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- Sohler, D., et al.
(författare)
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Yrast states of the proton drip line nucleus 106 Sb
- 1999
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Ingår i: Physical Review C - Nuclear Physics. - 2469-9985 .- 2469-9993 .- 0556-2813 .- 1089-490X. ; 59:3, s. 1324-1327
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Tidskriftsartikel (refereegranskat)abstract
- Yrast states of [Formula Presented] have been investigated in the [Formula Presented] reaction using in-beam [Formula Presented]-spectroscopic methods and in the [Formula Presented] reaction performing delayed [Formula Presented] and conversion electron studies. A new isomeric state was found at 103 keV with [Formula Presented] The number of states and transitions in the proposed level scheme have been doubled. The experimental results are discussed within the framework of the shell model. © 1999 The American Physical Society.
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- Lipoglavsek, M, et al.
(författare)
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E2 polarization charge in Sn-102
- 1998
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Ingår i: PHYSICS LETTERS B. - : ELSEVIER SCIENCE BV. ; 440:3-4, s. 246-250
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- The nucleus Sn-102, which is the lightest Sn isotope with known excited states, was investigated with the Cr-50(Ni-58, alpha 2n) reaction using delayed in-beam gamma-ray and conversion-electron spectroscopy. The experimental setup was designed to study th
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- Fischer, S M, et al.
(författare)
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Alignment additivity in the two-quasiparticle superdeformed bands of Tl-192
- 1996
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Ingår i: Physical Review C. Nuclear Physics. - 0556-2813 .- 1089-490X. ; 53:5, s. 2126-2133
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Tidskriftsartikel (refereegranskat)abstract
- Four superdeformed bands have been confirmed in Tl-192. Two of these bands have T-(2) dynamic moments of inertia which are nearly constant with rotational frequency HBAR omega. The other two bands show the characteristic rise of T-(2) with increasing HBAR omega seen in most superdeformed bands of the A = 190 region of superdeformation. From comparisons with the odd-A neighbors, it was found that the alignments of these bands relative to a Hg-192 core can be accounted for from the additive contributions of the assigned quasiproton and quasineutron orbitals.
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6. |
- Sohler, D, et al.
(författare)
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Yrast states of the proton drip line nucleus Sb-106
- 1999
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Ingår i: PHYSICAL REVIEW C-NUCLEAR PHYSICS. - : AMERICAN PHYSICAL SOC. - 0556-2813. ; 59:3, s. 1324-1327
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Yrast states of Sb-106 have been investigated in the Fe-54(Ni-58, alpha pn) reaction using in-beam gamma-spectroscopic methods and in the Cr-50(Ni-58,pn) reaction performing delayed gamma and conversion electron studies. A new isomeric state was found at
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7. |
- Adeva, B, et al.
(författare)
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Large enhancement of deuteron polarization with frequency modulated microwaves
- 1996
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Ingår i: NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT. - : ELSEVIER SCIENCE BV. - 0168-9002. ; 372:3, s. 339-343
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- We report a large enhancement of 1.7 in deuteron polarization up to values of 0.6 due to frequency modulation of the polarizing microwaves in a two liter polarized target using the method of dynamic nuclear polarization. This target was used during a deep
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8. |
- Ahmad, F, et al.
(författare)
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IL-3 and IL-4 activate cyclic nucleotide phosphodiesterases 3 (PDE3) and 4 (PDE4) by different mechanisms in FDCP2 myeloid cells
- 1999
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Ingår i: Journal of Immunology. - 1550-6606. ; 162:8, s. 4864-4875
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Tidskriftsartikel (refereegranskat)abstract
- In FDCP2 myeloid cells, IL-4 activated cyclic nucleotide phosphodiesterases PDE3 and PDE4, whereas IL-3, granulocyte-macrophage CSF (GM-CSF), and phorbol ester (PMA) selectively activated PDE4. IL-4 (not IL-3 or GM-CSF) induced tyrosine phosphorylation of insulin-receptor substrate-2 (IRS-2) and its association with phosphatidylinositol 3-kinase (PI3-K). TNF-alpha, AG-490 (Janus kinase inhibitor), and wortmannin (PI3-K inhibitor) inhibited activation of PDE3 and PDE4 by IL-4. TNF-alpha also blocked IL-4-induced tyrosine phosphorylation of IRS-2, but not of STAT6. AG-490 and wortmannin, not TNF-alpha, inhibited activation of PDE4 by IL-3. These results suggested that IL-4-induced activation of PDE3 and PDE4 was downstream of IRS-2/PI3-K, not STAT6, and that inhibition of tyrosine phosphorylation of IRS molecules might be one mechnism whereby TNF-alpha could selectively regulate activities of cytokines that utilized IRS proteins as signal transducers. RO31-7549 (protein kinase C (PKC) inhibitor) inhibited activation of PDE4 by PMA. IL-4, IL-3, and GM-CSF activated mitogen-activated protein (MAP) kinase and protein kinase B via PI3-K signals; PMA activated only MAP kinase via PKC signals. The MAP kinase kinase (MEK-1) inhibitor PD98059 inhibited IL-4-, IL-3-, and PMA-induced activation of MAP kinase and PDE4, but not IL-4-induced activation of PDE3. In FDCP2 cells transfected with constitutively activated MEK, MAP kinase and PDE4, not PDE3, were activated. Thus, in FDCP2 cells, PDE4 can be activated by overlapping MAP kinase-dependent pathways involving PI3-K (IL-4, IL-3, GM-CSF) or PKC (PMA), but selective activation of PDE3 by IL-4 is MAP kinase independent (but perhaps IRS-2/PI3-K dependent).
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- Eudy, James D., et al.
(författare)
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Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa
- 1998
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Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 280:5370, s. 1753-1757
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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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