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Träfflista för sökning "WFRF:(Jansson Mattias) srt2:(2005-2009)"

Sökning: WFRF:(Jansson Mattias) > (2005-2009)

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1.
  • Jansson, Nina, 1976, et al. (författare)
  • Down-regulation of placental transport of amino acids precedes the development of intrauterine growth restriction in rats fed a low protein diet.
  • 2006
  • Ingår i: The Journal of physiology. - : Wiley. - 0022-3751. ; 576:Pt 3, s. 935-46
  • Tidskriftsartikel (refereegranskat)abstract
    • Intrauterine growth restriction (IUGR) represents an important risk factor for perinatal complications and for adult disease. IUGR is associated with a down-regulation of placental amino acid transporters; however, whether these changes are primary events directly contributing to IUGR or a secondary consequence is unknown. We investigated the time course of changes in placental and fetal growth, placental nutrient transport in vivo and the expression of placental nutrient transporters in pregnant rats subjected to protein malnutrition, a model for IUGR. Pregnant rats were given either a low protein (LP) diet (n = 64) or an isocaloric control diet (n = 66) throughout pregnancy. Maternal insulin, leptin and IGF-I levels decreased, whereas maternal amino acid concentrations increased moderately in response to the LP diet. Fetal and placental weights in the LP group were unaltered compared to control diet at gestational day (GD) 15, 18 and 19 but significantly reduced at GD 21. Placental system A transport activity was reduced at GD 19 and 21 in response to a low protein diet. Placental protein expression of SNAT2 was decreased at GD 21. In conclusion, placental amino acid transport is down-regulated prior to the development of IUGR, suggesting that these placental transport changes are a cause, rather than a consequence, of IUGR. Reduced maternal levels of insulin, leptin and IGF-1 may link maternal protein malnutrition to reduced fetal growth by down-regulation of key placental amino acid transporters.
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2.
  • Andersson, Niklas, 1970, et al. (författare)
  • Variants of the interleukin-1 receptor antagonist gene are associated with fat mass in men
  • 2009
  • Ingår i: International Journal of Obesity. - : Springer Science and Business Media LLC. - 0307-0565 .- 1476-5497. ; 33:5, s. 525-533
  • Tidskriftsartikel (refereegranskat)abstract
    • Context: Immune functions seem to have connections to variations in body fat mass. Studies of knockout mice indicate that endogenous interleukin (IL)-1 can suppress mature-onset obesity. Objective: To systematically investigate our hypotheses that single- nucleotide polymorphisms (SNPs) and/or haplotypes variants in the IL-1 gene system are associated with fat mass. Subjects: The Gothenburg osteoporosis and obesity determinants (GOOD) study is a population-based cross-sectional study of 18-20 year-old men (n = 1068), from Gothenburg, Sweden. Major findings were confirmed in elderly men (n = 3014) from the Swedish part of the osteoporotic fractures in men (MrOS) multicenter population-based study. Main Outcome Measure: The genotype distributions and their association with body fat mass in different compartments, measured with dual-energy X-ray absorptiometry (DXA). Results: Out of 15 investigated SNPs in the IL-1 receptor antagonist (IL1RN) gene, a recently identified 30 untranslated region C4T (rs4252041, minor allele frequency 4%) SNP was associated with the primary outcome total fat mass (P = 0.003) and regional fat masses, but not with lean body mass or serum IL-1 receptor 1 (IL1RN) levels. This SNP was also associated with body fat when correcting the earlier reported IL1RN_2018 T4C (rs419598) SNP (in linkage disequilibrium with a well-studied variable number tandem repeat of 86 bp). The association between rs4252041 SNP and body fat was confirmed in the older MrOS population (P = 0.03). The rs4252041 SNP was part of three haplotypes consisting of five adjacent SNPs that were identified by a sliding window approach. These haplotypes had a highly significant global association with total body fat (P < 0.001). None of the other investigated members of the IL-1 gene family displayed any SNPs that have not been described previously to be significantly associated with body fat. Conclusions: The IL1RN gene, shown to enhance obesity by suppressing IL-1 effects in experimental animals, have no previously described gene polymorphisms and haplotypes that are associated with fat, but not lean mass in two populations of men. International Journal of Obesity (2009) 33, 525-533; doi: 10.1038/ijo.2009.47; published online 17 March 2009
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4.
