| scholarly article | Q13442814 |
| P50 | author | Suzanne L. Mansour | Q43175473 |
| P2093 | author name string | Gary C Schoenwolf | |
| Lisa D Urness | |||
| Xiaofen Wang | |||
| Christian N Paxton | |||
| P2860 | cites work | Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss | Q24300723 |
| Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) | Q24313229 | ||
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| Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier | Q28202651 | ||
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| A mutation in PDS causes non-syndromic recessive deafness | Q28264560 | ||
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| Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice | Q28505685 | ||
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| Identification of cis-element regulating expression of the mouse Fgf10 gene during inner ear development | Q28506880 | ||
| Inner ear and maternal reproductive defects in mice lacking the Hmx3 homeobox gene | Q28511865 | ||
| Requirements for FGF3 and FGF10 during inner ear formation | Q28585124 | ||
| Differential requirements for FGF3, FGF8 and FGF10 during inner ear development | Q28585590 | ||
| Fgf3 and Fgf10 are required for mouse otic placode induction | Q28585848 | ||
| Hmx2 homeobox gene control of murine vestibular morphogenesis | Q28587250 | ||
| Cloning, characterization, and mapping of the mouse homeobox gene Hmx1 | Q28588596 | ||
| Foxg1 is required for morphogenesis and histogenesis of the mammalian inner ear | Q28589083 | ||
| Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless | Q28589182 | ||
| Cthrc1 selectively activates the planar cell polarity pathway of Wnt signaling by stabilizing the Wnt-receptor complex | Q28590249 | ||
| Sox9 is required for invagination of the otic placode in mice | Q28591158 | ||
| Wnt-dependent regulation of inner ear morphogenesis is balanced by the opposing and supporting roles of Shh. | Q28591489 | ||
| Hmx2 and Hmx3 homeobox genes direct development of the murine inner ear and hypothalamus and can be functionally replaced by Drosophila Hmx | Q28593026 | ||
| FGF8 initiates inner ear induction in chick and mouse | Q28593974 | ||
| A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells | Q29614542 | ||
| Towards an integrated view of Wnt signaling in development | Q29615175 | ||
| Proximal events in Wnt signal transduction | Q29616162 | ||
| Rank products: a simple, yet powerful, new method to detect differentially regulated genes in replicated microarray experiments | Q29616371 | ||
| Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass | Q30489861 | ||
| Towards genetic genome projects: genomic library screening and gene-targeting vector construction in a single step | Q30719533 | ||
| The solute carrier 26 family of proteins in epithelial ion transport | Q31152083 | ||
| Fgf-dependent otic induction requires competence provided by Foxi1 and Dlx3b | Q33269857 | ||
| Identification of synergistic signals initiating inner ear development. | Q33927542 | ||
| Mouse FGF15 is the ortholog of human and chick FGF19, but is not uniquely required for otic induction. | Q34312959 | ||
| Mapping of Wnt, frizzled, and Wnt inhibitor gene expression domains in the avian otic primordium | Q34416692 | ||
| FGF signaling in ear development and innervation. | Q35607411 | ||
| Hmx homeobox gene function in inner ear and nervous system cell-type specification and development | Q36144920 | ||
| Planar cell polarity and a potential role for a Wnt morphogen gradient in stereociliary bundle orientation in the mammalian inner ear. | Q36206053 | ||
| Induction and specification of cranial placodes | Q36469493 | ||
| Conditional gene inactivation reveals roles for Fgf10 and Fgfr2 in establishing a normal pattern of epithelial branching in the mouse lung. | Q36511680 | ||
| Dusp6 (Mkp3) is a negative feedback regulator of FGF-stimulated ERK signaling during mouse development | Q36713660 | ||
| The preplacodal region: an ectodermal domain with multipotential progenitors that contribute to sense organs and cranial sensory ganglia. | Q36950092 | ||
| The first steps towards hearing: mechanisms of otic placode induction. | Q36950097 | ||
| Expression and functions of FGF ligands during early otic development. | Q36950101 | ||
| Axial patterning in the developing vertebrate inner ear. | Q36950114 | ||
| Deletion of the chloride transporter Slc26a9 causes loss of tubulovesicles in parietal cells and impairs acid secretion in the stomach | Q36972040 | ||
| Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus | Q37021446 | ||
| Conditional inactivation of Has2 reveals a crucial role for hyaluronan in skeletal growth, patterning, chondrocyte maturation and joint formation in the developing limb | Q37314413 | ||
