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ZNF462 haploinsufficiency is linked to Weiss-Kruszka Syndrome, a genetic disorder characterized by neurodevelopmental defects including Autism. Though conserved in vertebrates and essential for embryonic development the molecular functions of ZNF462 remain unclear. We identified its murine homolog Z...
ORGANISM(S): Mus musculus (Mouse) 
2023-05-10 | PXD037238 | Pride
Epigenetic processes are the main conductors of phenotypic variation in eukaryotes. The malaria parasite Plasmodium falciparum employs antigenic variation of the major surface antigen PfEMP1, encoded by 60 var genes, to evade acquired immune responses. PfEMP1 also mediates sequestration of infected ...
ORGANISM(S): Plasmodium falciparum 
ZFP462 safeguards neural lineage specification by targeting G9A/GLP mediated heterochromatin to silence enhancers
Loss of H3K9me3 heterochromatin at protein coding genes enables developmental lineage specification (srHC-seq)
ZFP462 safeguards neural lineage specification by targeting G9A/GLP mediated heterochromatin to silence enhancers [QuantSeq]
Loss of H3K9me3 heterochromatin at protein coding genes enables developmental lineage specification (RNA-Seq)
Loss of H3K9me3 heterochromatin at protein coding genes enables developmental lineage specification (ChIP-Seq)
ZFP462 safeguards neural lineage specification by targeting G9A/GLP mediated heterochromatin to silence enhancers [RNA-seq]
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