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Related Citations for PubMed (Select 10915776)


Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells.

Grayson C, Reid SN, Ellis JA, Rutherford A, Sowden JC, Yates JR, Farber DB, Trump D.

Hum Mol Genet. 2000 Jul 22;9(12):1873-9.


Retinoschisin, a photoreceptor-secreted protein, and its interaction with bipolar and muller cells.

Reid SN, Yamashita C, Farber DB.

J Neurosci. 2003 Jul 9;23(14):6030-40.


Expression of X-linked retinoschisis protein RS1 in photoreceptor and bipolar cells.

Molday LL, Hicks D, Sauer CG, Weber BH, Molday RS.

Invest Ophthalmol Vis Sci. 2001 Mar;42(3):816-25.


A retinal neuronal developmental wave of retinoschisin expression begins in ganglion cells during layer formation.

Takada Y, Fariss RN, Tanikawa A, Zeng Y, Carper D, Bush R, Sieving PA.

Invest Ophthalmol Vis Sci. 2004 Sep;45(9):3302-12.


Retinoschisin expression and localization in rodent and human pineal and consequences of mouse RS1 gene knockout.

Takada Y, Fariss RN, Muller M, Bush RA, Rushing EJ, Sieving PA.

Mol Vis. 2006 Sep 28;12:1108-16.


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.


Intracellular retention of mutant retinoschisin is the pathological mechanism underlying X-linked retinoschisis.

Wang T, Waters CT, Rothman AM, Jakins TJ, Römisch K, Trump D.

Hum Mol Genet. 2002 Nov 15;11(24):3097-105.


Retinoschisin is a peripheral membrane protein with affinity for anionic phospholipids and affected by divalent cations.

Vijayasarathy C, Takada Y, Zeng Y, Bush RA, Sieving PA.

Invest Ophthalmol Vis Sci. 2007 Mar;48(3):991-1000.


Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis.

Min SH, Molday LL, Seeliger MW, Dinculescu A, Timmers AM, Janssen A, Tonagel F, Tanimoto N, Weber BH, Molday RS, Hauswirth WW.

Mol Ther. 2005 Oct;12(4):644-51.


X-linked retinoschisis: a clinical and molecular genetic review.

Tantri A, Vrabec TR, Cu-Unjieng A, Frost A, Annesley WH Jr, Donoso LA.

Surv Ophthalmol. 2004 Mar-Apr;49(2):214-30. Review.


The Na/K-ATPase is obligatory for membrane anchorage of retinoschisin, the protein involved in the pathogenesis of X-linked juvenile retinoschisis.

Friedrich U, Stöhr H, Hilfinger D, Loenhardt T, Schachner M, Langmann T, Weber BH.

Hum Mol Genet. 2011 Mar 15;20(6):1132-42. doi: 10.1093/hmg/ddq557. Epub 2010 Dec 31.


Cell-specific expression of tubby gene family members (tub, Tulp1,2, and 3) in the retina.

Ikeda S, He W, Ikeda A, Naggert JK, North MA, Nishina PM.

Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2706-12.


CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene.

Langmann T, Lai CC, Weigelt K, Tam BM, Warneke-Wittstock R, Moritz OL, Weber BH.

Nucleic Acids Res. 2008 Nov;36(20):6523-34. doi: 10.1093/nar/gkn737. Epub 2008 Oct 16.


Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease.

Vijayasarathy C, Sui R, Zeng Y, Yang G, Xu F, Caruso RC, Lewis RA, Ziccardi L, Sieving PA.

Hum Mutat. 2010 Nov;31(11):1251-60. doi: 10.1002/humu.21350.


Truncation of retinoschisin protein associated with a novel splice site mutation in the RS1 gene.

Lesch B, Szabó V, Kánya M, Varsányi B, Somfai GM, Hargitai J, Vámos R, Fiedler O, Farkas A.

Mol Vis. 2008 Aug 25;14:1549-58.

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