Results 41 to 50 of about 167,650 (273)

Design, Synthesis, and Docking Study of Acyl Thiourea Derivatives as Possible Histone Deacetylase Inhibitors with a Novel Zinc Binding Group

open access: yesScientia Pharmaceutica, 2019
Histone deacetylase inhibitors with zinc binding groups often exhibit drawbacks like non-selectivity or toxic effects. Thus, there are continuous efforts to modify the currently available inhibitors or to discover new derivatives to overcome these ...
Duraid H. Al-Amily   +1 more
doaj   +1 more source

Histone deacetylase inhibitors

open access: yesJournal of Education, Health and Sport, 2020
The human genome is contained in chromatin, which is a complex macromolecular complex. It is made of DNA, histones and non-histone proteins. The structure of chromatin and the process of its rearrangement regulate the process of transcription, and hence ...
Marzena Baran   +2 more
doaj   +1 more source

Histone deacetylase 4 alters cartilage homeostasis in human osteoarthritis [PDF]

open access: yesBMC Musculoskeletal Disorders, 2014
Osteoarthritis (OA) is the most common degenerative joint disorder, and a major cause of pain and disability among the elderly. Histone deacetylase 4 (HDAC4) has been shown to be a key regulator of chondrocyte hypertrophy during skeletogenesis. The aims of present study were to investigate the expression of HDAC4 in normal and OA cartilage and its ...
Lu, Jingwei   +4 more
openaire   +2 more sources

Droxinostat, a Histone Deacetylase Inhibitor, Induces Apoptosis in Hepatocellular Carcinoma Cell Lines via Activation of the Mitochondrial Pathway and Downregulation of FLIP

open access: yesTranslational Oncology, 2016
Background: The current chemotherapeutic outcomes for hepatocellular carcinoma (HCC) are not encouraging, and long-term survival of this patient group remains poor.
Jing Liu   +9 more
doaj   +1 more source

Conditional deletion of HDAC4 from collagen type 2α1-expressing cells increases angiogenesis in vivo

open access: yesMolecular Medicine, 2020
Background HDAC4 is a key regulator of chondrocyte hypertrophy and skeletal development, but it is not clear whether the increase in vascular invasion at growth plates is related to HDAC4 expression.
Lilan Gao   +5 more
doaj   +1 more source

Histone deacetylase inhibition modulates cell fate decisions during myeloid differentiation

open access: yesHaematologica, 2010
Background The clinical use of chromatin-modulating drugs, such as histone deacetylase inhibitors, for the treatment of bone marrow failure and hematopoietic malignancies has increased dramatically over the last few years.
Marije Bartels   +4 more
doaj   +1 more source

Histone deacetylase HDA-4-mediated epigenetic regulation in space-flown C. elegans

open access: yesnpj Microgravity, 2021
Epigenetic changes during long-term spaceflight are beginning to be studied by NASA’s twin astronauts and other model organisms. Here, we evaluate the epigenetic regulation of gene expression in space-flown C.
Atsushi Higashitani   +8 more
doaj   +1 more source

Caspase-mediated Specific Cleavage of Human Histone Deacetylase 4 [PDF]

open access: yesJournal of Biological Chemistry, 2004
Histone deacetylase 4 (HDAC4) is a class II HDAC implicated in controlling gene expression important for diverse cellular functions, but little is known about how its expression and stability are regulated. We report here that this deacetylase is unusually unstable, with a half-life of less than 8 h.
Fang, Liu   +3 more
openaire   +2 more sources

Intermittent Fasting Protects against Alzheimer’s Disease Possible through Restoring Aquaporin-4 Polarity

open access: yesFrontiers in Molecular Neuroscience, 2017
The impairment of amyloid-β (Aβ) clearance in the brain plays a causative role in Alzheimer’s disease (AD). Polarity distribution of aquaporin-4 (AQP4) is important to remove Aβ from brain.
Jingzhu Zhang   +8 more
doaj   +1 more source

Valproate alters dopamine signaling in association with induction of Par-4 protein expression. [PDF]

open access: yesPLoS ONE, 2012
Chromatin remodeling through histone modifications has emerged as a key mechanism in the pathophysiology of psychiatric disorders. Valproate (VPA), a first-line medication for bipolar disorder, is known to have histone deacetylase (HDAC) inhibitor ...
Saebom Lee   +7 more
doaj   +1 more source

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