BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 21385326)

  • 1. Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.
    Furuta T; Teranishi M; Uchida Y; Nishio N; Kato K; Otake H; Yoshida T; Tagaya M; Suzuki H; Sugiura M; Sone M; Hiramatsu M; Sugiura S; Ando F; Shimokata H; Nakashima T
    Int J Immunogenet; 2011 Jun; 38(3):249-54. PubMed ID: 21385326
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.
    Teranishi M; Uchida Y; Nishio N; Kato K; Otake H; Yoshida T; Suzuki H; Sone M; Sugiura S; Ando F; Shimokata H; Nakashima T
    Free Radic Res; 2013 Jul; 47(6-7):498-506. PubMed ID: 23560644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss.
    Nishio N; Teranishi M; Uchida Y; Sugiura S; Ando F; Shimokata H; Sone M; Otake H; Kato K; Yoshida T; Tagaya M; Hibi T; Nakashima T
    Life Sci; 2013 Mar; 92(10):541-6. PubMed ID: 23352976
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population.
    Teranishi M; Uchida Y; Nishio N; Kato K; Otake H; Yoshida T; Suzuki H; Sone M; Sugiura S; Ando F; Shimokata H; Nakashima T
    DNA Cell Biol; 2012 Oct; 31(10):1555-62. PubMed ID: 22877234
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interleukin-1 gene cluster polymorphism in chagas disease in a Colombian case-control study.
    Flórez O; Zafra G; Morillo C; Martín J; González CI
    Hum Immunol; 2006 Sep; 67(9):741-8. PubMed ID: 17002905
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss.
    Uchida Y; Sugiura S; Ando F; Shimokata H; Nakashima T
    Laryngoscope; 2010 Apr; 120(4):791-5. PubMed ID: 20213658
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study.
    Uchida Y; Sugiura S; Nakashima T; Ando F; Shimokata H
    J Neurogenet; 2011 Oct; 25(3):82-7. PubMed ID: 21756056
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polymorphisms in genes involved in inflammatory pathways in patients with sudden sensorineural hearing loss.
    Hiramatsu M; Teranishi M; Uchida Y; Nishio N; Suzuki H; Kato K; Otake H; Yoshida T; Tagaya M; Suzuki H; Sone M; Sugiura S; Ando F; Shimokata H; Nakashima T
    J Neurogenet; 2012 Sep; 26(3-4):387-96. PubMed ID: 22385075
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Proinflammatory cytokine IL-1 β polymorphisms in sudden sensorineural hearing loss.
    Um JY; Jang CH; Kim HL; Cho YB; Park J; Lee SJ; Kim YB; Kim HJ; Ahn KS; Jang HJ; Lee SG; Lee H; Lee KM; Kim SJ; Hong SH
    Immunopharmacol Immunotoxicol; 2013 Feb; 35(1):52-6. PubMed ID: 23013363
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Glutathione s-transferase gene polymorphisms in Italian patients with sudden sensorineural hearing loss.
    Cadoni G; Boccia S; Scipione S; Arzani D; Cianfagna F; Ricciardi G; Paludetti G; Agostino S
    Otol Neurotol; 2006 Dec; 27(8):1166-9. PubMed ID: 16788422
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.
    Nishio N; Teranishi M; Uchida Y; Sugiura S; Ando F; Shimokata H; Sone M; Otake H; Kato K; Yoshida T; Tagaya M; Hibi T; Nakashima T
    Gene; 2012 May; 499(1):226-30. PubMed ID: 22426290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Steroid combination therapy and detoxification enzyme gene polymorphisms in sudden sensorineural hearing loss patients.
    Um JY; Jang CH; Kim SJ; Kim HL; Kim SY; Cho YB; Hong SH
    Otol Neurotol; 2011 Jul; 32(5):872-6. PubMed ID: 21389901
    [TBL] [Abstract][Full Text] [Related]  

  • 13. MICA-STR A.4 is associated with slower hearing loss progression in patients with Ménière's disease.
    Gazquez I; Moreno A; Aran I; Soto-Varela A; Santos S; Perez-Garrigues H; Lopez-Nevot A; Requena T; Lopez-Nevot MA; Lopez-Escamez JA
    Otol Neurotol; 2012 Feb; 33(2):223-9. PubMed ID: 22222578
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term middle ear pressure measurements in inner ear disorders.
    Park JJ; Luecke K; Luedeke I; Emmerling O; Westhofen M
    Acta Otolaryngol; 2012 Mar; 132(3):266-70. PubMed ID: 22201452
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of Obstructive Sleep Apnea With the Risk of Ménière's Disease and Sudden Sensorineural Hearing Loss: A Study Using Data From the Korean National Health Insurance Service.
    Kim JY; Ko I; Cho BJ; Kim DK
    J Clin Sleep Med; 2019 Sep; 15(9):1293-1301. PubMed ID: 31538600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case-control study on proinflammatory genetic polymorphisms on sudden sensorineural hearing loss.
    Cadoni G; Gaetani E; Picciotti PM; Arzani D; Quarta M; Giannantonio S; Paludetti G; Boccia S
    Laryngoscope; 2015 Jan; 125(1):E28-32. PubMed ID: 25345762
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Detection of humoral immune response to inner ear proteins in patients with sensorineural hearing loss].
    Naumann A; Hempel JM; Schorn K
    Laryngorhinootologie; 2001 May; 80(5):237-44. PubMed ID: 11417244
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chronic kidney disease is associated with increased risk of sudden sensorineural hearing loss and Ménière's disease: a nationwide cohort study.
    Kim JY; Lee S; Cha J; Son G; Kim DK
    Sci Rep; 2021 Oct; 11(1):20194. PubMed ID: 34642430
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Coexistence of IL-6 -572C/G and ICAM-1 K469E Polymorphisms among Patients with Sudden Sensorineural Hearing Loss.
    Tian G; Zhang S; Yang J
    Tohoku J Exp Med; 2018 May; 245(1):7-12. PubMed ID: 29695657
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
    Usami S; Takahashi K; Yuge I; Ohtsuka A; Namba A; Abe S; Fransen E; Patthy L; Otting G; Van Camp G
    Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.