-
1
-
-
77949482615
-
Intratympanic gentamicin treatment of patients with Meniere's disease with normal hearing
-
Silverstein H, Wazen J, Van Ess MJ, Daugherty J, Alameda YA (2010) Intratympanic gentamicin treatment of patients with Meniere's disease with normal hearing. Otolaryngol Head Neck Surg 142(4):570-575
-
(2010)
Otolaryngol Head Neck Surg
, vol.142
, Issue.4
, pp. 570-575
-
-
Silverstein, H.1
Wazen, J.2
Van Ess, M.J.3
Daugherty, J.4
Alameda, Y.A.5
-
3
-
-
0027226069
-
Mitochondrial ribosomal RNA mutation associated with both antibiotic- induced and non-syndromic deafness
-
DOI 10.1038/ng0793-289
-
Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ, Arnos KS, Cortopassi GA, Jaber L, Rotter JI et al (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic- induced and non-syndromic deafness. Nat Genet 4(3):289-294 (Pubitemid 23205179)
-
(1993)
Nature Genetics
, vol.4
, Issue.3
, pp. 289-294
-
-
Prezant, T.R.1
Agapian, J.V.2
Bohlman, M.C.3
Bu, X.4
Oztas, S.5
Qiu, W.-Q.6
Arnos, K.S.7
Cortopassi, G.A.8
Jaber, L.9
Rotter, J.I.10
Shohat, M.11
Fischel-Ghodsian, N.12
-
4
-
-
0347003512
-
Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNa Gene in a Large Chinese Family
-
DOI 10.1086/381133
-
Zhao H, Li R, Wang Q, Yan Q, Deng JH, Han D, Bai Y, Young WY, Guan MX (2004) Maternally inherited aminoglycosideinduced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet 74(1):139-152 (Pubitemid 38085245)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.1
, pp. 139-152
-
-
Zhao, H.1
Li, R.2
Wang, Q.3
Yan, Q.4
Deng, J.-H.5
Han, D.6
Bai, Y.7
Young, W.-Y.8
Guan, M.-X.9
-
5
-
-
59749096341
-
Prevalence of mitochondrial 1555A ? G mutation in adults of European descent
-
Vandebona H, Mitchell P, Manwaring N, Griffiths K, Gopinath B, Wang JJ, Sue CM (2009) Prevalence of mitochondrial 1555A ? G mutation in adults of European descent. N Engl J Med 360(6):642-644
-
(2009)
N Engl J Med
, vol.360
, Issue.6
, pp. 642-644
-
-
Vandebona, H.1
Mitchell, P.2
Manwaring, N.3
Griffiths, K.4
Gopinath, B.5
Wang, J.J.6
Sue, C.M.7
-
6
-
-
33750927660
-
Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA
-
DOI 10.1002/humu.20378
-
Ruiz-Pesini E, Wallace DC (2006) Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. Hum Mutat 27(11):1072-1081 (Pubitemid 44730502)
-
(2006)
Human Mutation
, vol.27
, Issue.11
, pp. 1072-1081
-
-
Ruiz-Pesini, E.1
Wallace, D.C.2
-
7
-
-
34447562896
-
Modulation of 16S rRNA function by ribosomal protein S12
-
DOI 10.1016/j.bbaexp.2007.04.004, PII S0167478107000735
-
Vila-Sanjurjo A, Lu Y, Aragonez JL, Starkweather RE, Sasikumar M, O'Connor M (2007) Modulation of 16S rRNA function by ribosomal protein S12. Biochim Biophys Acta 1769(7-8): 462-471. doi:10.1016/j.bbaexp.2007.04.004 (Pubitemid 47081203)
-
(2007)
Biochimica et Biophysica Acta - Gene Structure and Expression
, vol.1769
, Issue.7-8
, pp. 462-471
-
-
Vila-Sanjurjo, A.1
Lu, Y.2
Aragonez, J.L.3
Starkweather, R.E.4
Sasikumar, M.5
O'Connor, M.6
-
8
-
-
34547621748
-
Relative abundance of the human mitochondrial transcription system and distinct roles for h-mtTFB1 and h-mtTFB2 in mitochondrial biogenesis and gene expression
-
DOI 10.1093/nar/gkm424
-
Cotney J, Wang Z, Shadel GS (2007) Relative abundance of the human mitochondrial transcription system and distinct roles for h-mtTFB1 and h-mtTFB2 in mitochondrial biogenesis and gene expression. Nucleic Acids Res 35(12):4042-4054 (Pubitemid 47244625)
-
(2007)
Nucleic Acids Research
, vol.35
, Issue.12
, pp. 4042-4054
-
-
Cotney, J.1
Wang, Z.2
Shadel, G.S.3
-
9
-
-
0029047601
-
-
Equilibrium TCoHa, Committee on Hearing and Equilibrium guidelines for the evaluation of results of treatment of conductive hearing loss. American Academy of Otolaryngology- Head and Neck Surgery Foundation, Inc.
