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 *

67 related articles for article (PubMed ID: 22735573)

  • 1. The mitochondrial T1095C mutation increases gentamicin-mediated apoptosis.
    Muyderman H; Sims NR; Tanaka M; Fuku N; Raghupathi R; Thyagarajan D
    Mitochondrion; 2012 Jul; 12(4):465-71. PubMed ID: 22735573
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.
    Thyagarajan D; Bressman S; Bruno C; Przedborski S; Shanske S; Lynch T; Fahn S; DiMauro S
    Ann Neurol; 2000 Nov; 48(5):730-6. PubMed ID: 11079536
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
    Scrimshaw BJ; Faed JM; Tate WP; Yun K
    J Hum Genet; 1999; 44(6):388-90. PubMed ID: 10570910
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Screening for the 1555G mutation in mitochondrial DNA in pedigrees with aminoglycoside antibiotic induced deafness].
    Yuan H; Jiang S; Yang W
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1998 Apr; 33(2):67-70. PubMed ID: 11498854
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Topical gentamicin-induced hearing loss: a mitochondrial ribosomal RNA study of genetic susceptibility.
    Chen JM; Williamson PA; Hutchin T; Nedzelski JM; Cortopassi GA
    Am J Otol; 1996 Nov; 17(6):850-2. PubMed ID: 8915412
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.
    Guan MX; Fischel-Ghodsian N; Attardi G
    Hum Mol Genet; 1996 Jul; 5(7):963-71. PubMed ID: 8817331
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
    Dai P; Yuan Y; Huang D; Qian Y; Liu X; Han D; Yuan H; Wang X; Young WY; Guan MX
    Biochem Biophys Res Commun; 2006 Sep; 348(1):200-5. PubMed ID: 16875663
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.
    Guo ZF; Guo WS; Xiao L; Gao GQ; Lan F; Lu XG; Li K; Liao DF
    Appl Biochem Biotechnol; 2012 Jan; 166(1):234-42. PubMed ID: 22068689
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.
    Prezant TR; Agapian JV; Bohlman MC; Bu X; Oztas S; Qiu WQ; Arnos KS; Cortopassi GA; Jaber L; Rotter JI
    Nat Genet; 1993 Jul; 4(3):289-94. PubMed ID: 7689389
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 368(3):631-6. PubMed ID: 18261986
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: a cybrid study.
    Chen J; Hattori Y; Nakajima K; Eizawa T; Ehara T; Koyama M; Hirai T; Fukuda Y; Kinoshita M; Sugiyama A; Hayashi J; Onaya T; Kobayashi T; Tawata M
    Diabetes Res Clin Pract; 2006 Nov; 74(2):148-53. PubMed ID: 16828917
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [An extensive matrilineal nonsyndromic sensorineural deafness family and mtDNA 12SrRNA gene mutation].
    Yan M; Liu N; Shan X; Xin G; Pu X; Wu J; Yang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):321-4. PubMed ID: 10514542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Maternally inherited deafness associated with a T1095C mutation in the mDNA.
    Tessa A; Giannotti A; Tieri L; Vilarinho L; Marotta G; Santorelli FM
    Eur J Hum Genet; 2001 Feb; 9(2):147-9. PubMed ID: 11313749
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.
    Wang Q; Li R; Zhao H; Peters JL; Liu Q; Yang L; Han D; Greinwald JH; Young WY; Guan MX
    Am J Med Genet A; 2005 Feb; 133A(1):27-30. PubMed ID: 15637703
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
    Brown MD; Allen JC; Van Stavern GP; Newman NJ; Wallace DC
    Am J Med Genet; 2001 Dec; 104(4):331-8. PubMed ID: 11754070
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH; Reddy PP
    Int J Audiol; 2008 Nov; 47(11):702-7. PubMed ID: 19031229
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells.
    Inoue K; Takai D; Soejima A; Isobe K; Yamasoba T; Oka Y; Goto Y; Hayashi J
    Biochem Biophys Res Commun; 1996 Jun; 223(3):496-501. PubMed ID: 8687424
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy.
    Mariotti C; Tiranti V; Carrara F; Dallapiccola B; DiDonato S; Zeviani M
    J Clin Invest; 1994 Mar; 93(3):1102-7. PubMed ID: 8132749
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The relation between mitochondrial DNA mutation and aminogly- coside antibiotics-induced deafness].
    Zhang L; Lu M; Huang Y; Zhou X; Qiu D; Wang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):138-40. PubMed ID: 10359860
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial rRNA and tRNA and hearing function.
    Xing G; Chen Z; Cao X
    Cell Res; 2007 Mar; 17(3):227-39. PubMed ID: 17199108
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.