BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 35249537)

  • 1. A newly identified mutation (c.2029 C > T) in SLC26A4 gene is associated with enlarged vestibular aqueducts in a Chinese family.
    Wu T; Cui L; Mou Y; Guo W; Liu D; Qiu J; Xu C; Zhou J; Han F; Sun Y
    BMC Med Genomics; 2022 Mar; 15(1):49. PubMed ID: 35249537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Compound heterozygous variants of the SLC26A4 gene in a Chinese family with enlarged vestibular aqueducts.
    He X; Zhao S; Shi L; Lu Y; Yang Y; Zhang X
    BMC Med Genomics; 2022 Jul; 15(1):152. PubMed ID: 35804348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.
    Liang Y; Peng Q; Wang K; Zhu P; Wu C; Rao C; Chang J; Li S; Lu X
    Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():97-100. PubMed ID: 29501320
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct.
    Wang M; Zhang F; Xu L; Xiao Y; Li J; Fan Z; Sun Q; Bai X; Wang H
    Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():170-174. PubMed ID: 27729126
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct.
    Zhao X; Cheng X; Huang L; Wang X; Wen C; Wang X
    Biosci Trends; 2018; 12(5):502-506. PubMed ID: 30473558
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct.
    He X; Peng Q; Li S; Zhu P; Wu C; Rao C; Chang J; Xie M; Zhong B; Lu X
    Int J Pediatr Otorhinolaryngol; 2017 Apr; 95():104-108. PubMed ID: 28576516
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome.
    Zhang F; Bai X; Xiao Y; Zhang X; Zhang G; Li J; Xu L; Wang H
    Int J Pediatr Otorhinolaryngol; 2016 Jun; 85():75-9. PubMed ID: 27240500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.
    Huang S; Han D; Yuan Y; Wang G; Kang D; Zhang X; Yan X; Meng X; Dong M; Dai P
    J Transl Med; 2011 Sep; 9():167. PubMed ID: 21961810
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel compound heterozygous mutation of SLC26A4 in two Chinese families with nonsyndromic hearing loss and enlarged vestibular aqueducts.
    Zhu GJ; Shi LS; Zhou H; Yang Y; Chen J; Gao X
    Mol Med Rep; 2017 Dec; 16(6):9011-9016. PubMed ID: 28990112
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel SLC26A4 splicing mutation identified in two deaf Chinese twin sisters with enlarged vestibular aqueducts.
    Zhou K; Huang L; Feng M; Li X; Zhao Y; Liu F; Wei J; Qin D; Lu Q; Shi M; Qu S; Tang F
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1447. PubMed ID: 32770655
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct.
    Yao G; Li S; Chen D; Wang H; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
    Int J Pediatr Otorhinolaryngol; 2013 Apr; 77(4):544-9. PubMed ID: 23385134
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.
    Pang X; Chai Y; Chen P; He L; Wang X; Wu H; Yang T
    Int J Pediatr Otorhinolaryngol; 2015 Aug; 79(8):1351-3. PubMed ID: 26100058
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China.
    Yuan Y; Guo W; Tang J; Zhang G; Wang G; Han M; Zhang X; Yang S; He DZ; Dai P
    PLoS One; 2012; 7(11):e49984. PubMed ID: 23185506
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enlarged vestibular aqueduct: Audiological and genetical features in children and adolescents.
    Aimoni C; Ciorba A; Cerritelli L; Ceruti S; Skarżyński PH; Hatzopoulos S
    Int J Pediatr Otorhinolaryngol; 2017 Oct; 101():254-258. PubMed ID: 28780189
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Investigation of DFNB4 SLC26A4 mutation in patients with enlarged vestibular aquaduct.
    Kınoğlu K; Orhan KS; Kara H; Öztürk O; Polat B; Aydoğan H; Çelik M; Ceviz AB; Güldiken Y
    Int J Pediatr Otorhinolaryngol; 2020 Nov; 138():110379. PubMed ID: 33152970
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mutation analysis and prenatal diagnosis for 12 families affected with hereditary hearing loss and enlarged vestibular aqueduct].
    Xiang Y; Li H; Xu X; Xu C; Chen C; Lin X; Tang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):336-341. PubMed ID: 28604950
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families.
    Liu Y; Wen J; Sang S; Mei L; He C; Jiang L; Huang S; Feng Y
    Eur Arch Otorhinolaryngol; 2020 Dec; 277(12):3331-3339. PubMed ID: 32447495
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
    Muskett JA; Chattaraj P; Heneghan JF; Reimold FR; Shmukler BE; Brewer CC; King KA; Zalewski CK; Shawker TH; Butman JA; Kenna MA; Chien WW; Alper SL; Griffith AJ
    Laryngoscope; 2016 Jul; 126(7):E240-7. PubMed ID: 26485571
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss.
    Okamoto Y; Mutai H; Nakano A; Arimoto Y; Sugiuchi T; Masuda S; Morimoto N; Sakamoto H; Ogahara N; Takagi A; Taiji H; Kaga K; Ogawa K; Matsunaga T
    Laryngoscope; 2014 Apr; 124(4):E134-40. PubMed ID: 24105851
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Identification of a novel mutation of SLC26A4 gene with enlarged vestibular aqueduct syndrome].
    Chen J; Shi LS; Zhou H; Zhu GJ; Ma DB; Li JY; Gao X
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 May; 31(9):694-696. PubMed ID: 29871349
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.