Pages that link to "Q46157086"
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The following pages link to Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness (Q46157086):
Displaying 50 items.
- Mitochondrial DNA backgrounds might modulate diabetes complications rather than T2DM as a whole (Q21135340) (← links)
- Characterization and tRNA recognition of mammalian mitochondrial seryl-tRNA synthetase (Q22253892) (← links)
- Aminoglycosides and other nonsense suppression therapies for the treatment of dystrophinopathy (Q24240721) (← links)
- The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders (Q24291646) (← links)
- Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus (Q24336077) (← links)
- A human mitochondrial transcription factor is related to RNA adenine methyltransferases and binds S-adenosylmethionine (Q24537551) (← links)
- Human mtDNA haplogroups associated with high or reduced spermatozoa motility (Q24538797) (← links)
- A human mitochondrial GTP binding protein related to tRNA modification may modulate phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation (Q24540271) (← links)
- A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia (Q24561975) (← links)
- New developments in aminoglycoside therapy and ototoxicity (Q24599985) (← links)
- Platinum-induced ototoxicity in children: a consensus review on mechanisms, predisposition, and protection, including a new International Society of Pediatric Oncology Boston ototoxicity scale (Q24615296) (← links)
- Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations (Q24669653) (← links)
- Mitochondria (Q24671804) (← links)
- An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds (Q24675914) (← links)
- Mitochondrial DNA mutations in human disease (Q24676881) (← links)
- Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background (Q24678122) (← links)
- Nonsyndromic hearing impairment: unparalleled heterogeneity (Q24680416) (← links)
- A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. (Q24681680) (← links)
- Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss (Q24791654) (← links)
- High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss (Q24815450) (← links)
- Mitochondrial genetics (Q26849285) (← links)
- Inner ear symptoms and disease: pathophysiological understanding and therapeutic options (Q26997318) (← links)
- Mitochondrial genome changes and neurodegenerative diseases (Q27023750) (← links)
- The bacterial and mitochondrial ribosomal A-site molecular switches possess different conformational substates (Q27650094) (← links)
- Dissociation of antibacterial activity and aminoglycoside ototoxicity in the 4-monosubstituted 2-deoxystreptamine apramycin (Q27681169) (← links)
- 4′-O-substitutions determine selectivity of aminoglycoside antibiotics (Q27681495) (← links)
- Ribosome. The complete structure of the 55S mammalian mitochondrial ribosome (Q27700074) (← links)
- Dysregulated mitochondrial and chloroplast bioenergetics from a translational medical perspective (Review) (Q28066841) (← links)
- A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation (Q28082057) (← links)
- Assignment of 2'-O-methyltransferases to modification sites on the mammalian mitochondrial large subunit 16 S ribosomal RNA (rRNA) (Q28115977) (← links)
- Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family (Q28117356) (← links)
- Human mitochondrial transcription factor B1 methylates ribosomal RNA at a conserved stem-loop (Q28117937) (← links)
- Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations (Q28185082) (← links)
- Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands (Q28187639) (← links)
- Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene (Q28198184) (← links)
- Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation (Q28217558) (← links)
- Molecular physiology of bestrophins: multifunctional membrane proteins linked to best disease and other retinopathies (Q28275211) (← links)
- Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3 (Q28293107) (← links)
- Technical knockout, a Drosophila model of mitochondrial deafness (Q28354235) (← links)
- Irreversible sensorineural hearing loss as a result of azithromycin ototoxicity. A case report (Q28377492) (← links)
- Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder (Q28379261) (← links)
- Mechanisms of aminoglycoside ototoxicity and targets of hair cell protection (Q28393038) (← links)
- Identification of genetic and chemical modulators of zebrafish mechanosensory hair cell death (Q28472316) (← links)
- Toward a mtDNA locus-specific mutation database using the LOVD platform (Q28649774) (← links)
- Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening (Q28660527) (← links)
- Antibiotics May Trigger Mitochondrial Dysfunction Inducing Psychiatric Disorders (Q28816988) (← links)
- Drug-induced ototoxicity: Mechanisms, Pharmacogenetics, and protective strategies (Q30240026) (← links)
- Genetics: A New Frontier in Otology. (Q30362238) (← links)
- Overexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status or hearing (Q30397225) (← links)
- Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform (Q30438646) (← links)