Dahl HH - Search Results

1

Eeyore: a novel mouse model of hereditary deafness.

Miller KA, Williams LH, Dahl HH, Manji SS. Miller KA, et al. Among authors: dahl hh. PLoS One. 2013 Sep 23;8(9):e74243. doi: 10.1371/journal.pone.0074243. eCollection 2013. PLoS One. 2013. PMID: 24086324 Free PMC article.

2

A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.

Manji SS, Williams LH, Miller KA, Ooms LM, Bahlo M, Mitchell CA, Dahl HH. Manji SS, et al. Among authors: dahl hh. PLoS One. 2011 Mar 15;6(3):e17607. doi: 10.1371/journal.pone.0017607. PLoS One. 2011. PMID: 21423608 Free PMC article.

3

Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.

Manji SS, Miller KA, Williams LH, Dahl HH. Manji SS, et al. Among authors: dahl hh. Am J Pathol. 2012 Apr;180(4):1560-9. doi: 10.1016/j.ajpath.2011.12.034. Epub 2012 Feb 11. Am J Pathol. 2012. PMID: 22330676

4

Inner ear morphology is perturbed in two novel mouse models of recessive deafness.

Miller KA, Williams LH, Rose E, Kuiper M, Dahl HH, Manji SS. Miller KA, et al. Among authors: dahl hh. PLoS One. 2012;7(12):e51284. doi: 10.1371/journal.pone.0051284. Epub 2012 Dec 12. PLoS One. 2012. PMID: 23251483 Free PMC article.

5

Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.

Williams LH, Miller KA, Dahl HH, Manji SS. Williams LH, et al. Among authors: dahl hh. Hear Res. 2013 May;299:53-62. doi: 10.1016/j.heares.2013.02.006. Epub 2013 Feb 26. Hear Res. 2013. PMID: 23485424

6

Molecular characterization and expression of maternally expressed gene 3 (Meg3/Gtl2) RNA in the mouse inner ear.

Manji SS, Sørensen BS, Klockars T, Lam T, Hutchison W, Dahl HH. Manji SS, et al. Among authors: dahl hh. J Neurosci Res. 2006 Feb 1;83(2):181-90. doi: 10.1002/jnr.20721. J Neurosci Res. 2006. PMID: 16342203

7

Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) gene.

Hutchison WM, Thyagarajan D, Poulton J, Marchington DR, Kirby DM, Manji SS, Dahl HH. Hutchison WM, et al. Among authors: dahl hh. Arch Neurol. 2005 Dec;62(12):1920-3. doi: 10.1001/archneur.62.12.1920. Arch Neurol. 2005. PMID: 16344351

8

Detection of mutations in genes associated with hearing loss using a microarray-based approach.

Siemering K, Manji SS, Hutchison WM, Du Sart D, Phelan D, Dahl HH. Siemering K, et al. Among authors: dahl hh. J Mol Diagn. 2006 Sep;8(4):483-9; quiz 528. doi: 10.2353/jmoldx.2006.050147. J Mol Diagn. 2006. PMID: 16931589 Free PMC article.

9

Cochlear implants for DFNA17 deafness.

Hildebrand MS, de Silva MG, Gardner RJ, Rose E, de Graaf CA, Bahlo M, Dahl HH. Hildebrand MS, et al. Among authors: dahl hh. Laryngoscope. 2006 Dec;116(12):2211-5. doi: 10.1097/01.mlg.0000242089.72880.f8. Laryngoscope. 2006. PMID: 17146397

10

Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28.

Amor DJ, Dahl HH, Bahlo M, Bankier A. Amor DJ, et al. Among authors: dahl hh. Am J Med Genet A. 2007 Oct 1;143A(19):2236-41. doi: 10.1002/ajmg.a.31917. Am J Med Genet A. 2007. PMID: 17726694

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