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  • 1
    Electronic Resource
    Electronic Resource
    Localization of the humanRGR opsin gene to chromosome 10q23 (1996)
    Springer
    Human genetics 〈Berlin〉 97 (1996), S. 720-722 
    Details
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The humanRGR gene encodes an opsin protein (retinal G protein-coupled receptor), which is expressed in Müller cells and the retinal pigment epithelium and is thought to play a role in the visual process. To investigate a possible linkage of theRGR gene to retinal dystrophies, the locus of the gene was mapped on human metaphase chromosomes. Genomic and cDNA fragments of the humanRGR gene were used as probes for fluorescence in situ hybridization. Analysis of the fluorescence signals on high-resolution banded chromosomes showed that theRGR gene is localized to human chromosome lOq23. This result now provides for the rapid analysis of this gene with respect to inherited diseases of the retina.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02346179
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Localization of the human RGR opsin gene to chromosome 10q23 (1996)
    Springer
    Human genetics 〈Berlin〉 97 (1996), S. 720-722 
    Details
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The human RGR gene encodes an opsin protein (retinal G protein-coupled receptor), which is expressed in Müller cells and the retinal pigment epithelium and is thought to play a role in the visual process. To investigate a possible linkage of the RGR gene to retinal dystrophies, the locus of the gene was mapped on human metaphase chromosomes. Genomic and cDNA fragments of the human RGR gene were used as probes for fluorescence in situ hybridization. Analysis of the fluorescence signals on high-resolution banded chromosomes showed that the RGR gene is localized to human chromosome 10q23. This result now provides for the rapid analysis of this gene with respect to inherited diseases of the retina.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004390050126
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
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