Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Clinical Investigator Award (CIA) (K08)
Project #
1K08DC000119-01A1
Application #
2014216
Study Section
Communication Disorders Review Committee (CDRC)
Project Start
1997-01-01
Project End
2001-12-31
Budget Start
1997-01-01
Budget End
1997-12-31
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Friedman, R A; Adir, Y; Crenshaw, E B et al. (2000) A transgenic insertional inner ear mutation on mouse chromosome 1. Laryngoscope 110:489-96
Sue, C M; Tanji, K; Hadjigeorgiou, G et al. (1999) Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene. Neurology 52:1905-8
Angeli, S I; Naranjo, C; Friedman, R A et al. (1999) An analysis of a large postlingually deaf family with hereditary non-syndromic profound hearing loss. Acta Otolaryngol 119:158-62
Friedman, R A; Bykhovskaya, Y; Sue, C M et al. (1999) Maternally inherited nonsyndromic hearing loss. Am J Med Genet 84:369-72
Kozel, P J; Friedman, R A; Erway, L C et al. (1998) Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2. J Biol Chem 273:18693-6
Paradies, N E; Sanford, L P; Doetschman, T et al. (1998) Developmental expression of the TGF beta s in the mouse cochlea. Mech Dev 79:165-8