| Unraveling inner ear induction by gene manipulation using Pax2-Cre BAC transgenic mice | Q37407787 | ||
| Molecular and tissue interactions governing induction of cranial ectodermal placodes | Q37509335 | ||
| Expression and function of FGF10 in mammalian inner ear development | Q37524712 | ||
| Fgf3 is required for dorsal patterning and morphogenesis of the inner ear epithelium | Q38440251 | ||
| Expression of mouse fibroblast growth factor and fibroblast growth factor receptor genes during early inner ear development | Q38451515 | ||
| Inductive Processes in Embryonic Development | Q40033483 | ||
| A Cre/loxP-deleter transgenic line in mouse strain 129S1/SvImJ. | Q40744891 | ||
| The role of FGF-3 in early inner ear development: an analysis in normal and kreisler mutant mice | Q40946155 | ||
| Vertebrate Sprouty genes are induced by FGF signaling and can cause chondrodysplasia when overexpressed. | Q41692233 | ||
| Competence, specification and commitment in otic placode induction. | Q41748874 | ||
| Hyaluronan as a propellant for epithelial movement: the development of semicircular canals in the inner ear of Xenopus | Q42469567 | ||
| Three vertebrate hyaluronan synthases are expressed during mouse development in distinct spatial and temporal patterns | Q44178809 | ||
| Specification of the otic placode depends on Sox9 function in Xenopus | Q44844783 | ||
| Genetic interactions underlying otic placode induction and formation | Q44930068 | ||
| Regulative response of the cranial neural tube after neural fold ablation: spatiotemporal nature of neural crest regeneration and up-regulation of Slug. | Q46191821 | ||
| Pivotal role of hmx2 and hmx3 in zebrafish inner ear and lateral line development | Q47073338 | ||
| Fgf3 and Fgf8 dependent and independent transcription factors are required for otic placode specification | Q47073913 | ||
| Molecular anatomy of placode development in Xenopus laevis | Q47273875 | ||
| Characterization of avian frizzled genes in cranial placode development | Q47865505 | ||
| Cwnt-8C: a novel Wnt gene with a potential role in primitive streak formation and hindbrain organization. | Q48090895 | ||
| Expression of multiple novel Wnt-1/int-1-related genes during fetal and adult mouse development | Q48841883 | ||
| Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome. | Q50493197 | ||
| Nkx5-1 controls semicircular canal formation in the mouse inner ear. | Q50507452 | ||
| Progressive restriction of otic fate: the role of FGF and Wnt in resolving inner ear potential. | Q50776563 | ||
| Hyaluronate production by the inner ear during otic capsule and perilymphatic space formation. | Q50901236 | ||
| Foxg1 is required for proper separation and formation of sensory cristae during inner ear development. | Q51924168 | ||
| Expression of mouse Foxi class genes in early craniofacial development. | Q52087464 | ||
| Inner ear and lateral line expression of a zebrafish Nkx5-1 gene and its downregulation in the ears of FGF8 mutant, ace. | Q52164544 | ||
| The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos. | Q52211686 | ||
| Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function. | Q55119211 | ||
| The development of semicircular canals in the inner ear: role of FGFs in sensory cristae | Q61852088 | ||
| A new mouse member of the Wnt gene family, mWnt-8, is expressed during early embryogenesis and is ectopically induced by retinoic acid | Q62817996 | ||
| Two highly related homeodomain proteins, Nkx5-1 and Nkx5-2, display different DNA binding specificities | Q73137125 | ||
| Widespread recombinase expression using FLPeR (flipper) mice | Q73266365 | ||
| Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otic placode induction | Q82444181 | ||
| Wnt signals mediate a fate decision between otic placode and epidermis | Q82444199 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 595-604 | |
| P577 | publication date | 2010-02-18 | |
| P1433 | published in | Developmental Biology | Q3025402 |
| P1476 | title | FGF signaling regulates otic placode induction and refinement by controlling both ectodermal target genes and hindbrain Wnt8a | |
| P478 | volume | 340 |
| Q48312602 | 3D mouse embryonic stem cell culture for generating inner ear organoids. |
| Q55711979 | A Review of FOXI3 Regulation of Development and Possible Roles in Cancer Progression and Metastasis. |
| Q41094719 | A gene network regulated by FGF signalling during ear development |
| Q35224066 | A more efficient method to generate null mutants using Hprt-Cre with floxed alleles |
| Q33588427 | A systems-level approach reveals new gene regulatory modules in the developing ear |
| Q37140415 | An Fgf-Shh signaling hierarchy regulates early specification of the zebrafish skull. |
