Literature DB >> 10496072

Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutation.

S Usami1, S Abe, H Shinkawa, Y Inoue, T Yamaguchi.   

Abstract

The 1555A-->G point mutation is associated with a susceptibility to aminoglycoside antibiotics, and is of particular interest, as it may cause hearing loss even without aminoglycoside exposure. There may be a considerably large high-risk population in Japan, and to avoid possible side effects in this group, a rapid mass screening system and careful counseling are recommended. We are currently using the mutant allele specific amplification (MASA) method to detect the 1555A-->G mitochondrial mutation and we distribute a warning card to subjects found to bear this mutation.

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Year:  1999        PMID: 10496072     DOI: 10.1007/s100380050165

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  4 in total

1.  Prevalence of mitochondrial gene mutations among hearing impaired patients.

Authors:  S Usami; S Abe; J Akita; A Namba; H Shinkawa; M Ishii; S Iwasaki; T Hoshino; J Ito; K Doi; T Kubo; T Nakagawa; S Komiyama; T Tono; S Komune
Journal:  J Med Genet       Date:  2000-01       Impact factor: 6.318

2.  Herbal Medicine Containing Licorice May Be Contraindicated for a Patient with an HSD11B2 Mutation.

Authors:  Indra Sari Kusuma Harahap; Naoko Sasaki; Surini Yusoff; Myeong Jin Lee; Satoru Morikawa; Noriyuki Nishimura; Tomohiro Sasaki; Seiichiro Usuki; Midori Hirai; Mika Ohta; Yutaka Takaoka; Takashi Nishimoto; Hisahide Nishio
Journal:  Evid Based Complement Alternat Med       Date:  2011-02-20       Impact factor: 2.629

3.  In vitro gentamicin exposure alters caveolae protein profile in cochlear spiral ligament pericytes.

Authors:  Elisa Ghelfi; Yohann Grondin; Emil J Millet; Adam Bartos; Magda Bortoni; Clara Oliveira Gomes Dos Santos; Humberto J Trevino-Villarreal; Rosalinda Sepulveda; Rick Rogers
Journal:  Proteome Sci       Date:  2018-03-16       Impact factor: 2.480

4.  Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan.

Authors:  Yasunori Maeda; Akira Sasaki; Shuya Kasai; Shinichi Goto; Shin-Ya Nishio; Kaori Sawada; Itoyo Tokuda; Ken Itoh; Shin-Ichi Usami; Atsushi Matsubara
Journal:  Hum Genome Var       Date:  2020-09-18
  4 in total

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