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K Sandhoff

Showing results (231-240 of 256) with videos related to

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American Journal of Human Genetics|November 1, 1981
Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophyR L Stevens, A L Fluharty, H Kihara, et al.
Genomics|May 18, 1999
Genomic organization of the gene coding for TIRC7, a novel membrane protein essential for T cell activationT Heinemann, G C Bulwin, J Randall, et al.
The Journal of Biological Chemistry|July 14, 2001
Human acid ceramidase: processing, glycosylation, and lysosomal targetingK Ferlinz, G Kopal, K Bernardo, et al.
Human Molecular Genetics|June 1, 1996
Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipidsN Fujita, K Suzuki, M T Vanier, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
The Journal of Clinical Investigation|June 13, 1998
Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease miceF Norflus, C J Tifft, M P McDonald, et al.
Journal of Lipid Research|May 1, 1999
Transcription factors Sp1 and AP-2 mediate induction of acid sphingomyelinase during monocytic differentiationT Langmann, C Buechler, S Ries, et al.
The Journal of Biological Chemistry|March 21, 1997
Evidence for the involvement of Glu-355 in the catalytic action of human beta-hexosaminidase BM Pennybacker, C G Schuette, B Liessem, et al.
Nature Genetics|July 1, 1995
Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick diseaseK Horinouchi, S Erlich, D P Perl, et al.
FEBS Letters|July 14, 1997
Bcl-2 antagonizes apoptotic cell death induced by two new ceramide analoguesT Wieder, C C Geilen, T Kolter, et al.
Pageof 26

Showing results (231-240 of 256) with videos related to

Sort By:
Pageof 26
American Journal of Human Genetics|November 1, 1981
Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophyR L Stevens, A L Fluharty, H Kihara, et al.
Genomics|May 18, 1999
Genomic organization of the gene coding for TIRC7, a novel membrane protein essential for T cell activationT Heinemann, G C Bulwin, J Randall, et al.
The Journal of Biological Chemistry|July 14, 2001
Human acid ceramidase: processing, glycosylation, and lysosomal targetingK Ferlinz, G Kopal, K Bernardo, et al.
Human Molecular Genetics|June 1, 1996
Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipidsN Fujita, K Suzuki, M T Vanier, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
The Journal of Clinical Investigation|June 13, 1998
Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease miceF Norflus, C J Tifft, M P McDonald, et al.
Journal of Lipid Research|May 1, 1999
Transcription factors Sp1 and AP-2 mediate induction of acid sphingomyelinase during monocytic differentiationT Langmann, C Buechler, S Ries, et al.
The Journal of Biological Chemistry|March 21, 1997
Evidence for the involvement of Glu-355 in the catalytic action of human beta-hexosaminidase BM Pennybacker, C G Schuette, B Liessem, et al.
Nature Genetics|July 1, 1995
Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick diseaseK Horinouchi, S Erlich, D P Perl, et al.
FEBS Letters|July 14, 1997
Bcl-2 antagonizes apoptotic cell death induced by two new ceramide analoguesT Wieder, C C Geilen, T Kolter, et al.
Pageof 26