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Biorxiv : the Preprint Server for Biology
|
May 25, 2026
Clinically relevant AAV8- <i>PEX1</i> gene therapy preserves retinal integrity and function long-term in a murine model of Zellweger spectrum disorder
Samy Omri, Erminia Di Pietro, Devin S McDougald, et al.
Vision Research
|
April 2, 2003
Gene therapy for choroideremia: in vitro rescue mediated by recombinant adenovirus
Vibha Anand, Duarte C Barral, Yong Zeng, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy
Samuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 25, 2007
Gene transfer to ocular stem cells by early gestational intraamniotic injection of lentiviral vector
Masayuki Endo, Philip W Zoltick, Daniel C Chung, et al.
Molecular Therapy. Nucleic Acids
|
September 10, 2018
Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA
Scott J Dooley, Devin S McDougald, Krishna J Fisher, et al.
Molecular Vision
|
November 18, 2004
Effect of over-expression of pigment epithelium derived factor (PEDF) on developing retinal vasculature in the mouse
Wai T Wong, Tonia S Rex, Alberto Auricchio, et al.
Developmental Biology
|
November 11, 2008
Tie2Cre-mediated inactivation of plexinD1 results in congenital heart, vascular and skeletal defects
Ying Zhang, Manvendra K Singh, Karl R Degenhardt, et al.
The Journal of Gene Medicine
|
June 26, 2014
Adeno-associated virus 8-mediated gene therapy for choroideremia: preclinical studies in in vitro and in vivo models
Aaron Black, Vidyullatha Vasireddy, Daniel C Chung, et al.
Investigative Ophthalmology & Visual Science
|
July 29, 2003
Proapoptotic bcl-2 family members, Bax and Bak, are essential for developmental photoreceptor apoptosis
Paul Hahn, Tullia Lindsten, Gui-Shuang Ying, et al.
Ophthalmic Genetics
|
May 29, 2019
Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in <i>PNPLA6</i> mimicking choroideremia
Erin O'Neil, Leona Serrano, Drew Scoles, et al.
Page
of 18
Search research articles
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Showing results (71-80 of 175) with videos related to
Sort By:
Page
of 18
Biorxiv : the Preprint Server for Biology
|
May 25, 2026
Clinically relevant AAV8- <i>PEX1</i> gene therapy preserves retinal integrity and function long-term in a murine model of Zellweger spectrum disorder
Samy Omri, Erminia Di Pietro, Devin S McDougald, et al.
Vision Research
|
April 2, 2003
Gene therapy for choroideremia: in vitro rescue mediated by recombinant adenovirus
Vibha Anand, Duarte C Barral, Yong Zeng, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy
Samuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 25, 2007
Gene transfer to ocular stem cells by early gestational intraamniotic injection of lentiviral vector
Masayuki Endo, Philip W Zoltick, Daniel C Chung, et al.
Molecular Therapy. Nucleic Acids
|
September 10, 2018
Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA
Scott J Dooley, Devin S McDougald, Krishna J Fisher, et al.
Molecular Vision
|
November 18, 2004
Effect of over-expression of pigment epithelium derived factor (PEDF) on developing retinal vasculature in the mouse
Wai T Wong, Tonia S Rex, Alberto Auricchio, et al.
Developmental Biology
|
November 11, 2008
Tie2Cre-mediated inactivation of plexinD1 results in congenital heart, vascular and skeletal defects
Ying Zhang, Manvendra K Singh, Karl R Degenhardt, et al.
The Journal of Gene Medicine
|
June 26, 2014
Adeno-associated virus 8-mediated gene therapy for choroideremia: preclinical studies in in vitro and in vivo models
Aaron Black, Vidyullatha Vasireddy, Daniel C Chung, et al.
Investigative Ophthalmology & Visual Science
|
July 29, 2003
Proapoptotic bcl-2 family members, Bax and Bak, are essential for developmental photoreceptor apoptosis
Paul Hahn, Tullia Lindsten, Gui-Shuang Ying, et al.
Ophthalmic Genetics
|
May 29, 2019
Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in <i>PNPLA6</i> mimicking choroideremia
Erin O'Neil, Leona Serrano, Drew Scoles, et al.
Page
of 18