Results 1 to 10 of about 76,746 (287)

Differential effects of HDAC inhibitors in the Rho I255d mouse model for autosomal dominant retinitis pigmentosa [PDF]

open access: yesCell Death Discovery
Retinitis Pigmentosa (RP) is an inherited neurodegenerative disease which leads to loss of retinal photoreceptors and blindness. Histone deacetylases (HDAC) were previously found to be involved in photoreceptor cell death, and HDAC inhibitors have shown ...
Yu Zhu   +3 more
doaj   +2 more sources

Next-Generation HDAC Inhibitors: Advancing Zinc-Binding Group Design for Enhanced Cancer Therapy [PDF]

open access: yesCells
Histone deacetylases (HDACs) are pivotal epigenetic regulators that control gene expression, cell proliferation, and differentiation, and their dysregulation is closely associated with the onset and progression of multiple cancers.
Mohammed Hawash
doaj   +2 more sources

Analysis of the effect of HDAC inhibitors on the formation of the HIV reservoir [PDF]

open access: yesmBio
The HIV reservoir is more dynamic than previously thought with around 70% of the latent reservoir originating from viruses circulating within 1 year of the initiation of antiretroviral therapy (ART).
Lijun Ling   +13 more
doaj   +2 more sources

Targeted intervention of tumor microenvironment with HDAC inhibitors and their combination therapy strategies [PDF]

open access: yesEuropean Journal of Medical Research
Histone deacetylation represents a significant epigenetic mechanism that involves the removal of acetyl groups from histones, subsequently influencing gene transcription.
Wanli Zhang   +7 more
doaj   +2 more sources

DOT1L inhibition does not modify the sensitivity of cutaneous T cell lymphoma to pan-HDAC inhibitors in vitro

open access: yesFrontiers in Genetics, 2022
Cutaneous T-cell lymphomas (CTCLs) are a subset of T-cell malignancies presenting in the skin. The treatment options for CTCL, in particular in advanced stages, are limited.
Eliza Mari Kwesi-Maliepaard   +8 more
doaj   +1 more source

Discovery of 1-Benzhydryl-Piperazine-Based HDAC Inhibitors with Anti-Breast Cancer Activity: Synthesis, Molecular Modeling, In Vitro and In Vivo Biological Evaluation

open access: yesPharmaceutics, 2022
Isoform-selective histone deacetylase (HDAC) inhibition is promoted as a rational strategy to develop safer anti-cancer drugs compared to non-selective HDAC inhibitors.
Dusan Ruzic   +11 more
doaj   +1 more source

HDAC inhibitors: Targets for tumor therapy, immune modulation and lung diseases

open access: yesTranslational Oncology, 2022
Histone deacetylases (HDACs) are enzymes that play a key role in the epigenetic regulation of gene expression by remodeling chromatin. Inhibition of HDACs is a prospective therapeutic approach for reversing epigenetic alteration in several diseases.
Geetha Shanmugam   +2 more
doaj   +1 more source

Application of Ligand- and Structure-Based Prediction Models for the Design of Alkylhydrazide-Based HDAC3 Inhibitors as Novel Anti-Cancer Compounds

open access: yesPharmaceuticals, 2023
Histone deacetylases (HDAC) represent promising epigenetic targets for several diseases including different cancer types. The HDAC inhibitors approved to date are pan-HDAC inhibitors and most show a poor selectivity profile, side effects, and in ...
Emre F. Bülbül   +7 more
doaj   +1 more source

Metabolism, HDACs, and HDAC Inhibitors: A Systems Biology Perspective [PDF]

open access: yesMetabolites, 2021
Histone deacetylases (HDACs) are epigenetic enzymes that play a central role in gene regulation and are sensitive to the metabolic state of the cell. The cross talk between metabolism and histone acetylation impacts numerous biological processes including development and immune function.
Jacob King   +2 more
openaire   +3 more sources

Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors [PDF]

open access: yesRoyal Society Open Science, 2019
HDAC inhibitors have been developed very rapidly in clinical trials and even in approvals for treating several cancers. However, there are few reported HDAC inhibitors designed from Nɛ-acetyl lysine.
Fang Wang   +9 more
doaj   +1 more source

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