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J Fielding

Showing results (461-470 of 493) with videos related to

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Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 19, 2019
Heme binding to human CLOCK affects interactions with the E-boxSamuel L Freeman, Hanna Kwon, Nicola Portolano, et al.
Nature|December 5, 2008
Partial rupture of a locked patch of the Sumatra megathrust during the 2007 earthquake sequenceA Ozgun Konca, Jean-Philippe Avouac, Anthony Sladen, et al.
Plos One|September 10, 2015
Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome SequencingBruno Maranhao, Pooja Biswas, Alexander D H Gottsch, et al.
The British Journal of Ophthalmology|April 18, 2015
Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopiaThomas Chassine, Béatrice Bocquet, Vincent Daien, et al.
Science (New York, N.Y.)|July 12, 2014
Heme enzymes. Neutron cryo-crystallography captures the protonation state of ferryl heme in a peroxidaseCecilia M Casadei, Andrea Gumiero, Clive L Metcalfe, et al.
American Journal of Preventive Medicine|May 12, 2000
Developing the Guide to Community Preventive Services--overview and rationale. The Task Force on Community Preventive ServicesB I Truman, C K Smith-Akin, A R Hinman, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Analysis of ocular hypopigmentation in Rab38cht/cht miceBrian P Brooks, Denise M Larson, Chi-Chao Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 28, 2009
Expression profiling during ocular development identifies 2 Nlz genes with a critical role in optic fissure closureJacob D Brown, Sunit Dutta, Kapil Bharti, et al.
American Journal of Human Genetics|May 11, 2010
A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosaS Amer Riazuddin, Muhammad Iqbal, Yue Wang, et al.
Pageof 50

Showing results (461-470 of 493) with videos related to

Sort By:
Pageof 50
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 19, 2019
Heme binding to human CLOCK affects interactions with the E-boxSamuel L Freeman, Hanna Kwon, Nicola Portolano, et al.
Nature|December 5, 2008
Partial rupture of a locked patch of the Sumatra megathrust during the 2007 earthquake sequenceA Ozgun Konca, Jean-Philippe Avouac, Anthony Sladen, et al.
Plos One|September 10, 2015
Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome SequencingBruno Maranhao, Pooja Biswas, Alexander D H Gottsch, et al.
The British Journal of Ophthalmology|April 18, 2015
Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopiaThomas Chassine, Béatrice Bocquet, Vincent Daien, et al.
Science (New York, N.Y.)|July 12, 2014
Heme enzymes. Neutron cryo-crystallography captures the protonation state of ferryl heme in a peroxidaseCecilia M Casadei, Andrea Gumiero, Clive L Metcalfe, et al.
American Journal of Preventive Medicine|May 12, 2000
Developing the Guide to Community Preventive Services--overview and rationale. The Task Force on Community Preventive ServicesB I Truman, C K Smith-Akin, A R Hinman, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Analysis of ocular hypopigmentation in Rab38cht/cht miceBrian P Brooks, Denise M Larson, Chi-Chao Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 28, 2009
Expression profiling during ocular development identifies 2 Nlz genes with a critical role in optic fissure closureJacob D Brown, Sunit Dutta, Kapil Bharti, et al.
American Journal of Human Genetics|May 11, 2010
A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosaS Amer Riazuddin, Muhammad Iqbal, Yue Wang, et al.
Pageof 50