Results 111 to 120 of about 3,297,974 (375)
TAK1 restricts spontaneous NLRP3 activation and cell death to control myeloid proliferation
The NOD-like receptor (NLR)–P3 inflammasome is a global sensor of infection and stress. Elevated NLRP3 activation levels are associated with human diseases, but the mechanisms controlling NLRP3 inflammasome activation are largely unknown.
R. Malireddi+6 more
semanticscholar +1 more source
The inactivation of SLC35C1 (GDP‐fucose transporter) and enzymes involved in GDP‐fucose biosynthesis was studied. Fucose supplementation increases the level of GDP‐fucose to abnormal, millimolar values in the absence of the TSTA3 protein and SLC35C1 in contrast to the GMDS/SLC35C1 double mutant.
Edyta Skurska, Mariusz Olczak
wiley +1 more source
Abstract Purpose Palliative radiotherapy comprises a significant portion of the radiation treatment workload. Volumetric‐modulated arc therapy (VMAT) improves dose conformity and, in conjunction with flattening filter free (FFF) delivery, can decrease treatment times, both of which are desirable in a population with a high probability of retreatment ...
Madeleine L. Van de Kleut+2 more
wiley +1 more source
DESCRIPTION OF SOME SPONTANEUS SPECIES AND THE POSSIBILITIES OF USE THEM IN THE ROCKY GARDENS [PDF]
In Romania’s spontaneous flora are reported over 3759 species of plants, of which 3136 species are spontaneous [CIOCÂRLAN, 2000], 23 have been declared nature monuments, 74 are extinct, 39 endangered, 171 are vulnerable and 1253 are rare.
BUTA ERZSEBET+6 more
doaj
Abstract In radiation oncology, inter‐fractional dosimetry using optically stimulated luminescent detectors (OSLDs) ensures accurate plan delivery and patient safety. RadPro International GmbH's myOLSchip system, featuring a beryllium oxide (BeO) OSL dosimeter, reader, and eraser, was characterized and calibrated with a Varian Truebeam for in‐vivo ...
Heath Davis+3 more
wiley +1 more source
Spontaneous passage of ingested sewing needle: A case report
Key Clinical Message Sewing needle ingestion is a rare but potentially dangerous event that can affect people of all ages and backgrounds like this patient.
Yohannis Derbew Molla+4 more
doaj +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao+34 more
wiley +1 more source
Editorial: Halophytes: salt stress tolerance mechanisms and potential use
Raoudha Abdellaoui+6 more
doaj +1 more source
Spontaneous generation of eigenvalues
We show that the action of conformal vector fields on functions on the sphere determines the spectrum of the Laplacian (or the conformal Laplacian), without further input of information.
Beckner+7 more
core +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