Kiernan AE - Search Results

1

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. 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.

2

Mouse homologues for human deafness.

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

3

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. J Neurocytol. 1999 Oct-Nov;28(10-11):969-85. doi: 10.1023/a:1007090626294. J Neurocytol. 1999. PMID: 10900098

4

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson JA, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel KP, Voegeling S, Guenet JL, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher EM, Martin J, Rastan S, Brown SD, Hunter J. Nolan PM, et al. Nat Genet. 2000 Aug;25(4):440-3. doi: 10.1038/78140. Nat Genet. 2000. PMID: 10932191

5

Molecular genetics of pattern formation in the inner ear: do compartment boundaries play a role?

Brigande JV, Kiernan AE, Gao X, Iten LE, Fekete DM. Brigande JV, et al. Among authors: kiernan ae. Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):11700-6. doi: 10.1073/pnas.97.22.11700. Proc Natl Acad Sci U S A. 2000. PMID: 11050198 Free PMC article.

6

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: kiernan ae. Hum Mol Genet. 2001 Mar 1;10(5):507-12. doi: 10.1093/hmg/10.5.507. Hum Mol Genet. 2001. PMID: 11181574

7

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: kiernan ae. Dev Biol. 2001 Jun 1;234(1):244-60. doi: 10.1006/dbio.2001.0241. Dev Biol. 2001. PMID: 11356033 Free article.

8

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. Mamm Genome. 2002 Mar;13(3):142-8. doi: 10.1007/BF02684018. Mamm Genome. 2002. PMID: 11919684

9

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: kiernan ae. Development. 2003 May;130(9):2013-25. doi: 10.1242/dev.00376. Development. 2003. PMID: 12642503

10

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. Nature. 2005 Apr 21;434(7036):1031-5. doi: 10.1038/nature03487. Nature. 2005. PMID: 15846349

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