Results 141 to 150 of about 27,519 (289)

LSD1+8a is an RNA biomarker of neuroendocrine prostate cancer

open access: yesNeoplasia: An International Journal for Oncology Research
Background: Lysine-specific demethylase 1 (LSD1) is a histone demethylase and regulator of differentiation, including in cancer. A neuronal-specific isoform of LSD1—LSD1+8a—has been shown to play a key role in promoting neuronal differentiation in the ...
Anbarasu Kumaraswamy   +14 more
doaj   +1 more source

LSD1 inhibitors disrupt the GFI1 transcription repressor complex

open access: yesMolecular & Cellular Oncology, 2018
Pharmacologic inhibition of KDM1A (Lysine Demethylase 1A) induces differentiation in certain subtypes of acute myeloid leukemia. Our recent studies reveal this is dependent upon drug-induced disruption of the GFI1 (Growth Factor Independent 1 ...
Alba Maiques-Diaz   +3 more
doaj   +1 more source

LSD1 Interacts with Zfp516 to Promote UCP1 Transcription and Brown Fat Program

open access: yesCell Reports, 2016
Zfp516, a brown fat (BAT)-enriched and cold-inducible transcription factor, promotes transcription of UCP1 and other BAT-enriched genes for non-shivering thermogenesis. Here, we identify lysine-specific demethylase 1 (LSD1) as a direct binding partner of
Audrey Sambeat   +6 more
doaj   +1 more source

Histone H3 peptide based LSD1-selective inhibitors

open access: yesBioorganic & Medicinal Chemistry Letters, 2015
A series of candidates for the histone H3 peptide based LSD1-selective inhibitor were designed and synthesized. Among peptides 1a-c and 2a-c, peptide 1a, which has a phenylcyclopropylamine (PCPA) moiety at Lys-4 of the 21 amino acid residues of histone H3, was the most potent LSD1-selective inhibitor.
Taeko, Kakizawa   +4 more
openaire   +3 more sources

Cellular analysis of the action of epigenetics drugs and probes [PDF]

open access: yes, 2017
Small molecule drugs and probes are important tools in drug discovery, pharmacology, and cell biology. This is of course also true for epigenetic inhibitors.
A. Ganesan   +12 more
core   +1 more source

Lysine specific demethylase 1 inactivation enhances differentiation and promotes cytotoxic response when combined with all-trans retinoic acid in acute myeloid leukemia across subtypes

open access: yesHaematologica, 2019
Lysine specific demethylase 1 (LSD1) is a histone modifying enzyme that suppresses gene expression through demethylation of lysine 4 on histone H3. The anti-tumor activity of GSK2879552 and GSK-LSD1, potent, selective irreversible inactivators of LSD1 ...
Kimberly N. Smitheman   +19 more
doaj   +1 more source

Regulation of alphaherpesvirus infections by the ICP0 family of proteins [PDF]

open access: yes, 2013
Immediate-early protein ICP0 of herpes simplex virus type 1 (HSV-1) is important for the regulation of lytic and latent viral infection. Like the related proteins expressed by other alphaherpesviruses, ICP0 has a zinc-stabilized RING finger domain that ...
Boutell, Chris, Everett, Roger
core   +1 more source

Lysine-Specific Demethylase 1 Has Dual Functions as a Major Regulator of Androgen Receptor Transcriptional Activity

open access: yesCell Reports, 2014
Summary: Lysine-Specific Demethylase 1 (LSD1, KDM1A) functions as a transcriptional corepressor through demethylation of histone 3 lysine 4 (H3K4) but has a coactivator function on some genes through mechanisms that are unclear.
Changmeng Cai   +15 more
doaj   +1 more source

Supplementary Fig. 5 from Disruption of the MYC Superenhancer Complex by Dual Targeting of FLT3 and LSD1 in Acute Myeloid Leukemia

open access: gold, 2023
William M. Yashar   +14 more
openalex   +1 more source

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