BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 28918053)

  • 21. The USH2A c.2299delG mutation: dating its common origin in a Southern European population.
    Aller E; Larrieu L; Jaijo T; Baux D; Espinós C; González-Candelas F; Nájera C; Palau F; Claustres M; Roux AF; Millán JM
    Eur J Hum Genet; 2010 Jul; 18(7):788-93. PubMed ID: 20145675
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The usher syndromes.
    Keats BJ; Corey DP
    Am J Med Genet; 1999 Sep; 89(3):158-66. PubMed ID: 10704190
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
    Ebermann I; Scholl HP; Charbel Issa P; Becirovic E; Lamprecht J; Jurklies B; Millán JM; Aller E; Mitter D; Bolz H
    Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. CRISPR/Cas9: targeted genome editing for the treatment of hereditary hearing loss.
    Farooq R; Hussain K; Tariq M; Farooq A; Mustafa M
    J Appl Genet; 2020 Feb; 61(1):51-65. PubMed ID: 31912450
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
    Aparisi MJ; Aller E; Fuster-García C; García-García G; Rodrigo R; Vázquez-Manrique RP; Blanco-Kelly F; Ayuso C; Roux AF; Jaijo T; Millán JM
    Orphanet J Rare Dis; 2014 Nov; 9():168. PubMed ID: 25404053
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The CRISPR/Cas9 system produces specific and homozygous targeted gene editing in rice in one generation.
    Zhang H; Zhang J; Wei P; Zhang B; Gou F; Feng Z; Mao Y; Yang L; Zhang H; Xu N; Zhu JK
    Plant Biotechnol J; 2014 Aug; 12(6):797-807. PubMed ID: 24854982
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Site-directed mutagenesis in Petunia × hybrida protoplast system using direct delivery of purified recombinant Cas9 ribonucleoproteins.
    Subburaj S; Chung SJ; Lee C; Ryu SM; Kim DH; Kim JS; Bae S; Lee GJ
    Plant Cell Rep; 2016 Jul; 35(7):1535-44. PubMed ID: 26825596
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Detecting novel mutations and combined Klinefelter syndrome in Usher syndrome cases.
    Li X; Huang S; Yuan Y; Lu Y; Zhang D; Wang X; Yuan H; Han W; Dai P
    Acta Otolaryngol; 2019 Jun; 139(6):479-486. PubMed ID: 31035849
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CRISPR/Cas9-mediated genome editing of splicing mutation causing congenital hearing loss.
    Ryu N; Kim MA; Choi DG; Kim YR; Sonn JK; Lee KY; Kim UK
    Gene; 2019 Jun; 703():83-90. PubMed ID: 30898719
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. A Simple and Universal System for Gene Manipulation in
    Al Abdallah Q; Ge W; Fortwendel JR
    mSphere; 2017; 2(6):. PubMed ID: 29202040
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Efficient DNA-free genome editing of bread wheat using CRISPR/Cas9 ribonucleoprotein complexes.
    Liang Z; Chen K; Li T; Zhang Y; Wang Y; Zhao Q; Liu J; Zhang H; Liu C; Ran Y; Gao C
    Nat Commun; 2017 Jan; 8():14261. PubMed ID: 28098143
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG Mutation.
    Calzetti G; Levy RA; Cideciyan AV; Garafalo AV; Roman AJ; Sumaroka A; Charng J; Heon E; Jacobson SG
    Am J Ophthalmol; 2018 Sep; 193():114-129. PubMed ID: 29953849
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CRISPR/Cas9; A robust technology for producing genetically engineered plants.
    Farooq R; Hussain K; Nazir S; Javed MR; Masood N
    Cell Mol Biol (Noisy-le-grand); 2018 Nov; 64(14):31-38. PubMed ID: 30511631
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gene Therapy with CRISPR/Cas9 Coming to Age for HIV Cure.
    Soriano V
    AIDS Rev; 2017; 19(3):167-172. PubMed ID: 29019352
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Use of RNA-Protein Complexes for Genome Editing in Non-
    Grahl N; Demers EG; Crocker AW; Hogan DA
    mSphere; 2017; 2(3):. PubMed ID: 28657070
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two Distinct Approaches for CRISPR-Cas9-Mediated Gene Editing in Cryptococcus neoformans and Related Species.
    Wang P
    mSphere; 2018 Jun; 3(3):. PubMed ID: 29898980
    [No Abstract]   [Full Text] [Related]  

  • 39. Insertional Mutagenesis by CRISPR/Cas9 Ribonucleoprotein Gene Editing in Cells Targeted for Point Mutation Repair Directed by Short Single-Stranded DNA Oligonucleotides.
    Rivera-Torres N; Banas K; Bialk P; Bloh KM; Kmiec EB
    PLoS One; 2017; 12(1):e0169350. PubMed ID: 28052104
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.