| 1. |
- BERMÚDEZ,, Hermann Darío, et al.
(författare)
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The Cretaceous/Paleogene boundary deposits on Gorgonilla Island
- 2018
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Ingår i: The Geology of Colombia: Volume 3 Paleogene – Neogene. - Bogota : Servicio Geológico Colombiano. ; , s. 1-34
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Bokkapitel (refereegranskat)abstract
- A ~20 mm thick spherule bed representing Chicxulub impact ejecta deposits and marking the Cretaceous/Paleogene (K/Pg) boundary was recently discovered on Gorgonilla Island (Gorgona National Natural Park, Pacific of Colombia). This discovery represents the first confirmed record of the K/Pg event in Colombia, South America and the eastern Pacific Ocean. The deposit consists of extraordinarily well–preserved glass spherules (microtektites and microkrystites) reaching 1.1 mm in diameter. Importantly, the Gorgonilla spherule bed is unique relative to other K/Pg boundary sites in that up to 90% of the spherules are intact and not devitrified, and the bed is virtually devoid of lithic fragments and microfossils. The spherules were deposited in a deep marine environment, possibly below the calcite compensation depth. The preservation, normal size–gradation, presence of fine textures within the spherules, and absence of bioturbation or traction transport indicate that the Gorgonilla spherules settled within a water column with minimal disturbance. Thus, the spherule bed may represent one of the first parautochthonous primary deposits of the Chicxulub impact known to date. 40Ar/39Ar dating and micropaleontological analysis reveal that the Gorgonilla spherule bed resulted from the Chicxulub impact. Intense soft–sediment deformation and bed disruption in Maastrichtian sediments of the Gorgonilla Island K/Pg section provide evidence for seismic activity triggered by the Chicxulub bolide impact, 66 million years ago. It is also notable that the basal deposits of the Danian in the Colombian locality present the first evidence of a recovery vegetation, characterized by ferns from a tropical habitat, shortly following the end–Cretaceous event.
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| 2. |
- Bermúdez, Hermann, et al.
(författare)
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The Cretaceous/Paleogene Boundary Deposits on Gorgonilla Island
- 2019. - 1
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Ingår i: <em>The Geology of Colombia, Volume 3 Paleogene – Neogene </em><em></em>. - Bogota : Servicio Geológico Colombiano. ; , s. 1-19
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Bokkapitel (refereegranskat)abstract
- A ca. 20 mm thick spherule bed representing Chicxulub impact ejecta deposits and marking the Cretaceous/Paleogene (K/Pg) boundary was recently discovered on Gorgonilla Island (Gorgona National Natural Park, Pacific of Colombia). This discovery represents the first confirmed record of the K/Pg event in Colombia, South America and the eastern Pacific Ocean. The deposit consists of extraordinarily well–preserved glass spherules (microtektites and microkrystites) reaching 1.1 mm in diameter. Importantly, the Gorgonilla spherule bed is unique relative to other K/Pg boundary sites in that up to 90% of the spherules are intact and not devitrified, and the bed is virtually devoid of lithic fragments and microfossils. The spherules were deposited in a deep marine environment, possibly below the calcite compensation depth. The preservation, normal size–gradation, presence of fine textures within the spherules, and absence of bioturbation or traction transport indicate that the Gorgonilla spherules settled within a water column with minimal disturbance. The spherule bed may represent one of the first parautochthonous primary deposits of the Chicxulub impact known to date. 40Ar/39Ar dating and micropaleontological analysis reveal that the Gorgonilla spherule bed resulted from the Chicxulub impact. Intense soft–sediment deformation and bed disruption in Maastrichtian sediments of the Gorgonilla Island K/Pg section provide evidence for seismic activity triggered by the Chicxulub bolide impact, 66 million years ago. It is also notable that the basal deposits of the Danian in the Colombian locality present the first evidence of a recovery vegetation, characterized by ferns from a tropical habitat, shortly following the end–Cretaceous event.
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| 3. |
- Bossini-Castillo, Lara, et al.
