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Nature Communications
|
October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
Michael 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 Consortium
Terrence 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 hyperintensities
Wojciech 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 knockouts
Bret 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 knockouts
Bret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Nature Genetics
|
April 9, 2021
A resource of targeted mutant mouse lines for 5,061 genes
Marie-Christine Birling, Atsushi Yoshiki, David J Adams, et al.
Nature
|
September 15, 2016
High-throughput discovery of novel developmental phenotypes
Mary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Nature
|
November 17, 2017
Corrigendum: High-throughput discovery of novel developmental phenotypes
Mary 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.
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Search research articles
Search
Showing results (291-300 of 299) with videos related to
Sort By:
Page
of 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 dysfunction
Michael 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 Consortium
Terrence 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 hyperintensities
Wojciech 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 knockouts
Bret 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 knockouts
Bret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Nature Genetics
|
April 9, 2021
A resource of targeted mutant mouse lines for 5,061 genes
Marie-Christine Birling, Atsushi Yoshiki, David J Adams, et al.
Nature
|
September 15, 2016
High-throughput discovery of novel developmental phenotypes
Mary E Dickinson, Ann M Flenniken, Xiao Ji, et al.
Nature
|
November 17, 2017
Corrigendum: High-throughput discovery of novel developmental phenotypes
Mary 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.
Page
of 30