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Results: 1 to 20 of 21

Cited In for PubMed (Select 11181574)

1.

Numb is not a critical regulator of Notch-mediated cell fate decisions in the developing chick inner ear.

Eddison M, Weber SJ, Ariza-McNaughton L, Lewis J, Daudet N.

Front Cell Neurosci. 2015 Mar 12;9:74. doi: 10.3389/fncel.2015.00074. eCollection 2015.

2.

A murine model of neurofibromatosis type 2 that accurately phenocopies human schwannoma formation.

Gehlhausen JR, Park SJ, Hickox AE, Shew M, Staser K, Rhodes SD, Menon K, Lajiness JD, Mwanthi M, Yang X, Yuan J, Territo P, Hutchins G, Nalepa G, Yang FC, Conway SJ, Heinz MG, Stemmer-Rachamimov A, Yates CW, Wade Clapp D.

Hum Mol Genet. 2015 Jan 1;24(1):1-8. doi: 10.1093/hmg/ddu414. Epub 2014 Aug 11.

PMID:
25113746
3.

Segregating neural and mechanosensory fates in the developing ear: patterning, signaling, and transcriptional control.

Raft S, Groves AK.

Cell Tissue Res. 2015 Jan;359(1):315-32. doi: 10.1007/s00441-014-1917-6. Epub 2014 Jun 6.

PMID:
24902666
4.

The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organs.

Moayedi Y, Basch ML, Pacheco NL, Gao SS, Wang R, Harrison W, Xiao N, Oghalai JS, Overbeek PA, Mardon G, Groves AK.

PLoS Genet. 2014 Jan;10(1):e1004055. doi: 10.1371/journal.pgen.1004055. Epub 2014 Jan 2.

5.

Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice.

Hurd EA, Micucci JA, Reamer EN, Martin DM.

Mech Dev. 2012 Sep-Dec;129(9-12):308-23. doi: 10.1016/j.mod.2012.06.002. Epub 2012 Jun 15.

6.

Overactivation of Notch1 signaling induces ectopic hair cells in the mouse inner ear in an age-dependent manner.

Liu Z, Owen T, Fang J, Zuo J.

PLoS One. 2012;7(3):e34123. doi: 10.1371/journal.pone.0034123. Epub 2012 Mar 20.

7.

In vivo Notch reactivation in differentiating cochlear hair cells induces Sox2 and Prox1 expression but does not disrupt hair cell maturation.

Liu Z, Owen T, Fang J, Srinivasan RS, Zuo J.

Dev Dyn. 2012 Apr;241(4):684-96. doi: 10.1002/dvdy.23754. Epub 2012 Feb 21.

8.

Canonical and non-canonical Notch ligands.

D'Souza B, Meloty-Kapella L, Weinmaster G.

Curr Top Dev Biol. 2010;92:73-129. doi: 10.1016/S0070-2153(10)92003-6. Review.

9.

Specification of cell fate in the mammalian cochlea.

Driver EC, Kelley MW.

Birth Defects Res C Embryo Today. 2009 Sep;87(3):212-21. doi: 10.1002/bdrc.20154. Review.

10.

Building the world's best hearing aid; regulation of cell fate in the cochlea.

Puligilla C, Kelley MW.

Curr Opin Genet Dev. 2009 Aug;19(4):368-73. doi: 10.1016/j.gde.2009.06.004. Epub 2009 Jul 13. Review.

11.

The canonical Notch signaling pathway: unfolding the activation mechanism.

Kopan R, Ilagan MX.

Cell. 2009 Apr 17;137(2):216-33. doi: 10.1016/j.cell.2009.03.045. Review.

12.

Hes5 expression in the postnatal and adult mouse inner ear and the drug-damaged cochlea.

Hartman BH, Basak O, Nelson BR, Taylor V, Bermingham-McDonogh O, Reh TA.

J Assoc Res Otolaryngol. 2009 Sep;10(3):321-40. doi: 10.1007/s10162-009-0162-2. Epub 2009 Apr 17.

13.

Hesr1 and Hesr2 may act as early effectors of Notch signaling in the developing cochlea.

Hayashi T, Kokubo H, Hartman BH, Ray CA, Reh TA, Bermingham-McDonogh O.

Dev Biol. 2008 Apr 1;316(1):87-99. doi: 10.1016/j.ydbio.2008.01.006. Epub 2008 Jan 18.

14.

Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous mice.

Kiernan AE, Li R, Hawes NL, Churchill GA, Gridley T.

Genetics. 2007 Sep;177(1):307-11.

15.

Basic helix-loop-helix gene Hes6 delineates the sensory hair cell lineage in the inner ear.

Qian D, Radde-Gallwitz K, Kelly M, Tyrberg B, Kim J, Gao WQ, Chen P.

Dev Dyn. 2006 Jun;235(6):1689-700.

16.

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

Kiernan AE, Xu J, Gridley T.

PLoS Genet. 2006 Jan;2(1):e4. Epub 2006 Jan 13.

17.

Molecular and comparative genetics of mental retardation.

Inlow JK, Restifo LL.

Genetics. 2004 Feb;166(2):835-81.

18.
19.

Focusing on the genetics of hearing: you ain't heard nothin' yet.

Parkinson N, Brown SD.

Genome Biol. 2002;3(6):COMMENT2006. Epub 2002 May 28. Review.

20.

Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.

Le Caignec C, Lefevre M, Schott JJ, Chaventre A, Gayet M, Calais C, Moisan JP.

Am J Hum Genet. 2002 Jul;71(1):180-6. Epub 2002 May 17.

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