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Todd E Scheetz

Showing results (31-40 of 129) with videos related to

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Journal of Glaucoma|June 16, 2023
Thrombospondin Mutations and Patients With Primary Congenital Glaucoma in a United States PopulationErin A Boese, Wallace L M Alward, Young H Kwon, et al.
Current Biology : CB|February 6, 2004
Migration of the plastid genome to the nucleus in a peridinin dinoflagellateJeremiah D Hackett, Hwan Su Yoon, M Bento Soares, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
A Hyperactive Transposase Promotes Persistent Gene Transfer of a piggyBac DNA TransposonErin R Burnight, Janice M Staber, Pavel Korsakov, et al.
Medical Research Archives|February 20, 2018
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the EyeKatie Weihbrecht, Wesley A Goar, Thomas Pak, et al.
Scientific Reports|October 21, 2016
Corrigendum: Automated Axon Counting in Rodent Optic Nerve Sections with AxonJKasra Zarei, Todd E Scheetz, Mark Christopher, et al.
Scientific Reports|May 27, 2016
Automated Axon Counting in Rodent Optic Nerve Sections with AxonJKasra Zarei, Todd E Scheetz, Mark Christopher, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2010
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencingA Eliot Shearer, Adam P DeLuca, Michael S Hildebrand, et al.
Molecular Vision|April 13, 2017
LADD syndrome with glaucoma is caused by a novel geneAllie Simpson, Armin Avdic, Ben R Roos, et al.
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Ophthalmic Genetics|September 27, 2017
Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphismKathleen R Chirco, Carly J Lewis, Todd E Scheetz, et al.
Pageof 13

Showing results (31-40 of 129) with videos related to

Sort By:
Pageof 13
Journal of Glaucoma|June 16, 2023
Thrombospondin Mutations and Patients With Primary Congenital Glaucoma in a United States PopulationErin A Boese, Wallace L M Alward, Young H Kwon, et al.
Current Biology : CB|February 6, 2004
Migration of the plastid genome to the nucleus in a peridinin dinoflagellateJeremiah D Hackett, Hwan Su Yoon, M Bento Soares, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
A Hyperactive Transposase Promotes Persistent Gene Transfer of a piggyBac DNA TransposonErin R Burnight, Janice M Staber, Pavel Korsakov, et al.
Medical Research Archives|February 20, 2018
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the EyeKatie Weihbrecht, Wesley A Goar, Thomas Pak, et al.
Scientific Reports|October 21, 2016
Corrigendum: Automated Axon Counting in Rodent Optic Nerve Sections with AxonJKasra Zarei, Todd E Scheetz, Mark Christopher, et al.
Scientific Reports|May 27, 2016
Automated Axon Counting in Rodent Optic Nerve Sections with AxonJKasra Zarei, Todd E Scheetz, Mark Christopher, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2010
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencingA Eliot Shearer, Adam P DeLuca, Michael S Hildebrand, et al.
Molecular Vision|April 13, 2017
LADD syndrome with glaucoma is caused by a novel geneAllie Simpson, Armin Avdic, Ben R Roos, et al.
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Ophthalmic Genetics|September 27, 2017
Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphismKathleen R Chirco, Carly J Lewis, Todd E Scheetz, et al.
Pageof 13