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 *

162 related articles for article (PubMed ID: 28790396)

  • 1. A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss.
    Lin YH; Lin YH; Lu YC; Liu TC; Chen CY; Hsu CJ; Chen PL; Wu CC
    Sci Rep; 2017 Aug; 7(1):7551. PubMed ID: 28790396
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families.
    Bai X; Zhang F; Xiao Y; Jin Y; Zheng Q; Wang H; Xu L
    J Cell Mol Med; 2020 Jun; 24(12):6978-6987. PubMed ID: 32390314
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Missense Mutation in
    Gao X; Xu JC; Wang WQ; Yuan YY; Bai D; Huang SS; Wang GJ; Su Y; Li J; Kang DY; Zhang MG; Lin X; Dai P
    Biomed Res Int; 2018; 2018():5370802. PubMed ID: 29850532
    [TBL] [Abstract][Full Text] [Related]  

  • 4. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss.
    Kitano T; Miyagawa M; Nishio SY; Moteki H; Oda K; Ohyama K; Miyazaki H; Hidaka H; Nakamura KI; Murata T; Matsuoka R; Ohta Y; Nishiyama N; Kumakawa K; Furutate S; Iwasaki S; Yamada T; Ohta Y; Uehara N; Noguchi Y; Usami SI
    PLoS One; 2017; 12(5):e0177636. PubMed ID: 28545070
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Missense
    Bai D; Zhang X; Li Y; Ni J; Lan K
    Biomed Res Int; 2021; 2021():5574136. PubMed ID: 34250087
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.
    Cai XZ; Li Y; Xia L; Peng Y; He CF; Jiang L; Feng Y; Xia K; Liu XZ; Mei LY; Hu ZM
    J Hum Genet; 2017 Feb; 62(2):317-320. PubMed ID: 27535032
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Four Novel Variants in
    Cui TY; Gao X; Huang SS; Sun YY; Zhang SQ; Jiang XX; Yang YZ; Kang DY; Zhu QW; Yuan YY
    Neural Plast; 2020; 2020():6137083. PubMed ID: 32684921
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding.
    Collin RW; Chellappa R; Pauw RJ; Vriend G; Oostrik J; van Drunen W; Huygen PL; Admiraal R; Hoefsloot LH; Cremers FP; Xiang M; Cremers CW; Kremer H
    Hum Mutat; 2008 Apr; 29(4):545-54. PubMed ID: 18228599
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation in the Hair Cell Specific Gene
    He L; Pang X; Chen P; Wu H; Yang T
    Neural Plast; 2016; 2016():9890827. PubMed ID: 28053790
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss.
    Freitas ÉL; Oiticica J; Silva AG; Bittar RS; Rosenberg C; Mingroni-Netto RC
    Eur J Med Genet; 2014 Mar; 57(4):125-8. PubMed ID: 24556497
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.
    Lee HK; Park HJ; Lee KY; Park R; Kim UK
    Biochem Biophys Res Commun; 2010 Jun; 396(3):626-30. PubMed ID: 20434433
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The DFNA15 deafness mutation affects POU4F3 protein stability, localization, and transcriptional activity.
    Weiss S; Gottfried I; Mayrose I; Khare SL; Xiang M; Dawson SJ; Avraham KB
    Mol Cell Biol; 2003 Nov; 23(22):7957-64. PubMed ID: 14585957
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Novel Nonsense Mutation of
    Zhang C; Wang M; Xiao Y; Zhang F; Zhou Y; Li J; Zheng Q; Bai X; Wang H
    Neural Plast; 2016; 2016():1512831. PubMed ID: 27999687
    [No Abstract]   [Full Text] [Related]  

  • 14. Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects.
    Lee SY; Kim MY; Han JH; Park SS; Yun Y; Jee SC; Han JJ; Lee JH; Seok H; Choi BY
    Sci Rep; 2023 Aug; 13(1):12584. PubMed ID: 37537203
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).
    Kim HJ; Won HH; Park KJ; Hong SH; Ki CS; Cho SS; Venselaar H; Vriend G; Kim JW
    PLoS One; 2013; 8(11):e79063. PubMed ID: 24260153
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses.
    Singh S; Penney C; Griffin A; Woodland G; Werdyani S; Benteau TA; Abdelfatah N; Squires J; King B; Houston J; Dyer MJ; Roslin NM; Vincent D; Marquis P; O'Rielly DD; Hodgkinson K; Burt T; Baker A; Stanton SG; Young TL
    Eur J Hum Genet; 2023 Jul; 31(7):815-823. PubMed ID: 37072551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.
    de Heer AM; Huygen PL; Collin RW; Kremer H; Cremers CW
    Ann Otol Rhinol Laryngol; 2009 Apr; 118(4):313-20. PubMed ID: 19462854
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.
    Pauw RJ; van Drunen FJ; Collin RW; Huygen PL; Kremer H; Cremers CW
    Arch Otolaryngol Head Neck Surg; 2008 Mar; 134(3):294-300. PubMed ID: 18347256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
    Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T
    Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.