187 related articles for article (PubMed ID: 20386946)
1. CD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear.
Hertzano R; Puligilla C; Chan SL; Timothy C; Depireux DA; Ahmed Z; Wolf J; Eisenman DJ; Friedman TB; Riazuddin S; Kelley MW; Strome SE
J Assoc Res Otolaryngol; 2010 Sep; 11(3):407-18. PubMed ID: 20386946
[TBL] [Abstract][Full Text] [Related]
2. Loss of Fgfr3 leads to excess hair cell development in the mouse organ of Corti.
Hayashi T; Cunningham D; Bermingham-McDonogh O
Dev Dyn; 2007 Feb; 236(2):525-33. PubMed ID: 17117437
[TBL] [Abstract][Full Text] [Related]
3. Sprouty2, a mouse deafness gene, regulates cell fate decisions in the auditory sensory epithelium by antagonizing FGF signaling.
Shim K; Minowada G; Coling DE; Martin GR
Dev Cell; 2005 Apr; 8(4):553-64. PubMed ID: 15809037
[TBL] [Abstract][Full Text] [Related]
4. Hearing loss in a mouse model of Muenke syndrome.
Mansour SL; Twigg SR; Freeland RM; Wall SA; Li C; Wilkie AO
Hum Mol Genet; 2009 Jan; 18(1):43-50. PubMed ID: 18818193
[TBL] [Abstract][Full Text] [Related]
5. Progressive deafness and altered cochlear innervation in knock-out mice lacking prosaposin.
Akil O; Chang J; Hiel H; Kong JH; Yi E; Glowatzki E; Lustig LR
J Neurosci; 2006 Dec; 26(50):13076-88. PubMed ID: 17167097
[TBL] [Abstract][Full Text] [Related]
6. Selective ablation of pillar and deiters' cells severely affects cochlear postnatal development and hearing in mice.
Mellado Lagarde MM; Cox BC; Fang J; Taylor R; Forge A; Zuo J
J Neurosci; 2013 Jan; 33(4):1564-76. PubMed ID: 23345230
[TBL] [Abstract][Full Text] [Related]
7. Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasia.
Pannier S; Couloigner V; Messaddeq N; Elmaleh-Bergès M; Munnich A; Romand R; Legeai-Mallet L
Biochim Biophys Acta; 2009 Feb; 1792(2):140-7. PubMed ID: 19073250
[TBL] [Abstract][Full Text] [Related]
8. Localization of septin proteins in the mouse cochlea.
Yoshida A; Yamamoto N; Kinoshita M; Hiroi N; Hiramoto T; Kang G; Trimble WS; Tanigaki K; Nakagawa T; Ito J
Hear Res; 2012 Jul; 289(1-2):40-51. PubMed ID: 22575789
[TBL] [Abstract][Full Text] [Related]
9. Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.
Colvin JS; Bohne BA; Harding GW; McEwen DG; Ornitz DM
Nat Genet; 1996 Apr; 12(4):390-7. PubMed ID: 8630492
[TBL] [Abstract][Full Text] [Related]
10. MicroRNA gene expression in the mouse inner ear.
Weston MD; Pierce ML; Rocha-Sanchez S; Beisel KW; Soukup GA
Brain Res; 2006 Sep; 1111(1):95-104. PubMed ID: 16904081
[TBL] [Abstract][Full Text] [Related]
11. Calbindin and S100 protein expression in the developing inner ear in mice.
Buckiová D; Syka J
J Comp Neurol; 2009 Apr; 513(5):469-82. PubMed ID: 19226521
[TBL] [Abstract][Full Text] [Related]
12. Glial fibrillary acidic protein expression and promoter activity in the inner ear of developing and adult mice.
Rio C; Dikkes P; Liberman MC; Corfas G
J Comp Neurol; 2002 Jan; 442(2):156-62. PubMed ID: 11754168
[TBL] [Abstract][Full Text] [Related]
13. MAP3K1 function is essential for cytoarchitecture of the mouse organ of Corti and survival of auditory hair cells.
Yousaf R; Meng Q; Hufnagel RB; Xia Y; Puligilla C; Ahmed ZM; Riazuddin S
Dis Model Mech; 2015 Dec; 8(12):1543-53. PubMed ID: 26496772
[TBL] [Abstract][Full Text] [Related]
14. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.
Robertson NG; Cremers CW; Huygen PL; Ikezono T; Krastins B; Kremer H; Kuo SF; Liberman MC; Merchant SN; Miller CE; Nadol JB; Sarracino DA; Verhagen WI; Morton CC
Hum Mol Genet; 2006 Apr; 15(7):1071-85. PubMed ID: 16481359
[TBL] [Abstract][Full Text] [Related]
15. Genetic rescue of Muenke syndrome model hearing loss reveals prolonged FGF-dependent plasticity in cochlear supporting cell fates.
Mansour SL; Li C; Urness LD
Genes Dev; 2013 Nov; 27(21):2320-31. PubMed ID: 24145799
[TBL] [Abstract][Full Text] [Related]
16. Fibroblast growth factor signaling regulates pillar cell development in the organ of corti.
Mueller KL; Jacques BE; Kelley MW
J Neurosci; 2002 Nov; 22(21):9368-77. PubMed ID: 12417662
[TBL] [Abstract][Full Text] [Related]
17. De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness.
Schrauwen I; Kari E; Mattox J; Llaci L; Smeeton J; Naymik M; Raible DW; Knowles JA; Crump JG; Huentelman MJ; Friedman RA
Hum Genet; 2018 Jul; 137(6-7):459-470. PubMed ID: 29955957
[TBL] [Abstract][Full Text] [Related]
18. Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear.
Burns JC; Kelly MC; Hoa M; Morell RJ; Kelley MW
Nat Commun; 2015 Oct; 6():8557. PubMed ID: 26469390
[TBL] [Abstract][Full Text] [Related]
19. RNA microarray analysis in prenatal mouse cochlea reveals novel IGF-I target genes: implication of MEF2 and FOXM1 transcription factors.
Sanchez-Calderon H; Rodriguez-de la Rosa L; Milo M; Pichel JG; Holley M; Varela-Nieto I
PLoS One; 2010 Jan; 5(1):e8699. PubMed ID: 20111592
[TBL] [Abstract][Full Text] [Related]
20. Fgf8 induces pillar cell fate and regulates cellular patterning in the mammalian cochlea.
Jacques BE; Montcouquiol ME; Layman EM; Lewandoski M; Kelley MW
Development; 2007 Aug; 134(16):3021-9. PubMed ID: 17634195
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
