Combinations of isoform-targeted histone deacetylase inhibitors and bryostatin analogues display remarkable potency to activate latent HIV without global T-cell activation.
about
Class 1-selective histone deacetylase inhibitors enhance HIV latency reversal while preserving the activity of HDAC isoforms necessary for maximal HIV gene expression.REDOR NMR Reveals Multiple Conformers for a Protein Kinase C Ligand in a Membrane Environment.Characterization of designed, synthetically accessible bryostatin analog HIV latency reversing agents.Mesenchymal stem cells are attracted to latent HIV-1-infected cells and enable virus reactivation via a non-canonical PI3K-NFκB signaling pathway
P2860
Combinations of isoform-targeted histone deacetylase inhibitors and bryostatin analogues display remarkable potency to activate latent HIV without global T-cell activation.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Combinations of isoform-target ...... hout global T-cell activation.
@en
type
label
Combinations of isoform-target ...... hout global T-cell activation.
@en
prefLabel
Combinations of isoform-target ...... hout global T-cell activation.
@en
P2093
P2860
P1433
P1476
Combinations of isoform-target ...... thout global T-cell activation
@en
P2093
Austin Niu
Brice J Albert
Garland R Marshall
Lee Ratner
Paul A Wender
Rashmi Ramani
Robert M Williams
P2860
P2888
P356
10.1038/S41598-017-07814-4
P407
P577
2017-08-07T00:00:00Z