(författare)
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A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort
- 2011
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Ingår i: Annals of the Rheumatic Diseases. - : BMJ. - 1468-2060 .- 0003-4967. ; 70:4, s. 638-641
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Tidskriftsartikel (refereegranskat)abstract
- Objectives The aim of this study was to confirm the influence of TNFSF4 polymorphisms on systemic sclerosis (SSc) susceptibility and phenotypic features. Methods A total of 8 European populations of Caucasian ancestry were included, comprising 3014 patients with SSc and 3125 healthy controls. Four genetic variants of TNFSF4 gene promoter (rs1234314, rs844644, rs844648 and rs12039904) were selected as genetic markers. Results A pooled analysis revealed the association of rs1234314 and rs12039904 polymorphisms with SSc (OR 1.15, 95% CI 1.02 to 1.31; OR 1.18, 95% CI 1.08 to 1.29, respectively). Significant association of the four tested variants with patients with limited cutaneous SSc (lcSSc) was revealed (rs1234314 OR 1.22, 95% CI 1.07 to 1.38; rs844644 OR 0.91, 95% CI 0.83 to 0.99; rs844648 OR 1.10, 95% CI 1.01 to 1.20 and rs12039904 OR 1.20, 95% CI 1.09 to 1.33). Association of rs1234314, rs844648 and rs12039904 minor alleles with patients positive for anti-centromere antibodies (ACA) remained significant (OR 1.23, 95% CI 1.10 to 1.37; OR 1.12, 95% CI 1.01 to 1.25; OR 1.22, 95% CI 1.07 to 1.38, respectively). Haplotype analysis confirmed a protective haplotype associated with SSc, lcSSc and ACA positive subgroups (OR 0.88, 95% CI 0.82 to 0.96; OR 0.88, 95% CI 0.80 to 0.96; OR 0.86, 95% CI 0.77 to 0.97, respectively) and revealed a new risk haplotype associated with the same groups of patients (OR 1.14, 95% CI 1.03 to 1.26; OR 1.20, 95% CI 1.08 to 1.35; OR 1.23, 95% CI 1.07 to 1.42, respectively). Conclusions The data confirm the influence of TNFSF4 polymorphisms in SSc genetic susceptibility, especially in subsets of patients positive for lcSSc and ACA.
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| 4. |
- Cruz, Raquel, et al.
(författare)
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Novel genes and sex differences in COVID-19 severity
- 2022
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Ingår i: Human Molecular Genetics. - : Oxford University Press. - 0964-6906 .- 1460-2083. ; 31:22, s. 3789-3806
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Tidskriftsartikel (refereegranskat)abstract
- Here, we describe the results of a genome-wide study conducted in 11 939 coronavirus disease 2019 (COVID-19) positive cases with an extensive clinical information that were recruited from 34 hospitals across Spain (SCOURGE consortium). In sex-disaggregated genome-wide association studies for COVID-19 hospitalization, genome-wide significance (P < 5 × 10−8) was crossed for variants in 3p21.31 and 21q22.11 loci only among males (P = 1.3 × 10−22 and P = 8.1 × 10−12, respectively), and for variants in 9q21.32 near TLE1 only among females (P = 4.4 × 10−8). In a second phase, results were combined with an independent Spanish cohort (1598 COVID-19 cases and 1068 population controls), revealing in the overall analysis two novel risk loci in 9p13.3 and 19q13.12, with fine-mapping prioritized variants functionally associated with AQP3 (P = 2.7 × 10−8) and ARHGAP33 (P = 1.3 × 10−8), respectively. The meta-analysis of both phases with four European studies stratified by sex from the Host Genetics Initiative (HGI) confirmed the association of the 3p21.31 and 21q22.11 loci predominantly in males and replicated a recently reported variant in 11p13 (ELF5, P = 4.1 × 10−8). Six of the COVID-19 HGI discovered loci were replicated and an HGI-based genetic risk score predicted the severity strata in SCOURGE. We also found more SNP-heritability and larger heritability differences by age (<60 or ≥60 years) among males than among females. Parallel genome-wide screening of inbreeding depression in SCOURGE also showed an effect of homozygosity in COVID-19 hospitalization and severity and this effect was stronger among older males. In summary, new candidate genes for COVID-19 severity and evidence supporting genetic disparities among sexes are provided.
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| 5. |
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| 6. |
- Gretarsdottir, Solveig, et al.
(författare)
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Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
- 2010
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Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 42:8, s. 71-692
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Tidskriftsartikel (refereegranskat)abstract
- We performed a genome-wide association study on 1,292 individuals with abdominal aortic aneurysms (AAAs) and 30,503 controls from Iceland and The Netherlands, with a follow-up of top markers in up to 3,267 individuals with AAAs and 7,451 controls. The A allele of rs7025486 on 9q33 was found to associate with AAA, with an odds ratio (OR) of 1.21 and P = 4.6 x 10(-10). In tests for association with other vascular diseases, we found that rs7025486[A] is associated with early onset myocardial infarction (OR = 1.18, P = 3.1 x 10(-5)), peripheral arterial disease (OR = 1.14, P = 3.9 x 10(-5)) and pulmonary embolism (OR = 1.20, P = 0.00030), but not with intracranial aneurysm or ischemic stroke. No association was observed between rs7025486[A] and common risk factors for arterial and venous diseases-that is, smoking, lipid levels, obesity, type 2 diabetes and hypertension. Rs7025486 is located within DAB2IP, which encodes an inhibitor of cell growth and survival.
