SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Anderson K.) "

Sökning: WFRF:(Anderson K.)

  • Resultat 1291-1300 av 1492
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1291.
  • Kyle, R. A., et al. (författare)
  • Monoclonal gammopathy of undetermined significance (MGUS) and smoldering (asymptomatic) multiple myeloma: IMWG consensus perspectives risk factors for progression and guidelines for monitoring and management
  • 2010
  • Ingår i: Leukemia. - : Springer Science and Business Media LLC. - 1476-5551 .- 0887-6924. ; 24:6, s. 1121-1127
  • Forskningsöversikt (refereegranskat)abstract
    • Monoclonal gammopathy of undetermined significance (MGUS) was identified in 3.2% of 21 463 residents of Olmsted County, Minnesota, 50 years of age or older. The risk of progression to multiple myeloma, Waldenstrom's macroglobulinemia, AL amyloidosis or a lymphoproliferative disorder is approximately 1% per year. Low-risk MGUS is characterized by having an M protein < 15 g/l, IgG type and a normal free light chain (FLC) ratio. Patients should be followed with serum protein electrophoresis at six months and, if stable, can be followed every 2-3 years or when symptoms suggestive of a plasma cell malignancy arise. Patients with intermediate and high-risk MGUS should be followed in 6 months and then annually for life. The risk of smoldering (asymptomatic) multiple myeloma (SMM) progressing to multiple myeloma or a related disorder is 10% per year for the first 5 years, 3% per year for the next 5 years and 1-2% per year for the next 10 years. Testing should be done 2-3 months after the initial recognition of SMM. If the results are stable, the patient should be followed every 4-6 months for 1 year and, if stable, every 6-12 months. Leukemia (2010) 24, 1121-1127; doi:10.1038/leu.2010.60; published online 22 April 2010
  •  
1292.
  • Kärnbratt, Joakim, 1982, et al. (författare)
  • Self-Assembly of Linear Porphyrin Oligomers into Well-Defined Aggregates
  • 2012
  • Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 116:37, s. 19630-19635
  • Tidskriftsartikel (refereegranskat)abstract
    • Conjugated zinc porphyrin oligomers of various lengths are shown to form well-defined planar aggregates at low temperatures. The aggregation occurs over a narrow temperature interval (170-150 K) and is accompanied by dramatic changes in the electronic absorption and emission spectra. Similar changes are found in J-aggregates in which the transition dipole moments of aggregated chromophores couple to form a new and intense transition in the absorption spectrum, red shifted from the monomeric chromophore band. For the present porphyrin oligomers, the dramatic absorption changes are not associated with the formation of large aggregates, but rather with the dimerization accompanied by planarization of the oligomers. Free oligomers have a broad distribution of porphyrin porphyrin dihedral angles and show a broad and unstructured absorption spectrum. As the oligomers stack to form aggregates, they planarize and the width of the conformational distribution is reduced to include virtually only the planar conformers, resulting in the observed change of the absorption spectrum. No experimental evidence for the formation of large aggregates was found, while a small aggregate, probably only dimer, is supported by the minor changes of the fluorescence rate constant upon aggregation and the fact that pyridine has no significant effect on the formation of this aggregate, which otherwise is very effective for inhibiting aggregation of zinc porphyrin oligomers. Compared to most porphyrin aggregates, which show broad absorption spectra and quenched fluorescence, these aggregates give sharp absorption and emission spectra with little change in the fluorescence quantum yield. Similar aggregates were also observed for oligomers substituted with both a fullerene electron acceptor and a ferrocene donor. The results presented here will be potentially useful as tools to understand how electron transfer and delocalization processes are influenced by molecular order/disorder transitions.
  •  
1293.
  •  
1294.
