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/vufind/Search/Results?lookfor=%22YUAN+HUIJUN%22&type=Person&page=18
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PubPharm (179)
171
Prevention of rabies virus infection in dogs by a recombinant canine adenovirus type-2 encoding the rabies virus glycoprotein
enthalten in:
Microbes and infection
| 2006
von
Hu, R.
|
Zhang, S.
|
Fooks, A.
| +6
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172
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss. How to cite this article: Young W-Y, Zhao L, Qian Y, Li R, Chen J, Yuan H, Dai P, Zhai S, Han D, Guan M-X. 2006. Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss. Am J Med Genet Part A 140A:2188-2197.
enthalten in:
American journal of medical genetics / C
| 2006
von
Young, W.
|
Zhao, L.
|
Qian, Y.
| +7
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173
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss
enthalten in:
American journal of medical genetics. Part A
| 2005
von
Yuan, H.
|
Qian, Y.
|
Xu, Y.
| +12
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174
Modulation of nano-selenium on tetrodotoxin-sensitive voltage-gated sodium currents in rat dorsal root ganglion neurons
enthalten in:
Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference
| 2005
von
Yuan, H.
|
Lan, T.
|
Lin, J.
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175
Cosegregation of the G7444A mutation in the mitochondrial COI-tRNASer(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss
enthalten in:
American journal of medical genetics / C
| 2005
von
Yuan, H.
|
Qian, Y.
|
Xu, Y.
| +6
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176
Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees
enthalten in:
Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology
| 2004
von
Li, W.
|
Han, D.
|
Yuan, H.
| +1
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177
Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis
enthalten in:
Acta oto-laryngologica
| 2004
von
Dai, P.
|
Yang, W.
|
Jiang, S.
| +5
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178
Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis
enthalten in:
Acta oto-laryngologica
| 2004
von
Dai, P.
|
Yang, W.
|
Jiang, S.
| +5
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179
Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2002
von
Li, W.
|
Han, D.
|
Yuan, H.
| +4
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127120-53-0
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Connexin 26
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RNA, Ribosomal
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GJB2 protein, human
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RNA, ribosomal, 12S
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Membrane Transport Proteins
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SLC26A4 protein, human
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mutation
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