BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 24831256)

  • 1. Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
    Rong W; Chen X; Zhao K; Liu Y; Liu X; Ha S; Liu W; Kang X; Sheng X; Zhao C
    PLoS One; 2014; 9(5):e97808. PubMed ID: 24831256
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology.
    Qu LH; Jin X; Xu HW; Li SY; Yin ZQ
    Mol Genet Genomics; 2015 Feb; 290(1):353-63. PubMed ID: 25252889
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder.
    Xia H; Hu P; Yuan L; Xiong W; Xu H; Yi J; Yang Z; Deng X; Guo Y; Deng H
    Mol Med Rep; 2017 Oct; 16(4):4241-4246. PubMed ID: 28731162
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.
    Liu F; Li P; Liu Y; Li W; Wong F; Du R; Wang L; Li C; Jiang F; Tang Z; Liu M
    Mol Vis; 2013; 19():695-701. PubMed ID: 23559863
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genotype-phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials.
    Galbis-Martínez L; Blanco-Kelly F; García-García G; Ávila-Fernández A; Jaijo T; Fuster-García C; Perea-Romero I; Zurita-Muñoz O; Jimenez-Rolando B; Carreño E; García-Sandoval B; Millán JM; Ayuso C
    Acta Ophthalmol; 2021 Dec; 99(8):922-930. PubMed ID: 33576163
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.
    Ben-Rebeh I; Grati M; Bonnet C; Bouassida W; Hadjamor I; Ayadi H; Ghorbel A; Petit C; Masmoudi S
    Mol Vis; 2016; 22():827-35. PubMed ID: 27440999
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family.
    Gao X; Wang GJ; Yuan YY; Xin F; Han MY; Lu JQ; Zhao H; Yu F; Xu JC; Zhang MG; Dong J; Lin X; Dai P
    PLoS One; 2014; 9(7):e103415. PubMed ID: 25080338
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
    Kumar A; Babu M; Kimberling WJ; Venkatesh CP
    Mol Vis; 2004 Nov; 10():910-6. PubMed ID: 15592175
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations.
    Eandi CM; Dallorto L; Spinetta R; Micieli MP; Vanzetti M; Mariottini A; Passerini I; Torricelli F; Alovisi C; Marchese C
    Sci Rep; 2017 Nov; 7(1):15681. PubMed ID: 29142287
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree.
    Kooshavar D; Razipour M; Movasat M; Keramatipour M
    Int J Pediatr Otorhinolaryngol; 2018 Jan; 104():10-13. PubMed ID: 29287847
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Compound heterozygous MYO7A mutations segregating Usher syndrome type 2 in a Han family.
    Zong L; Chen K; Wu X; Liu M; Jiang H
    Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():150-155. PubMed ID: 27729122
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1.
    Nakanishi H; Ohtsubo M; Iwasaki S; Hotta Y; Takizawa Y; Hosono K; Mizuta K; Mineta H; Minoshima S
    J Hum Genet; 2010 Dec; 55(12):796-800. PubMed ID: 20844544
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.
    Khalaileh A; Abu-Diab A; Ben-Yosef T; Raas-Rothschild A; Lerer I; Alswaiti Y; Chowers I; Banin E; Sharon D; Khateb S
    Invest Ophthalmol Vis Sci; 2018 Feb; 59(2):1095-1104. PubMed ID: 29490346
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family.
    He X; Peng Q; Li S; Zhu P; Wu C; Rao C; Lin J; Lu X
    Int J Pediatr Otorhinolaryngol; 2017 Aug; 99():40-43. PubMed ID: 28688563
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndrome.
    Ouarhache M; Kettani O; Fizazi KE; Bouguenouch L; Ouldim K
    Mol Biol Rep; 2024 May; 51(1):683. PubMed ID: 38796585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel mutations in the USH1C gene in Usher syndrome patients.
    Aparisi MJ; García-García G; Jaijo T; Rodrigo R; Graziano C; Seri M; Simsek T; Simsek E; Bernal S; Baiget M; Pérez-Garrigues H; Aller E; Millán JM
    Mol Vis; 2010 Dec; 16():2948-54. PubMed ID: 21203349
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
    Ben Rebeh I; Morinière M; Ayadi L; Benzina Z; Charfedine I; Feki J; Ayadi H; Ghorbel A; Baklouti F; Masmoudi S
    Mol Vis; 2010 Sep; 16():1898-906. PubMed ID: 21031134
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome.
    Sodi A; Mariottini A; Passerini I; Murro V; Tachyla I; Bianchi B; Menchini U; Torricelli F
    Mol Vis; 2014; 20():1717-31. PubMed ID: 25558175
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations.
    Ramzan K; Al-Owain M; Huma R; Al-Hazzaa SAF; Al-Ageel S; Imtiaz F; Al-Sayed M
    Int J Pediatr Otorhinolaryngol; 2018 May; 108():17-21. PubMed ID: 29605349
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss.
    Shahzad M; Sivakumaran TA; Qaiser TA; Schultz JM; Hussain Z; Flanagan M; Bhinder MA; Kissell D; Greinwald JH; Khan SN; Friedman TB; Zhang K; Riazuddin S; Riazuddin S; Ahmed ZM
    Otolaryngol Head Neck Surg; 2013 Sep; 149(3):478-87. PubMed ID: 23770805
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.