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- Balpande, A. R., et al.
(författare)
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Excellent specific strength-ductility synergy in novel complex concentrated alloy after suction casting
- 2024
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Ingår i: Materials and Design. - 1873-4197 .- 0264-1275. ; 242
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Tidskriftsartikel (refereegranskat)abstract
- Lightweight alloys are known to improve the fuel efficiency of the structural components due to high strength-to-weight ratio, however, they lack formability at room temperature. This major limitation of poor formability is most of the time overcome by post-fabrication processing and treatments thereby increasing their cost exponentially. We present a novel Ti50V16Zr16Nb10Al5Mo3 (all in at. %) complex concentrated alloy (Ti-CCA) designed based on the combination of valence electron concentration theory and the high entropy approach. The optimal selection of constituent elements has led to a density of 5.63 gm/cc for Ti-CCA after suction casting (SC). SC Ti-CCA displayed exceptional room temperature strength (UTS ∼ 1.25 GPa) and ductility (ε ∼ 35 %) with a yield strength (YS) of ∼ 1.1 GPa (Specific YS = 191 MPa/gm/cc) without any post-processing treatments. The exceptional YS in Ti-CCA is attributed to hetero grain size microstructure, whereas enormous strength-ductility synergy is due to the concurrent occurrence of slip and deformation band formation in the early stages of deformation followed by prolonged necking event due to delayed void nucleation and growth. The proposed philosophy of Ti-CCA design overcomes the conventional notion of strength-ductility trade-off in such alloy systems by retaining their inherent characteristics.
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| 2. |
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| 3. |
- Elfawy, Hasnaa A., et al.
(författare)
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Molecular toxicity of Benzo(a)pyrene mediated by elicited oxidative stress infer skeletal deformities and apoptosis in embryonic zebrafish
- 2021
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Ingår i: Science of the Total Environment. - : Elsevier. - 0048-9697 .- 1879-1026. ; 789
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Tidskriftsartikel (refereegranskat)abstract
- Benzo(a)pyrene (BaP) has become an integral component of disposed of plastic waste, organic pollutants, and remnants of combustible materials in the aquatic environment due to their persistent nature. The accumulation and integration of these polycyclic aromatic hydrocarbons (PAHs) have raised concern to human health and ecological safety. This study assessed the BaP-induced in vivo molecular toxicity with embryonic zebrafish inferred by oxidative stress and apoptosis. BaP was found to induce morphological and physiological abnormalities like delayed hatching (p < 0.05). Computational analysis demonstrated the high-affinity interaction of BaP with the zebrafish hatching enzyme (ZHE1) with Arg, Cys, Ala, Tyr, and Phe located at the active site revealing the influence of BaP on delayed hatching due to alteration of the enzyme structure. RT-PCR analysis revealed significant down-regulation of the skeletal genes Sox9a, SPP1/OPN, and Col1a1 (p < 0.05) genes. The cellular investigations unraveled that the toxicity of BaP extends to the skeletal regions of zebrafish (head, backbone, and tail) because of the elicited oxidative stress leading to apoptosis. The study extended the horizon of understanding of BaP toxicity at the molecular level which will enhance the indulgent and designing of techniques for better ecological sustainability.
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| 6. |
- Pirazzi, Carlo, et al.
(författare)
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PNPLA3 has retinyl-palmitate lipase activity in human hepatic stellate cells
- 2014
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Ingår i: Human Molecular Genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 23:15, s. 4077-4085
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Tidskriftsartikel (refereegranskat)abstract
- Retinoids are micronutrients that are stored as retinyl esters in the retina and hepatic stellate cells (HSCs). HSCs are key players in fibrogenesis in chronic liver diseases. The enzyme responsible for hydrolysis and release of retinyl esters from HSCs is unknown and the relationship between retinoid metabolism and liver disease remains unclear. We hypothesize that the patatin-like phospholipase domain-containing 3 (PNPLA3) protein is involved in retinol metabolism in HSCs. We tested our hypothesis both in primary human HSCs and in a human cohort of subjects with non-alcoholic fatty liver disease (N = 146). Here we show that PNPLA3 is highly expressed in human HSCs. Its expression is regulated by retinol availability and insulin, and increased PNPLA3 expression results in reduced lipid droplet content. PNPLA3 promotes extracellular release of retinol from HSCs in response to insulin. We also show that purified wild-type PNPLA3 hydrolyzes retinyl palmitate into retinol and palmitic acid. Conversely, this enzymatic activity is markedly reduced with purified PNPLA3 148M, a common mutation robustly associated with liver fibrosis and hepatocellular carcinoma development. We also find the PNPLA3 I148M genotype to be an independent (P = 0.009 in a multivariate analysis) determinant of circulating retinol-binding protein 4, a reliable proxy for retinol levels in humans. This study identifies PNPLA3 as a lipase responsible for retinyl-palmitate hydrolysis in HSCs in humans. Importantly, this indicates a potential novel link between HSCs, retinoid metabolism and PNPLA3 in determining the susceptibility to chronic liver disease.
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