-
Equilibrium TCoHa (1995) Committee on Hearing and Equilibrium guidelines for the evaluation of results of treatment of conductive hearing loss. American Academy of Otolaryngology- Head and Neck Surgery Foundation, Inc. Otolaryngol Head Neck Surg 113:186-187
-
(1995)
Otolaryngol Head Neck Surg
, vol.113
, pp. 186-187
-
-
-
10
-
-
77955364142
-
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups
-
Gomez-Duran A, Pacheu-Grau D, Lopez-Gallardo E, Diez-Sanchez C, Montoya J, Lopez-Perez MJ, Ruiz-Pesini E (2009) Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Hum Mol Genet 19(17):3343-3353
-
(2009)
Hum Mol Genet
, vol.19
, Issue.17
, pp. 3343-3353
-
-
Gomez-Duran, A.1
Pacheu-Grau, D.2
Lopez-Gallardo, E.3
Diez-Sanchez, C.4
Montoya, J.5
Lopez-Perez, M.J.6
Ruiz-Pesini, E.7
-
11
-
-
33846094306
-
An enhanced MITOMAP with a global mtDNA mutational phylogeny
-
DOI 10.1093/nar/gkl927
-
Ruiz-Pesini E, Lott MT, Procaccio V, Poole JC, Brandon MC, Mishmar D, Yi C, Kreuziger J, Baldi P, Wallace DC (2007) An enhanced MITOMAP with a global mtDNA mutational phylogeny. Nucleic Acids Res 35(Database issue):D823-D828 (Pubitemid 46056316)
-
(2007)
Nucleic Acids Research
, vol.35
, Issue.SUPPL. 1
-
-
Ruiz-Pesini, E.1
Lott, M.T.2
Procaccio, V.3
Poole, J.C.4
Brandon, M.C.5
Mishmar, D.6
Yi, C.7
Kreuziger, J.8
Baldi, P.9
Wallace, D.C.10
-
12
-
-
58149397990
-
Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy
-
Alonso-Montes C, Castro MG, Reguero JR, Perrot A, Ozcelik C, Geier C, Posch MG, Moris C, Alvarez V, Ruiz-Ortega M, Coto E (2008) Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophy. Dis Markers 25(3):131-139
-
(2008)
Dis Markers
, vol.25
, Issue.3
, pp. 131-139
-
-
Alonso-Montes, C.1
Castro, M.G.2
Reguero, J.R.3
Perrot, A.4
Ozcelik, C.5
Geier, C.6
Posch, M.G.7
Moris, C.8
Alvarez, V.9
Ruiz-Ortega, M.10
Coto, E.11
-
13
-
-
34548781484
-
Mitochondrial DNA haplogroups and age-related hearing loss
-
DOI 10.1001/archotol.133.9.929
-
Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Newall P, Mitchell P, Sue CM (2007) Mitochondrial DNA haplogroups and age-related hearing loss. Arch Otolaryngol Head Neck Surg 133(9):929-933 (Pubitemid 47437282)
-
(2007)
Archives of Otolaryngology - Head and Neck Surgery
, vol.133
, Issue.9
, pp. 929-933
-
-
Manwaring, N.1
Jones, M.M.2
Jie, J.W.3
Rochtchina, E.4
Howard, C.5
Newall, P.6
Mitchell, P.7
Sue, C.M.8
-
14
-
-
77953264623
-
Binding of aminoglycoside antibiotics to helix 69 of 23S rRNA
-
Scheunemann AE, Graham WD, Vendeix FA, Agris PF (2010) Binding of aminoglycoside antibiotics to helix 69 of 23S rRNA. Nucleic Acids Res 38(9):3094-3105
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.9
, pp. 3094-3105
-
-
Scheunemann, A.E.1
Graham, W.D.2
Vendeix, F.A.3
Agris, P.F.4
-
15
-
-
0035344453
-
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families
-
doi:10.1002/humu.1122
-
Shah ZH, Toompuu M, Hakkinen T, Rovio AT, van Ravenswaay C, De Leenheer EM, Smith RJ, Cremers FP, Cremers CW, Jacobs HT (2001) Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families. Hum Mutat 17(5):433-434. doi:10.1002/humu.1122
-
(2001)
Hum Mutat
, vol.17
, Issue.5
, pp. 433-434
-
-
Shah, Z.H.1
Toompuu, M.2
Hakkinen, T.3
Rovio, A.T.4
Van Ravenswaay, C.5
De Leenheer, E.M.6
Smith, R.J.7
Cremers, F.P.8
Cremers, C.W.9
Jacobs, H.T.10
-
16
-
-
73749087417
-
Mitochondrial pharmacogenomics: Barcode for antibiotic therapy
-
