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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.