang Z., Neural Plast. July 2, 2020; 2020 3570732.
	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):
	Stabilization of Gaze during Early Xenopus Development by Swimming-Related Utricular Signals., Lambert FM., Curr Biol. February 24, 2020; 30 (4): 746-753.e4.
	Topologically correct central projections of tetrapod inner ear afferents require Fzd3., Duncan JS., Sci Rep. July 16, 2019; 9 (1): 10298.
	Transplantation of Ears Provides Insights into Inner Ear Afferent Pathfinding Properties., Gordy C., Dev Neurobiol. November 1, 2018; 78 (11): 1064-1080.
	Semicircular Canal Influences on the Developmental Tuning of the Translational Vestibulo-Ocular Reflex., Branoner F., Front Neurol. June 5, 2018; 9 404.
	Sonic hedgehog antagonists reduce size and alter patterning of the frog inner ear., Zarei S., Dev Neurobiol. December 1, 2017; 77 (12): 1385-1400.
	no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development., Nakayama T., Dev Biol. June 15, 2017; 426 (2): 472-486.
	A novel role of the organizer gene Goosecoid as an inhibitor of Wnt/PCP-mediated convergent extension in Xenopus and mouse., Ulmer B., Sci Rep. February 21, 2017; 7 43010.
	Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians., Cortese M., Proc Natl Acad Sci U S A. February 21, 2017; 114 (8): 2054-2059.
	Metabolomic approach for identifying and visualizing molecular tissue markers in tadpoles of Xenopus tropicalis by mass spectrometry imaging., Goto-Inoue N., Biol Open. September 15, 2016; 5 (9): 1252-9.
	Sex differences and endocrine regulation of auditory-evoked, neural responses in African clawed frogs (Xenopus)., Hall IC., J Comp Physiol A Neuroethol Sens Neural Behav Physiol. January 1, 2016; 202 (1): 17-34.
	RNA Extraction from Xenopus Auditory and Vestibular Organs for Molecular Cloning and Expression Profiling with RNA-Seq and Microarrays., Trujillo-Provencio C., Methods Mol Biol. January 1, 2016; 1427 73-92.
	Ear manipulations reveal a critical period for survival and dendritic development at the single-cell level in Mauthner neurons., Elliott KL., Dev Neurobiol. December 1, 2015; 75 (12): 1339-51.
	RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.
	Semicircular canal-dependent developmental tuning of translational vestibulo-ocular reflexes in Xenopus laevis., Branoner F., Dev Neurobiol. October 1, 2015; 75 (10): 1051-67.
	Spinal corollary discharge modulates motion sensing during vertebrate locomotion., Chagnaud BP., Nat Commun. September 4, 2015; 6 7982.
	Inner ear development: building a spiral ganglion and an organ of Corti out of unspecified ectoderm., Fritzsch B., Cell Tissue Res. July 1, 2015; .
	The nuclease FAN1 is involved in DNA crosslink repair in Arabidopsis thaliana independently of the nuclease MUS81., Herrmann NJ., Nucleic Acids Res. April 20, 2015; 43 (7): 3653-66.
	The frog inner ear: picture perfect?, Mason MJ., J Assoc Res Otolaryngol. April 1, 2015; 16 (2): 171-88.
	ERK7 regulates ciliogenesis by phosphorylating the actin regulator CapZIP in cooperation with Dishevelled., Miyatake K., Nat Commun. March 31, 2015; 6 6666.
	Sensory afferent segregation in three-eared frogs resemble the dominance columns observed in three-eyed frogs., Elliott KL., Sci Rep. February 9, 2015; 5 8338.
	Opportunities and limits of the one gene approach: the ability of Atoh1 to differentiate and maintain hair cells depends on the molecular context., Jahan I., Front Cell Neurosci. February 5, 2015; 9 26.
	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.
	A novel function for Egr4 in posterior hindbrain development., Bae CJ., Sci Rep. January 12, 2015; 5 7750.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	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.
	Vertebrate Cranial Placodes as Evolutionary Innovations-The Ancestor's Tale., Schlosser G., Curr Top Dev Biol. January 1, 2015; 111 235-300.
	SPAK and OSR1 Sensitive Cell Membrane Protein Abundance and Activity of KCNQ1/E1 K+ Channels., Elvira B., Cell Physiol Biochem. January 1, 2015; 37 (5): 2032-42.
	Evolutionary innovation and conservation in the embryonic derivation of the vertebrate skull., Piekarski N., Nat Commun. December 1, 2014; 5 5661.
	I-J loop involvement in the pharmacological profile of CLC-K channels expressed in Xenopus oocytes., Gradogna A., Biochim Biophys Acta. November 1, 2014; 1838 (11): 2745-56.
	Embryological manipulations in the developing Xenopus inner ear reveal an intrinsic role for Wnt signaling in dorsal-ventral patterning., Forristall CA., Dev Dyn. October 1, 2014; 243 (10): 1262-74.
	Early expression of aromatase and the membrane estrogen receptor GPER in neuromasts reveals a role for estrogens in the development of the frog lateral line system., Hamilton CK., Gen Comp Endocrinol. September 1, 2014; 205 242-50.
	Transport of boron by the tassel-less1 aquaporin is critical for vegetative and reproductive development in maize., Durbak AR., Plant Cell. July 1, 2014; 26 (7): 2978-95.
	Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
	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.
	Label-free determination of hemodynamic parameters in the microcirculaton with third harmonic generation microscopy., Dietzel S., PLoS One. January 1, 2014; 9 (6): e99615.
	Early embryonic specification of vertebrate cranial placodes., Schlosser G., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
	Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene., Geng FS., Development. November 1, 2013; 140 (21): 4362-74.
	Subtype-selective activation of K(v)7 channels by AaTXKβ₂₋₆₄, a novel toxin variant from the Androctonus australis scorpion venom., Landoulsi Z., Mol Pharmacol. November 1, 2013; 84 (5): 763-73.
	A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome., Rienhoff HY., Am J Med Genet A. August 1, 2013; 161A (8): 2040-6.
	The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity., Mhaske PV., Am J Physiol Cell Physiol. June 15, 2013; 304 (12): C1150-8.

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