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- Morganti, Michelangelo, et al.
(författare)
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Effect of light-level geolocators on apparent survival of two highly aerial swift species
- 2018
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Ingår i: Journal of Avian Biology. - : Wiley. - 0908-8857. ; 49:1
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Tidskriftsartikel (refereegranskat)abstract
- Light-level geolocators are currently widely used to track the migration of small-sized birds, but their potentially detrimental effects on survival of highly aerial species have been poorly investigated so far. We recorded capture–recapture histories of 283 common swifts Apus apus and 107 pallid swifts Apus pallidus breeding in 14 colonies in Italy, Spain, Sweden and Switzerland that were equipped with 10 different types of geolocators (‘geolocator birds’), and compared their survival with that of, respectively, 215 common and 101 pallid swifts not equipped with geolocators (‘control birds’). Data were analysed using both GLMMs with return rate as a proxy for survival and mark–recapture models to estimate survival while accounting for recapture probability. In all the analyses, geolocator birds showed reduced apparent survival compared to controls. Geolocator weight was always lower than 3% of body mass, and did not affect survival per se. Geolocators with a light-stalk, which is used in some geolocator models to reduce light sensor shading by feathers, decreased apparent survival more than models without light-stalk. Apparent survival of geolocator birds significantly varied among sites, being much higher in northern Europe. Despite in our analyses we could only partly account for variable recapture probabilities among sites and for inter-annual variability in survival, our results generally showed that equipping swifts with geolocators decreased their survival prospects, but also that the magnitude of this effect may depend on species-specific traits. These conclusions are in line with those of other studies on aerial foragers. We suggest that future studies tracking the movements of aerial insectivorous birds should use devices designed to minimize drag.
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| 2. |
- Bozkurt, Murat Fani, et al.
(författare)
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Guideline for PET/CT imaging of neuroendocrine neoplasms with Ga-68-DOTA-conjugated somatostatin receptor targeting peptides and F-18-DOPA
- 2017
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Ingår i: European Journal of Nuclear Medicine and Molecular Imaging. - : SPRINGER. - 1619-7070 .- 1619-7089. ; 44:9, s. 1588-1601
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Tidskriftsartikel (refereegranskat)abstract
- Purpose & Methods Neuroendocrine neoplasms are a heterogenous group of tumours, for which nuclear medicine plays an important role in the diagnostic work-up as well as in the targeted therapeutic options. This guideline is aimed to assist nuclear medicine physicians in recommending, performing, reporting and interpreting the results of somatostatin receptor (SSTR) PET/CT imaging using Ga-68-DOTA-conjugated peptides, as well as F-18-DOPA imaging for various neuroendocrine neoplasms. Results & Conclusion The previous procedural guideline by EANM regarding the use PET/CT tumour imaging with Ga-68-conjugated peptides has been revised and updated with the relevant and recent literature in the field with contribution of distinguished experts.
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| 3. |
- Sighel, Denise, et al.
(författare)
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Inhibition of mitochondrial translation suppresses glioblastoma stem cell growth
- 2021
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Ingår i: Cell Reports. - : Elsevier BV. - 2211-1247. ; 35:4
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Tidskriftsartikel (refereegranskat)abstract
- Glioblastoma stem cells (GSCs) resist current glioblastoma (GBM) therapies. GSCs rely highly on oxidative phosphorylation (OXPHOS), whose function requires mitochondrial translation. Here we explore the therapeutic potential of targeting mitochondrial translation and report the results of high-content screening with putative blockers of mitochondrial ribosomes. We identify the bacterial antibiotic quinupristin/dalfopristin (Q/D) as an effective suppressor of GSC growth. Q/D also decreases the clonogenicity of GSCs in vitro, consequently dysregulating the cell cycle and inducing apoptosis. Cryoelectron microscopy (cryo-EM) reveals that Q/D binds to the large mitoribosomal subunit, inhibiting mitochondrial protein synthesis and functionally dysregulating OXPHOS complexes. These data suggest that targeting mitochondrial translation could be explored to therapeutically suppress GSC growth in GBM and that Q/D could potentially be repurposed for cancer treatment.
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