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RNA-seq on K562 cells treated with an shRNA knockdown against NUP35. (NUP35-BGKLV38-C) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_External_Users_03-07-14.pdf
ORGANISM(S): Homo sapiens 
2021-06-15 | GSE177933 | GEO
SMPD4 is a neutral sphingomylinase implicated in a specific type of congenital microcephaly. Although not intensively studied, SMPD4 deficiency has also been found to cause cell division defects. This suggests a role for SMPD4 in cell cycle and differentiation. In order to explore this role we used ...
ORGANISM(S): Homo sapiens (Human) 
2022-10-25 | PXD037694 | Pride
RNA-seq on HepG2 cells treated with an shRNA knockdown against NUP35. (NUP35_BGHLV27) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_External_Users_03-07-14.pdf
ORGANISM(S): Homo sapiens 
2016-11-08 | GSE88285 | GEO
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