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Träfflista för sökning "WFRF:(Adolfsson Rolf) srt2:(2005-2009)"

Sökning: WFRF:(Adolfsson Rolf) > (2005-2009)

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  • Adolfsson, Petra, 1970, et al. (författare)
  • Ordning och komplexitet - offentlig sektor till vardags och i princip
  • 2009
  • Ingår i: Adolfsson, P. & Solli, R. (red.) (2009) Offentlig sektor och komplexitet. Om hantering av mål, strategier och professioner. - Lund : Studentlitteratur. - 9789144057804 ; , s. 17-36
  • Bokkapitel (övrigt vetenskapligt/konstnärligt)
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4.
  • Adolfsson, Rolf (författare)
  • A review of Swedish crop residue statistics used in the greenhouse gas inventory
  • 2005
  • Rapport (övrigt vetenskapligt/konstnärligt)abstract
    • Factors for recalculating primary crops into the nitrogen content of crop residues for different arable crops are compiled and summarised here. The data is included in the calculation of nitrous oxide from the turnover in crop residues and was used in the inventory of greenhouse gases in the 2006 Submission. The data is compared to data for both Denmark and Finland. In addition, sources of uncertainty are discussed. The suggested revision decreases the estimated emissions from crop residues by 18 % in 2003. The emissions from crop residues correspond to 6 % of the N2O emissions from agriculture in this year.
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5.
  • Adolfsson,, Rolf (författare)
  • A review of Swedish crop residue statistics used in the greenhouse gas inventory
  • 2005
  • Rapport (övrigt vetenskapligt/konstnärligt)abstract
    • The IPCC (Intergovernmental Panel on Climate Change) calculation model for nitrous oxide (N2O) emissions from agricultural land includes emissions from the nitrogen turnover in crop residues. The nitrogen content of crop residues is calculated using primary crop statistics in combination with recalculation factors, that is, the ratios of crop residue/primary crop and the nitrogen content in crop residues. In addition, information on removed crop residues is used to subtract that part of the crop residues that is not turned over on agricultural land.A comparison between data used in different countries reveals great differences.1 Variations in climate, soil fertility and production methods across different countries partly explain some of the differences. Nevertheless, it is likely that these differences also depend on different definitions as well as on variations in the trial data. A more systematic comparison of the recalculations for different countries requires well-documented sources of information
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6.
  • Alaerts, Maaike, et al. (författare)
  • Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population
  • 2009
  • Ingår i: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. - : John Wiley & Sons, Inc. - 1552-4841 .- 1552-485X. ; 150B:4, s. 585-592
  • Tidskriftsartikel (refereegranskat)abstract
    • Through active reuptake of serotonin into presynaptic neurons, the serotonin transporter (5-HTT) plays an important role in regulating serotonin concentrations in the brain, and it is the site of binding for tricyclic antidepressants and selective serotonin reuptake inhibitors (SSRIs). Therefore it has been hypothesized that this transporter is involved in the etiology of bipolar (BP) disorder. Inconsistent association study results for the SLC6A4 gene encoding 5-HTT reported in literature emphasize the need for more systematic and detailed analyses of this candidate gene. We performed an extensive analysis of SLC6A4 on DNA of 254 BPI patients and 364 control individuals from a Northern Swedish isolated population. This analysis consisted of a HapMap LD-based association study including three widely investigated polymorphisms (5-HTTVNTR, 5-HTTLPR, and rs3813034), a copy-number variation (CNV) analysis and a mutation analysis of the complete coding sequence and the 3'-UTR of SLC6A4. No single marker showed statistically significant association with BPI, nor did any of the haplotypes. In the mutation analysis 13 novel variants were detected, including 2 amino acid substitutions M389V and 1587L, but these are probably not implicated in risk for BP. No deletions or duplications were detected in the CNV analysis. We conclude that variation in the SLC6A4 gene or its regulatory regions does not contribute to the susceptibility for BP disorder in the Northern Swedish population.
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7.
