A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness. - Wikidata - awgldk - TriplyDB

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.

http://www.wikidata.org/entity/Q37072839

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Study of streptomycin-induced ototoxicity: protocol for a longitudinal study.Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth Rapid method for identification of six common species of mycobacteria based on multiplex SNP analysis.Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants.Identification and genotyping of Mycobacterium tuberculosis complex species by use of a SNaPshot Minisequencing-based assay.Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: a report from Nigeria.A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides?Pediatric TB: issues related to current and future treatment options.Safety and tolerability profile of second-line anti-tuberculosis medications.The safety and tolerability of the second-line injectable antituberculosis drugs in children.Multidrug-resistant tuberculosis (MDR-TB) treatment in the UK: a study of injectable use and toxicity in practice.Adverse Effects and Choice between the Injectable Agents Amikacin and Capreomycin in Multidrug-Resistant Tuberculosis.Genetics of non syndromic hearing loss in the republic of macedonia.PharmGKB summary: very important pharmacogene information for MT-RNR1.Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.

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A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.

http://www.wikidata.org/entity/Q37072839

description

article científic

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bilimsel makale

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scientific article published on 13 January 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

A rapid method for detection o ...... inoglycoside-induced deafness.

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A rapid method for detection o ...... inoglycoside-induced deafness.

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A rapid method for detection o ...... inoglycoside-induced deafness.

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A rapid method for detection o ...... inoglycoside-induced deafness.

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A rapid method for detection o ...... inoglycoside-induced deafness.

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A rapid method for detection o ...... inoglycoside-induced deafness.

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BMC Medical Genetics

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A rapid method for detection o ...... inoglycoside-induced deafness.

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Greetje de Jong

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Gwynneth Hefke

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H Simon Schaaf

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Hannique Human

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Johan Fagan

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John H Greinwald

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Rene Veikondis

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Soraya Bardien

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Tashneem Harris

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P2860

Primer3 on the WWW for general users and for biologist programmers

Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?

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

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.

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

Mitochondrial deafness alleles confer misreading of the genetic code

Mitochondrial rRNA and tRNA and hearing function.

Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.

A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy.

A novel mitochondrial mutation, 1556C --> T, in a Japanese patient with streptomycin-induced tinnitus.

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2

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scholarly article

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10.1186/1471-2350-10-2

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10

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Lize van der Merwe

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2009-01-13T00:00:00Z

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23788211

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1044737562

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19144107

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2630920

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