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.


PUBMED FOR HANDHELDS

Journal Abstract Search


222 related items for PubMed ID: 32377700

  • 1. Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNASer(UCN) mutations.
    Peng W, Zhong Y, Zhao X, Yuan J.
    Mol Med Rep; 2020 Jul; 22(1):77-86. PubMed ID: 32377700
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
    Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, Sun D, Tao Z, Tsushima A, Wu G, Xu L, Chen C, Yi B, Cai J, Tang X, Wang J, Li D, Yuan Q, Liao Z, Chen J, Li Z, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2007 Sep 14; 361(1):133-9. PubMed ID: 17659260
    [Abstract] [Full Text] [Related]

  • 3. Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.
    Zhu Y, Qian Y, Tang X, Wang J, Yang L, Liao Z, Li R, Ji J, Li Z, Chen J, Choo DI, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Apr 14; 342(3):843-50. PubMed ID: 16500624
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.
    Tang X, Zheng J, Ying Z, Cai Z, Gao Y, He Z, Yu H, Yao J, Yang Y, Wang H, Chen Y, Guan MX.
    Mitochondrion; 2015 Jul 14; 23():17-24. PubMed ID: 25968158
    [Abstract] [Full Text] [Related]

  • 5. Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
    Yuan H, Chen J, Liu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dai P, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2007 Oct 12; 362(1):94-100. PubMed ID: 17698030
    [Abstract] [Full Text] [Related]

  • 6. [Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].
    Yang AF, Zhu Y, Lu JX, Yang L, Zhao JY, Sun DM.
    Yi Chuan; 2008 Jun 12; 30(6):728-34. PubMed ID: 18550495
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial COI/tRNASer(UCN) G7444A mutation may be associated with aminoglycoside-induced and non-syndromic hearing impairment.
    Liu Q, Liu P, Ding Y, Dong XJ, Wang ZX, Qian YE, Wang Q, Yang GC.
    Mol Med Rep; 2015 Dec 12; 12(6):8176-8. PubMed ID: 26497601
    [Abstract] [Full Text] [Related]

  • 8. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
    Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX.
    Am J Med Genet A; 2005 Oct 01; 138A(2):133-40. PubMed ID: 16152638
    [Abstract] [Full Text] [Related]

  • 9. [Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family].
    Zhao JY, Tang XW, Lan JS, Lv JX, Yang L, Li ZY, Zhu Y, Sun DM, Yang AF, Wang JD, Xu J, Guan MX.
    Yi Chuan; 2008 Dec 01; 30(12):1557-62. PubMed ID: 19073569
    [Abstract] [Full Text] [Related]

  • 10. Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation.
    Fan W, Zheng J, Kong W, Cui L, Aishanjiang M, Yi Q, Wang M, Cang X, Tang X, Chen Y, Mo JQ, Sondheimer N, Ge W, Guan MX.
    J Biol Chem; 2019 Dec 13; 294(50):19292-19305. PubMed ID: 31685661
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial COI/tRNASer(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family.
    Ding Y, Xia BH, Teng YS, Zhuo GC, Leng JH.
    Int J Clin Exp Pathol; 2017 Dec 13; 10(9):9496-9502. PubMed ID: 31966824
    [Abstract] [Full Text] [Related]

  • 12. The Mitochondrial COI/tRNASER(UCN) G7444A Mutation may be Associated with Hearing Impairment in a Han Chinese Family.
    Y D, B-H X, Y-S T, G-C Z, J-H L.
    Balkan J Med Genet; 2017 Dec 13; 20(2):43-50. PubMed ID: 29876232
    [Abstract] [Full Text] [Related]

  • 13. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients.
    Abreu-Silva RS, Lezirovitz K, Braga MC, Spinelli M, Pirana S, Della-Rosa VA, Otto PA, Mingroni-Netto RC.
    Braz J Med Biol Res; 2006 Feb 13; 39(2):219-26. PubMed ID: 16470309
    [Abstract] [Full Text] [Related]

  • 14. Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.
    Mkaouar-Rebai E, Tlili A, Masmoudi S, Louhichi N, Charfeddine I, Ben Amor M, Lahmar I, Driss N, Drira M, Ayadi H, Fakhfakh F.
    Biochem Biophys Res Commun; 2006 Feb 24; 340(4):1251-8. PubMed ID: 16406239
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
    Tang X, Yang L, Zhu Y, Liao Z, Wang J, Qian Y, Tao Z, Hu L, Wu G, Lan J, Wang X, Ji J, Wu J, Ji Y, Feng J, Chen J, Li Z, Zhang X, Lu J, Guan MX.
    Gene; 2007 May 15; 393(1-2):11-9. PubMed ID: 17341440
    [Abstract] [Full Text] [Related]

  • 17. Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.
    Chen J, Yuan H, Lu J, Liu X, Wang G, Zhu Y, Cheng J, Wang X, Han B, Yang L, Yang S, Yang A, Sun Q, Kang D, Zhang X, Dai P, Zhai S, Han D, Young WY, Guan MX.
    Mitochondrion; 2008 Sep 15; 8(4):285-92. PubMed ID: 18639500
    [Abstract] [Full Text] [Related]

  • 18. The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.
    Ding Y, Teng YS, Zhuo GC, Xia BH, Leng JH.
    Curr Mol Med; 2019 Sep 15; 19(2):136-146. PubMed ID: 30854964
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
    Lu J, Qian Y, Li Z, Yang A, Zhu Y, Li R, Yang L, Tang X, Chen B, Ding Y, Li Y, You J, Zheng J, Tao Z, Zhao F, Wang J, Sun D, Zhao J, Meng Y, Guan MX.
    Mitochondrion; 2010 Jan 15; 10(1):69-81. PubMed ID: 19818876
    [Abstract] [Full Text] [Related]

  • 20. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.
    Yuan Y, You Y, Huang D, Cui J, Wang Y, Wang Q, Yu F, Kang D, Yuan H, Han D, Dai P.
    J Transl Med; 2009 Sep 10; 7():79. PubMed ID: 19744334
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 12.