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A gradient of Bmp7 specifies the tonotopic axis in the developing inner ear

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-010x(19981215)282:6<628::aid-jez2>3.0.co;2-nopenalex-snapshot

The proximo-distal sequence of origin of the parts of the chick wing and the role of the ectoderm

inferredcites →https://doi.org/10.1002/aja.1001950404openalex-snapshot

A series of normal stages in the development of the chick embryo

inferredcites →https://doi.org/10.1002/cne.902880402openalex-snapshot

Development of location‐specific hair cell stereocilia in denervated embryonic ears

inferredcites →https://doi.org/10.1002/dneu.22015openalex-snapshot

Dorsal–ventral patterning of the neural tube: A tale of three signals

inferredcites →https://doi.org/10.1002/dvdy.10182openalex-snapshot

Rethinking axial patterning in amphibians

inferredcites →https://doi.org/10.1002/dvdy.21750openalex-snapshot

MAP3Ks as central regulators of cell fate during development

inferredcites →https://doi.org/10.1002/jez.1401080304openalex-snapshot

The proximo‐distal sequence of origin of the parts of the chick wing and the role of the ectoderm

inferredcites →https://doi.org/10.1002/jmor.1050880104openalex-snapshot

A series of normal stages in the development of the chick embryo

inferredcites →https://doi.org/10.1006/dbio.1998.8850openalex-snapshot

Local Inhibitory Action of BMPs and Their Relationships with Activators in Feather Formation: Implications for Periodic Patterning

inferredcites →https://doi.org/10.1007/s00114-005-0050-5openalex-snapshot

Audiogram, body mass, and basilar papilla length: correlations in birds and predictions for extinct archosaurs

inferredcites →https://doi.org/10.1007/s10162-011-0265-4openalex-snapshot

TAK1 Expression in the Cochlea: A Specific Marker for Adult Supporting Cells

inferredcites →https://doi.org/10.1007/s101620010071openalex-snapshot

Topological and Developmental Gradients of Calbindin Expression in the Chick's Inner Ear

inferredcites →https://doi.org/10.1016/0012-1606(86)90047-3openalex-snapshot

Actin filaments, stereocilia, and hair cells of the bird cochlea

inferredcites →https://doi.org/10.1016/0012-1606(90)90251-dopenalex-snapshot

Epithelial autonomy in the development of the inner ear of a bird embryo

inferredcites →https://doi.org/10.1016/0092-8674(94)90008-6openalex-snapshot

Ectopic expression of Sonic hedgehog alters dorsal-ventral patterning of somites

inferredcites →https://doi.org/10.1016/0378-5955(87)90151-1openalex-snapshot

Development of hair cell stereocilia in the avian cochlea

inferredcites →https://doi.org/10.1016/j.ceb.2011.11.005openalex-snapshot

Gradients of signalling in the developing limb

inferredcites →https://doi.org/10.1016/j.ceb.2011.12.010openalex-snapshot

Integration of morphogen signalling within the growth regulatory network

inferredcites →https://doi.org/10.1016/j.cell.2010.06.010openalex-snapshot

TGF-β Signaling Specifies Axons during Brain Development

inferredcites →https://doi.org/10.1016/j.febslet.2012.02.035openalex-snapshot

Spatial regulation of BMP activity

inferredcites →https://doi.org/10.1016/j.gde.2011.09.001openalex-snapshot

Systems control of BMP morphogen flow in vertebrate embryos

inferredcites →https://doi.org/10.1016/j.heares.2011.01.011openalex-snapshot

Development of tonotopy in the auditory periphery

inferredcites →https://doi.org/10.1016/j.heares.2012.04.008openalex-snapshot

Atoh1 expression and function during auditory hair cell regeneration in post-hatch chickens

inferredcites →https://doi.org/10.1016/j.heares.2012.04.018openalex-snapshot

Fgf signaling regulates development and transdifferentiation of hair cells and supporting cells in the basilar papilla

inferredcites →https://doi.org/10.1016/j.jmb.2013.11.022openalex-snapshot

Limb Patterning: From Signaling Gradients to Molecular Oscillations

inferredcites →https://doi.org/10.1016/j.matbio.2007.05.004openalex-snapshot

The bone morphogenetic protein 1/Tolloid-like metalloproteinases

inferredcites →https://doi.org/10.1016/s0006-3495(02)75374-5openalex-snapshot

Modeling Hair Cell Tuning by Expression Gradients of Potassium Channel β Subunits

