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Matthew B Johnson

Showing results (91-100 of 103) with videos related to

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Nature Genetics|November 17, 2023
Primate-specific ZNF808 is essential for pancreatic development in humansElisa De Franco, Nick D L Owens, Hossam Montaser, et al.
Nature|October 28, 2011
Spatio-temporal transcriptome of the human brainHyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, et al.
Cell|May 15, 2012
Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortexKenneth Y Kwan, Mandy M S Lam, Matthew B Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
<i>MAFA</i> missense mutation causes familial insulinomatosis and diabetes mellitusDonato Iacovazzo, Sarah E Flanagan, Emily Walker, et al.
Brain, Behavior, and Immunity|March 29, 2024
CSMD1 regulates brain complement activity and circuit developmentMatthew L Baum, Daniel K Wilton, Rachel G Fox, et al.
Nature|April 13, 2018
Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical sizeMatthew B Johnson, Xingshen Sun, Andrew Kodani, et al.
Nature Genetics|November 5, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinismMatthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, et al.
The Journal of Experimental Medicine|April 18, 2024
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiencyMatthew B Johnson, Masato Ogishi, Clara Domingo-Vila, et al.
Neuron|September 3, 2021
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regionsKelly M Girskis, Andrew B Stergachis, Ellen M DeGennaro, et al.
Cell Death & Disease|May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformationsElizabeth A Werren, Emily R Peirent, Henna Jantti, et al.
Pageof 11

Showing results (91-100 of 103) with videos related to

Sort By:
Pageof 11
Nature Genetics|November 17, 2023
Primate-specific ZNF808 is essential for pancreatic development in humansElisa De Franco, Nick D L Owens, Hossam Montaser, et al.
Nature|October 28, 2011
Spatio-temporal transcriptome of the human brainHyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, et al.
Cell|May 15, 2012
Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortexKenneth Y Kwan, Mandy M S Lam, Matthew B Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
<i>MAFA</i> missense mutation causes familial insulinomatosis and diabetes mellitusDonato Iacovazzo, Sarah E Flanagan, Emily Walker, et al.
Brain, Behavior, and Immunity|March 29, 2024
CSMD1 regulates brain complement activity and circuit developmentMatthew L Baum, Daniel K Wilton, Rachel G Fox, et al.
Nature|April 13, 2018
Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical sizeMatthew B Johnson, Xingshen Sun, Andrew Kodani, et al.
Nature Genetics|November 5, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinismMatthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, et al.
The Journal of Experimental Medicine|April 18, 2024
Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiencyMatthew B Johnson, Masato Ogishi, Clara Domingo-Vila, et al.
Neuron|September 3, 2021
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regionsKelly M Girskis, Andrew B Stergachis, Ellen M DeGennaro, et al.
Cell Death & Disease|May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformationsElizabeth A Werren, Emily R Peirent, Henna Jantti, et al.
Pageof 11