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Biological Chemistry Hoppe-Seyler|July 1, 1991
Transient expression of wild type and mutant human apolipoprotein AI in COS cellsW Stoffel, E BinczekBiological Chemistry Hoppe-Seyler|September 1, 1988
Structural requirements of human preproapolipoprotein AI for translocation and processing studied by site-directed mutagenesis in vitroW Stoffel, E BinczekGenomics|July 1, 1996
Molecular cloning and characterization of the mouse CGT gene encoding UDP-galactose ceramide-galactosyltransferase (cerebroside synthetase)A Bosio, E Binczek, W StoffelProceedings of the National Academy of Sciences of the United States of America|November 12, 1996
Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesisA Bosio, E Binczek, W StoffelBiological Chemistry Hoppe-Seyler|April 1, 1992
Mouse apolipoprotein AI. cDNA-derived primary structure, gene organisation and complete nucleotide sequenceW Stoffel, R Müller, E Binczek, et al.Journal of Neurochemistry|January 9, 1998
Composition and biophysical properties of myelin lipid define the neurological defects in galactocerebroside- and sulfatide-deficient miceA Bosio, E Binczek, W F Haupt, et al.Genomics|May 15, 1996
The human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26A Bosio, E Binczek, M M Le Beau, et al.Pageof 1