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 *

259 related articles for article (PubMed ID: 25999548)

  • 41. A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment.
    Wolf A; Frohne A; Allen M; Parzefall T; Koenighofer M; Schreiner MM; Schoefer C; Frei K; Lucas T
    Otol Neurotol; 2017 Feb; 38(2):173-179. PubMed ID: 27861301
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
    Bazazzadegan N; Nikzat N; Fattahi Z; Nishimura C; Meyer N; Sahraian S; Jamali P; Babanejad M; Kashef A; Yazdan H; Sabbagh Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Reyhanifar F; Nouri N; Smith RJ; Kahrizi K; Najmabadi H
    Int J Pediatr Otorhinolaryngol; 2012 Aug; 76(8):1164-74. PubMed ID: 22695344
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations.
    Wu CM; Ko HC; Tsou YT; Lin YH; Lin JL; Chen CK; Chen PL; Wu CC
    PLoS One; 2015; 10(9):e0138575. PubMed ID: 26397989
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients.
    de Moraes VC; dos Santos NZ; Ramos PZ; Svidnicki MC; Castilho AM; Sartorato EL
    Int J Pediatr Otorhinolaryngol; 2013 Mar; 77(3):410-3. PubMed ID: 23273637
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [DNA microarray screening analysis in children with profound hearing impairment in Hubei province].
    Zhan Y; Wu X; Hu Y; Huang X; Duan J; Chen H; Jin J; Li D; Xie W; Kong W
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2014 May; 28(10):680-4. PubMed ID: 25129964
    [TBL] [Abstract][Full Text] [Related]  

  • 46. GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness.
    Fang Y; Gu M; Wang C; Suo F; Wang G; Xia Y
    Cell Biochem Biophys; 2015 Sep; 73(1):41-4. PubMed ID: 25649612
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Analysis of p.V37I compound heterozygous mutations in the GJB2 gene in Chinese infants and young children.
    Du Y; Huang L; Cheng X; Zhao L; Ruan Y; Ni T
    Biosci Trends; 2016 Jul; 10(3):220-6. PubMed ID: 27350192
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population.
    Koohiyan M
    Int J Pediatr Otorhinolaryngol; 2019 Oct; 125():1-5. PubMed ID: 31228605
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [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]  

  • 51. [Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].
    Dai P; Han B; Yuan YY; Jin ZC; Wang Y; Xiang Y; Yu F; Liu X; Wang GJ; Kang DY; Zhang X; Li M; Zhai SQ; Huang DL; Han DY
    Zhonghua Yi Xue Za Zhi; 2007 Apr; 87(16):1088-92. PubMed ID: 17672986
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort.
    Carvalho SDCES; Grangeiro CHP; Picanço-Albuquerque CG; Dos Anjos TO; De Molfetta GA; Silva WA; Ferraz VEF
    BMC Res Notes; 2018 Aug; 11(1):546. PubMed ID: 30068397
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.
    Azadegan-Dehkordi F; Ahmadi R; Koohiyan M; Hashemzadeh-Chaleshtori M
    Ann Hum Genet; 2019 Jan; 83(1):1-10. PubMed ID: 30175840
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Screening of hot-spot deafness gene mutations among 277 cochlear implantation patients in Sichuan province].
    Jiang TF; Peng JJ; Zheng H; Chen XL; Kong WL
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Aug; 32(15):1177-1182. PubMed ID: 30282152
    [No Abstract]   [Full Text] [Related]  

  • 56. Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations.
    Moteki H; Naito Y; Fujiwara K; Kitoh R; Nishio SY; Oguchi K; Takumi Y; Usami S
    Acta Otolaryngol; 2011 Nov; 131(11):1232-6. PubMed ID: 21728752
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The responsible genes in Japanese deafness patients and clinical application using Invader assay.
    Usami S; Wagatsuma M; Fukuoka H; Suzuki H; Tsukada K; Nishio S; Takumi Y; Abe S
    Acta Otolaryngol; 2008 Apr; 128(4):446-54. PubMed ID: 18368581
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [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]  

  • 59. Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
    Riahi Z; Hammami H; Ouragini H; Messai H; Zainine R; Bouyacoub Y; Romdhane L; Essaid D; Kefi R; Rhimi M; Bedoui M; Dhaouadi A; Feldmann D; Jonard L; Besbes G; Abdelhak S
    Gene; 2013 Aug; 525(1):1-4. PubMed ID: 23680645
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.
    Wang ZT; Chen Y; Chen DY; Chai YC; Pang XH; Sun LH; Wang XW; Yang T; Wu H
    Int J Pediatr Otorhinolaryngol; 2014 Sep; 78(9):1513-6. PubMed ID: 25015771
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.