BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

220 related articles for article (PubMed ID: 30826590)

  • 21. 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]  

  • 22. Genetics of Usher Syndrome: New Insights From a Meta-analysis.
    Jouret G; Poirsier C; Spodenkiewicz M; Jaquin C; Gouy E; Arndt C; Labrousse M; Gaillard D; Doco-Fenzy M; Lebre AS
    Otol Neurotol; 2019 Jan; 40(1):121-129. PubMed ID: 30531642
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Searching for evidence of DFNB2.
    Astuto LM; Kelley PM; Askew JW; Weston MD; Smith RJ; Alswaid AF; Al-Rakaf M; Kimberling WJ
    Am J Med Genet; 2002 May; 109(4):291-7. PubMed ID: 11992483
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.
    Niepokój K; Rygiel AM; Jurczak P; Kujko AA; Śniegórska D; Sawicka J; Grabarczyk A; Bal J; Wertheim-Tysarowska K
    J Appl Genet; 2018 Feb; 59(1):67-72. PubMed ID: 29151245
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Variation analysis of genes associated with Usher syndrome type 1 in 136 Chinese deafness families].
    Ren SM; Wu QH; Chen YB; Jiao ZH; Kong XD
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Mar; 56(3):236-241. PubMed ID: 33730806
    [No Abstract]   [Full Text] [Related]  

  • 26. Genetic screening of Russian Usher syndrome patients toward selection for gene therapy.
    Ivanova ME; Trubilin VN; Atarshchikov DS; Demchinsky AM; Strelnikov VV; Tanas AS; Orlova OM; Machalov AS; Overchenko KV; Markova TV; Golenkova DM; Anoshkin KI; Volodin IV; Zaletaev DV; Pulin AA; Nadelyaeva II; Kalinkin AI; Barh D
    Ophthalmic Genet; 2018 Dec; 39(6):706-713. PubMed ID: 30358468
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Assessment of different virus-mediated approaches for retinal gene therapy of Usher 1B.
    Lopes VS; Diemer T; Williams DS
    Adv Exp Med Biol; 2014; 801():725-31. PubMed ID: 24664764
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Third-generation lentiviral gene therapy rescues function in a mouse model of Usher 1B.
    Schott JW; Huang P; Morgan M; Nelson-Brantley J; Koehler A; Renslo B; Büning H; Warnecke A; Schambach A; Staecker H
    Mol Ther; 2023 Dec; 31(12):3502-3519. PubMed ID: 37915173
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I.
    Oshima A; Jaijo T; Aller E; Millan JM; Carney C; Usami S; Moller C; Kimberling WJ
    Hum Mutat; 2008 Jun; 29(6):E37-46. PubMed ID: 18429043
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spectrum of
    Kabahuma RI; Schubert WD; Labuschagne C; Yan D; Blanton SH; Pepper MS; Liu XZ
    Genes (Basel); 2021 Feb; 12(2):. PubMed ID: 33671976
    [No Abstract]   [Full Text] [Related]  

  • 32. 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]  

  • 33. Identification of a novel compound heterozygous pathogenic variant in
    Zhang Y; Guo X; Hao L; Tian M; Ma Y; Tang Y
    J Int Med Res; 2023 Dec; 51(12):3000605231218924. PubMed ID: 38141656
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population.
    Souissi A; Ben Said M; Ben Ayed I; Elloumi I; Bouzid A; Mosrati MA; Hasnaoui M; Belcadhi M; Idriss N; Kamoun H; Gharbi N; Gibriel AA; Tlili A; Masmoudi S
    J Adv Res; 2021 Jul; 31():13-24. PubMed ID: 34194829
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B.
    Hashimoto T; Gibbs D; Lillo C; Azarian SM; Legacki E; Zhang XM; Yang XJ; Williams DS
    Gene Ther; 2007 Apr; 14(7):584-94. PubMed ID: 17268537
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A.
    Lopes VS; Williams DS
    Cold Spring Harb Perspect Med; 2015 Jan; 5(6):. PubMed ID: 25605753
    [TBL] [Abstract][Full Text] [Related]  

  • 37. New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family.
    Lin Q; Yang D; Shen Z; Zhou X
    Int Ophthalmol; 2023 Jun; 43(6):2091-2099. PubMed ID: 36484953
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of a novel MYO7A mutation in Usher syndrome type 1.
    Cheng L; Yu H; Jiang Y; He J; Pu S; Li X; Zhang L
    Oncotarget; 2018 Jan; 9(2):2295-2303. PubMed ID: 29416772
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.
    Libby RT; Steel KP
    Invest Ophthalmol Vis Sci; 2001 Mar; 42(3):770-8. PubMed ID: 11222540
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.