↓ Direkt till sidans innehåll
↓ Direkt till sidans sekundära innehåll (sidomenyn)

Träfflista för sökning "WFRF:(Vissers M.) srt2:(2010-2014)"

Search: WFRF:(Vissers M.) > (2010-2014)

Result 1-6 of 6

Sort/group result

Sort by: Hits per page:

Enumeration	Reference	Cover	Find
1.	Frisk Kockum, Anton, 1987, et al. (author) Detailed modelling of the susceptibility of a thermally populated, strongly driven circuit-QED system 2013 In: Journal of Physics B: Atomic, Molecular and Optical Physics. - : IOP Publishing. - 1361-6455 .- 0953-4075. ; 46:22 Journal article (peer-reviewed)abstract We present measurements and modelling of the susceptibility of a 2D microstrip cavity coupled to a driven transmon qubit. We are able to fit the response of the cavity to a weak probe signal with high accuracy in the strong coupling, low detuning, i.e., non-dispersive, limit over a wide bandwidth. The observed spectrum is rich in multi-photon processes for the doubly dressed transmon. These features are well explained by including the higher transmon levels in the driven Jaynes-Cummings model and solving the full master equation to calculate the susceptibility of the cavity.
2.	Helsmoortel, Celine, et al. (author) A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP 2014 In: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 46:4, s. 380- Journal article (peer-reviewed)abstract Despite the high heritability of autism spectrum disorders (ASD), characterized by persistent deficits in social communication and interaction and restricted, repetitive patterns of behavior, interests or activities(1), a genetic diagnosis can be established in only a minority of patients. Known genetic causes include chromosomal aberrations, such as the duplication of the 15q11-13 region, and monogenic causes, as in Rett and fragile- X syndromes. The genetic heterogeneity within ASD is striking, with even the most frequent causes responsible for only 1% of cases at the most. Even with the recent developments in nextgeneration sequencing, for the large majority of cases no molecular diagnosis can be established(2-7). Here, we report ten patients with ASD and other shared clinical characteristics, including intellectual disability and facial dysmorphisms caused by a mutation in ADNP, a transcription factor involved in the SWI/ SNF remodeling complex. We estimate this gene to be mutated in at least 0.17% of ASD cases, making it one of the most frequent ASD- associated genes known to date.
3.	Hoogland, A. M., et al. (author) CRISP-3 AND B-MSP ON PROSTATE CANCER NEEDLE-BIOPSIES DO NOT HAVE PREDICTIVE VALUE FOR SUBSEQUENT PROSTATECTOMY OUTCOME 2011 In: European Urology Supplements. - 1569-9056. ; 10:2, s. 237-238 Conference paper (peer-reviewed)
4.	Wortmann, SB, et al. (author) Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness 2012 In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 44:7, s. 797-U231 Journal article (peer-reviewed)
5.	Baron, R, et al. (author) Refractory Chronic Pain Screening Tool (RCPST): a feasibility study to assess practicality and validity of identifying potential neurostimulation candidates 2014 In: Pain medicine (Malden, Mass.). - : Oxford University Press (OUP). - 1526-4637 .- 1526-2375. ; 15:2, s. 281-291 Journal article (peer-reviewed)
6.	Vissers, DCJ, et al. (author) An economic evaluation of short-acting opioids for treatment of breakthrough pain in patients with cancer 2011 In: Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research. - : Elsevier BV. - 1524-4733. ; 14:2, s. 274-281 Journal article (peer-reviewed)

Skapa referenser, mejla, bekava och länka

Permalink

Result 1-6 of 6

Refine your search

Type of publication: journal article (5); conference paper (1)

Type of content: peer-reviewed (6)

Author/Editor: Hansson, P. (1); Frisk Kockum, Anton, ... (1); Johansson, Göran, 19 ... (1); van Bokhoven, H (1); Sandberg, M (1); Gilissen, C (1); show more...; Klein, C. (1); Baron, R (1); Jacobs, M (1); Bjartell, Anders (1); Annerén, Göran (1); Jakobsson, J. (1); Nordgren, Ann (1); Taylor, RS (1); Spelbrink, JN (1); Attal, N (1); Cruccu, G (1); Kulik, W (1); Baric, I (1); Backonja, MM (1); Eldridge, P (1); Levy, R (1); Vissers, K (1); Buchser, E (1); De Andres, J (1); Loeser, JD (1); Prager, JP (1); Hicks, MS (1); Regnault, A (1); Van den Abeele, C (1); Vissers, M. R. (1); Malmgren, Helena (1); Schuurs-Hoeijmakers, ... (1); Roobol, M J (1); Naess, K (1); Eichler, Evan E. (1); Bosco, Paolo (1); Kleefstra, Tjitske (1); Grunewald, A (1); Dahlman, Anna K (1); Vaz, FM (1); Rodenburg, RJ (1); Vissers, LELM (1); de Vries, Bert B A (1); Yntema, Helger G (1); Gao, J. S. (1); Pappas, D. P. (1); Wortmann, SB (1); van Hasselt, PM (1); Schroder, F. H. (1); show less...

University: Karolinska Institutet (4); Uppsala University (1); Lund University (1); Chalmers University of Technology (1)

Language: English (6)

Research subject (UKÄ/SCB): Medical and Health Sciences (2); Natural sciences (1)

Year

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.

Copyright © LIBRIS - National Library Systems
LIBRIS.kb.se

pil uppåt

Close

Copy and save the link in order to return to this view