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 *

149 related articles for article (PubMed ID: 23562982)

  • 21. Autosomal dominant auditory neuropathy and variant DIAPH3 (c.-173C>T).
    Sánchez-Martínez A; Benito-Orejas JI; Tellería-Orriols JJ; Alonso-Ramos MJ
    Acta Otorrinolaringol Esp (Engl Ed); 2017; 68(3):183-185. PubMed ID: 27658576
    [No Abstract]   [Full Text] [Related]  

  • 22. Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss.
    Lee J; Baek JI; Choi JY; Kim UK; Lee SH; Lee KY
    Gene; 2013 Dec; 532(2):276-80. PubMed ID: 23958653
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutations in the OTOF gene in Taiwanese patients with auditory neuropathy.
    Chiu YH; Wu CC; Lu YC; Chen PJ; Lee WY; Liu AY; Hsu CJ
    Audiol Neurootol; 2010; 15(6):364-74. PubMed ID: 20224275
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Targeted next generation sequencing reveals OTOF mutations in auditory neuropathy spectrum disorder.
    Chen K; Liu M; Wu X; Zong L; Jiang H
    Int J Pediatr Otorhinolaryngol; 2018 Dec; 115():19-23. PubMed ID: 30368385
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Preparing for Otoferlin gene therapy trials: A survey of NHS Paediatric Audiology and Cochlear Implant services on diagnosis and management of Auditory Neuropathy Spectrum Disorder.
    Spyridakou C; Chan J; Tan J; Clement E; Nash R; Hall A; Mehta N; Schilder AG
    Int J Pediatr Otorhinolaryngol; 2024 Feb; 177():111870. PubMed ID: 38290274
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families.
    Zhai R; Feng H; Li Q; Lu W; Liu D; Tian Y; Liu H; Li R; Zuo B; Tang W; Xu H; Chen B
    Biomed Res Int; 2020; 2020():8843539. PubMed ID: 33426078
    [TBL] [Abstract][Full Text] [Related]  

  • 27. ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy.
    Han KH; Oh DY; Lee S; Lee C; Han JH; Kim MY; Park HR; Park MK; Kim NKD; Lee J; Yi E; Kim JM; Kim JW; Chae JH; Oh SH; Park WY; Choi BY
    Sci Rep; 2017 Nov; 7(1):16504. PubMed ID: 29184165
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.
    Collin RW; Kalay E; Oostrik J; Caylan R; Wollnik B; Arslan S; den Hollander AI; Birinci Y; Lichtner P; Strom TM; Toraman B; Hoefsloot LH; Cremers CW; Brunner HG; Cremers FP; Karaguzel A; Kremer H
    Hum Mutat; 2007 Jul; 28(7):718-23. PubMed ID: 17373699
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel OTOF gene mutations identified using a massively parallel DNA sequencing technique in DFNB9 deafness.
    Wang Y; Lu Y; Cheng J; Zhang L; Han D; Yuan H
    Acta Otolaryngol; 2018 Oct; 138(10):865-870. PubMed ID: 30073893
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Auditory nerve disease and auditory neuropathy spectrum disorders.
    Kaga K
    Auris Nasus Larynx; 2016 Feb; 43(1):10-20. PubMed ID: 26209259
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans.
    Morlet T; Rabinowitz MR; Looney LR; Riegner T; Greenwood LA; Sherman EA; Achilly N; Zhu A; Yoo E; O'Reilly RC; Jinks RN; Puffenberger EG; Heaps A; Morton H; Strauss KA
    Laryngoscope; 2014 Mar; 124(3):E95-103. PubMed ID: 23946138
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing.
    Sun L; Lin Z; Zhang J; Shen J; Wang X; Yang J
    Front Neurol; 2022; 13():1026695. PubMed ID: 36570450
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A nonsense
    Jang MW; Oh DY; Yi E; Liu X; Ling J; Kim N; Sharma K; Kim TY; Lee S; Kim AR; Kim MY; Kim MA; Lee M; Han JH; Han JJ; Park HR; Kim BJ; Lee SY; Woo DH; Oh J; Oh SJ; Du T; Koo JW; Oh SH; Shin HW; Seong MW; Lee KY; Kim UK; Shin JB; Sang S; Cai X; Mei L; He C; Blanton SH; Chen ZY; Chen H; Liu X; Nourbakhsh A; Huang Z; Kang KW; Park WY; Feng Y; Lee CJ; Choi BY
    Proc Natl Acad Sci U S A; 2021 Jun; 118(22):. PubMed ID: 34050020
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.
    Woo HM; Park HJ; Park MH; Kim BY; Shin JW; Yoo WG; Koo SK
    BMC Med Genet; 2014 Apr; 15():46. PubMed ID: 24767429
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy.
    Wang DY; Wang YC; Weil D; Zhao YL; Rao SQ; Zong L; Ji YB; Liu Q; Li JQ; Yang HM; Shen Y; Benedict-Alderfer C; Zheng QY; Petit C; Wang QJ
    BMC Med Genet; 2010 May; 11():79. PubMed ID: 20504331
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutations.
    Li L; Xiao X; Li S; Jiao X; Hejtmancik JF; Zhang Q
    Mol Vis; 2011; 17():3326-32. PubMed ID: 22219627
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Central auditory maturation and behavioral outcomes after cochlear implantation in prelingual auditory neuropathy spectrum disorder related to OTOF variants (DFNB9): Lessons from pilot study.
    Lee SY; Han JH; Song HK; Kim NJ; Yi N; Kyong JS; Choi BY
    PLoS One; 2021; 16(6):e0252717. PubMed ID: 34097718
    [TBL] [Abstract][Full Text] [Related]  

  • 38. NADH improves AIF dimerization and inhibits apoptosis in iPSCs-derived neurons from patients with auditory neuropathy spectrum disorder.
    Qiu Y; Wang H; Pan H; Ding X; Guan J; Zhuang Q; Wu K; Lei Z; Cai H; Dong Y; Zhou H; Lin A; Wang Q; Yan Q
    Hear Res; 2024 Jan; 441():108919. PubMed ID: 38043402
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Temperature sensitive auditory neuropathy.
    Zhang Q; Lan L; Shi W; Yu L; Xie LY; Xiong F; Zhao C; Li N; Yin Z; Zong L; Guan J; Wang D; Sun W; Wang Q
    Hear Res; 2016 May; 335():53-63. PubMed ID: 26778470
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss.
    Sagong B; Baek JI; Bok J; Lee KY; Kim UK
    Int J Pediatr Otorhinolaryngol; 2016 Jan; 80():78-81. PubMed ID: 26746617
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.