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Published in 2020 at "Neuroradiology"
DOI: 10.1007/s00234-020-02466-0
Abstract: Purpose Endovascular therapy to the spinal dural arteriovenous fistula (SDAVF) with a common origin of the radiculomedullary artery and the feeder of the shunt has the risk of spinal cord infarction. This study aimed to…
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Keywords:
feeder;
common origin;
artery feeder;
radiculomedullary artery ... See more keywords
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Published in 2018 at "Astronomy and Astrophysics"
DOI: 10.1051/0004-6361/201833929
Abstract: Context. It has been suggested that the well-studied giant HII regions M16 and M17 may have had a common origin, being an example of large-scale triggered star formation. While some features of the distribution of…
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Keywords:
m16 m17;
common origin;
red supergiants;
spectroscopy ... See more keywords
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Published in 2020 at "Journal of Cosmology and Astroparticle Physics"
DOI: 10.1088/1475-7516/2020/12/024
Abstract: We consider a cosmological scenario where a relativistic particle and a stable massive particle are simultaneously produced from the decay of a late-decaying particle after Big-Bang Nucleosynthesis but before matter-radiation equality. The relativistic and massive…
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Keywords:
common origin;
cosmology;
matter;
dark ... See more keywords
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Published in 2019 at "Monthly Notices of the Royal Astronomical Society"
DOI: 10.1093/mnras/stz2147
Abstract: The origin of the molecular clouds orbiting SgrA* is one of the most debated questions about our Galactic Centre. Here, we present the hydrodynamic simulation of a molecular cloud infalling towards SgrA*, performed with the…
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Keywords:
common origin;
molecular clouds;
circumnuclear disc;
galactic centre ... See more keywords
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Published in 2023 at "Biomolecules"
DOI: 10.3390/biom13030455
Abstract: The protein C is a small viral protein encoded in an overlapping frame of the P gene in the subfamily Orthoparamyxovirinae. This protein, expressed by alternative translation initiation, is a virulence factor that regulates viral…
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Keywords:
common structural;
orthoparamyxovirinae proteins;
protein;
origin common ... See more keywords
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Published in 2023 at "Genes"
DOI: 10.3390/genes14040928
Abstract: Pathogenic variants in the SLC26A4 gene leading to nonsyndromic recessive deafness (DFNB4), or Pendred syndrome, are some of the most common causes of hearing loss worldwide. Earlier, we found a high proportion of SLC26A4-related hearing…
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Keywords:
slc26a4 gene;
pathogenic variant;
hearing loss;
variant 919 ... See more keywords