| 1. |
- O'Donnell, D., et al.
(författare)
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First observation of excited states in Hg-175(95)
- 2009
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Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 79:5, s. 051304-
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Tidskriftsartikel (refereegranskat)abstract
- Excited states of the neutron-deficient nucleus Hg-175, populated using fusion-evaporation reactions, are reported for the first time. The spin and parity of the ground state has been determined to be I-pi=7/2(-) through measurements of the alpha decay to the daughter nucleus Pt-171. A structure based on an isomeric state [T-1/2=0.34(3) mu s] with I-pi=13/2(+) and its decay path to the ground state have been established. The observed structures are interpreted in terms of single-particle configurations, and the trends of coexisting shapes in neighboring nuclei are discussed.
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| 2. |
- Hornillos, M. B. G., et al.
(författare)
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gamma-ray spectroscopy approaching the limits of existence of atomic nuclei : A study of the excited states of Pt-168 and Pt-169
- 2009
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Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 79:6
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Tidskriftsartikel (refereegranskat)abstract
- Excited states in the N=90 and N=91 Pt nuclei have been investigated using the JUROGAM and GREAT spectrometers in conjunction with the RITU gas-filled separator. These nuclei were populated via the reactions Mo-92(Kr-78,2n) and Mo-94(Kr-78,3n) at 335 and 348 MeV, respectively. The recoil-decay tagging technique has been used to correlate prompt gamma radiation with the characteristic alpha decays of Pt-168 and Pt-169. A gamma-gamma analysis has allowed a level scheme for Pt-168 to be reported for the first time and the level scheme for Pt-169 to be extended. The excitation energies of the proposed positive-parity yrast states of Pt-168 are compared with calculations based on the interacting boson model and found to be in excellent agreement. These data show a continuation of the trend toward vibrational nuclei as the N=82 shell gap is approached. In addition, new excited states constituting two decay paths have been discovered in Pt-169. .
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| 3. |
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| 4. |
- Heard-Costa, Nancy L, et al.
(författare)
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NRXN3 is a novel locus for waist circumference : a genome-wide association study from the CHARGE Consortium
- 2009
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Ingår i: PLoS genetics. - : Public Library of Science (PLoS). - 1553-7404. ; 5:6, s. e1000539-
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Tidskriftsartikel (refereegranskat)abstract
- Central abdominal fat is a strong risk factor for diabetes and cardiovascular disease. To identify common variants influencing central abdominal fat, we conducted a two-stage genome-wide association analysis for waist circumference (WC). In total, three loci reached genome-wide significance. In stage 1, 31,373 individuals of Caucasian descent from eight cohort studies confirmed the role of FTO and MC4R and identified one novel locus associated with WC in the neurexin 3 gene [NRXN3 (rs10146997, p = 6.4×10−7)]. The association with NRXN3 was confirmed in stage 2 by combining stage 1 results with those from 38,641 participants in the GIANT consortium (p = 0.009 in GIANT only, p = 5.3×10−8 for combined analysis, n = 70,014). Mean WC increase per copy of the G allele was 0.0498 z-score units (0.65 cm). This SNP was also associated with body mass index (BMI) [p = 7.4×10−6, 0.024 z-score units (0.10 kg/m2) per copy of the G allele] and the risk of obesity (odds ratio 1.13, 95% CI 1.07–1.19; p = 3.2×10−5 per copy of the G allele). The NRXN3 gene has been previously implicated in addiction and reward behavior, lending further evidence that common forms of obesity may be a central nervous system-mediated disorder. Our findings establish that common variants in NRXN3 are associated with WC, BMI, and obesity.
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| 5. |
- Newton-Cheh, Christopher, et al.
