SwePub
Sök i SwePub databas

  Utökad sökning

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

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

  • Resultat 1-6 av 6
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Frisk Kockum, Anton, 1987, et al. (författare)
  • Detailed modelling of the susceptibility of a thermally populated, strongly driven circuit-QED system
  • 2013
  • Ingår i: Journal of Physics B: Atomic, Molecular and Optical Physics. - : IOP Publishing. - 1361-6455 .- 0953-4075. ; 46:22
  • Tidskriftsartikel (refereegranskat)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. (författare)
  • A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
  • 2014
  • Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 46:4, s. 380-
  • Tidskriftsartikel (refereegranskat)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.
  •  
4.
  •  
5.
  •  
6.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-6 av 6

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