R01 DC005230-02S1/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

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2004	1
2005	2
2025	0

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Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.

Li R, Ishikawa K, Deng JH, Heman-Ackah S, Tamagawa Y, Yang L, Bai Y, Ichimura K, Guan MX. Li R, et al. Biochem Biophys Res Commun. 2005 Mar 4;328(1):32-7. doi: 10.1016/j.bbrc.2004.12.140. Biochem Biophys Res Commun. 2005. PMID: 15670746

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

Zhao L, Young WY, Li R, Wang Q, Qian Y, Guan MX. Zhao L, et al. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1503-8. doi: 10.1016/j.bbrc.2004.10.199. Biochem Biophys Res Commun. 2004. PMID: 15555598

Biochemical characterization of the deafness-associated mitochondrial tRNASer(UCN) A7445G mutation in osteosarcoma cell cybrids.

Li X, Zhang LS, Fischel-Ghodsian N, Guan MX. Li X, et al. Biochem Biophys Res Commun. 2005 Mar 11;328(2):491-8. doi: 10.1016/j.bbrc.2005.01.006. Biochem Biophys Res Commun. 2005. PMID: 15694374

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