BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 24941117)

  • 1. Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China.
    Xu BC; Bian PP; Liu XW; Zhu YM; Yang XL; Ma JL; Chen XJ; Wang YL; Guo YF
    Acta Otolaryngol; 2014 Sep; 134(9):924-9. PubMed ID: 24941117
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China.
    Duan SH; Zhu YM; Wang YL; Guo YF
    Acta Otolaryngol; 2015 Jun; 135(6):586-91. PubMed ID: 25761933
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China.
    Xin F; Yuan Y; Deng X; Han M; Wang G; Zhao J; Gao X; Liu J; Yu F; Han D; Dai P
    J Transl Med; 2013 Dec; 11():312. PubMed ID: 24341454
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Analysis of the hereditary etiology of 336 patients with non-syndromic sensorineural hearing loss from Ningxia Hui Autonomous Region of China].
    Wang YL; Zhu YM; Liu XW; Xu BC; Guo YF; Wang QJ
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep; 47(9):760-3. PubMed ID: 23141447
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 122():185-190. PubMed ID: 31035178
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.
    Jiang Y; Huang S; Deng T; Wu L; Chen J; Kang D; Xu X; Li R; Han D; Dai P
    PLoS One; 2015; 10(8):e0135088. PubMed ID: 26252218
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Analysis of deafness-related gene mutations in 100 non-syndromic hearing loss patients in Henan province].
    Yang A; Geng M; Zhang H; Guo X; Tang J; Han F
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1959-62. PubMed ID: 26911058
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Comparative analysis of the recurrent mutations between Uigur and Han ethnic deaf group in Xinjiang region of China].
    Li Q; Fang R; Huang D; Wang G; Liu X; Dai P
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Jan; 24(1):11-5. PubMed ID: 20235449
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Common gene mutations study in Uyghur population with deafness in Kashgar region of Xinjiang].
    Chen Y; Tudi M; Lu HL; Jiang D; Zhao J; Hu B; Kuyaxi P; Zhang H
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Mar; 46(3):205-8. PubMed ID: 21575411
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 108():49-54. PubMed ID: 29605365
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
    Qing J; Zhou Y; Lai R; Hu P; Ding Y; Wu W; Xiao Z; Ho PT; Liu Y; Liu J; Du L; Yan D; Goldstein BJ; Liu X; Xie D
    Genet Test Mol Biomarkers; 2015 Jan; 19(1):52-8. PubMed ID: 25493717
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
    Luo J; Bai X; Zhang F; Xiao Y; Gu L; Han Y; Fan Z; Li J; Xu L; Wang H
    Ann Hum Genet; 2017 Nov; 81(6):258-266. PubMed ID: 28786104
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China.
    Bian P; Xu B; Zhao X; Zhu Y; Chen C; Chen X; Liu X; Wang Y; Guo Y
    Inquiry; 2022; 59():469580211055571. PubMed ID: 35212567
    [No Abstract]   [Full Text] [Related]  

  • 14. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.
    Ji YB; Han DY; Lan L; Wang DY; Zong L; Zhao FF; Liu Q; Benedict-Alderfer C; Zheng QY; Wang QJ
    Acta Otolaryngol; 2011 Feb; 131(2):124-9. PubMed ID: 21162657
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic mutations in non-syndromic deafness patients of Uyghur and Han Chinese ethnicities in Xinjiang, China: a comparative study.
    Chen Y; Tudi M; Sun J; He C; Lu HL; Shang Q; Jiang D; Kuyaxi P; Hu B; Zhang H
    J Transl Med; 2011 Sep; 9():154. PubMed ID: 21917135
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].
    Ji YB; Han DY; Wang DY; Zhou Y; Zhao C; Wang H; Lan L; Wang QJ
    Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(36):2531-5. PubMed ID: 20137612
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.
    Pan J; Xu P; Tang W; Cui Z; Feng M; Wang C
    Int J Pediatr Otorhinolaryngol; 2017 Jul; 98():39-42. PubMed ID: 28583500
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India.
    Adhikary B; Ghosh S; Paul S; Bankura B; Pattanayak AK; Biswas S; Maity B; Das M
    Gene; 2015 Dec; 573(2):239-45. PubMed ID: 26188157
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].
    Yuan YY; Dai P; Zhu XH; Kang DY; Zhang X; Huang DL
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Apr; 44(4):292-6. PubMed ID: 19558834
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Epidemiological analysis of GJB2,SLC26A4,mtRNA,GJB3 in nonsyndromic hearing loss in Kashi in Xinjiang].
    Sun J; Chen Y; Zhang H; Wen H
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Apr; 31(8):619-622. PubMed ID: 29871328
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.