Results 191 to 200 of about 394,248 (332)
This work presents the development of efficient blue thermally activated delayed fluorescent (TADF) materials that perform well without doping, enabling simplified, matrix‐free hyperfluorescence (MFHF) OLEDs. When combined with encapsulated narrow‐band emitters, the TADF materials serve as effective hosts resulting in pure blue, ultranarrow emission ...
Hwan‐Hee Cho+5 more
wiley +1 more source
Identification and characterization of new structured RNA classes in plants. [PDF]
Sack M+6 more
europepmc +1 more source
Assembly of pre-mRNA splicing complex is cap dependent [PDF]
Erik Patzelt+4 more
openalex +1 more source
Optical Chaos Generation and Applications
This review comprehensively examines optical chaos generation via feedback, injection, and optoelectronic methods, emphasizing bandwidth enhancement and time‐delay suppression. Applications include chaos‐synchronized secure communication, physical random number generation, chaotic lidar for cm‐level detection, distributed fiber sensing, and terahertz ...
Wenhui Chen+8 more
wiley +1 more source
<i>BRCA2</i> Pre-mRNA Differential 5' Splicing: A Rescue of Functional Protein Properties from Pathogenic Gene Variants and a Lifeline for Fanconi Anemia D1 Patients. [PDF]
Paredes R+8 more
europepmc +1 more source
Genetic Engineering Methods in Primary T Cells
Primary T cells can be engineered to confer them with novel therapeutic functions, allowing them to treat a variety of conditions. Genetic engineering can be either stable or transient, aiming to either express or inhibit a target gene. This review discusses the various genetic engineering tools available as well as their characteristics and ...
Anthony Youssef, Hui‐Shan Li
wiley +1 more source
A New High Penetrant Intronic Pathogenic Variant Related to Long QT Syndrome Type 2. [PDF]
Rodríguez-Junquera M+11 more
europepmc +1 more source
Control of adenovirus E1B mRNA synthesis by a shift in the activities of RNA splice sites.
Craig Montell+3 more
openalex +1 more source
Current preclinical studies of AAV‐mediated gene therapy explore different strategies based on the characteristics of inner ear diseases. For genetic hearing loss, approaches include the replacement of a “good gene,” removal of a “bad gene,” or direct correction of mutations through base editing.
Fan Wu+7 more
wiley +1 more source