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Context-specific functions of chromatin remodellers in development and disease
Chromatin remodellers were once thought to be highly redundant and nonspecific in their
actions. However, recent human genetic studies demonstrate remarkable biological …
actions. However, recent human genetic studies demonstrate remarkable biological …
Satellite DNA: an evolving topic
MA Garrido-Ramos - Genes, 2017 - mdpi.com
Satellite DNA represents one of the most fascinating parts of the repetitive fraction of the
eukaryotic genome. Since the discovery of highly repetitive tandem DNA in the 1960s, a lot …
eukaryotic genome. Since the discovery of highly repetitive tandem DNA in the 1960s, a lot …
[HTML][HTML] Strength in diversity: Understanding the pathways to herpes simplex virus reactivation
JB Suzich, AR Cliffe - Virology, 2018 - Elsevier
Herpes simplex virus (HSV) establishes a latent infection in peripheral neurons and can
periodically reactivate to cause disease. Reactivation can be triggered by a variety of stimuli …
periodically reactivate to cause disease. Reactivation can be triggered by a variety of stimuli …
Epigenetic etiology of intellectual disability
Intellectual disability (ID) is a prevailing neurodevelopmental condition associated with
impaired cognitive and adaptive behaviors. Many chromatin-modifying enzymes and other …
impaired cognitive and adaptive behaviors. Many chromatin-modifying enzymes and other …
The role of ATRX in glioma biology
The current World Health Organization classification of CNS tumors has made a tremendous
leap from past editions by incorporating molecular criteria in addition to the pre-existing …
leap from past editions by incorporating molecular criteria in addition to the pre-existing …
Transcription of tandemly repetitive DNA: functional roles
MA Biscotti, A Canapa, M Forconi, E Olmo… - Chromosome …, 2015 - Springer
A considerable fraction of the eukaryotic genome is made up of satellite DNA constituted of
tandemly repeated sequences. These elements are mainly located at centromeres …
tandemly repeated sequences. These elements are mainly located at centromeres …
HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome
Mutations in CDCA7, the SNF2 family protein HELLS (LSH), or the DNA methyltransferase
DNMT3b cause immunodeficiency–centromeric instability–facial anomalies (ICF) syndrome …
DNMT3b cause immunodeficiency–centromeric instability–facial anomalies (ICF) syndrome …
[HTML][HTML] Time-resolved global and chromatin proteomics during herpes simplex virus type 1 (HSV-1) infection
Herpes simplex virus (HSV-1) lytic infection results in global changes to the host cell
proteome and the proteins associated with host chromatin. We present a system level …
proteome and the proteins associated with host chromatin. We present a system level …
The many faces of H3. 3 in regulating chromatin in embryonic stem cells and beyond
LRZ Cohen, E Meshorer - Trends in Cell Biology, 2024 - cell.com
H3. 3 is a highly conserved nonreplicative histone variant. H3. 3 is enriched in promoters
and enhancers of active genes, but it is also found within suppressed heterochromatin …
and enhancers of active genes, but it is also found within suppressed heterochromatin …
Stalled replication forks within heterochromatin require ATRX for protection
Expansive growth of neural progenitor cells (NPCs) is a prerequisite to the temporal waves
of neuronal differentiation that generate the six-layered neocortex, while also placing a …
of neuronal differentiation that generate the six-layered neocortex, while also placing a …