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- Sargeson, A. M., et al.
(författare)
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Names and symbols for the transfermium elements
- 1997
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Ingår i: Pure and Applied Chemistry. - : Walter de Gruyter GmbH. - 0033-4545 .- 1365-3075. ; 69:12, s. 2471-2473
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Tidskriftsartikel (refereegranskat)abstract
- The recommendations (ref. 1) of the Commission on Nomenclature of Inorganic Chemistry (CNIC) on the nomenclature of the transfermium elements (101-109, inclusive) were considered by the IUPAC Bureau at Guildford (UK) in September 1995. As a result of the various criticisms of the recommendations and theway that they had been processed, the Bureau decided to adopt the recommendations as provisional and to circulate them to national/regional nomenclature centres in the normal way, with notices to be published innational/regional chemistry journals and magazines, requesting submission of comments to CNIC. In particular, the National Adhering Organizations (NAOs) were invited to express their views concerning the extant proposals for the names of these elements and the principles and traditions used to derive them. The response from the general chemical community was small, and the bulk of the replies came from nuclear scientists.
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- Fraile, LM, et al.
(författare)
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Octupole correlations in Ra-229
- 1999
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Ingår i: NUCLEAR PHYSICS A. - : ELSEVIER SCIENCE BV. - 0375-9474. ; 657:4, s. 355-390
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Tidskriftsartikel (refereegranskat)abstract
- The structure of Ra-229 has been studied in the beta(-) decay of Fr-229. Spins and parities have been determined from the conversion electron measurements, while half-lives for the 137.5, 142.7, 168.8, 213.0 and 479.0 keV levels have been measured in the
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- Garcia-Guzman, M, et al.
(författare)
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Characterization of recombinant human P2X4 receptor reveals pharmacological differences to the rat homologue.
- 1997
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Ingår i: Molecular Pharmacology. - 0026-895X .- 1521-0111. ; 51:1, s. 109-18
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Tidskriftsartikel (refereegranskat)abstract
- We isolated a cDNA from human brain encoding a purinergic receptor that shows a high degree of homology to the rat P2X4 receptor (87% identity). By fluorescence in situ hybridization, the human P2X4 gene has been mapped to region q24.32 of chromosome 12. Tissue distribution analysis of human P2X4 transcripts demonstrates a broad expression pattern in that the mRNA was detected not only in brain but also in all tissues tested. Heterologous expression of the human P2X4 receptor in Xenopus laevis oocytes and human embryonic kidney 293 cells evoked an ATP-activated channel. Simultaneous whole-cell current and Fura-2 fluorescence measurements in human embronic kidney 293 cells transfected with human P2X4 cDNA allowed us to determine the fraction of the current carried by Ca2: this was approximately 8%, demonstrating a high Ca2+ permeability. Low extracellular Zn2+ concentrations (5-10 microM) increase the apparent gating efficiency of human P2X4 by ATP without affecting the maximal response. However, raising the concentration of the divalent cation (> 100 microM) inhibits the ATP-evoked current in a non-voltage-dependent manner. The human P2X4 receptor displays a very similar agonist potency profile to that of rat P2X4 (ATP > > 2-methylthio-ATP > or = CTP > alpha, beta-methylene-ATP > dATP) but has a notably higher sensitivity for the antagonists suramin, pyridoxal-phosphate-6-azophenyl-2',4'-disulfonic acid, and bromphenol blue. Chimeric constructs between human and rat isoforms as well as single-point mutations were engineered to map the regions responsible for the different sensitivity to suramin and pyridoxal-phosphate-6-azophenyl-2'4'-disulfonic acid.
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- Olin, Håkan, et al.
(författare)
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Conductance quantization in gold nanowires at low temperature
- 1997
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Konferensbidrag (populärvet., debatt m.m.)abstract
- When a scanning tunnelling microscope (STM) tip is driven into a metallic sample surface a nanometer sized wire (nanowire) is formed during the subsequent retraction. The electrical conduction measured during this retraction process shows signs of quantized conductance in units of 2e(2)/h. Due to the inherent non-reproducibility of the measured conductance curves a standard technique is to build histograms from a large number of curves. Such histograms, built with conductance experiments on gold nanowires at room temperature, show 3-4 peaks at integer values of 2e(2)/h, while in a low temperature mechanically controlled break junction study only the first peak is reported. In this work, histograms made up of thousands of consecutive curves at 4K are presented, showing up to 5 conductance peaks. An explanation for this discrepancy could be a higher nanowire temperature resulting from the higher retraction speed used in our measurements. However, a simple estimation, where we used macroscopic heat transport theory, resulted in a very low temperature increase, less than 1 mu k, ruling out this possibility. Thus, no significant difference with previous room temperature studies were observed, pointing to a conductance quantization that is the same at room and low temperature.
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- Rubio, F. T., et al.
(författare)
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BDNF gene transfer to the mammalian brain using CNS-derived neural precursors
- 1999
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Ingår i: Gene Therapy. - : Springer Science and Business Media LLC. - 0969-7128 .- 1476-5462. ; 6:11, s. 1851-1866
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Tidskriftsartikel (refereegranskat)abstract
- Neural stem cell lines represent a homogeneous source of cells for genetic, developmental, and gene transfer and repair studies in the nervous system. Since both gene transfer of neurotrophic factors and cell replacement strategies are of immediate interest for therapeutical purposes, we have generated BDNF-secreting neural stem cell lines and investigated to what extent different endogenous levels of BDNF expression affect in vitro survival, proliferation and differentiation of these cells. Also we have investigated the in vivo effects of such BDNF gene transfer procedure in the rat neostriatum. Hippocampus- and cerebellum-derived cell lines reacted differently to manipulations aimed at varying their levels of BDNF production. Overexpression of BDNF enhanced survival of both cell types, in a serum-deprivation assay. Conversely, and ruling out unspecific effects, expression of an antisense version of BDNF resulted in compromised survival of cerebellum-derived cells, and in a lethal phenotype in hippocampal progenitors. These data indicate that endogenous BDNF level strongly influences the in vitro survival of these cells. These effects are more pronounced for hippocampus- than for cerebellum-derived progenitors. Hippocampus-derived BDNF overproducers showed no major change in their capacity to differentiate towards a neuronal phenotype in vitro. In contrast cerebellar progenitors overproducing BDNF did not differentiate into neurons, whereas cells expressing the antisense BDNF construct generated cells with morphological features of neurons and expressing immunological neuronal markers. Taken together these results provide evidence that BDNF controls both the in vitro survival and differentiation of neural stem cells. After in vivo transplantation of BDNF-overproducing cells to the rat neostriatum, these survived better than the control ones, and induced the expected neurotrophic effects on cholinergic neurons. However, long-term (3 months) administration of BDNF resulted in detrimental effects, at this location. These findings may be of importance for the understanding of brain development, for the design of therapeutic neuro-regenerative strategies, and for cell replacement and gene therapy studies.
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