BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 28918053)

  • 1. USH2A Gene Editing Using the CRISPR System.
    Fuster-García C; García-García G; González-Romero E; Jaijo T; Sequedo MD; Ayuso C; Vázquez-Manrique RP; Millán JM; Aller E
    Mol Ther Nucleic Acids; 2017 Sep; 8():529-541. PubMed ID: 28918053
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome Editing in Patient iPSCs Corrects the Most Prevalent
    Sanjurjo-Soriano C; Erkilic N; Baux D; Mamaeva D; Hamel CP; Meunier I; Roux AF; Kalatzis V
    Mol Ther Methods Clin Dev; 2020 Jun; 17():156-173. PubMed ID: 31909088
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells.
    Liu X; Lillywhite J; Zhu W; Huang Z; Clark AM; Gosstola N; Maguire CT; Dykxhoorn D; Chen ZY; Yang J
    Genes (Basel); 2021 May; 12(6):. PubMed ID: 34070435
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments.
    Aller E; Nájera C; Millán JM; Oltra JS; Pérez-Garrigues H; Vilela C; Navea A; Beneyto M
    Eur J Hum Genet; 2004 May; 12(5):407-10. PubMed ID: 14970843
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The effect of the common c.2299delG mutation in USH2A on RNA splicing.
    Lenassi E; Saihan Z; Bitner-Glindzicz M; Webster AR
    Exp Eye Res; 2014 May; 122():9-12. PubMed ID: 24607488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Natural history of Usher type 2 with the c.2299delG mutation of
    Meunier A; Zanlonghi X; Roux AF; Fils JF; Caspers L; Migeotte I; Abramowicz M; Meunier I
    Ophthalmic Genet; 2022 Aug; 43(4):470-475. PubMed ID: 35345973
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation.
    Slijkerman RW; Vaché C; Dona M; García-García G; Claustres M; Hetterschijt L; Peters TA; Hartel BP; Pennings RJ; Millan JM; Aller E; Garanto A; Collin RW; Kremer H; Roux AF; Van Wijk E
    Mol Ther Nucleic Acids; 2016 Nov; 5(10):e381. PubMed ID: 27802265
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In Vivo Assessment of Potential Therapeutic Approaches for USH2A-Associated Diseases.
    Pendse ND; Lamas V; Pawlyk BS; Maeder ML; Chen ZY; Pierce EA; Liu Q
    Adv Exp Med Biol; 2019; 1185():91-96. PubMed ID: 31884594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II.
    Dreyer B; Brox V; Tranebjaerg L; Rosenberg T; Sadeghi AM; Möller C; Nilssen O
    Hum Mutat; 2008 Mar; 29(3):451. PubMed ID: 18273898
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.
    Dreyer B; Tranebjaerg L; Brox V; Rosenberg T; Möller C; Beneyto M; Weston MD; Kimberling WJ; Cremers CW; Liu XZ; Nilssen O
    Am J Hum Genet; 2001 Jul; 69(1):228-34. PubMed ID: 11402400
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Usher syndrome in Denmark: mutation spectrum and some clinical observations.
    Dad S; Rendtorff ND; Tranebjærg L; Grønskov K; Karstensen HG; Brox V; Nilssen Ø; Roux AF; Rosenberg T; Jensen H; Møller LB
    Mol Genet Genomic Med; 2016 Sep; 4(5):527-539. PubMed ID: 27957503
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational spectrum in Usher syndrome type II.
    Ouyang XM; Hejtmancik JF; Jacobson SG; Li AR; Du LL; Angeli S; Kaiser M; Balkany T; Liu XZ
    Clin Genet; 2004 Apr; 65(4):288-93. PubMed ID: 15025721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
    Reiners J; Nagel-Wolfrum K; Jürgens K; Märker T; Wolfrum U
    Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New CRISPR Tools to Correct Pathogenic Mutations in Usher Syndrome.
    Major L; McClements ME; MacLaren RE
    Int J Mol Sci; 2022 Oct; 23(19):. PubMed ID: 36232969
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectrum of mutations in USH2A in British patients with Usher syndrome type II.
    Leroy BP; Aragon-Martin JA; Weston MD; Bessant DA; Willis C; Webster AR; Bird AC; Kimberling WJ; Payne AM; Bhattacharya SS
    Exp Eye Res; 2001 May; 72(5):503-9. PubMed ID: 11311042
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of intragenic USH2A copy number variation unveils broad spectrum of unique and recurrent variants.
    Austin-Tse CA; Mandelker DL; Oza AM; Mason-Suares H; Rehm HL; Amr SS
    Eur J Med Genet; 2018 Oct; 61(10):621-626. PubMed ID: 29655801
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.
    Jiang L; Liang X; Li Y; Wang J; Zaneveld JE; Wang H; Xu S; Wang K; Wang B; Chen R; Sui R
    Orphanet J Rare Dis; 2015 Sep; 10():110. PubMed ID: 26338283
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa.
    Hartel BP; Löfgren M; Huygen PL; Guchelaar I; Lo-A-Njoe Kort N; Sadeghi AM; van Wijk E; Tranebjærg L; Kremer H; Kimberling WJ; Cremers CW; Möller C; Pennings RJ
    Hear Res; 2016 Sep; 339():60-8. PubMed ID: 27318125
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report.
    Zhou C; Xiao Y; Xie H; Liu S; Wang J
    BMC Med Genomics; 2021 Aug; 14(1):200. PubMed ID: 34376197
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High-efficient and precise base editing of C•G to T•A in the allotetraploid cotton (Gossypium hirsutum) genome using a modified CRISPR/Cas9 system.
    Qin L; Li J; Wang Q; Xu Z; Sun L; Alariqi M; Manghwar H; Wang G; Li B; Ding X; Rui H; Huang H; Lu T; Lindsey K; Daniell H; Zhang X; Jin S
    Plant Biotechnol J; 2020 Jan; 18(1):45-56. PubMed ID: 31116473
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.