  • Landegren, Nils, et al. (författare)
  • Transglutaminase 4 as a prostate autoantigen in male subfertility
  • 2015
  • Ingår i: Science Translational Medicine. - : American Association for the Advancement of Science. - 1946-6234 .- 1946-6242. ; 7:292
  • Tidskriftsartikel (refereegranskat)abstract
    • Autoimmune polyendocrine syndrome type 1 (APS1), a monogenic disorder caused by AIRE gene mutations, features multiple autoimmune disease components. Infertility is common in both males and females with APS1. Although female infertility can be explained by autoimmune ovarian failure, the mechanisms underlying male infertility have remained poorly understood. We performed a proteome-wide autoantibody screen in APS1 patient sera to assess the autoimmune response against the male reproductive organs. By screening human protein arrays with male and female patient sera and by selecting for gender-imbalanced autoantibody signals, we identified transglutaminase 4 (TGM4) as a male-specific autoantigen. Notably, TGM4 is a prostatic secretory molecule with critical role in male reproduction. TGM4 autoantibodies were detected in most of the adult male APS1 patients but were absent in all the young males. Consecutive serum samples further revealed that TGM4 autoantibodies first presented during pubertal age and subsequent to prostate maturation. We assessed the animal model for APS1, the Aire-deficient mouse, and found spontaneous development of TGM4 autoantibodies specifically in males. Aire-deficient mice failed to present TGM4 in the thymus, consistent with a defect in central tolerance for TGM4. In the mouse, we further link TGM4 immunity with a destructive prostatitis and compromised secretion of TGM4. Collectively, our findings in APS1 patients and Aire-deficient mice reveal prostate autoimmunity as a major manifestation of APS1 with potential role in male subfertility.
  •  
1295.
  •  
1296.
  •  
1297.
  • Laskar, Ruhina S, et al. (författare)
  • Sex specific associations in genome wide association analysis of renal cell carcinoma.
  • 2019
  • Ingår i: European Journal of Human Genetics. - : Springer Science and Business Media LLC. - 1018-4813 .- 1476-5438. ; 27:10, s. 1589-1598
  • Tidskriftsartikel (refereegranskat)abstract
    • Renal cell carcinoma (RCC) has an undisputed genetic component and a stable 2:1 male to female sex ratio in its incidence across populations, suggesting possible sexual dimorphism in its genetic susceptibility. We conducted the first sex-specific genome-wide association analysis of RCC for men (3227 cases, 4916 controls) and women (1992 cases, 3095 controls) of European ancestry from two RCC genome-wide scans and replicated the top findings using an additional series of men (2261 cases, 5852 controls) and women (1399 cases, 1575 controls) from two independent cohorts of European origin. Our study confirmed sex-specific associations for two known RCC risk loci at 14q24.2 (DPF3) and 2p21(EPAS1). We also identified two additional suggestive male-specific loci at 6q24.3 (SAMD5, male odds ratio (ORmale) = 0.83 [95% CI = 0.78-0.89], Pmale = 1.71 × 10-8 compared with female odds ratio (ORfemale) = 0.98 [95% CI = 0.90-1.07], Pfemale = 0.68) and 12q23.3 (intergenic, ORmale = 0.75 [95% CI = 0.68-0.83], Pmale = 1.59 × 10-8 compared with ORfemale = 0.93 [95% CI = 0.82-1.06], Pfemale = 0.21) that attained genome-wide significance in the joint meta-analysis. Herein, we provide evidence of sex-specific associations in RCC genetic susceptibility and advocate the necessity of larger genetic and genomic studies to unravel the endogenous causes of sex bias in sexually dimorphic traits and diseases like RCC.
  •  
1298.
  • Le Nours, K, et al. (författare)
  • The structure and characterization of a modular endo-beta-1,4-mannanase from Cellulomonas fimi
  • 2005
  • Ingår i: Biochemistry. - : American Chemical Society (ACS). - 0006-2960 .- 1520-4995. ; 44:38, s. 12700-12708
  • Tidskriftsartikel (refereegranskat)abstract
    • The endo-beta-1,4-mannanase from the soil bacterium Cellulomonas fimi is a modular plant cell wall degrading enzyme involved in the hydrolysis of the backbone of mannan, one of the most abundant polysaccharides of the hemicellulosic network in the plant cell wall. The crystal structure of a recombinant truncated endo-beta-1,4-mannanase from C. fimi (CMan26A-50K) was determined by X-ray crystallography to 2.25 angstrom resolution using the molecular replacement technique. The overall structure of the enzyme consists of a core (beta/alpha)(8)-barrel catalytic module characteristic of clan GH-A, connected via a linker to an immunoglobulin-like module of unknown function. A complex with the oligosaccharide mannotriose to 2.9 angstrom resolution has also been obtained. Both the native structure and the complex show a cacodylate ion bound at the -1 subsite, while subsites -2, -3, and -4 are occupied by mannotriose in the complex. Enzyme kinetic analysis and the analysis of hydrolysis products from manno-oligosaccharides and mannopentitol suggest five important active-site cleft subsites. CfMan26A-50K has a high affinity -3 subsite with Phe325 as an aromatic platform, which explains the mannose releasing property of the enzyme. Structural differences with the homologous Cellvibrio japonicus beta-1,4-mannanase (CjMan26A) at the -2 and -3 subsites may explain the poor performance of CfMan26A mutants as "glycosynthases".
