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Journal Abstract Search

314 related items for PubMed ID: 20061330

  • 21. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis.
    Zeng Y, Takada Y, Kjellstrom S, Hiriyanna K, Tanikawa A, Wawrousek E, Smaoui N, Caruso R, Bush RA, Sieving PA.
    Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):3279-85. PubMed ID: 15326152
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  • 22. Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse.
    Park TK, Wu Z, Kjellstrom S, Zeng Y, Bush RA, Sieving PA, Colosi P.
    Gene Ther; 2009 Jul; 16(7):916-26. PubMed ID: 19458650
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  • 25. Genetic variations in the hotspot region of RS1 gene in Indian patients with juvenile X-linked retinoschisis.
    Suganthalakshmi B, Shukla D, Rajendran A, Kim R, Nallathambi J, Sundaresan P.
    Mol Vis; 2007 Apr 19; 13():611-7. PubMed ID: 17515881
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  • 29. Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 gene.
    Hayashi T, Omoto S, Takeuchi T, Kozaki K, Ueoka Y, Kitahara K.
    Am J Ophthalmol; 2004 Nov 19; 138(5):788-98. PubMed ID: 15531314
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  • 31. Clinical features of X linked juvenile retinoschisis in Chinese families associated with novel mutations in the RS1 gene.
    Li X, Ma X, Tao Y.
    Mol Vis; 2007 Jun 07; 13():804-12. PubMed ID: 17615541
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  • 33. Synaptic pathology in retinoschisis knockout (Rs1-/y) mouse retina and modification by rAAV-Rs1 gene delivery.
    Takada Y, Vijayasarathy C, Zeng Y, Kjellstrom S, Bush RA, Sieving PA.
    Invest Ophthalmol Vis Sci; 2008 Aug 07; 49(8):3677-86. PubMed ID: 18660429
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  • 37. Mouse models of X-linked juvenile retinoschisis have an early onset phenotype, the severity of which varies with genotype.
    Liu Y, Kinoshita J, Ivanova E, Sun D, Li H, Liao T, Cao J, Bell BA, Wang JM, Tang Y, Brydges S, Peachey NS, Sagdullaev BT, Romano C.
    Hum Mol Genet; 2019 Sep 15; 28(18):3072-3090. PubMed ID: 31174210
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  • 38. Retinal organoids with X-linked retinoschisis RS1 (E72K) mutation exhibit a photoreceptor developmental delay and are rescued by gene augmentation therapy.
    Duan C, Ding C, Sun X, Mao S, Liang Y, Liu X, Ding X, Chen J, Tang S.
    Stem Cell Res Ther; 2024 May 31; 15(1):152. PubMed ID: 38816767
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  • 39. Structural analysis of X-linked retinoschisis mutations reveals distinct classes which differentially effect retinoschisin function.
    Ramsay EP, Collins RF, Owens TW, Siebert CA, Jones RPO, Wang T, Roseman AM, Baldock C.
    Hum Mol Genet; 2016 Dec 15; 25(24):5311-5320. PubMed ID: 27798099
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