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Noa Henig

Showing results (1-10 of 5) with videos related to

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Plos One|April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cellsNoa Henig, Nili Avidan, Ilana Mandel, et al.
Current Protocols in Molecular Biology|July 6, 2017
NEBNext Direct: A Novel, Rapid, Hybridization-Based Approach for the Capture and Library Conversion of Genomic Regions of InterestAmy B Emerman, Sarah K Bowman, Andrew Barry, et al.
Elife|October 2, 2024
The zinc-finger transcription factor Sfp1 imprints specific classes of mRNAs and links their synthesis to cytoplasmic decayMoran Kelbert, Antonio Jordán-Pla, Lola de Miguel-Jiménez, et al.
American Journal of Human Genetics|March 31, 2022
De novo variants in ATP2B1 lead to neurodevelopmental delayMeer Jacob Rahimi, Nicole Urban, Meret Wegler, et al.
American Journal of Human Genetics|May 30, 2024
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignatureRemzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Plos One|April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cellsNoa Henig, Nili Avidan, Ilana Mandel, et al.
Current Protocols in Molecular Biology|July 6, 2017
NEBNext Direct: A Novel, Rapid, Hybridization-Based Approach for the Capture and Library Conversion of Genomic Regions of InterestAmy B Emerman, Sarah K Bowman, Andrew Barry, et al.
Elife|October 2, 2024
The zinc-finger transcription factor Sfp1 imprints specific classes of mRNAs and links their synthesis to cytoplasmic decayMoran Kelbert, Antonio Jordán-Pla, Lola de Miguel-Jiménez, et al.
American Journal of Human Genetics|March 31, 2022
De novo variants in ATP2B1 lead to neurodevelopmental delayMeer Jacob Rahimi, Nicole Urban, Meret Wegler, et al.
American Journal of Human Genetics|May 30, 2024
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignatureRemzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
Pageof 1