Search Results - (Author, Cooperation:S. Makova)

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  1. 1
    M. T. Boskovski ; S. Yuan ; N. B. Pedersen ; C. K. Goth ; S. Makova ; H. Clausen ; M. Brueckner ; M. K. Khokha
    Nature Publishing Group (NPG)
    Published 2013
    Staff View
    Publication Date:
    2013-11-15
    Publisher:
    Nature Publishing Group (NPG)
    Print ISSN:
    0028-0836
    Electronic ISSN:
    1476-4687
    Topics:
    Biology
    Chemistry and Pharmacology
    Medicine
    Natural Sciences in General
    Physics
    Keywords:
    ADAM Proteins/metabolism ; Amino Acid Sequence ; Animals ; *Body Patterning ; Cilia/metabolism/*physiology ; Embryo, Nonmammalian/embryology/metabolism ; Glycosylation ; Heterotaxy Syndrome/*genetics ; Humans ; Mice ; Molecular Sequence Data ; N-Acetylgalactosaminyltransferases/deficiency/genetics/*metabolism ; Peptide Fragments/chemistry/metabolism ; Receptor, Notch1/chemistry/deficiency/genetics/*metabolism ; *Signal Transduction ; Xenopus/embryology/genetics ; Xenopus Proteins/deficiency/genetics/*metabolism
    Published by:
    http://www.nature.com/

    Latest Papers from Table of Contents or Articles in Press
  2. 2
    Gol'dshleger, N. F. ; Makova, S. Z. ; Shul'ga, Yu. M.
    Springer
    Published 1992
    Staff View
    ISSN:
    1573-9171
    Keywords:
    Rhodium(III) trifluoroacetate ; norbornadiene ; reduction
    Source:
    Springer Online Journal Archives 1860-2000
    Topics:
    Chemistry and Pharmacology
    Notes:
    Abstract It was shown that the action of heat on rhodium(III) trifluoroacetate with norbornadiene (NBD) leads to its reduction and the formation of red crystals of [Rh(CF3COO)NBD]2. The formation of the complex was confirmed by elemental analysis and IR, electronic, and x-ray photoelectron spectra. The reaction shows that Rh-Rh compounds can disproportionate under the influence of NBD with the formation of Rh(I) and Rh(III).
    Type of Medium:
    Electronic Resource
    URL:
    http://dx.doi.org/10.1007/BF00866602

    Articles: DFG German National Licenses
  3. 3
    Borovkov, V. V. ; Evstigneeva, R. P. ; Makova, S. Z.
    Springer
    Published 1992
    Staff View
    ISSN:
    1573-8353
    Source:
    Springer Online Journal Archives 1860-2000
    Topics:
    Chemistry and Pharmacology
    Notes:
    Abstract Diquinone derivatives of deuteroporphyrin IX containing covalent bridges of different lengths between the chromophores have been synthesized. The compounds were prepared by the condensation of hydroxy-quinones with deuteroporphyrin IX using a mixed anhydride method which employed the system di-tert-butyl pyrocarbonate — 4-dimethylaminopyridine. A spectral study of the resulting porphyrin-quinones was carried out.
    Type of Medium:
    Electronic Resource
    URL:
    http://dx.doi.org/10.1007/BF00473932

    Articles: DFG German National Licenses