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 *

177 related articles for article (PubMed ID: 36225977)

  • 1. A Novel Missense
    Ma J; Wang R; Zhang L; Wang S; Tong S; Bai X; Lu Z
    Biomed Res Int; 2022; 2022():5068869. PubMed ID: 36225977
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.
    Guan J; Wang H; Lan L; Wu Y; Chen G; Zhao C; Wang D; Wang Q
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1367. PubMed ID: 32567228
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.
    Niu Z; Feng Y; Hu Z; Li J; Sun J; Chen H; He C; Wang X; Jiang L; Liu Y; Cai X; Wang L; Cai Y; Liu X; Mei L
    Int J Pediatr Otorhinolaryngol; 2017 Sep; 100():1-7. PubMed ID: 28802351
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment.
    Tsai HT; Wang YP; Chung SF; Lin HC; Ho GM; Shu MT
    BMC Med Genet; 2007 May; 8():26. PubMed ID: 17517145
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss.
    Sun Y; Cheng J; Lu Y; Li J; Lu Y; Jin Z; Dai P; Wang R; Yuan H
    J Genet Genomics; 2011 Feb; 38(2):71-6. PubMed ID: 21356526
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.
    Bespalova IN; Van Camp G; Bom SJ; Brown DJ; Cryns K; DeWan AT; Erson AE; Flothmann K; Kunst HP; Kurnool P; Sivakumaran TA; Cremers CW; Leal SM; Burmeister M; Lesperance MM
    Hum Mol Genet; 2001 Oct; 10(22):2501-8. PubMed ID: 11709537
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese.
    Fukuoka H; Kanda Y; Ohta S; Usami SI
    J Hum Genet; 2007; 52(6):510-515. PubMed ID: 17492394
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Missense Variant of Endoplasmic Reticulum Region of
    Li J; Xu H; Sun J; Tian Y; Liu D; Qin Y; Liu H; Li R; Neng L; Deng X; Xue B; Yu C; Tang W
    Biomed Res Int; 2021; 2021():6624744. PubMed ID: 34258273
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings.
    Bramhall NF; Kallman JC; Verrall AM; Street VA
    BMC Med Genet; 2008 Jun; 9():48. PubMed ID: 18518985
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype and Phenotype Analyses of a Novel
    Velde HM; Huizenga XJJ; Yntema HG; Haer-Wigman L; Beynon AJ; Oostrik J; Pegge SAH; Kremer H; Lanting CP; Pennings RJE
    Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833385
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family.
    Komatsu K; Nakamura N; Ghadami M; Matsumoto N; Kishino T; Ohta T; Niikawa N; Yoshiura K
    J Hum Genet; 2002; 47(8):395-9. PubMed ID: 12181639
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WFS1 and GJB2 mutations in patients with bilateral low-frequency sensorineural hearing loss.
    Kasakura-Kimura N; Masuda M; Mutai H; Masuda S; Morimoto N; Ogahara N; Misawa H; Sakamoto H; Saito K; Matsunaga T
    Laryngoscope; 2017 Sep; 127(9):E324-E329. PubMed ID: 28271504
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1.
    Hildebrand MS; Sorensen JL; Jensen M; Kimberling WJ; Smith RJ
    Am J Med Genet A; 2008 Sep; 146A(17):2258-65. PubMed ID: 18688868
    [TBL] [Abstract][Full Text] [Related]  

  • 14. WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case.
    Gonçalves AC; Matos TD; Simões-Teixeira HR; Pimenta Machado M; Simão M; Dias OP; Andrea M; Fialho G; Caria H
    Gene; 2014 Apr; 538(2):288-91. PubMed ID: 24462758
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a novel missense mutation in the WFS1 gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequencies.
    Bai X; Lv H; Zhang F; Liu J; Fan Z; Xu L; Han Y; Chai R; Li J; Wang H
    Am J Med Genet A; 2014 Dec; 164A(12):3052-60. PubMed ID: 25250959
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A PCR-RFLP assay for the A716T mutation in the WFS1 gene, a common cause of low-frequency sensorineural hearing loss.
    Sivakumaran TA; Lesperance MM
    Genet Test; 2002; 6(3):229-31. PubMed ID: 12490066
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.
    Noguchi Y; Yashima T; Hatanaka A; Uzawa M; Yasunami M; Kimura A; Kitamura K
    Acta Otolaryngol; 2005 Nov; 125(11):1189-94. PubMed ID: 16353398
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel
    Li Q; Liang P; Wang S; Li W; Wang J; Yang Y; An X; Chen J; Zha D
    Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33846771
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel WFS1 mutations in patients with low-to-middle frequency hearing loss.
    Guo L; Gu X; Sun Q; Zhang Y; Li H; Du Q
    Int J Pediatr Otorhinolaryngol; 2023 Apr; 167():111484. PubMed ID: 36958120
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss.
    Wang M; Zhou Y; Zhang F; Fan Z; Bai X; Wang H
    BMC Med Genet; 2020 Jul; 21(1):154. PubMed ID: 32711451
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.