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H Lazar

Showing results (71-80 of 85) with videos related to

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Genome Biology|December 19, 2014
Conserved syntenic clusters of protein coding genes are missing in birdsPeter V Lovell, Morgan Wirthlin, Larry Wilhelm, et al.
Pathogens (Basel, Switzerland)|November 24, 2020
COVID-19 as a Trigger of Recurrent Guillain-Barré SyndromeErin P McDonnell, Nicole J Altomare, Yesha H Parekh, et al.
Genome Research|June 20, 2018
Epigenetic maintenance of topological domains in the highly rearranged gibbon genomeNathan H Lazar, Kimberly A Nevonen, Brendan O'Connell, et al.
Investigative Ophthalmology & Visual Science|December 18, 2014
Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in IsraelCsilla H Lazar, Mousumi Mutsuddi, Adva Kimchi, et al.
Plos Computational Biology|October 1, 2024
Building, benchmarking, and exploring perturbative maps of transcriptional and morphological dataSafiye Celik, Jan-Christian Hütter, Sandra Melo Carlos, et al.
American Journal of Respiratory Cell and Molecular Biology|August 17, 2004
Plasminogen activator inhibitor-1 impairs alveolar epithelial repair by binding to vitronectinMichael H Lazar, Paul J Christensen, Ming Du, et al.
Nature Genetics|May 29, 2024
High-resolution genome-wide mapping of chromosome-arm-scale truncations induced by CRISPR-Cas9 editingNathan H Lazar, Safiye Celik, Lu Chen, et al.
American Journal of Human Genetics|November 5, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing LossPrasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Genome Research|January 27, 2019
Single-cell sequencing of primate preimplantation embryos reveals chromosome elimination via cellular fragmentation and blastomere exclusionBrittany L Daughtry, Jimi L Rosenkrantz, Nathan H Lazar, et al.
American Journal of Human Genetics|September 3, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing LossPrasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Genome Biology|December 19, 2014
Conserved syntenic clusters of protein coding genes are missing in birdsPeter V Lovell, Morgan Wirthlin, Larry Wilhelm, et al.
Pathogens (Basel, Switzerland)|November 24, 2020
COVID-19 as a Trigger of Recurrent Guillain-Barré SyndromeErin P McDonnell, Nicole J Altomare, Yesha H Parekh, et al.
Genome Research|June 20, 2018
Epigenetic maintenance of topological domains in the highly rearranged gibbon genomeNathan H Lazar, Kimberly A Nevonen, Brendan O'Connell, et al.
Investigative Ophthalmology & Visual Science|December 18, 2014
Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in IsraelCsilla H Lazar, Mousumi Mutsuddi, Adva Kimchi, et al.
Plos Computational Biology|October 1, 2024
Building, benchmarking, and exploring perturbative maps of transcriptional and morphological dataSafiye Celik, Jan-Christian Hütter, Sandra Melo Carlos, et al.
American Journal of Respiratory Cell and Molecular Biology|August 17, 2004
Plasminogen activator inhibitor-1 impairs alveolar epithelial repair by binding to vitronectinMichael H Lazar, Paul J Christensen, Ming Du, et al.
Nature Genetics|May 29, 2024
High-resolution genome-wide mapping of chromosome-arm-scale truncations induced by CRISPR-Cas9 editingNathan H Lazar, Safiye Celik, Lu Chen, et al.
American Journal of Human Genetics|November 5, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing LossPrasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Genome Research|January 27, 2019
Single-cell sequencing of primate preimplantation embryos reveals chromosome elimination via cellular fragmentation and blastomere exclusionBrittany L Daughtry, Jimi L Rosenkrantz, Nathan H Lazar, et al.
American Journal of Human Genetics|September 3, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing LossPrasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Pageof 9