Results 171 to 180 of about 102,789 (325)
Improving Plasma-Catalytic Ammonia Synthesis Using a Coaxial Double-Helix-Electrode Reactor. [PDF]
Xian S +7 more
europepmc +1 more source
Sensing and Reprogramming Surface Receptor Activation With Synthetic Transcriptional Circuits
A synthetic receptor‐signalling induced transcription (RESIT) circuit is designed based on receptor activation mediated split protease complementation and release of membrane‐tethered synthetic transcriptional modules. The RESIT system enables probing Ca2+ entry, receptor tyrosine kinase (RTK) activities and Ras activation, and reprogramming RTK ...
Fei Liu +5 more
wiley +1 more source
Therapeutic Potential of Mitochondrial Transplantation with Focus on DBD. [PDF]
Guo C +9 more
europepmc +1 more source
ABSTRACT DEAF1‐associated neurodevelopmental disorder (DAND) is a neurodevelopmental spectrum disorder caused by two methods of inheritance: the autosomal dominant intellectual disability syndrome (Vulto‐van Silfout‐de Vries syndrome (VSVS), OMIM #615828), and the autosomal recessive Neurodevelopmental disorder with hypotonia and impaired expressive ...
Kylie Katz, Philip Jensik, Milen Velinov
wiley +1 more source
Rhesus Antagonism Is Associated With Non-Anastomotic Biliary Strictures After Orthotopic Liver Transplantation From Brain-Death Donors. [PDF]
Broekman LDN +5 more
europepmc +1 more source
A New Conditional Transcription Factor for Use in Toxoplasma Gondii
Graphical Abstract and Lay Summary A new conditional transcription factor (CTF) for Toxoplasma gondii reversibly regulates a reporter gene, achieving an outstanding signal‐to‐noise ratio. Gene expression is robust in the absence and nearly abolished in the presence of rapamycin, and the tool's modular design will facilitate application to varied genes ...
Mohammad Farouq Sharifpour +12 more
wiley +1 more source
Multisite Phosphorylation Regulates the Structure and Auto-Inhibitory Function of the Intrinsically Disordered N‑Terminal Domain of p53. [PDF]
Fu L +8 more
europepmc +1 more source
ABSTRACT A novel AR frameshift mutation (c.2023_2035del) was identified in a 17‐year‐old phenotypic female with Complete Androgen Insensitivity Syndrome (CAIS). This report emphasizes the necessity of molecular characterization and multidisciplinary management to address diagnosis, surgical timing, and psychological well‐being in disorder of sex ...
Astorino Maria Francesca +10 more
wiley +1 more source
Deceased Donation after Brain Death (DBD)
openaire +3 more sources

