Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear. - Wikidata - wikimedia - TriplyDB

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

http://www.wikidata.org/entity/Q30490970

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Segregating neural and mechanosensory fates in the developing ear: patterning, signaling, and transcriptional control.How to bury the dead: elimination of apoptotic hair cells from the hearing organ of the mouse Hearing loss and hair cell death in mice given the cholesterol-chelating agent hydroxypropyl-β-cyclodextrin Functional hair cell mechanotransducer channels are required for aminoglycoside ototoxicity Co-administration of cisplatin and furosemide causes rapid and massive loss of cochlear hair cells in mice.Application of Mouse Models to Research in Hearing and Balance Notch inhibition induces mitotically generated hair cells in mammalian cochleae via activating the Wnt pathway Co-regulation of the Notch and Wnt signaling pathways promotes supporting cell proliferation and hair cell regeneration in mouse utricles.Characterization of the Transcriptomes of Lgr5+ Hair Cell Progenitors and Lgr5- Supporting Cells in the Mouse Cochlea.Supporting cells remove and replace sensory receptor hair cells in a balance organ of adult mice.Characterization of Lgr5+ progenitor cell transcriptomes in the apical and basal turns of the mouse cochlea.Characterization of a unique cell population marked by transgene expression in the adult cochlea of nestin-CreER(T2)/tdTomato-reporter mice.c-Jun N-Terminal Phosphorylation: Biomarker for Cellular Stress Rather than Cell Death in the Injured Cochlea.Manipulating cell fate in the cochlea: a feasible therapy for hearing loss.Genome-wide demethylation by 5-aza-2'-deoxycytidine alters the cell fate of stem/progenitor cells.In Vivo Cochlear Hair Cell Generation and Survival by Coactivation of β-Catenin and Atoh1 Selective deletion of cochlear hair cells causes rapid age-dependent changes in spiral ganglion and cochlear nucleus neurons Lgr5+ cells regenerate hair cells via proliferation and direct transdifferentiation in damaged neonatal mouse utricle Systemic lipopolysaccharide induces cochlear inflammation and exacerbates the synergistic ototoxicity of kanamycin and furosemide.Comparative analysis of combination kanamycin-furosemide versus kanamycin alone in the mouse cochlea.Spontaneous hair cell regeneration in the neonatal mouse cochlea in vivo Inner ear supporting cells protect hair cells by secreting HSP70.Regulated reprogramming in the regeneration of sensory receptor cells.Changes in the regulation of the Notch signaling pathway are temporally correlated with regenerative failure in the mouse cochlea A review of gene delivery and stem cell based therapies for regenerating inner ear hair cells Development of an ototoxicity model in the adult CBA/CaJ mouse and determination of a golden window of corticosteroid intervention for otoprotection Inner ear supporting cells: rethinking the silent majority.Atoh1 induces auditory hair cell recovery in mice after ototoxic injury.Changes in the adult vertebrate auditory sensory epithelium after trauma.Notch inhibition induces cochlear hair cell regeneration and recovery of hearing after acoustic trauma.Tympanic border cells are Wnt-responsive and can act as progenitors for postnatal mouse cochlear cells.Notch signaling limits supporting cell plasticity in the hair cell-damaged early postnatal murine cochlea Generation of human inner ear prosensory-like cells via epithelial-to-mesenchymal transition.MYC gene delivery to adult mouse utricles stimulates proliferation of postmitotic supporting cells in vitro.TAK1 expression in the cochlea: a specific marker for adult supporting cells.Inhibition of Notch activity promotes nonmitotic regeneration of hair cells in the adult mouse utricles Sox2 up-regulation and glial cell proliferation following degeneration of spiral ganglion neurons in the adult mouse inner ear.Defining the cellular environment in the organ of Corti following extensive hair cell loss: a basis for future sensory cell replacement in the Cochlea.Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse ear.Notch signaling and Atoh1 expression during hair cell regeneration in the mouse utricle.

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Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

http://www.wikidata.org/entity/Q30490970

description

2007 nî lūn-bûn

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2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

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2007年学术文章

@wuu

2007年学术文章

@zh-cn

2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

name

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

@ast

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

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type

label

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

@ast

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

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prefLabel

Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

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Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

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Sox2 and JAGGED1 expression in normal and drug-damaged adult mouse inner ear.

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Andrew Forge

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Clifford R Hume

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Elizabeth C Oesterle

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Ruth R Taylor

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Sean Campbell

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P2860

Mammalian cochlear supporting cells can divide and trans-differentiate into hair cells

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

Gene disruption of p27(Kip1) allows cell proliferation in the postnatal and adult organ of corti.

The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear

Expression of Delta1 and Serrate1 (Jagged1) in the mouse inner ear

Notch/Notch ligands and Math1 expression patterns in the organ of Corti of wild-type and Hes1 and Hes5 mutant mice

Inhibitors of differentiation and DNA binding (Ids) regulate Math1 and hair cell formation during the development of the organ of Corti

Sox2 deficiency causes neurodegeneration and impaired neurogenesis in the adult mouse brain

Progressive hearing loss in mice lacking the cyclin-dependent kinase inhibitor Ink4d

Notch ligands with contrasting functions: Jagged1 and Delta1 in the mouse inner ear

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