  • Alaerts, Maaike, et al. (författare)
  • Lack of association of an insertion/deletion polymorphism in the G protein-coupled receptor 50 with bipolar disorder in a Northern Swedish population
  • 2006
  • Ingår i: Psychiatric Genetics. - : Lippincott Williams & Wilkins. - 0955-8829 .- 1473-5873. ; 16:6, s. 235-236
  • Tidskriftsartikel (refereegranskat)abstract
    • GPR50 is a G protein-coupled receptor, located on Xq28 and related to the melatonin receptor family. It is suggested as a functional and positional candidate gene for bipolar disorder (BP). Recently an insertion/deletion polymorphism in GPR50, Delta502-505, was found to be associated with BP in a Scottish association sample (P=0.007). When the analysis was restricted to female subjects, the association increased in significance (P=0.00023). We attempted to replicate this finding in a Northern Swedish association sample, but no significant association was detected (P=0.7, women only: P=0.65).
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8.
  • Alaerts, Maaike, et al. (författare)
  • Support for NRG1 as a Susceptibility Factor for Schizophrenia in a Northern Swedish Isolated Population
  • 2009
  • Ingår i: Archives of General Psychiatry. - : American Medical Association. - 0003-990X .- 1538-3636. ; 66:8, s. 828-837
  • Tidskriftsartikel (refereegranskat)abstract
    • Context: Neuregulin 1 (NRG1), a growth factor involved in neurodevelopment, myelination, neurotransmitter receptor expression, and synaptic plasticity, first joined the list of candidate genes for schizophrenia when a 7-marker haplotype at the 5' end of the gene (Hap(ICE)) was shown to be associated with the disorder in the Icelandic population. Since then, more genetic and functional evidence has emerged, which supports a role for NRG1 in the development of schizophrenia.Objective: To determine the contribution of NRG1 to susceptibility for schizophrenia in a northern Swedish isolated population.Design: Detailed linkage disequilibrium (LD)-based patient- control association study. This is the first study to type and analyze the 7 Hap(ICE) markers and a set of 32 HapMap tagging single-nucleotide polymorphisms (SNPs) that represents variants with a minor allele frequency of at least 1% and fully characterizes the LD structure of the 5' part of NRG1.Setting: Outpatient and inpatient hospitals.Participants: A total of 486 unrelated patients with schizophrenia and 514 unrelated control individuals recruited from a northern Swedish isolated population.Main Outcome Measures: Association between markers and disease.Results: Analysis of the Hap(ICE) markers showed the association of a 7-marker and 2-microsatellite haplotype, different from the haplotypes associated in the Icelandic population and overrepresented in northern Swedish control individuals. Subsequently, a more detailed analysis that included all 37 genotyped SNPs was performed by investigating haplotypic association, dependent and independent of LD block structure. We found significant association with 5 SNPs located in the second intron of NRG1 (.007 <= P <= .04). Also, 2-, 3-, and 4-SNP windows that comprise these SNPs were associated (P < 3 x 10(-4)). One protective haplotype (0% vs 1.8%; P < 5 x 10(-5)) and 1 disease risk-causing haplotype (40.4% vs 34.9%, P=.02) were defined.Conclusion: The NRG1 gene contributes to the susceptibility for schizophrenia in the northern Swedish population.
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9.
  • Angst, Jules, et al. (författare)
  • The HCL-32 : towards a self-assessment tool for hypomanic symptoms in outpatients
  • 2005
  • Ingår i: Journal of Affective Disorders. - Amsterdam : Elsevier. - 0165-0327 .- 1573-2517. ; 88:2, s. 217-233
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Bipolar disorders (BP) are frequently diagnosed and treated as pure depression initially; accurate diagnosis often being delayed by 8 to 10 years. In prospective studies, the presence of hypomanic symptoms in adolescence is strongly predictive of later bipolar disorders. As such, an instrument for self-assessment of hypomanic symptoms might increase the detection of suspected and of manifest, but under-treated, cases of bipolar disorders.Methods: The multi-lingual hypomania checklist (HCL-32) has been developed and is being tested internationally. This preliminary paper reports the performance of the scale in distinguishing individuals with BP (N=266) from those with major depressive disorder (MDD; N= 160). The samples were adult psychiatry patients recruited in Italy (N= 186) and Sweden (N=240).Results: The samples reported similar clinical profiles and the structure for the HCL-32 demonstrated two main factors identified as "active/elated" hypomania and "risk-taking/irritable" hypomania. The HCL-32 distinguished between BP and MDD with a sensitivity of 80% and a specificity of 51%.Limitations: Although the HCL-32 is a sensitive instrument for hypomanic symptoms, it does not distinguish between BP-1 and BP-11 disorders.Conclusions: Future studies should test if different combinations of items. possibly recording the consequences of hypomania, can distinguish between these BP subtypes.
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