Pacheu-Grau D, Gomez-Duran A, Lopez-Perez MJ, Montoya J, Ruiz-Pesini E (2010) Mitochondrial pharmacogenomics: barcode for antibiotic therapy. Drug Discov Today 15(1-2):33-39
-
(2010)
Drug Discov Today
, vol.15
, Issue.1-2
, pp. 33-39
-
-
Pacheu-Grau, D.1
Gomez-Duran, A.2
Lopez-Perez, M.J.3
Montoya, J.4
Ruiz-Pesini, E.5
-
17
-
-
77957129708
-
Influence of mtDNA genetic variation on antibiotic therapy
-
Pacheu-Grau D, Gomez-Duran A, Montoya J, Ruiz-Pesini E (2010) Influence of mtDNA genetic variation on antibiotic therapy. Pharmacogenomics 11(9):1185-1187
-
(2010)
Pharmacogenomics
, vol.11
, Issue.9
, pp. 1185-1187
-
-
Pacheu-Grau, D.1
Gomez-Duran, A.2
Montoya, J.3
Ruiz-Pesini, E.4
-
18
-
-
0029974154
-
Topical gentamicin-induced hearing loss: A mitochondrial ribosomal RNA study of genetic susceptibility
-
Chen JM, Williamson PA, Hutchin T, Nedzelski JM, Cortopassi GA (1996) Topical gentamicin-induced hearing loss: a mitochondrial ribosomal RNA study of genetic susceptibility. Am J Otol 17(6):850-852 (Pubitemid 26379247)
-
(1996)
American Journal of Otology
, vol.17
, Issue.6
, pp. 850-852
-
-
Chen, J.M.1
Williamson, P.A.2
Hutchin, T.3
Nedzelski, J.M.4
Cortopassi, G.A.5
-
19
-
-
0035092355
-
Unpredictable hearing loss after intratympanic gentamicin treatment for vertigo. A new theory
-
DOI 10.1080/000164801300006254
-
Walsted A (2001) Unpredictable hearing loss after intratympanic gentamicin treatment for vertigo. A new theory. Acta Otolaryngol 121(1):42-44 (Pubitemid 32205024)
-
(2001)
Acta Oto-Laryngologica
, vol.121
, Issue.1
, pp. 42-44
-
-
Walsted, A.1
-
20
-
-
33746559647
-
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations
-
DOI 10.1086/506389
-
Guan MX, Yan Q, Li X, Bykhovskaya Y, Gallo-Teran J, Hajek P, Umeda N, Zhao H, Garrido G, Mengesha E, Suzuki T, del Castillo I, Peters JL, Li R, Qian Y, Wang X, Ballana E, Shohat M, Lu J, Estivill X, Watanabe K, Fischel-Ghodsian N (2006) Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations. Am J Hum Genet 79(2):291-302. doi:10.1086/506389 (Pubitemid 44141827)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.2
, pp. 291-302
-
-
Guan, M.-X.1
Yan, Q.2
Li, X.3
Bykhovskaya, Y.4
Gallo-Teran, J.5
Hajek, P.6
Umeda, N.7
Zhao, H.8
Garrido, G.9
Mengesha, E.10
Suzuki, T.11
Del Castillo, I.12
Peters, J.L.13
Li, R.14
Qian, Y.15
Wang, X.16
Ballana, E.17
Shohat, M.18
Lu, J.19
Estivill, X.20
Watanabe, K.21
Fischel-Ghodsian, N.22
more..
-
21
-
-
0036158877
-
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy
-
DOI 10.1002/mus.10012
-
Campos Y, Garcia A, Lopez A, Jimenez S, Rubio JC, Del Hoyo P, Bustos F, Martin MA, Cabello A, Ricoy JR, Arenas J (2002) Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy. Muscle Nerve 25(2):185-188. doi:10.1002/mus.10012 (Pubitemid 34117064)
-
(2002)
Muscle and Nerve
, vol.25
, Issue.2
, pp. 185-188
-
-
Campos, Y.1
Garcia, A.2
Lopez, A.3
Jimenez, S.4
Rubio, J.C.5
Del Hoyo, P.6
Bustos, F.7
Martin, M.A.8
Cabello, A.9
Ricoy, J.R.10
Arenas, J.11
-
22
-
-
57149125444
-
Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families
-
doi:10.1097/FPC.0b013e3283131661
-
Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX (2008) Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenet Genomics 18(12):1059-1070. doi:10.1097/FPC. 0b013e3283131661
-
(2008)
Pharmacogenet Genomics
, vol.18
, Issue.12
, pp. 1059-1070
-
-
Wang, X.1
Lu, J.2
Zhu, Y.3
Yang, A.4
Yang, L.5
Li, R.6
Chen, B.7
Qian, Y.8
Tang, X.9
Wang, J.10
Zhang, X.11
Guan, M.X.12
|