Suchergebnisse - "YUAN HUIJUN"

PubPharm (13)

1

Gene Therapy for Leber Hereditary Optic Neuropathy : Low- and Medium-Dose Visual Results

enthalten in: Ophthalmology | 2017

von Guy, J. | Feuer, W. | Davis, J. | +6

CommentIn: Ophthalmology. 2018 Feb;125(2):e14-e15. - PMID 29389412

2

Gene Therapy for Leber Hereditary Optic Neuropathy : Initial Results

enthalten in: Ophthalmology | 2016

von Feuer, W. | Schiffman, J. | Davis, J. | +7

CommentIn: Ophthalmology. 2016 Jul;123(7):e44-5. - PMID 27342337

3

A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss

enthalten in: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery | 2016

von Zhang, D. | Duan, H. | Lin, P. | +9

4

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

enthalten in: BMC genetics | 2014

von Zhu, Y. | Huang, S. | Kang, D. | +7

5

Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation

enthalten in: Mitochondrion | 2009

von Zhu, Y. | Li, Q. | Chen, Z. | +7

6

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

enthalten in: Journal of translational medicine | 2009

von Yuan, Y. | You, Y. | Huang, D. | +8

7

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss

enthalten in: Mitochondrion | 2008

von Chen, J. | Yuan, H. | Lu, J. | +17

8

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

9

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families

enthalten in: Biochemical and biophysical research communications | 2006

von Dai, P. | Yuan, Y. | Huang, D. | +7

10

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