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| 7. |
- Hueyuek, Tayfun, et al.
(författare)
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Conceptual design of the early implementation of the NEutron Detector Array (NEDA) with AGATA
- 2016
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Ingår i: European Physical Journal A. - : Springer-Verlag New York. - 1434-6001 .- 1434-601X. ; 52:3
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Tidskriftsartikel (refereegranskat)abstract
- The NEutron Detector Array (NEDA) project aims at the construction of a new high-efficiency compact neutron detector array to be coupled with large gamma-ray arrays such as AGATA. The application of NEDA ranges from its use as selective neutron multiplicity filter for fusion-evaporation reaction to a large solid angle neutron tagging device. In the present work, possible configurations for the NEDA coupled with the Neutron Wall for the early implementation with AGATA has been simulated, using Monte Carlo techniques, in order to evaluate their performance figures. The goal of this early NEDA implementation is to improve, with respect to previous instruments, efficiency and capability to select multiplicity for fusion-evaporation reaction channels in which 1, 2 or 3 neutrons are emitted. Each NEDA detector unit has the shape of a regular hexagonal prism with a volume of about 3.23 l and it is filled with the EJ301 liquid scintillator, that presents good neutron-gamma discrimination properties. The simulations have been performed using a fusion-evaporation event generator that has been validated with a set of experimental data obtained in the Ni-58 + Fe-56 reaction measured with the Neutron Wall detector array.
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| 8. |
- López-Isac, Elena, et al.
(författare)
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Brief Report : IRF4 Newly Identified as a Common Susceptibility Locus for Systemic Sclerosis and Rheumatoid Arthritis in a Cross-Disease Meta-Analysis of Genome-Wide Association Studies
- 2016
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Ingår i: Arthritis & Rheumatology. - : Wiley. - 2326-5191 .- 2326-5205. ; 68:9, s. 2338-2344
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Tidskriftsartikel (refereegranskat)abstract
- Objective: Systemic sclerosis (SSc) and rheumatoid arthritis (RA) are autoimmune diseases that have similar clinical and immunologic characteristics. To date, several shared SSc–RA genetic loci have been identified independently. The aim of the current study was to systematically search for new common SSc–RA loci through an interdisease meta–genome-wide association (meta-GWAS) strategy. Methods: The study was designed as a meta-analysis combining GWAS data sets of patients with SSc and patients with RA, using a strategy that allowed identification of loci with both same-direction and opposite-direction allelic effects. The top single-nucleotide polymorphisms were followed up in independent SSc and RA case–control cohorts. This allowed an increase in the sample size to a total of 8,830 patients with SSc, 16,870 patients with RA, and 43,393 healthy controls. Results: This cross-disease meta-analysis of the GWAS data sets identified several loci with nominal association signals (P < 5 × 10−6) that also showed evidence of association in the disease-specific GWAS scans. These loci included several genomic regions not previously reported as shared loci, as well as several risk factors that were previously found to be associated with both diseases. Follow-up analyses of the putatively new SSc–RA loci identified IRF4 as a shared risk factor for these 2 diseases (Pcombined = 3.29 × 10−12). Analysis of the biologic relevance of the known SSc–RA shared loci identified the type I interferon and interleukin-12 signaling pathways as the main common etiologic factors. Conclusion: This study identified a novel shared locus, IRF4, for the risk of SSc and RA, and highlighted the usefulness of a cross-disease GWAS meta-analysis strategy in the identification of common risk loci.
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| 9. |
- Mendez-Sanchez, Daniel, et al.
(författare)
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Chemoenzymatic Deracemization of Secondary Alcohols by using a TEMPO-Iodine-Alcohol Dehydrogenase System
- 2015
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Ingår i: ChemCatChem. - : Wiley. - 1867-3880. ; 7:24, s. 4016-4020
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Tidskriftsartikel (refereegranskat)abstract
- A deracemization system for secondary alcohols was established after the analysis of individual steps and their compatibility in one pot. The chemical oxidation and bioreduction occurred in a sequential manner to yield 1-arylethanols and lineal aliphatic alcohols with excellent conversions and enantiomeric excess values. The oxidation step was performed by using 2,2,6,6-tetramethylpiperidin-1-oxyl and iodine. This chemical process was extremely favored by sonication, which allowed quantitative formation of the corresponding ketone intermediates after just 1h. Simple destruction of iodine in the same pot allowed sequential bioreduction of the ketones by using either Prelog or antiPrelog enzymes, which led to the preparation of the enantiopure alcohols in excellent yields.
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| 10. |
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