  • Birk, Wolfgang, et al. (författare)
  • Threat assessment for unexpected events
  • 2008
  • Patent (populärvet., debatt m.m.)abstract
    • The invention relates to an onboard warning system for a host vehicle (1), a system comprising a sensor system detecting a presence of external objects (2) within a sensor detection area (3) and an external object movement determination unit (5) arranged to determine a measure of a relative movement of said external objects to said host vehicle. The invention is characterized in that the warning system further includes: a host vehicle movement determination unit (4) arranged to determine a relative movement of said host vehicle to a ground-fixed coordinate system; a unit (6) for determination of a measure of a absolute acceleration of said external objects to said ground-fixed coordinate system by transformation of the measure of the relative movement of said external objects to said host vehicle into said ground-fixed coordinate system using the relative movement of said host vehicle determined by said host vehicle movement determination unit; and a warning signal generator (7) arranged to generate a warning signal when said measure of absolute acceleration of said external objects relative to said fixed ground acceleration system in the sensor detection area exceeds a threshold value.
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5.
  • Brännström, Mattias, et al. (författare)
  • Rear end collision mitigation system for an automotive vehicle : patent pending
  • 2006
  • Patent (populärvet., debatt m.m.)abstract
    • The present invention relates to a system (1) and method for autonomous rear impact mitigation in a host vehicle (2) having a brake system (4) and a steering system (5). The relative motion parameters between the host vehicle (2) and a second vehicle (11) behind the host vehicle (2) are established. While the host vehicle (2) has a positive velocity, the brake system (4) of the host vehicle (2) is selectively activated based on the determined relative motion parameters.
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6.
  • Casper, C, et al. (författare)
  • Coreceptor usage of primary HIV type 1 isolates obtained from different lymph node subsets
  • 2005
  • Ingår i: AIDS Research and Human Retroviruses. - : Mary Ann Liebert Inc. - 1931-8405 .- 0889-2229. ; 21:12, s. 1003-1010
  • Tidskriftsartikel (refereegranskat)abstract
    • Biological characteristics of virus quantitatively rescued from different cell types present in lymph nodes of HIV-1-infected individuals in various stages of their disease were determined, not including patients with AIDS defining illness. Viruses were obtained by cocultivation with donor monocyte-derived macrophages and T-lymphocytes and their biological phenotype compared to viruses obtained from the peripheral blood mononuclear cells of the same patient. The biological phenotype was determined on established cell lines (U937-2, CEM, and MT-2) and on the U87.CD4 coreceptor indicator cell lines and variable region 3 (V3) of the envelope was subjected to direct sequencing. All isolates obtained from lymph node subsets used CCR5 as coreceptor. Furthermore, these viruses were also sensitive to inhibition by beta-chemokines as analyzed for viruses of one patient. All 12 V3 regions showed a unique sequence indicating compartmentalization within each patient. The biological phenotype of CCR5-dependent (R5) HIV-1 isolates obtained from PBMC resembles the phenotype of viruses isolated from different lymph node cell subsets.
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7.
