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  • 1995-1999  (4)
  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 384 (1996), S. 404-404 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] SIR — Since the Chinese Maternal and Infant Health Care Law, previously called the "eugenics and health protection law", was first proposed in December 1993, and finally promulgated on 27 October 1994, it has provoked widespread concern in the international scientific community (see Nature ...
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Sir — Williams syndrome (WS) is believed to be a contiguous gene syndrome caused by deletion of elastin and of other unknown genes1,2 on chromosome 7. WS is generally sporadic with an incidence of 1/20,000-1/50,000 live births, although rare familial (autosomal dominant) cases have been ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature genetics 17 (1997), S. 20-20 
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Your editorial1 provided a thoughtful i and informative overview of widespread concerns regarding eugenic legislation in China and elsewhere. However, one statement in this editorial— “…in the face of eugenic law, the genetical is political”— is likely to remind ...
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-7373
    Keywords: alleletyping ; oligodendrocyte-type-2 astrocyte ; glioblastoma multiforme ; loss of heterozygosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We have conducted alleletyping of two novel cell lines derived from glioblastoma multiforme, which appear to have arisen from different glial lineages, by using 76 fluorescently labeled oligonucleotide primers amplifying microsatellite loci covering the entire human genome. One cell line, Hu-O-2A/Gb1, expresses antigens and metabolic profiles characteristic of the oligodendrocyte-type-2 astrocyte (0-2A) lineage of the rat central nervous system. This cell line generated, in vitro, cells with characteristics of 0-2A progenitor cells, oligodendrocytes and astrocytes. The second cell line, IN1434, is derived from an astrocyte or a precursor cell restricted to astrocytic differentiation. Hu-O-2A/Gb1 cells show allelic losses of loci on chromosomes 2, 5, 6, 7, 8, 9, 10, 11, 13, 15, 16, 17, 20 and 21. IN1434 cells are likely to have allelic losses of loci on chromosomes 1, 3, 8 and 10, although no control DNA is available for this cell line. These results, for the first time, provide a detailed information of the molecular genetic defects occurring in Hu-O-2A/Gb1 and IN1434.
    Type of Medium: Electronic Resource
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