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 *

402 related articles for article (PubMed ID: 32995707)

  • 21. Genetic screening revealed usher syndrome in a paediatric Chinese patient.
    Qu C; Liang F; Long Q; Zhao M; Shang H; Fan L; Wang L; Foster J; Yan D; Liu X
    Hearing Balance Commun; 2017; 15(2):98-106. PubMed ID: 30800556
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular updates on Usher syndrome].
    Roux AF
    J Fr Ophtalmol; 2005 Jan; 28(1):93-7. PubMed ID: 15767904
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Current updates on genetic spectrum of usher syndrome.
    Ullah F; Zeeshan Ali M; Ahmad S; Muzammal M; Khan S; Khan J; Ahmad Khan M
    Nucleosides Nucleotides Nucleic Acids; 2024 May; ():1-24. PubMed ID: 38718411
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bardet-Biedl syndrome and Usher syndrome.
    Koenig R
    Dev Ophthalmol; 2003; 37():126-40. PubMed ID: 12876834
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic Testing Leading to Early Identification of Childhood Ocular Manifestations of Usher Syndrome.
    Brodie KD; Moore AT; Slavotinek AM; Meyer AK; Nadaraja GS; Conrad DE; Weinstein JE; Chan DK
    Laryngoscope; 2021 Jun; 131(6):E2053-E2059. PubMed ID: 33111992
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Usher Syndrome: Genetics and Molecular Links of Hearing Loss and Directions for Therapy.
    Whatley M; Francis A; Ng ZY; Khoh XE; Atlas MD; Dilley RJ; Wong EYM
    Front Genet; 2020; 11():565216. PubMed ID: 33193648
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Disease mechanisms and gene therapy for Usher syndrome.
    Géléoc GGS; El-Amraoui A
    Hear Res; 2020 Sep; 394():107932. PubMed ID: 32199721
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.
    Rosenberg T; Haim M; Hauch AM; Parving A
    Clin Genet; 1997 May; 51(5):314-21. PubMed ID: 9212179
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.
    Aller E; Jaijo T; Oltra S; Alió J; Galán F; Nájera C; Beneyto M; Millán JM
    Clin Genet; 2004 Dec; 66(6):525-9. PubMed ID: 15521980
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa.
    Pieke-Dahl S; Ohlemiller KK; McGee J; Walsh EJ; Kimberling WJ
    Hear Res; 1997 Oct; 112(1-2):1-12. PubMed ID: 9367224
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Molecular genetic study of Usher syndrome in Spain].
    Jaijo T; Aller E; Beneyto M; Nájera C; Millán JM
    Acta Otorrinolaringol Esp; 2005; 56(7):285-9. PubMed ID: 16240916
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel mutations in MYO7A and USH2A in Usher syndrome.
    Maubaret C; Griffoin JM; Arnaud B; Hamel C
    Ophthalmic Genet; 2005 Mar; 26(1):25-9. PubMed ID: 15823922
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A Review of Gene, Drug and Cell-Based Therapies for Usher Syndrome.
    French LS; Mellough CB; Chen FK; Carvalho LS
    Front Cell Neurosci; 2020; 14():183. PubMed ID: 32733204
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotypic characterization of retinitis pigmentosa associated with deafness.
    Paredes ÁC; López G; Gelvez N; Tamayo ML
    Biomedica; 2022 May; 42(Sp. 1):130-143. PubMed ID: 35866736
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The retinal phenotype of Usher syndrome: pathophysiological insights from animal models.
    El-Amraoui A; Petit C
    C R Biol; 2014 Mar; 337(3):167-77. PubMed ID: 24702843
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the
    Zhang L; Cheng J; Zhou Q; Khan MA; Fu J; Duan C; Sun S; Lv H; Fu J
    Front Genet; 2020; 11():422. PubMed ID: 32425987
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic Screening of the Usher Syndrome in Cuba.
    Santana EE; Fuster-García C; Aller E; Jaijo T; García-Bohórquez B; García-García G; Millán JM; Lantigua A
    Front Genet; 2019; 10():501. PubMed ID: 31231422
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dual-AAV vector-mediated expression of
    Lau SC; Grati M; Isgrig K; Sinan M; Calabro KR; Zhu J; Ishibashi Y; Ozgur Z; Wafa T; Belyantseva IA; Fitzgerald T; Friedman TB; Boye SL; Boye SE; Chien WW
    Mol Ther Methods Clin Dev; 2023 Sep; 30():534-545. PubMed ID: 37693946
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.