inferredcites →https://doi.org/10.1016/s0022-5193(69)80016-0openalex-snapshot

Positional information and the spatial pattern of cellular differentiation

inferredcites →https://doi.org/10.1038/376333a0openalex-snapshot

Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus

inferredcites →https://doi.org/10.1038/377757a0openalex-snapshot

Correction: Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus

inferredcites →https://doi.org/10.1038/nature07059openalex-snapshot

Scaling of the BMP activation gradient in Xenopus embryos

inferredcites →https://doi.org/10.1038/nn.2332openalex-snapshot

Tonotopic reorganization of developing auditory brainstem circuits

inferredcites →https://doi.org/10.1073/pnas.1100179108openalex-snapshot

Negative feedback in the bone morphogenetic protein 4 (BMP4) synexpression group governs its dynamic signaling range and canalizes development

inferredcites →https://doi.org/10.1083/jcb.96.3.807openalex-snapshot

Actin filaments, stereocilia, and hair cells of the bird cochlea. I. Length, number, width, and distribution of stereocilia of each hair cell are related to the position of the hair cell on the cochlea.

inferredcites →https://doi.org/10.1085/jgp.105.1.49openalex-snapshot

The calcium-activated potassium channels of turtle hair cells.

inferredcites →https://doi.org/10.1093/bioinformatics/btp120openalex-snapshot

TopHat: discovering splice junctions with RNA-Seq

inferredcites →https://doi.org/10.1098/rspb.1990.0123openalex-snapshot

Preferential expression of transient potassium current ( I A ) by 'short' hair cells of the chick’s cochlea

inferredcites →https://doi.org/10.1101/cshperspect.a001339openalex-snapshot

Vertebrate Limb Development: Moving from Classical Morphogen Gradients to an Integrated 4-Dimensional Patterning System

inferredcites →https://doi.org/10.1101/cshperspect.a001701openalex-snapshot

Systems Biology of the Self-regulating Morphogenetic Gradient of the Xenopus Gastrula

inferredcites →https://doi.org/10.1111/j.1365-2818.1987.tb02821.xopenalex-snapshot

Preparation of the mammalian organ of Corti for scanning electron microscopy*

inferredcites →https://doi.org/10.1113/jphysiol.1990.sp018271openalex-snapshot

Potassium currents in hair cells isolated from the cochlea of the chick.

inferredcites →https://doi.org/10.1113/jphysiol.2002.029785openalex-snapshot

Variation in Large‐Conductance, Calcium‐Activated Potassium Channels from Hair Cells Along the Chicken Basilar Papilla

inferredcites →https://doi.org/10.1126/science.283.5399.215openalex-snapshot

A Molecular Mechanism for Electrical Tuning of Cochlear Hair Cells

inferredcites →https://doi.org/10.1146/annurev.cb.08.110192.001353openalex-snapshot

Actin Filaments, Stereocilia, and Hair Cells: How Cells Count and Measure

inferredcites →https://doi.org/10.1146/annurev.physiol.61.1.809openalex-snapshot

MECHANISMS OF HAIR CELL TUNING

inferredcites →https://doi.org/10.1152/jn.01028.2012openalex-snapshot

Electrical tuning and transduction in short hair cells of the chicken auditory papilla

inferredcites →https://doi.org/10.1182/blood-2012-03-416198openalex-snapshot

TAK1 kinase signaling regulates embryonic angiogenesis by modulating endothelial cell survival and migration

inferredcites →https://doi.org/10.1242/dev.01589openalex-snapshot

Two contrasting roles for Notch activity in chick inner ear development:specification of prosensory patches and lateral inhibition of hair-cell differentiation

inferredcites →https://doi.org/10.1242/dev.02333openalex-snapshot

The TGFβ activated kinase TAK1 regulates vascular development in vivo

inferredcites →https://doi.org/10.1242/dev.036335openalex-snapshot

BMP7 promotes proliferation of nephron progenitor cells via a JNK-dependent mechanism

inferredcites →https://doi.org/10.1242/dev.074476openalex-snapshot

Delta-like 1 and lateral inhibition during hair cell formation in the chicken inner ear: evidence against cis-inhibition

inferredcites →https://doi.org/10.1371/journal.pbio.0020092openalex-snapshot

Neural Induction in Xenopus: Requirement for Ectodermal and Endomesodermal Signals via Chordin, Noggin, β-Catenin, and Cerberus

inferredcites →https://doi.org/10.1371/journal.pbio.1000248openalex-snapshot

Patterning of the Dorsal-Ventral Axis in Echinoderms: Insights into the Evolution of the BMP-Chordin Signaling Network

inferredcites →https://doi.org/10.1371/journal.pone.0048704openalex-snapshot

MYC Gene Delivery to Adult Mouse Utricles Stimulates Proliferation of Postmitotic Supporting Cells In Vitro

inferredcites →https://doi.org/10.14712/fb2004050030107openalex-snapshot

The RCAS vector system.

