Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
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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 diseaseScreening 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.
P2860
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P2860
Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@en
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@nl
type
label
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@en
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@nl
prefLabel
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@en
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@nl
P2860
P1476
Genetics of aminoglycoside-ind ...... hearing impairment: a review.
@en
P2093
L Hema Bindu
P2860
P304
P356
10.1080/14992020802215862
P577
2008-11-01T00:00:00Z