Results 41 to 50 of about 1,616,869 (326)
Characterization of ribosome heterogeneity during endothelial to hematopoietic transition
FEBS Open Bio, EarlyView.The panorama of ribosome heterogeneity during embryonic hematopoiesis has not yet been portrayed. In this study, utilizing dual‐omics data, the heterogenous dynamic of ribosome during endothelial‐to‐hematopoietic transition has been systemically described. Moreover, stage‐specific upregulation and peripheral localization of RPL27 and RACK1 in hemogenic
Xitong Tian +4 more
wiley +1 more source
Microfluidic electro‐viscoelastic manipulation of extracellular vesicles
FEBS Open Bio, EarlyView.The electro‐viscoelastic manipulation as a potential method for separation of particles based on size. The particles introduced as a sheath flow migrate to the channel center under the influence of simultaneously applied electric field and pressure driven flow.
Seyedamirhosein Abdorahimzadeh +7 more
wiley +1 more source
Radiology Case Reports, 2021 Crossed cerebellar diaschisis is a rare clinical entity of hemispheric cerebellar depression subsequent to a contralateral cerebral cortical lesion, described to be the result of excessive neuronal excitatory synaptic activity within cortico-cerebellar ...
Rachid Belfkih, Professor of neurology +3 more
doaj +1 more source
Genetics in Medicine, 2017 Purpose:Implementation of novel genetic diagnostic tests is generally driven by technological advances because they promise shorter turnaround times and/or higher diagnostic yields.
L. Vissers +13 more
semanticscholar +1 more source
Report on the 2nd MObility for Vesicle research in Europe (MOVE) symposium—2024
FEBS Open Bio, EarlyView.The 2nd MObility for Vesicle research in Europe (MOVE) Symposium in Belgrade brought over 280 attendees from 28 countries to advance extracellular vesicle (EV) research. Featuring keynotes, presentations, and industry sessions, it covered EV biogenesis, biomarkers, therapies, and manufacturing.
Dorival Mendes Rodrigues‐Junior +5 more
wiley +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra +17 more
wiley +1 more source
Expanding the duration of the neurology clerkship – does it matter?
Brain Disorders, 2021 Objective: The standard duration of the core neurology clerkship at our institution is four weeks. However, the optimal length to provide sufficient exposure to medical students remains unknown.
Zafer Keser +7 more
doaj +1 more source
What's happening in Neurology® Neuroimmunology & Neuroinflammation
Neurology, 2018 Articles appearing in the January 2018 ...
semanticscholar +1 more source