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Bo Chang

Showing results (281-290 of 290) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|October 15, 2005
Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosisJi-jing Pang, Bo Chang, Ashok Kumar, et al.
Human Molecular Genetics|April 25, 2006
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouseBo Chang, Hemant Khanna, Norman Hawes, et al.
Molecular Vision|January 11, 2007
Tool from ancient pharmacopoeia prevents vision lossJeffrey H Boatright, Anisha G Moring, Clinton McElroy, et al.
Visual Neuroscience|April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesBo Chang, John R Heckenlively, Philippa R Bayley, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 2020
Chronic Dicer1 deficiency promotes atrophic and neovascular outer retinal pathologies in miceCharles B Wright, Hironori Uehara, Younghee Kim, et al.
Virology|May 13, 2015
Genomic characterization of emergent pseudorabies virus in China reveals marked sequence divergence: Evidence for the existence of two major genotypesChao Ye, Qing-Zhan Zhang, Zhi-Jun Tian, et al.
The Journal of Physiology|August 9, 2008
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responsesDennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.
American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 2010
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 miceJames S Friedman, Bo Chang, Daniel S Krauth, et al.
Genome Research|April 29, 2015
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disordersHeather Fairfield, Anuj Srivastava, Guruprasad Ananda, et al.
Pageof 29

Showing results (281-290 of 290) with videos related to

Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 290 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 15, 2005
Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosisJi-jing Pang, Bo Chang, Ashok Kumar, et al.
Human Molecular Genetics|April 25, 2006
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouseBo Chang, Hemant Khanna, Norman Hawes, et al.
Molecular Vision|January 11, 2007
Tool from ancient pharmacopoeia prevents vision lossJeffrey H Boatright, Anisha G Moring, Clinton McElroy, et al.
Visual Neuroscience|April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesBo Chang, John R Heckenlively, Philippa R Bayley, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 2020
Chronic Dicer1 deficiency promotes atrophic and neovascular outer retinal pathologies in miceCharles B Wright, Hironori Uehara, Younghee Kim, et al.
Virology|May 13, 2015
Genomic characterization of emergent pseudorabies virus in China reveals marked sequence divergence: Evidence for the existence of two major genotypesChao Ye, Qing-Zhan Zhang, Zhi-Jun Tian, et al.
The Journal of Physiology|August 9, 2008
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responsesDennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.
American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 2010
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 miceJames S Friedman, Bo Chang, Daniel S Krauth, et al.
Genome Research|April 29, 2015
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disordersHeather Fairfield, Anuj Srivastava, Guruprasad Ananda, et al.
Pageof 29