Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review. - Wikidata - wikimedia - TriplyDB

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

http://www.wikidata.org/entity/Q37334174

about

Assessment of nutrient supplement to reduce gentamicin-induced ototoxicity.The zebrafish merovingian mutant reveals a role for pH regulation in hair cell toxicity and function.The challenge of hair cell regeneration.Gentamicin rapidly inhibits mitochondrial metabolism in high-frequency cochlear outer hair cells.Imaging of sensorineural hearing loss: a pattern-based approach to diseases of the inner ear and cerebellopontine angle.Cochleo-vestibular clinical findings among drug resistant Tuberculosis Patients on therapy-a pilot study.The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential.ER-mitochondrial calcium flow underlies vulnerability of mechanosensory hair cells to damage.Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads.Aminoglycoside stress together with the 12S rRNA 1494C>T mutation leads to mitophagy.A modern approach to the treatment of mitochondrial disease Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss.Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.Empiric therapy for gram-negative pathogens in nosocomial and health care-associated pneumonia: starting with the end in mind.The clinical and audiologic features of hearing loss due to mitochondrial mutations.Effect of streptomycin on melanogenesis and antioxidant status in melanocytes.Language Evolution: Constraints and Opportunities From Modern Genetics.Adverse Effects and Choice between the Injectable Agents Amikacin and Capreomycin in Multidrug-Resistant Tuberculosis.The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease.Audiological and radiological characteristics of a family with T961G mitochondrial mutation.Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.Causes of hearing impairment in the Norwegian paediatric cochlear implant program.Impact of kanamycin on melanogenesis and antioxidant enzymes activity in melanocytes--an in vitro study.Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.

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P2860

Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.

http://www.wikidata.org/entity/Q37334174

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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2008年學術文章

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name

Genetics of aminoglycoside-ind ...... hearing impairment: a review.

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Genetics of aminoglycoside-ind ...... hearing impairment: a review.

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type

label

Genetics of aminoglycoside-ind ...... hearing impairment: a review.

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Genetics of aminoglycoside-ind ...... hearing impairment: a review.

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prefLabel

Genetics of aminoglycoside-ind ...... hearing impairment: a review.

@en

Genetics of aminoglycoside-ind ...... hearing impairment: a review.

@nl

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14992020802215862

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International Journal of Audiology

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Genetics of aminoglycoside-ind ...... hearing impairment: a review.

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L Hema Bindu

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P P Reddy

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P2860

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations

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

Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.

Genetics, genomics and gene discovery in the auditory system.

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.

Ribosomal RNA and translation.

A molecular basis for human hypersensitivity to aminoglycoside antibiotics.

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702-707

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scholarly article

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10.1080/14992020802215862

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11

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47

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