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 *

145 related articles for article (PubMed ID: 30173967)

  • 41. Genetics of non syndromic hearing loss in the republic of macedonia.
    Sukarova Stefanovska E; Cakar M; Filipce I; Plaseska Karanfilska D
    Balkan J Med Genet; 2012 Dec; 15(Suppl):57-9. PubMed ID: 24052745
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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; 340(2):583-8. PubMed ID: 16380089
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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; 340(1):194-9. PubMed ID: 16375862
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Rapid screening for the mitochondrial DNA C1494T mutation in a deaf population in China using real-time quantitative PCR.
    Li Q; Yuan YY; Huang DL; Han DY; Dai P
    Acta Otolaryngol; 2012 Aug; 132(8):814-8. PubMed ID: 22497215
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Genetic and clinical analysis of nonsyndromic hearing impairment in pediatric and adult cases.
    Xing J; Liu X; Tian Y; Tan J; Zhao H
    Balkan J Med Genet; 2016 Jul; 19(1):35-42. PubMed ID: 27785406
    [TBL] [Abstract][Full Text] [Related]  

  • 46. GJB2 sequencing in deaf and profound sensorineural hearing loss children.
    Mielczarek M; Zakrzewska A; Olszewski J
    Otolaryngol Pol; 2016 Jun; 70(3):21-5. PubMed ID: 27386929
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.
    Vivero RJ; Ouyang X; Yan D; Du L; Liu W; Angeli SI; Liu XZ
    Genet Test Mol Biomarkers; 2012 Sep; 16(9):1146-8. PubMed ID: 22853457
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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; 79(5):388-91. PubMed ID: 9779807
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Novel mutations affecting the secondary structure of MT-RNR1 gene: a causal relationship with profound nonsyndromic hearing impairment.
    Padma G; Ramchander PV; Nandur VU; Kumar KR; Padma T
    Genet Test Mol Biomarkers; 2012 Sep; 16(9):1092-7. PubMed ID: 22852811
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Pharmacogenetic screening of A1555G and C1494T mitochondrial mutations and the use of ototoxic drugs among Jordanians.
    Yehya A; Al-Trad B; Bani-Hmoud M; Rababa'h AM
    Eur Rev Med Pharmacol Sci; 2021 Sep; 25(18):5684-5689. PubMed ID: 34604960
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.
    Maniglia LP; Moreira BCL; da Silva MAOM; Piatto VB; Maniglia JV
    Braz J Otorhinolaryngol; 2008; 74(5):731-736. PubMed ID: 19082356
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment.
    Hutchin TP; Parker MJ; Young ID; Davis AC; Pulleyn LJ; Deeble J; Lench NJ; Markham AF; Mueller RF
    J Med Genet; 2000 Sep; 37(9):692-4. PubMed ID: 10978361
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Mitochondrial DNA A1555G mutation analysis in 802 nonsyndromic hearing impairment patients].
    Liu XW; Guo YF; Han DY; Zhao YL; Lan L; Zhao C; Wang QJ
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Oct; 42(10):739-42. PubMed ID: 18229583
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.
    Guaran V; Astolfi L; Castiglione A; Simoni E; Olivetto E; Galasso M; Trevisi P; Busi M; Volinia S; Martini A
    Int J Mol Med; 2013 Oct; 32(4):785-94. PubMed ID: 23969527
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Molecular genetic analysis of mitochondrial DNA C1494T mutation in non-syndromic hearing loss of Chinese population].
    Tian G; Liu YH; Ma YN; Li YJ; Zhang Y; Niu SL; Xu YE; Pei P; Wang ST; Bu DF; Du BR; Zhou X; Ke XM; Qi Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):464-6. PubMed ID: 17680545
    [TBL] [Abstract][Full Text] [Related]  

  • 56. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
    Postal M; Palodeto B; Sartorato EL; Oliveira CA
    Braz J Otorhinolaryngol; 2009; 75(6):884-7. PubMed ID: 20209292
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss.
    Fassad MR; Desouky LM; Asal S; Abdalla EM
    Int J Mol Epidemiol Genet; 2014; 5(4):200-4. PubMed ID: 25755848
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel multiplex primer extension and denaturing high-performance liquid chromatography for genotyping of the deafness gene mutations.
    Men M; Xue J; Jiang L; Wang H; Pan Q; Feng Y
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Nov; 36(11):1079-84. PubMed ID: 22169721
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Molecular study of hearing loss in Minas Gerais, Brazil.
    Schüffner ROA; Nascimento KL; Dias FA; Silva PHTD; Pires WGB; Cipriano NM; Santos LLD
    Braz J Otorhinolaryngol; 2020; 86(3):327-331. PubMed ID: 30837189
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.