inferredcites →https://doi.org/10.1523/jneurosci.08-07-02460.1988openalex-snapshot

Electrical tuning in hair cells isolated from the chick cochlea

inferredcites →https://doi.org/10.1523/jneurosci.18-09-03327.1998openalex-snapshot

Development of the Mouse Inner Ear and Origin of Its Sensory Organs

inferredcites →https://doi.org/10.1523/jneurosci.3042-10.2010openalex-snapshot

Supporting Cells Eliminate Dying Sensory Hair Cells to Maintain Epithelial Integrity in the Avian Inner Ear

inferredcites →https://doi.org/10.1523/jneurosci.5513-08.2009openalex-snapshot

Effects of Restricted Basilar Papillar Lesions and Hair Cell Regeneration on Auditory Forebrain Frequency Organization in Adult European Starlings

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/subtbiol.52.155412zenodo-depositor-declared

Contributions of molecular and cranial specializations for sensory adaptation in the subterranean blind mole rats (Nannospalax xanthodon)

inferred← citeshttps://doi.org/10.1002/bies.202300058openalex-snapshot

Cochlear tonotopy from proteins to perception

inferred← citeshttps://doi.org/10.1002/cne.70103openalex-snapshot

Timing of Delamination of Inner Ear Neurons Specifies Their Topography and Target Innervation

inferred← citeshttps://doi.org/10.1002/dvdy.111openalex-snapshot

Fate‐mapping analysis using Rorb‐IRES‐Cre reveals apical‐to‐basal gradient of Rorb expression in mouse cochlea

inferred← citeshttps://doi.org/10.1002/wdev.202openalex-snapshot

Developmental regulation of planar cell polarity and hair‐bundle morphogenesis in auditory hair cells: lessons from human and mouse genetics

inferred← citeshttps://doi.org/10.1007/978-3-319-52073-5_3openalex-snapshot

New Directions in Cochlear Development

inferred← citeshttps://doi.org/10.1007/s00018-016-2257-3openalex-snapshot

The role of post-translational modifications in hearing and deafness

inferred← citeshttps://doi.org/10.1007/s00441-019-03115-6openalex-snapshot

Early appearance of key transcription factors influence the spatiotemporal development of the human inner ear

inferred← citeshttps://doi.org/10.1007/s11427-024-2672-1openalex-snapshot

The single-cell transcriptomic landscape of the topological differences in mammalian auditory receptors

inferred← citeshttps://doi.org/10.1016/j.bbadis.2024.167619openalex-snapshot

Canonical MAPK signaling in auditory neuropathy

inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108900openalex-snapshot

Cell-type identity of the avian cochlea

inferred← citeshttps://doi.org/10.1016/j.cophys.2020.06.010openalex-snapshot

Tonotopy of cochlear hair cell biophysics (excl. mechanotransduction)

inferred← citeshttps://doi.org/10.1016/j.cophys.2020.09.010openalex-snapshot

Cochlear development, cellular patterning and tonotopy

inferred← citeshttps://doi.org/10.1016/j.devcel.2024.03.028openalex-snapshot

3D reconstruction of the mouse cochlea from scRNA-seq data suggests morphogen-based principles in apex-to-base specification

inferred← citeshttps://doi.org/10.1016/j.gde.2015.02.006openalex-snapshot

Development of the inner ear

inferred← citeshttps://doi.org/10.1016/j.gep.2021.119214openalex-snapshot

Spatial and temporal expression of PORCN is highly dynamic in the developing mouse cochlea

inferred← citeshttps://doi.org/10.1016/j.heares.2025.109256openalex-snapshot

Hearing restoration through hair cell regeneration: A review of recent advancements and current limitations

inferred← citeshttps://doi.org/10.1016/j.isci.2024.109069openalex-snapshot

Mapping the developmental potential of mouse inner ear organoids at single-cell resolution

inferred← citeshttps://doi.org/10.1016/j.tins.2019.12.003openalex-snapshot

Diverse Mechanisms of Sound Frequency Discrimination in the Vertebrate Cochlea

inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.09.004openalex-snapshot

HMGA2 links opposing morphogen signaling to long-term low-frequency auditory function in the cochlea

