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

PUBMED FOR HANDHELDS

Journal Abstract Search

572 related items for PubMed ID: 16375862

  • 1. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
    Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 10; 340(2):583-8. PubMed ID: 16380089
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
    Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM.
    Biochem Biophys Res Commun; 2008 Apr 11; 368(3):631-6. PubMed ID: 18261986
    [Abstract] [Full Text] [Related]

  • 8. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].
    YANG AF, ZHENG J, LV JX, GUAN MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr 11; 28(2):165-71. PubMed ID: 21462128
    [Abstract] [Full Text] [Related]

  • 9. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
    Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Aug 11; 346(4):1131-5. PubMed ID: 16782057
    [Abstract] [Full Text] [Related]

  • 12. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
    Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX.
    Pharmacogenet Genomics; 2008 Dec 02; 18(12):1059-70. PubMed ID: 18820594
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.
    Liao Z, Zhao J, Zhu Y, Yang L, Yang A, Sun D, Zhao Z, Wang X, Tao Z, Tang X, Wang J, Guan M, Chen J, Li Z, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2007 Oct 26; 362(3):670-6. PubMed ID: 17723226
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
    Casano RA, Bykhovskaya Y, Johnson DF, Hamon M, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Med Genet; 1998 Oct 12; 79(5):388-91. PubMed ID: 9779807
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 29.