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Jon Lees

Showing results (1-10 of 11) with videos related to

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Plos One|August 20, 2015
Gene Function Prediction from Functional Association Networks Using Kernel Partial Least Squares RegressionSonja Lehtinen, Jon Lees, Jürg Bähler, et al.
Elife|October 3, 2023
Broad functional profiling of fission yeast proteins using phenomics and machine learningMaría Rodríguez-López, Nicola Bordin, Jon Lees, et al.
Journal of Muscle Research and Cell Motility|July 22, 2023
Zebrafish as a model for cardiac disease; Cryo-EM structure of native cardiac thin filaments from Danio RerioMarston Bradshaw, John M Squire, Edward Morris, et al.
Journal of Medicinal Chemistry|March 20, 2026
<i>In Silico</i> Discovery and Characterization of a Novel Nuclear Transcription Factor-Y (NF-Y) Inhibitor with Antimitogenic PropertiesReza Ebrahimighaei, Jon Lees, Robin A Corey, et al.
Nucleic Acids Research|November 25, 2020
CATH: increased structural coverage of functional spaceIan Sillitoe, Nicola Bordin, Natalie Dawson, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Medrxiv : the Preprint Server for Health Sciences|September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Nature Genetics|April 23, 2026
Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Nature Genetics|March 30, 2026
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Nature Genetics|April 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Plos One|August 20, 2015
Gene Function Prediction from Functional Association Networks Using Kernel Partial Least Squares RegressionSonja Lehtinen, Jon Lees, Jürg Bähler, et al.
Elife|October 3, 2023
Broad functional profiling of fission yeast proteins using phenomics and machine learningMaría Rodríguez-López, Nicola Bordin, Jon Lees, et al.
Journal of Muscle Research and Cell Motility|July 22, 2023
Zebrafish as a model for cardiac disease; Cryo-EM structure of native cardiac thin filaments from Danio RerioMarston Bradshaw, John M Squire, Edward Morris, et al.
Journal of Medicinal Chemistry|March 20, 2026
<i>In Silico</i> Discovery and Characterization of a Novel Nuclear Transcription Factor-Y (NF-Y) Inhibitor with Antimitogenic PropertiesReza Ebrahimighaei, Jon Lees, Robin A Corey, et al.
Nucleic Acids Research|November 25, 2020
CATH: increased structural coverage of functional spaceIan Sillitoe, Nicola Bordin, Natalie Dawson, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Medrxiv : the Preprint Server for Health Sciences|September 5, 2025
Biallelic variants in <i>RNU2-2</i> cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Nature Genetics|April 23, 2026
Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Nature Genetics|March 30, 2026
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorderDaniel Greene, Rodrigo Mendez, Jon Lees, et al.
Nature Genetics|April 10, 2025
Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Pageof 2