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Journal Abstract Search

107 related items for PubMed ID: 21838605

  • 1. Critical reassessment of a five-generation Chinese family carrying deafness-associated mitochondrial 1555A>G mutation.
    Ding Y, Leng J, Zheng J.
    Acta Otolaryngol; 2011 Nov; 131(11):1239-40. PubMed ID: 21838605
    [No Abstract] [Full Text] [Related]

  • 2. Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.
    Men M, Jiang L, Wang H, Liu Y, Hu Z, He C, Feng Y.
    Acta Otolaryngol; 2011 Sep; 131(9):970-5. PubMed ID: 21504270
    [Abstract] [Full Text] [Related]

  • 3. 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; 10(1):69-81. PubMed ID: 19818876
    [Abstract] [Full Text] [Related]

  • 4. A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.
    Bai Y, Wang Z, Dai W, Li Q, Chen G, Cong N, Guan M, Li H.
    BMC Med Genet; 2010 Sep 07; 11():129. PubMed ID: 20822538
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. [Mitochondrial 12S rRNA variants studies in 456 subjects with hearing loss in seven schools for deaf and mutes in Zhejiang province].
    Peng GH, Fang F, Zheng J, Zheng BJ, Yu X, Wu Y, Liang LZ, Zhang QM, Zhu Y, Tang XW, Chen BB.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Dec 15; 47(12):996-1003. PubMed ID: 23328039
    [Abstract] [Full Text] [Related]

  • 7. Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations.
    Ding Y, Xia BH, Liu Q, Li MY, Huang SX, Zhuo GC.
    Gene; 2016 Oct 10; 591(1):148-152. PubMed ID: 27397648
    [Abstract] [Full Text] [Related]

  • 8. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
    Xiang YB, Tang SH, Li HZ, Xu CY, Chen C, Xu YZ, Ding LR, Xu XQ.
    Int J Pediatr Otorhinolaryngol; 2019 Jul 10; 122():185-190. PubMed ID: 31035178
    [Abstract] [Full Text] [Related]

  • 9. Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.
    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 02; 293(9):3321-3334. PubMed ID: 29348176
    [Abstract] [Full Text] [Related]

  • 10. [Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis].
    Lyu K, Xiong Y, Yu H, Zou L, Ran L, Liu D, Yin Q, Xu Y, Fang X, Song Z, Huang L, Tan D, Zhang Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct 02; 31(5):547-52. PubMed ID: 25297577
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
    Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Zhao J, Chen Y, Guan M, Wang X, Li R, Tang X, Wang J, Tao Z, Lu J, Guan MX.
    Am J Med Genet A; 2008 May 15; 146A(10):1248-58. PubMed ID: 18386806
    [Abstract] [Full Text] [Related]

  • 12. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.
    Ji Y, Liang M, Zhang J, Zhang M, Zhu J, Meng X, Zhang S, Gao M, Zhao F, Wei QP, Jiang P, Tong Y, Liu X, Qin Mo J, Guan MX.
    J Hum Genet; 2014 Mar 15; 59(3):134-40. PubMed ID: 24430572
    [Abstract] [Full Text] [Related]

  • 13. [Mitochondrial tRNA(Thr)T15943C mutation may be a new position that affects the phenotypic expression of deafness associated 12s rRNA A1555G mutation].
    Xiao H, He Z, Gao Y, Yang Y, Zheng J, Cai Z, Zheng B, Tang X, Guan M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 15; 32(2):163-8. PubMed ID: 25863077
    [Abstract] [Full Text] [Related]

  • 14. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
    Huang B, Han M, Wang G, Huang S, Zeng J, Yuan Y, Dai P.
    Int J Pediatr Otorhinolaryngol; 2018 May 15; 108():49-54. PubMed ID: 29605365
    [Abstract] [Full Text] [Related]

  • 15. Clinical and genetic characterization of a Chinese family with CSNB1.
    Sui R, Li F, Zhao J, Jiang R.
    Adv Exp Med Biol; 2008 May 15; 613():245-52. PubMed ID: 18188951
    [No Abstract] [Full Text] [Related]

  • 16. [Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].
    Peng GH, Zheng BJ, Fang F, Wu Y, Liang LZ, Zheng J, Nan BY, Yu X, Tang XW, Zhu Y, Lu JX, Chen BB, Guan MX.
    Yi Chuan; 2013 Jan 15; 35(1):62-72. PubMed ID: 23357266
    [Abstract] [Full Text] [Related]

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  • 19. [Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].
    Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug 15; 29(4):382-7. PubMed ID: 22875491
    [Abstract] [Full Text] [Related]

  • 20. Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.
    Wei Q, Xu D, Chen Z, Li H, Lu Y, Liu C, Bu X, Xing G, Cao X.
    Int J Audiol; 2013 Feb 15; 52(2):98-103. PubMed ID: 23237192
    [Abstract] [Full Text] [Related]

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