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A structural role for histone methyltransferase MET-2 represses transcription independent of H3K9me catalysis [RNA-seq]
PubMed Full text in PMC Similar studies SRA Run Selector
A structural role for histone methyltransferase MET-2 represses transcription independent of H3K9me catalysis
PubMed Full text in PMC Similar studies
A structural role for histone methyltransferase MET-2 represses transcription independent of H3K9me catalysis [ChIP-seq]
An unstructured MET-2/SETDB1 cofactor ensures H3K9me2, focus formation and perinuclear anchoring
An unstructured MET-2/SETDB1 cofactor ensures H3K9me2, focus formation and perinuclear anchoring [RNA-seq]
An unstructured MET-2/SETDB1 cofactor ensures H3K9me2, focus formation and perinuclear anchoring [ChIP-seq]
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (smallRNA-seq)
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (RNA-seq)
Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (ChIP-seq)
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity [RNA-seq]
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity [CUT&RUN; ChICseq]
H3K9me blocks transcription factor activity in differentiated cells to ensure tissue integrity [ATAC-seq]
Loss of a heterochromatin anchor rescues altered genome organization and EDMD muscle defects triggered by a laminopathy mutation
RNA-seq: Loss of a heterochromatin anchor rescues altered genome organization and EDMD muscle defects triggered by a laminopathy mutation
DamID: Loss of a heterochromatin anchor rescues altered genome organization and EDMD muscle defects triggered by a laminopathy mutation
Histone H3K9 methylation promotes formation of genome compartments in C. elegans via chromosome compaction and perinuclear anchoring
Histone H3K9 methylation promotes formation of genome compartments in C. elegans via chromosome compaction and perinuclear anchoring (Hi-C)
Histone H3K9 methylation promotes formation of genome compartments in C. elegans via chromosome compaction and perinuclear anchoring (ChIP-seq)
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