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Träfflista för sökning "(WFRF:(Ma J)) conttype:(refereed) srt2:(1995-1999)"

Sökning: (WFRF:(Ma J)) conttype:(refereed) > (1995-1999)

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1.
  • Dunham, I, et al. (författare)
  • The DNA sequence of human chromosome 22
  • 1999
  • Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 402:6761, s. 489-495
  • Tidskriftsartikel (refereegranskat)
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  • Guo, J.H., et al. (författare)
  • Resonant excitation x-ray-fluorescence from C-60
  • 1995
  • Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 52, s. 10681-
  • Tidskriftsartikel (refereegranskat)abstract
    • X-ray fluorescence of condensed C-60 has been recorded in high resolution using monochromatic synchrotron radiation excitation. Strong intensity modulation of constituent spectral features is observed with varying excitation energy up to 10 eV above threshold. The energy dependence is interpreted as due to resonant inelastic x-ray scattering, leading to symmetry selection rules governing the two-photon process in the fully symmetric molecule.
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  • BERNSTEIN, LA, et al. (författare)
  • ONSET OF COLLECTIVITY IN NEUTRON-DEFICIENT PO-196,PO-198
  • 1995
  • Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 52:2, s. 621-627
  • Tidskriftsartikel (refereegranskat)abstract
    • We have studied via in-beam gamma-ray spectroscopy Po-196 and Po-198, which are the first neutron-deficient Po isotopes to exhibit a collective low-lying structure. The ratios of yrast state energies and the E2 branching ratios of transitions from non-yrast to yrast states are indicative of a low-lying vibrational structure. The onset of collective motion in these isotopes can be attributed to the opening of the neutron i(13/2) orbital at N approximate to 112 and the resulting large overlap between the two valence protons in the h(9/2) orbital and the valence neutrons in the i(13/2) orbital.
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  • CLARK, RM, et al. (författare)
  • SUPERDEFORMATION IN THE BISMUTH NUCLEI
  • 1995
  • Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 51:3, s. R1052-R1056
  • Tidskriftsartikel (refereegranskat)
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10.
  • Eudy, James D., et al. (författare)
  • Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa
  • 1998
  • Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 280:5370, s. 1753-1757
  • Tidskriftsartikel (refereegranskat)abstract
    • Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268ZD1 and AFM144XF2. Three biologically important mutations in Usher syndrome type IIa patients were identified in a gene (USH2A) isolated from this critical region. The USH2A gene encodes a protein with a predicted size of 171.5 kilodaltons that has laminin epidermal growth factor and fibronectin type III motifs; these motifs are most commonly observed in proteins comprising components of the basal lamina and extracellular matrixes and in cell adhesion molecules.
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  • Resultat 1-10 av 58

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