PREDICTION OF CREEP FAILURES OF LEAD IN BENDING FROM TENSILE DATA
David L. Platus, Blake Cotton
openalex +2 more sources
Machine stability and dosimetry for ultra‐high dose rate FLASH radiotherapy human clinical protocol
Abstract Background The FLASH effect, induced by ultra‐high dose rate (UHDR) irradiations, offers the potential to spare normal tissue while effectively treating tumors. It is important to achieve precise and accurate dose delivery and to establish reliable detector systems, particularly for clinical trials needed to help the clinical transfer of FLASH‐
Patrik Gonçalves Jorge+9 more
wiley +1 more source
Analysis of tire contact stresses and asphalt pavement rutting under gradient temperature and typical driving conditions. [PDF]
Guo M, Liu P, Feng W, Li X, Ge H.
europepmc +1 more source
Creep Resistance and Microstructure Evolution in P23/P91 Welds. [PDF]
Vodárek V+5 more
europepmc +1 more source
A nonlinear creep model of hard structural planes. [PDF]
Cui A+6 more
europepmc +1 more source
Experimental investigation on mechanical properties and strength criteria of frozen soft rock. [PDF]
Wang Z, Wang Z, Li D, Jia Z, Liu X.
europepmc +1 more source
Brassinosteroids Render Cell Walls Softer but Less Extensible in Growing Arabidopsis Hypocotyls. [PDF]
Suslov DV+5 more
europepmc +1 more source
Skin calcium deposits in primary familial brain calcification: A novel potential biomarker
Abstract Objective Primary Familial Brain Calcification (PFBC) is a rare neurodegenerative disorder characterized by small vessel calcifications in the basal ganglia. PFBC is caused by pathogenic variants in different genes and its physiopathology is still largely unknown. Skin vascular calcifications have been detected in single PFBC cases, suggesting
Aron Emmi+8 more
wiley +1 more source
Tilting deformation analysis and instability prediction of arch-locked-segment landslides induced by rainfall. [PDF]
Liu J, Liu H, Luo J, Chen J, Wang H.
europepmc +1 more source
UDP‐glucose dehydrogenase variants cause dystroglycanopathy
Abstract UDP‐glucose dehydrogenase (UGDH) variants have been associated with hypotonia, developmental delay, and epilepsy. We report the first pathologic evidence of dystroglycanopathy in siblings with UGDH variants. Both presented around 6 months with developmental delay and elevated creatinine kinase.
Anna M. Reelfs+8 more
wiley +1 more source