These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 22223843)

  • 1. Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study.
    Rahman S; Ecob R; Costello H; Sweeney MG; Duncan AJ; Pearce K; Strachan D; Forge A; Davis A; Bitner-Glindzicz M
    BMJ Open; 2012; 2(1):e000411. PubMed ID: 22223843
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC; Chiu YH; Chen PJ; Hsu CJ
    Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants.
    Göpel W; Berkowski S; Preuss M; Ziegler A; Küster H; Felderhoff-Müser U; Gortner L; Mögel M; Härtel C; Herting E;
    BMC Pediatr; 2014 Aug; 14():210. PubMed ID: 25155176
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment.
    Kaheel H; Breß A; Hassan MA; Shah AA; Amin M; Bakhit YHY; Kniper M
    BMC Ear Nose Throat Disord; 2018; 18():7. PubMed ID: 29942192
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced Deafness.
    Ding Y; Teng Y; Guo Q; Leng J
    Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292680
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial m.1584A 12S m62A rRNA methylation in families with m.1555A>G associated hearing loss.
    O'Sullivan M; Rutland P; Lucas D; Ashton E; Hendricks S; Rahman S; Bitner-Glindzicz M
    Hum Mol Genet; 2015 Feb; 24(4):1036-44. PubMed ID: 25305075
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Contribution of the tRNA
    Meng F; He Z; Tang X; Zheng J; Jin X; Zhu Y; Ren X; Zhou M; Wang M; Gong S; Mo JQ; Shu Q; Guan MX
    J Biol Chem; 2018 Mar; 293(9):3321-3334. PubMed ID: 29348176
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Audio profiles in mitochondrial deafness m.1555A>G and m.3243A>G show distinct differences.
    Iwanicka-Pronicka K; Pollak A; Skórka A; Lechowicz U; Korniszewski L; Westfal P; Skarżyński H; Płoski R
    Med Sci Monit; 2015 Mar; 21():694-700. PubMed ID: 25744662
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated?
    Al-Malky G; Suri R; Sirimanna T; Dawson SJ
    Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):969-73. PubMed ID: 24703164
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Mitochondrial DNA mutations in matrilineal nonsyndromic deafness pedigrees of southwest China].
    Zhang N; Qiao X; Wang L; Liang C
    Hua Xi Yi Ke Da Xue Xue Bao; 2001 Dec; 32(4):596-8, 626. PubMed ID: 12528560
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Is deafness mutation screening required in cystic fibrosis patients?
    Abusamra R; McShane D
    Paediatr Respir Rev; 2016 Aug; 20 Suppl():24-6. PubMed ID: 27427311
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
    Igumnova V; Veidemane L; Vīksna A; Capligina V; Zole E; Ranka R
    J Hum Genet; 2019 Mar; 64(3):199-206. PubMed ID: 30523288
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients.
    Chen C; Guan MX
    Hum Mol Genet; 2022 Sep; 31(18):3068-3082. PubMed ID: 35467742
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.
    Joo SY; Jang SH; Kim JA; Kim SJ; Kim B; Kim HY; Choi JY; Gee HY; Jung J
    J Korean Med Sci; 2023 Dec; 38(48):e355. PubMed ID: 38084023
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Improvement of a Rapid and Highly Sensitive Method for the Diagnosis of the Mitochondrial m.1555A>G Mutation Based on a Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip.
    Isaka Y; Nishio SY; Hishinuma E; Hiratsuka M; Usami SI
    Genet Test Mol Biomarkers; 2021 Jan; 25(1):79-83. PubMed ID: 33372830
    [No Abstract]   [Full Text] [Related]  

  • 16. Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of China.
    Guo YF; Liu XW; Xu BC; Zhu YM; Wang YL; Zhao FF; Wang DY; Zhao YL; Ji YB; Wang QJ
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):527-31. PubMed ID: 20662562
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.
    Rydzanicz M; Cywińska K; Wróbel M; Pollak A; Gawęcki W; Wojsyk-Banaszak I; Lechowicz U; Mueller-Malesińska M; Ołdak M; Płoski R; Skarżyński H; Szyfter K; Szyfter W
    Mol Genet Metab; 2011; 104(1-2):153-9. PubMed ID: 21621438
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of mitochondrial gene mutations among hearing impaired patients.
    Usami S; Abe S; Akita J; Namba A; Shinkawa H; Ishii M; Iwasaki S; Hoshino T; Ito J; Doi K; Kubo T; Nakagawa T; Komiyama S; Tono T; Komune S
    J Med Genet; 2000 Jan; 37(1):38-40. PubMed ID: 10633132
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.
    Subathra M; Ramesh A; Selvakumari M; Karthikeyen NP; Srisailapathy CR
    Ann Hum Genet; 2016 Sep; 80(5):257-73. PubMed ID: 27530448
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation.
    Lu SY; Nishio S; Tsukada K; Oguchi T; Kobayashi K; Abe S; Usami S
    Clin Genet; 2009 May; 75(5):480-4. PubMed ID: 19475720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.