Steel KP - Search Results

1

Sox2 is required for sensory organ development in the mammalian inner ear.

Kiernan AE, Pelling AL, Leung KK, Tang AS, Bell DM, Tease C, Lovell-Badge R, Steel KP, Cheah KS. Kiernan AE, et al. Among authors: steel kp. Nature. 2005 Apr 21;434(7036):1031-5. doi: 10.1038/nature03487. Nature. 2005. PMID: 15846349

2

Ectopic expression of activated notch or SOX2 reveals similar and unique roles in the development of the sensory cell progenitors in the mammalian inner ear.

Pan W, Jin Y, Chen J, Rottier RJ, Steel KP, Kiernan AE. Pan W, et al. Among authors: steel kp. J Neurosci. 2013 Oct 9;33(41):16146-57. doi: 10.1523/JNEUROSCI.3150-12.2013. J Neurosci. 2013. PMID: 24107947 Free PMC article.

3

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.

Kiernan AE, Erven A, Voegeling S, Peters J, Nolan P, Hunter J, Bacon Y, Steel KP, Brown SD, Guénet JL. Kiernan AE, et al. Among authors: steel kp. Mamm Genome. 2002 Mar;13(3):142-8. doi: 10.1007/BF02684018. Mamm Genome. 2002. PMID: 11919684

4

Mouse homologues for human deafness.

Kiernan AE, Steel KP. Kiernan AE, et al. Among authors: steel kp. Adv Otorhinolaryngol. 2000;56:233-43. doi: 10.1159/000059107. Adv Otorhinolaryngol. 2000. PMID: 10868240 Review. No abstract available.

5

The Notch ligand Jagged1 is required for inner ear sensory development.

Kiernan AE, Ahituv N, Fuchs H, Balling R, Avraham KB, Steel KP, Hrabé de Angelis M. Kiernan AE, et al. Among authors: steel kp. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3873-8. doi: 10.1073/pnas.071496998. Epub 2001 Mar 20. Proc Natl Acad Sci U S A. 2001. PMID: 11259677 Free PMC article.

6

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

Kiernan AE, Zalzman M, Fuchs H, Hrabe de Angelis M, Balling R, Steel KP, Avraham KB. Kiernan AE, et al. Among authors: steel kp. J Neurocytol. 1999 Oct-Nov;28(10-11):969-85. doi: 10.1023/a:1007090626294. J Neurocytol. 1999. PMID: 10900098

7

Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects.

Steffes G, Lorente-Cánovas B, Pearson S, Brooker RH, Spiden S, Kiernan AE, Guénet JL, Steel KP. Steffes G, et al. Among authors: steel kp. PLoS One. 2012;7(11):e51065. doi: 10.1371/journal.pone.0051065. Epub 2012 Nov 30. PLoS One. 2012. PMID: 23226461 Free PMC article.

8

The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.

Alavizadeh A, Kiernan AE, Nolan P, Lo C, Steel KP, Bucan M. Alavizadeh A, et al. Among authors: steel kp. Dev Biol. 2001 Jun 1;234(1):244-60. doi: 10.1006/dbio.2001.0241. Dev Biol. 2001. PMID: 11356033 Free article.

9

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

Tsai H, Hardisty RE, Rhodes C, Kiernan AE, Roby P, Tymowska-Lalanne Z, Mburu P, Rastan S, Hunter AJ, Brown SD, Steel KP. Tsai H, et al. Among authors: steel kp. Hum Mol Genet. 2001 Mar 1;10(5):507-12. doi: 10.1093/hmg/10.5.507. Hum Mol Genet. 2001. PMID: 11181574

10

Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice.

Hulander M, Kiernan AE, Blomqvist SR, Carlsson P, Samuelsson EJ, Johansson BR, Steel KP, Enerbäck S. Hulander M, et al. Among authors: steel kp. Development. 2003 May;130(9):2013-25. doi: 10.1242/dev.00376. Development. 2003. PMID: 12642503

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

231 results

Search Page

Filters