inferred← citeshttps://doi.org/10.1038/ncomms4840openalex-snapshot

Retinoic acid signalling regulates the development of tonotopically patterned hair cells in the chicken cochlea

inferred← citeshttps://doi.org/10.1038/ncomms5591openalex-snapshot

Correction: Corrigendum: A gradient of Bmp7 specifies the tonotopic axis in the developing inner ear

inferred← citeshttps://doi.org/10.1038/s41467-025-58557-0openalex-snapshot

Junctional force patterning drives both positional order and planar polarity in the auditory epithelia

inferred← citeshttps://doi.org/10.1039/c4cs00185kopenalex-snapshot

Jack of all trades: versatile catechol crosslinking mechanisms

inferred← citeshttps://doi.org/10.1073/pnas.1417856112openalex-snapshot

Conserved role of Sonic Hedgehog in tonotopic organization of the avian basilar papilla and mammalian cochlea

inferred← citeshttps://doi.org/10.1073/pnas.2213099120openalex-snapshot

Follistatin regulates the specification of the apical cochlea responsible for low-frequency hearing in mammals

inferred← citeshttps://doi.org/10.1093/molbev/msw001openalex-snapshot

“Reverse Genomics” Predicts Function of Human Conserved Noncoding Elements

inferred← citeshttps://doi.org/10.1097/aud.0000000000001782openalex-snapshot

Echoes of Renewal: Rebuilding the Mammalian Inner Ear

inferred← citeshttps://doi.org/10.1101/2024.03.04.583298openalex-snapshot

Mitochondrial dynamics regulate cell size in the developing cochlea

inferred← citeshttps://doi.org/10.1101/262832openalex-snapshot

DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory organ of Corti

inferred← citeshttps://doi.org/10.1111/joa.12314openalex-snapshot

Where hearing starts: the development of the mammalian cochlea

inferred← citeshttps://doi.org/10.1111/joa.12376openalex-snapshot

Gene expression profiling of the inner ear

inferred← citeshttps://doi.org/10.1155/2016/5836143openalex-snapshot

Identification of a Novel ENU-Induced Mutation in MouseTbx1Linked to Human DiGeorge Syndrome

inferred← citeshttps://doi.org/10.1242/dev.162263openalex-snapshot

Development of the cochlea

inferred← citeshttps://doi.org/10.1242/dev.202845openalex-snapshot

Mitochondrial dynamics regulate cell morphology in the developing cochlea

inferred← citeshttps://doi.org/10.1242/dev.204533openalex-snapshot

Targets of the transcription factor Six1 identify previously unreported candidate deafness genes

inferred← citeshttps://doi.org/10.1371/journal.pgen.1005037openalex-snapshot

Tfap2a Promotes Specification and Maturation of Neurons in the Inner Ear through Modulation of Bmp, Fgf and Notch Signaling

inferred← citeshttps://doi.org/10.1371/journal.pone.0132796openalex-snapshot

Expression and Misexpression of the miR-183 Family in the Developing Hearing Organ of the Chicken

inferred← citeshttps://doi.org/10.1371/journal.pone.0166146openalex-snapshot

Genome-Wide Detection of Selective Signatures in Chicken through High Density SNPs

inferred← citeshttps://doi.org/10.1371/journal.pone.0186667openalex-snapshot

Age-dependent gene expression in the inner ear of big brown bats (Eptesicus fuscus)

inferred← citeshttps://doi.org/10.1523/jneurosci.1554-17.2017openalex-snapshot

Wnt9a Can Influence Cell Fates and Neural Connectivity across the Radial Axis of the Developing Cochlea

inferred← citeshttps://doi.org/10.1631/jzus.b1800084openalex-snapshot

Bone morphogenetic proteins and inner ear development

inferred← citeshttps://doi.org/10.3389/fcell.2023.1143428openalex-snapshot

Alternative splicing in shaping the molecular landscape of the cochlea

inferred← citeshttps://doi.org/10.3389/fmolb.2021.726976openalex-snapshot

Position Specific Alternative Splicing and Gene Expression Profiles Along the Tonotopic Axis of Chick Cochlea

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Génération de progéniteurs otiques dérivés de cellules souches pluripotentes induites humaines (hiPSC) : application à la thérapie cellulaire dans l'oreille interne

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Gradients of glucose metabolism regulate morphogen signalling required for specifying tonotopic organisation in the chicken cochlea

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