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Experimental Eye Research|October 5, 2017
Long-term photoreceptor rescue in two rodent models of retinitis pigmentosa by adeno-associated virus delivery of Stanniocalcin-1Gavin W Roddy, Douglas Yasumura, Michael T Matthes, et al.
European Journal of Clinical Investigation|December 22, 2006
Expression of the target receptor CD33 in CD34+/CD38-/CD123+ AML stem cellsA W Hauswirth, S Florian, D Printz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 21, 2010
Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by lightEkaterina S Lobanova, Rolf Herrmann, Stella Finkelstein, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 28, 2011
ACE2 and Ang-(1-7) confer protection against development of diabetic retinopathyAmrisha Verma, Zhiying Shan, Bo Lei, et al.
Gene Therapy|November 28, 2014
AAV-mediated and pharmacological induction of Hsp70 expression stimulates survival of retinal ganglion cells following axonal injuryJ M K Kwong, L Gu, N Nassiri, et al.
Annals of Hematology|May 28, 2011
Prolonged progression-free survival in patients with chronic lymphocytic leukemia receiving granulocyte colony-stimulating factor during treatment with fludarabine, cyclophosphamide, and rituximabMichaela Gruber, Karin Fleiss, Edit Porpaczy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 11, 2008
High-efficiency transduction of the mouse retina by tyrosine-mutant AAV serotype vectorsHilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.
Neurobiology of Aging|March 15, 2011
AAV5-mediated sFLT01 gene therapy arrests retinal lesions in Ccl2(-/-)/Cx3cr1(-/-) miceJingsheng Tuo, Ji-Jing Pang, Xiaoguang Cao, et al.
Cells|January 8, 2023
Identification of CD203c as a New Basophil-Specific Flow-Marker in Ph+ Chronic Myeloid LeukemiaIrina Sadovnik, Daniel Ivanov, Dubravka Smiljkovic, et al.
Molecular Vision|October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosisAlejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
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