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Showing results (291-300 of 299) with videos related to

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Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Nature Genetics|June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping ConsortiumTerrence F Meehan, Nathalie Conte, David B West, et al.
American Journal of Human Genetics|July 2, 2013
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensitiesWojciech Wiszniewski, Jill V Hunter, Neil A Hanchard, et al.
Communications Biology|December 28, 2018
Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Communications Biology|March 12, 2019
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Nature Genetics|April 9, 2021
A resource of targeted mutant mouse lines for 5,061 genesMarie-Christine Birling, Atsushi Yoshiki, David J Adams, et al.
Nature|September 15, 2016
High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Nature|November 17, 2017
Corrigendum: High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Autophagy|January 23, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Pageof 30

Showing results (291-300 of 299) with videos related to

Sort By:
Pageof 30
You have reached the last page of results.This site can display upto 299 results.
Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Nature Genetics|June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping ConsortiumTerrence F Meehan, Nathalie Conte, David B West, et al.
American Journal of Human Genetics|July 2, 2013
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensitiesWojciech Wiszniewski, Jill V Hunter, Neil A Hanchard, et al.
Communications Biology|December 28, 2018
Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Communications Biology|March 12, 2019
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Nature Genetics|April 9, 2021
A resource of targeted mutant mouse lines for 5,061 genesMarie-Christine Birling, Atsushi Yoshiki, David J Adams, et al.
Nature|September 15, 2016
High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Nature|November 17, 2017
Corrigendum: High-throughput discovery of novel developmental phenotypesMary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Autophagy|January 23, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Pageof 30