نتایج جستجو برای: histone demethylases

تعداد نتایج: 43210  

2017
Yang Xu Shuang Zhang Shaofeng Lin Yaping Guo Wankun Deng Ying Zhang Yu Xue

In this work, we developed a database WERAM (http://weram.biocuckoo.org/) for histone acetyltransferases, histone deacetylases, histone methyltransferases, histone demethylases and acetyl- or methyl-binding proteins, which catalyze, remove and recognize histone acetylation and methylation sites as 'writers', 'erasers' and 'readers', and synergistically determine the 'histone code'. From the sci...

Journal: :Journal of Immunology 2021

Abstract GFI1 is a DNA-binding transcription factor that regulates hematopoiesis by repressing target genes through its association with complexes containing histone demethylases such as KDM1A (LSD1) and deacetylases (HDACs). To study the consequences of disruption complex between histone-modifying enzymes, we have used knock-in mice harboring P2A mutation in coding region renders it unable to ...

Journal: :Cardiovascular research 2011
Kisho Ohtani Stefanie Dimmeler

Epigenetic control mechanisms play a key role in the regulation of embryonic development and tissue homeostasis and modulate cardiovascular diseases. Increasing evidence suggests that lineage commitment of stem/progenitor cells is tightly regulated by epigenetic mechanisms. These epigenetic control mechanisms include DNA and histone modifications, which modulate the chromatin structure thereby ...

2015
Yasunao F. Kamikawa Mary E. Donohoe Qiang Wu

Epigenetic reprogramming is exemplified by the remarkable changes observed in cellular differentiation and X-chromosome inactivation (XCI) in mammalian female cells. Histone 3 lysine 27 trimethylation (H3K27me3) is a modification that suppresses gene expression in multiple contexts including embryonic stem cells (ESCs) and decorates the entire inactive X-chromosome. The conversion of female som...

Journal: :American journal of human genetics 2012
Damien Lederer Bernard Grisart Maria Cristina Digilio Valérie Benoit Marianne Crespin Sophie Claire Ghariani Isabelle Maystadt Bruno Dallapiccola Christine Verellen-Dumoulin

Kabuki syndrome (KS) is a rare genetic disease that causes developmental delay and congenital anomalies. Since the identification of MLL2 mutations as the primary cause of KS, such mutations have been identified in 56%-76% of affected individuals, suggesting that there may be additional genes associated with KS. Here, we describe three KS individuals with de novo partial or complete deletions o...

2014
Rachel Schiller Giuseppe Scozzafava Anthony Tumber James R Wickens Jacob T Bush Ganesha Rai Clarisse Lejeune Hwanho Choi Tzu-Lan Yeh Mun Chiang Chan Bryan T Mott James S O McCullagh David J Maloney Christopher J Schofield Akane Kawamura

The 2-oxoglutarate (2OG)-dependent Jumonji C domain (JmjC) family is the largest family of histone lysine demethylases. There is interest in developing small-molecule probes that modulate JmjC activity to investigate their biological roles. 5-Carboxy-8-hydroxyquinoline (IOX1) is the most potent broad-spectrum inhibitor of 2OG oxygenases, including the JmjC demethylases, reported to date; howeve...

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