  •  
1299.
  •  
1300.
  • Leavitt, Peter R., et al. (författare)
  • Paleolimnological evidence of the effects on lakes of energy and mass transfer from climate and humans
  • 2009
  • Ingår i: Limnology and Oceanography. - 0024-3590 .- 1939-5590. ; 54:6, s. 2330-2348
  • Forskningsöversikt (refereegranskat)abstract
    • The premise of this article is that climate effects on lakes can be quantified most effectively by the integration of process-oriented limnological studies with paleolimnological research, particularly when both disciplines operate within a common conceptual framework. To this end, the energy (E)-mass (m) flux framework (Em flux) is developed and applied to selected retrospective studies to demonstrate that climate variability regulates lake structure and function over diverse temporal and spatial scales through four main pathways: rapid direct transfer of E to the lake surface by irradiance, heat, and wind; slow indirect effects of E via changes in terrestrial development and subsequent m subsidies to lakes; direct influx of m as precipitation, particles, and solutes from the atmosphere; and indirect influx of water, suspended particles, and dissolved substances from the catchment. Sedimentary analyses are used to illustrate the unique effects of each pathway on lakes but suggest that interactions among mechanisms are complex and depend on the landscape position of lakes, catchment characteristics, the range of temporal variation of individual pathways, ontogenetic changes in lake basins, and the selective effects of humans on m transfers. In particular, preliminary synthesis suggests that m influx can overwhelm the direct effects of E transfer to lakes, especially when anthropogenic activities alter m subsidies from catchments.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1291-1300 av 1492
Typ av publikation
tidskriftsartikel (1252)
konferensbidrag (61)
forskningsöversikt (32)
bokkapitel (5)
rapport (3)
annan publikation (3)
visa fler...
doktorsavhandling (1)
visa färre...
Typ av innehåll
refereegranskat (1390)
övrigt vetenskapligt/konstnärligt (86)
populärvet., debatt m.m. (1)
Författare/redaktör
Moore, R. W. (562)
Garcia, C. (554)
Lokajicek, M. (554)
De, K. (552)
Fox, H. (551)
Jakobs, K. (550)
visa fler...
Meyer, J. (549)
Quadt, A. (549)
Chakraborty, D. (548)
Vachon, B. (548)
Burdin, S. (547)
Cheu, E. (547)
Evans, H. (547)
Haas, A. (547)
Kehoe, R. (547)
Kupco, A. (547)
Piegaia, R. (547)
Qian, J. (547)
Sawyer, L. (547)
Schwartzman, A. (547)
Sosebee, M. (547)
Abbott, B. (546)
Borissov, G. (546)
Brandt, A. (546)
Cooke, M. (546)
Fiedler, F. (546)
Hauser, R. (546)
Owen, M. (546)
Pleier, M. -A. (546)
Schaile, D. (546)
Snyder, S. (546)
Stark, J. (546)
Trefzger, T. (546)
Watts, G. (546)
Wermes, N. (546)
Andeen, T. (545)
Brock, R. (545)
Duflot, L. (545)
Khanov, A. (545)
Shamim, M. (545)
Simak, V. (545)
Strauss, M. (545)
Brooijmans, G. (544)
Hohlfeld, M. (544)
Mitrevski, J. (544)
Protopopescu, S. (544)
Rijssenbeek, M. (544)
Schwienhorst, R. (544)
Shabalina, E. (544)
von Toerne, E. (544)
visa färre...
Lärosäte
Uppsala universitet (619)
Stockholms universitet (546)
Lunds universitet (499)
Kungliga Tekniska Högskolan (427)
Karolinska Institutet (373)
Göteborgs universitet (151)
visa fler...
Chalmers tekniska högskola (69)
Umeå universitet (43)
Luleå tekniska universitet (27)
Linköpings universitet (27)
Linnéuniversitetet (24)
Högskolan Dalarna (20)
Örebro universitet (15)
Sveriges Lantbruksuniversitet (11)
Mittuniversitetet (6)
Högskolan Kristianstad (4)
Jönköping University (4)
Malmö universitet (4)
Södertörns högskola (4)
RISE (3)
Naturhistoriska riksmuseet (3)
Karlstads universitet (2)
Högskolan i Gävle (1)
Mälardalens universitet (1)
Högskolan i Skövde (1)
visa färre...
Språk
Engelska (1490)
Svenska (2)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (814)
Medicin och hälsovetenskap (239)
Teknik (41)
Samhällsvetenskap (29)
Lantbruksvetenskap (6)
Humaniora (3)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy