Search research articles
Contact Us
Filters
Showing results (31-40 of 256) with videos related to
Page
of 26
Sort By:
Advances in Experimental Medicine and Biology
|
January 1, 1980
The specificity of human N-acetyl-beta-D-hexosaminidases towards glycosphincolipids is determined by an activator protein
E Conzelmann, K Sandhoff
Archiv Fur Psychiatrie Und Nervenkrankheiten
|
April 30, 1976
[Sphingolipid storage disease as an example of a molecular neuropathology (author's transl)]
H Jatzkewitz, K Sandhoff
Advances in Enzymology and Related Areas of Molecular Biology
|
January 1, 1987
Glycolipid and glycoprotein degradation
E Conzelmann, K Sandhoff
Acta Neuropathologica
|
March 26, 1974
[Juvenile GM2 gangliosidosis with altered substrate specificity of hexosaminidase A (author's transl)]
J Zerfowski, K Sandhoff
Biochimica Et Biophysica Acta
|
June 5, 1992
Activator proteins and topology of lysosomal sphingolipid catabolism
W Fürst, K Sandhoff
Glycobiology
|
November 18, 1997
Sialic acids--why always alpha-linked?
T Kolter, K Sandhoff
Developmental Neuroscience
|
January 1, 1991
Biochemical basis of late-onset neurolipidoses
E Conzelmann, K Sandhoff
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1978
Membrane-bound neuraminidase from calf brain: regulation of oligosialoganglioside degradation by membrane fluidity and membrane components
K Sandhoff, B Pallmann
Journal of Neurochemistry
|
November 1, 1971
Age-dependent variations of the human N-acetyl- -D-hexosaminidases
K Harzer, K Sandhoff
Progress in Brain Research
|
January 1, 1994
Ganglioside metabolism: enzymology, topology and regulation
K Sandhoff, G van Echten
Page
of 26
Search research articles
Search
Showing results (31-40 of 256) with videos related to
Sort By:
Page
of 26
Advances in Experimental Medicine and Biology
|
January 1, 1980
The specificity of human N-acetyl-beta-D-hexosaminidases towards glycosphincolipids is determined by an activator protein
E Conzelmann, K Sandhoff
Archiv Fur Psychiatrie Und Nervenkrankheiten
|
April 30, 1976
[Sphingolipid storage disease as an example of a molecular neuropathology (author's transl)]
H Jatzkewitz, K Sandhoff
Advances in Enzymology and Related Areas of Molecular Biology
|
January 1, 1987
Glycolipid and glycoprotein degradation
E Conzelmann, K Sandhoff
Acta Neuropathologica
|
March 26, 1974
[Juvenile GM2 gangliosidosis with altered substrate specificity of hexosaminidase A (author's transl)]
J Zerfowski, K Sandhoff
Biochimica Et Biophysica Acta
|
June 5, 1992
Activator proteins and topology of lysosomal sphingolipid catabolism
W Fürst, K Sandhoff
Glycobiology
|
November 18, 1997
Sialic acids--why always alpha-linked?
T Kolter, K Sandhoff
Developmental Neuroscience
|
January 1, 1991
Biochemical basis of late-onset neurolipidoses
E Conzelmann, K Sandhoff
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1978
Membrane-bound neuraminidase from calf brain: regulation of oligosialoganglioside degradation by membrane fluidity and membrane components
K Sandhoff, B Pallmann
Journal of Neurochemistry
|
November 1, 1971
Age-dependent variations of the human N-acetyl- -D-hexosaminidases
K Harzer, K Sandhoff
Progress in Brain Research
|
January 1, 1994
Ganglioside metabolism: enzymology, topology and regulation
K Sandhoff, G van Echten
Page
of 26