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/vufind/Search/Results?lookfor=%22Cao%2C+Juyang%22&type=Person&sort=year
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PubPharm (15)
1
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
enthalten in:
Nucleic acids research
| 2013
von
Zhao, H.
|
Young, W.
|
Yan, Q.
| +7
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2
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss
enthalten in:
Biochemical and biophysical research communications
| 2007
von
Yuan, H.
|
Chen, J.
|
Liu, X.
| +11
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3
Genotypic analysis of familial dilated vestibular aqueduct syndrome
enthalten in:
Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology
| 2006
von
Dai, P.
|
Han, D.
|
Cao, J.
| +10
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4
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families : implication for early detection and prevention of deafness
enthalten in:
Biochemical and biophysical research communications
| 2006
von
Dai, P.
|
Liu, X.
|
Han, D.
| +17
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5
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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6
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
enthalten in:
Nucleic acids research
| 2005
von
Zhao, H.
|
Young, W.
|
Yan, Q.
| +7
Wird geladen...
7
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
enthalten in:
Nucleic acids research
| 2005
von
Zhao, H.
|
Young, W.
|
Yan, Q.
| +6
Wird geladen...
8
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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9
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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10
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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1
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15
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Lin chuang er bi yan hou ke za zhi = Journal of...
3
Nucleic acids research
2
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2
Zhonghua er bi yan hou ke za zhi
1
American journal of medical genetics / C
1
American journal of medical genetics. Part A
1
Zhonghua yi xue yi chuan xue za zhi = Zhonghua ...
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Thema
11
Journal Article
7
Research Support, Non-U.S. Gov't
5
DNA, Mitochondrial
5
English Abstract
5
RNA, Ribosomal
5
RNA, ribosomal, 12S
3
RNA, Transfer, Ser
3
Research Support, N.I.H., Extramural
2
63231-63-0
2
Aminoglycosides
2
RNA
2
RNA, Mitochondrial
2
Research Support, U.S. Gov't, P.H.S.
1
452VLY9402
1
61JJC8N5ZK
1
9014-25-9
1
Klinische Studie
1
Comparative Study
1
Cyclooxygenase 1
1
EC 1.14.99.1
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Erscheinungszeitraum
1
2010-2019
14
2000-2009
Erscheinungsjahr(e)
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Sprache
6
Chinesisch
5
Englisch
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