Results 181 to 190 of about 75,018 (265)
Molecular basis for the regulation of retroviral nucleosomal integration by chromatin compaction. [PDF]
Lapaillerie D +10 more
europepmc +1 more source
This study aimed to determine whether personalized selection of effective drugs for SMARCB1/INI1‐deficient tumors is feasible using in vitro drug sensitivity profiling. Drug sensitivity was assessed using a short‐term collagen gel–embedded three‐dimensional drug sensitivity test (3D‐DST) in tumors derived from SMARCB1/INI1‐deficient tumor cell line ...
Hiroaki Goto +12 more
wiley +1 more source
FACT-(H3-H4) complex stimulates Pol α activity to coordinate DNA synthesis with nucleosome assembly. [PDF]
Zhang W +11 more
europepmc +1 more source
This study reports a female proband with a de novo 9q34.11 deletion affecting SET, who underwent a 28‐year diagnostic odyssey after an atypical Rett syndrome clinical diagnosis. Genomic and proteomics analyses confirmed SET haploinsufficiency, refining the critical 9q34.11 region, and supporting speech therapy benefits in improving meaningful ...
Angelo Condell +14 more
wiley +1 more source
Multi-omic cell free DNA profiles of cerebral spinal fluid from lung cancer metastasis to the brain. [PDF]
Chen T +6 more
europepmc +1 more source
KU80 suppresses endonuclease G activity to preserve genomic integrity
Under normal conditions, EndoG remains restricted to mitochondria and the genome remains intact. When KU80 is absent, EndoG translocates into the nucleus, where it promotes DNA fragmentation and genomic instability. Thus, this work highlights the importance of KU80 in tightly controlling EndoG localization to preserve genome stability.
Jargalan Batsaikhan +8 more
wiley +1 more source
Cnp1 N-terminal dynamics regulate L1 loop recognition by Mis15 to orchestrate kinetochore assembly in Schizosaccharomyces pombe. [PDF]
Xiong Y +8 more
europepmc +1 more source
Spatially resolved mapping of histones reveals selective neuronal response in Rett syndrome
Rett syndrome (RTT) is a severe neurological disorder caused by loss‐of‐function mutations in the X‐linked MECP2 gene that causes profound life‐long neurological dysfunction. MeCP2 regulates chromatin, yet its influence on histone composition and dynamics is unclear.
Frederike Schäfer +6 more
wiley +1 more source
Poly(ADP-Ribose) polymerase1 Has Potential to Facilitate the Nucleosome Disassembly. [PDF]
Alekseev AA +7 more
europepmc +1 more source