  • de Woul, Mattias, 1972- (författare)
  • Response of glaciers to climate change : Mass balance sensitivity, sea level rise and runoff
  • 2008
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • The purpose of this study is to enhance our understanding of the response of glaciers to climate change. Global sea level is affected by changes in glacier ice volume, and melt-water from glaciers is a principal water source in many regions. This study applies glacier mass balance modelling, with varying complexity and spatial resolution, ranging from individual glaciers to regional and global assessments of glacier mass losses. Glaciers located in maritime environments generally show considerably higher mass balance sensitivities than those in continental settings. On average, an assumed increase in annual precipitation of +10% tends to offset the effect of an annual temperature change of +1 K, by roughly 20%. Two case studies, at Storglaciären, Sweden, and Hofsjökull, Iceland, involve model results of future mass balance change and glacier melt induced changes in runoff. Applying a temperature and precipitation scenario for Iceland in 2050 results in increased total runoff from Hofsjökull by roughly one third, and results emphasize the role of the firn layer in delaying water flow through glaciers, yielding a redistribution of discharge within the year. Based on a global gridded data set of glacierized area, the sea level equivalent from all mountain glaciers and ice caps outside the ice sheets in Greenland and Antarctica during 1961–2004, caused by changes in temperature and precipitation, is estimated to be 0.58±0.34 mm a–1. The mountain glaciers and ice caps around Antarctica alone contribute almost 40% of the global estimate, and hence their contribution is considerably larger than previously assumed.
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8.
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9.
  • Eden, Mattias, et al. (författare)
  • Al and O substitutions in BaS-phases, Ba2AlxSi12-xN16-xO2+x : A TEM, XRD and solid-state NMR study
  • 2008
  • Ingår i: Solid State Sciences. - : Elsevier BV. - 1293-2558 .- 1873-3085. ; 10:1, s. 50-60
  • Tidskriftsartikel (refereegranskat)abstract
    • In a series of Ba-based oxonitrido-silicate S-phases (Ba2AlxSi12-xN16-xO2+x) spanning a compositional range up to x approximate to 3, we examine the incorporation of Al and O by Si-29 and Al-27 magic-angle spinning (MAS) solid state nuclear magnetic resonance (NMR) and Al-27 triple-quantum MAS (3QMAS). The 3QMAS spectra reveal Al-27 signals from two distinct structural environments, assigned to AlN4 or AlN3O tetrahedra, respectively, and with their relative amounts depending on the S-phase substitution parameter x. Si-29 NMR show variable fractions of SiN4 and SiN3O environments. The NMR results accord overall with a structural substitution model for which O enters at one crystallographic position (occupied according to N4-xOx), in conjunction with a random Al for Si substitution at two distinct crystallographic positions. This leads to S-phase frameworks built from SiN4, SiN3O, AlN4 and AlN3O tetrahedra.
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10.
  • Fransson, Mattias, et al. (författare)
  • Expression of Toll-like receptor 9 in nose, peripheral blood and bone marrow during symptomatic allergic rhinitis.
  • 2007
  • Ingår i: Respiratory research. - : Springer Science and Business Media LLC. - 1465-993X .- 1465-9921. ; 8
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Allergic rhinitis is an inflammatory disease of the upper airway mucosa that also affects leukocytes in bone marrow and peripheral blood. Toll-like receptor 9 (TLR9) is a receptor for unmethylated CpG dinucleotides found in bacterial and viral DNA. The present study was designed to examine the expression of TLR9 in the nasal mucosa and in leukocytes derived from different cellular compartments during symptomatic allergic rhinitis. METHODS: The study was based on 32 patients with seasonal allergic rhinitis and 18 healthy subjects, serving as controls. Nasal biopsies were obtained before and after allergen challenge. Bone marrow, peripheral blood and nasal lavage fluid were sampled outside and during pollen season. The expression of TLR9 in tissues and cells was analyzed using immunohistochemistry and flow cytometry, respectively. RESULTS: TLR9 was found in several cell types in the nasal mucosa and in different leukocyte subpopulations derived from bone marrow, peripheral blood and nasal lavage fluid. The leukocyte expression was generally higher in bone marrow than in peripheral blood, and not affected by symptomatic allergic rhinitis. CONCLUSION: The widespread expression of TLR9 in the nasal mucosa along with its rich representation in leukocytes in different compartments, demonstrate the possibility for cells involved in allergic airway inflammation to directly interact with bacterial and viral DNA.
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