(författare)
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Genome-wide association study identifies eight loci associated with blood pressure
- 2009
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Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 41:6, s. 666-676
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Tidskriftsartikel (refereegranskat)abstract
- Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood pressure has proven challenging. We tested 2.5 million genotyped and imputed SNPs for association with systolic and diastolic blood pressure in 34,433 subjects of European ancestry from the Global BPgen consortium and followed up findings with direct genotyping (N <= 71,225 European ancestry, N <= 12,889 Indian Asian ancestry) and in silico comparison (CHARGE consortium, N 29,136). We identified association between systolic or diastolic blood pressure and common variants in eight regions near the CYP17A1 (P = 7 x 10(-24)), CYP1A2 (P = 1 x 10(-23)), FGF5 (P = 1 x 10(-21)), SH2B3 (P = 3 x 10(-18)), MTHFR (P = 2 x 10(-13)), c10orf107 (P = 1 x 10(-9)), ZNF652 (P = 5 x 10(-9)) and PLCD3 (P = 1 x 10(-8)) genes. All variants associated with continuous blood pressure were associated with dichotomous hypertension. These associations between common variants and blood pressure and hypertension offer mechanistic insights into the regulation of blood pressure and may point to novel targets for interventions to prevent cardiovascular disease.
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| 6. |
- O'Donnell, D., et al.
(författare)
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Spectroscopy of the neutron-deficient nucleus Os-167(91)
- 2009
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Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 79:6
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Tidskriftsartikel (refereegranskat)abstract
- Excited states of the nucleus Os-167 have been populated by the reaction Mo-92(Kr-78,2pn). The JUROGAM gamma-ray detector array has been used in conjunction with the RITU gas-filled separator and the GREAT spectrometer to observe prompt gamma rays in coincidence with recoiling fusion-evaporation residues and their subsequent decay by alpha particle emission. By correlating prompt gamma radiation with the characteristic alpha radioactivity of Os-167, it has been possible to extend the level scheme for this nucleus significantly. In particular, an extension of the yrast band and four previously unobserved bands are reported. In addition, the recoil distance Doppler-shift method was used to determine a lifetime of tau=20(4) ps for The I-pi=17/2(+) state in Os-167. Hence, the level of collectivity and magnitude of deformation of the low spin yrast band of this nucleus is established. .
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| 7. |
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| 8. |
- Bäckhed, Fredrik, 1973, et al.
(författare)
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Postnatal lymphatic partitioning from the blood vasculature in the small intestine requires fasting-induced adipose factor
- 2007
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Ingår i: Proc Natl Acad Sci U S A. ; 104:2, s. 606-611
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Tidskriftsartikel (refereegranskat)abstract
- Lymphatic vessels develop from specialized venous endothelial cells. Using knockout mice, we found that fasting-induced adipose factor (Fiaf) is required for functional partitioning of postnatal intestinal lymphatic and blood vessels. In wild-type animals, levels of intestinal Fiaf expression rise during the first postnatal day and peak at day 2, which coincides with the onset of the lymphatico-venous partitioning abnormality in Fiaf-/- mutants on a mixed 129/SvJ:C57BL/6 genetic background. Fiaf deficiency is not associated with disruption of the blood vasculature or with lymphatic endothelial recruitment of smooth muscle cells. We identified Prox1, a critical regulator of lymphangiogenesis, as a downstream target for Fiaf signaling in the intestinal lymphatic endothelium. This organ-specific lymphovascular abnormality can be rescued by allowing embryonic Fiaf-/- intestinal isografts to develop in Fiaf+/+ recipients.
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| 9. |
- Soranzo, Nicole, et al.
(författare)
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A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
- 2009
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Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 41:11, s. 38-1182
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Tidskriftsartikel (refereegranskat)abstract
- The number and volume of cells in the blood affect a wide range of disorders including cancer and cardiovascular, metabolic, infectious and immune conditions. We consider here the genetic variation in eight clinically relevant hematological parameters, including hemoglobin levels, red and white blood cell counts and platelet counts and volume. We describe common variants within 22 genetic loci reproducibly associated with these hematological parameters in 13,943 samples from six European population-based studies, including 6 associated with red blood cell parameters, 15 associated with platelet parameters and 1 associated with total white blood cell count. We further identified a long-range haplotype at 12q24 associated with coronary artery disease and myocardial infarction in 9,479 cases and 10,527 controls. We show that this haplotype demonstrates extensive disease pleiotropy, as it contains known risk loci for type 1 diabetes, hypertension and celiac disease and has been spread by a selective sweep specific to European and geographically nearby populations.
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