نتایج جستجو برای: آنزیم g9a

تعداد نتایج: 12176  

2010
Taoufik Bouezmarni Mhamed Mesfioui Abdelouahid Tajar Chunsheng Ma

1 Department of Economics, McGill University, Leacock Building, 855 Sherbrooke Street West, C.P. 6128, succursale Centre-ville Montreal, QC, Canada H3A 2T7 2 Département de Mathématiques et d’Informatique, Universitédu Québec à Trois-Rivières, Pavillon Ringuet, local 3060, C.P. 500, Trois-Rivières, QC, Canada G9A 5H7 3 ARC Epidemiology Unit, The University of Manchester, Oxford Road, Manchester...

Journal: :Journal of the American Chemical Society 2010
Eriko Iwasa Yoshitaka Hamashima Shinya Fujishiro Eisuke Higuchi Akihiro Ito Minoru Yoshida Mikiko Sodeoka

The first total synthesis of (+)-chaetocin has been accomplished in nine steps starting from known N-Cbz-N-Me-serine using radical alpha-bromination reaction of diketopiperazine 10 and Co(I)-mediated reductive dimerization reaction of 12 as key reactions. The enantiomers show comparable inhibitory activity toward histone methyltransferase (HMT) G9a, but analogues without the sulfur functionalit...

2017
Wenhua Jiang Pengfei Liu Xiaodong Li

Breast cancer (BC) is the most common type of malignancy in females worldwide, however, its underlying mechanisms remain poorly understood. The present study aimed to investigate the mechanisms behind the development and progression of BC and identify potential biomarkers for it. The chromatin immunoprecipitation-DNA sequencing (ChIP-Seq) dataset GSM1642516 and gene expression dataset GSE34925 ...

2017
Tom S Koemans Tjitske Kleefstra Melissa C Chubak Max H Stone Margot R F Reijnders Sonja de Munnik Marjolein H Willemsen Michaela Fenckova Connie T R M Stumpel Levinus A Bok Margarita Sifuentes Saenz Kyna A Byerly Linda B Baughn Alexander P A Stegmann Rolph Pfundt Huiqing Zhou Hans van Bokhoven Annette Schenck Jamie M Kramer

Kleefstra syndrome, caused by haploinsufficiency of euchromatin histone methyltransferase 1 (EHMT1), is characterized by intellectual disability (ID), autism spectrum disorder (ASD), characteristic facial dysmorphisms, and other variable clinical features. In addition to EHMT1 mutations, de novo variants were reported in four additional genes (MBD5, SMARCB1, NR1I3, and KMT2C), in single individ...

Journal: :international journal of pediatrics 0
moein farshchian department of biology, faculty of science, ferdowsi university of mashhad, mashhad, iran. mahtab dastpak cell and molecular biotechnology research group, institute of biotechnology ferdowsi university of mashhad, mashhad, iran. maryam m. matin cell and molecular biotechnology research group, institute of biotechnology ferdowsi university of mashhad, mashhad, iran. dirk geerts department of pediatric oncology / hematology, erasmus university medical center, rotterdam, the netherlands. ahmad reza bahrami department of biology, faculty of science, ferdowsi university of mashhad, mashhad, iran.

elucidating the critical epigenetics events involved in differentiation and reprogramming of cells to primordial germ cells (pgcs) is among the interesting issues in stem cell research. here, i will talk about critical transcription factors and global hypomethylation in development of germ cells. evidence strongly suggests that the earliest pgcs emerging in the e7.25 mouse embryo epiblast have ...

2016
Olof Gidlöf Andrea L. Johnstone Kerstin Bader Bohdan B. Khomtchouk Jiaqi J. O'Reilly Selvi Celik Derek J. Van Booven Claes Wahlestedt Bernhard Metzler David Erlinge

BACKGROUND Ischemic preconditioning (IPC) protects the heart from prolonged ischemic insult and reperfusion injury through a poorly understood mechanism. Post-translational modifications of histone residues can confer rapid and drastic switches in gene expression in response to various stimuli, including ischemia. The aim of this study was to investigate the effect of histone methylation in the...

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