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Plos One
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April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells
Noa 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 Interest
Amy 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 decay
Moran 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 delay
Meer 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 episignature
Remzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Plos One
|
April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells
Noa 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 Interest
Amy 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 decay
Moran 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 delay
Meer 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 episignature
Remzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
Page
of 1