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Search: WFRF:(Ozawa K.) > (2020-2023)

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1.
  • Horio, M., et al. (author)
  • Influence of oxygen coordination number on the electronic structure of single-layer La-based cuprates
  • 2023
  • In: Physical Review B. - 2469-9950. ; 108:3
  • Journal article (peer-reviewed)abstract
    • We present an angle-resolved photoemission spectroscopy study of the single-layer T∗-type structured cuprate SmLa1-xSrxCuO4 with unique fivefold pyramidal oxygen coordination. Upon varying oxygen content, T∗-SmLa1-xSrxCuO4 evolved from a Mott-insulating to a metallic state where the Luttinger sum rule breaks down under the assumption of a large holelike Fermi surface. This is in contrast with the known doping evolution of the structural isomer La2-xSrxCuO4 with sixfold octahedral coordination. In addition, quantitatively characterized Fermi surface suggests that the empirical Tc rule for octahedral oxygen-coordination systems does not apply to T∗-SmLa1-xSrxCuO4. The present results highlight unique properties of the T∗-type cuprates possibly rooted in its oxygen coordination, and necessitate thorough investigation with careful evaluation of disorder effects.
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2.
  • Mizumaki, H, et al. (author)
  • A frequent nonsense mutation in exon 1 across certain HLA-A and -B alleles in leukocytes of patients with acquired aplastic anemia
  • 2021
  • In: Haematologica. - : Ferrata Storti Foundation (Haematologica). - 1592-8721 .- 0390-6078. ; 106:6, s. 1581-1590
  • Journal article (peer-reviewed)abstract
    • Leukocytes that lack HLA allelic expression are frequently detected in patients with acquired aplastic anemia (AA) who respond to immunosuppressive therapy (IST), although the exact mechanisms underlying the HLA loss and HLA allele repertoire likely to acquire loss-of-function mutations are unknown. We identified a common nonsense mutation at position 19 (c.19C>T, p.R7X) in exon 1 (Exon1mut) of different HLA-A and -B alleles in HLA-lacking granulocytes from AA patients. A droplet digital PCR (ddPCR) assay capable of detecting as few as 0.07% Exon1mut HLA alleles in total DNA revealed the mutation was present in 29% (101/353) of AA patients, with a median allele frequency of 0.42% (range, 0.071% to 21.3%). Exon1mut occurred in only 12 different HLA-A (n=4) and HLA-B (n=8) alleles, including B*40:02 (n=31) and A*02:06 (n=15), which correspond to 4 HLA supertypes (A02, A03, B07, and B44). The percentages of patients who possessed at least one of these 12 HLA alleles were significantly higher in the 353 AA patients (92%, P
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  • Result 1-6 of 6

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