| Q34565185 | Analysis of FGF-dependent and FGF-independent pathways in otic placode induction |
| Q28728513 | Characterization of a novel fibroblast growth factor 10 (Fgf10) knock-in mouse line to target mesenchymal progenitors during embryonic development |
| Q30411351 | Cochlear progenitor number is controlled through mesenchymal FGF receptor signaling |
| Q41955252 | Compensatory regulation of the size of the inner ear in response to excess induction of otic progenitors by fibroblast growth factor signaling |
| Q39094885 | Concise Review: Regeneration in Mammalian Cochlea Hair Cells: Help from Supporting Cells Transdifferentiation |
| Q30666987 | Cooperative and independent functions of FGF and Wnt signaling during early inner ear development |
| Q38070804 | Development of cranial placodes: insights from studies in chick |
| Q38365010 | Early steps in inner ear development: induction and morphogenesis of the otic placode |
| Q47744057 | Effects of genetic variants of the bovine WNT8A gene on nine important growth traits in beef cattle |
| Q46613599 | Embryological manipulations in the developing Xenopus inner ear reveal an intrinsic role for Wnt signaling in dorsal-ventral patterning |
| Q90191234 | Enhancer activation by FGF signalling during otic induction |
| Q45586427 | FGF signaling: diverse roles during cochlear development. |
| Q64072320 | FGF10-FGFR2B Signaling Generates Basal Cells and Drives Alveolar Epithelial Regeneration by Bronchial Epithelial Stem Cells after Lung Injury |
| Q27302948 | Fgf10 is required for specification of non-sensory regions of the cochlear epithelium. |
| Q47094771 | Fgf3 and Fgf16 expression patterns define spatial and temporal domains in the developing chick inner ear. |
| Q41168846 | Foxi3 is necessary for the induction of the chick otic placode in response to FGF signaling |
| Q24318296 | Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9 |
| Q38592408 | Gene expression profiling of the inner ear. |
| Q54339414 | Generating Inner Ear Organoids from Mouse Embryonic Stem Cells. |
| Q30439081 | Genetic rescue of Muenke syndrome model hearing loss reveals prolonged FGF-dependent plasticity in cochlear supporting cell fates |
| Q90295004 | Hindbrain induction and patterning during early vertebrate development |
| Q50043702 | Lsd1 interacts with cMyb to demethylate repressive histone marks and maintain inner ear progenitor identity. |
| Q30391988 | MAP3K1 function is essential for cytoarchitecture of the mouse organ of Corti and survival of auditory hair cells |
| Q30415959 | Making sense of Wnt signaling-linking hair cell regeneration to development |
| Q43126190 | Mesodermal Fgf10b cooperates with other fibroblast growth factors during induction of otic and epibranchial placodes in zebrafish |
| Q27323045 | Modulation of Wnt Signaling Enhances Inner Ear Organoid Development in 3D Culture |
| Q26865155 | Molecular mechanisms of inner ear development |
| Q92977349 | Notch signalling regulates epibranchial placode patterning and segregation |
| Q39007241 | Otic placode cell specification and proliferation are regulated by Notch signaling in avian development |
| Q35842582 | Overactivation of Notch1 signaling induces ectopic hair cells in the mouse inner ear in an age-dependent manner |
| Q35484934 | Parabronchial smooth muscle constitutes an airway epithelial stem cell niche in the mouse lung after injury |
| Q28511597 | Pax2 contributes to inner ear patterning and optic nerve trajectory |
| Q34559489 | Pax6 interactions with chromatin and identification of its novel direct target genes in lens and forebrain |
| Q35127060 | Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development |
| Q30467210 | Regeneration of Hair Cells: Making Sense of All the Noise |
| Q35755137 | Role of FGF/FGFR signaling in skeletal development and homeostasis: learning from mouse models |
| Q33997378 | Serial analysis of gene expression in the chicken otocyst |
| Q28741138 | Shaping sound in space: the regulation of inner ear patterning |
| Q36009264 | Signaling in cell differentiation and morphogenesis |
| Q90027737 | Spatial and temporal inhibition of FGFR2b ligands reveals continuous requirements and novel targets in mouse inner ear morphogenesis |
| Q30466690 | Sprouty genes are essential for the normal development of epibranchial ganglia in the mouse embryo |
| Q34785950 | Sprouty1 and Sprouty2 limit both the size of the otic placode and hindbrain Wnt8a by antagonizing FGF signaling |
| Q34467171 | The Fibroblast Growth Factor signaling pathway |
| Q30691838 | The mouse Foxi3 transcription factor is necessary for the development of posterior placodes. |
| Q30401498 | The role of foxi family transcription factors in the development of the ear and jaw. |
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