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American Journal of Human Genetics
|
November 1, 1981
Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy
R 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 activation
T Heinemann, G C Bulwin, J Randall, et al.
The Journal of Biological Chemistry
|
July 14, 2001
Human acid ceramidase: processing, glycosylation, and lysosomal targeting
K 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 sphingolipids
N 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 Europe
S 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 mice
F 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 differentiation
T 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 B
M 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 disease
K Horinouchi, S Erlich, D P Perl, et al.
FEBS Letters
|
July 14, 1997
Bcl-2 antagonizes apoptotic cell death induced by two new ceramide analogues
T Wieder, C C Geilen, T Kolter, et al.
Page
of 26
Search research articles
Search
Showing results (231-240 of 256) with videos related to
Sort By:
Page
of 26
American Journal of Human Genetics
|
November 1, 1981
Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophy
R 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 activation
T Heinemann, G C Bulwin, J Randall, et al.
The Journal of Biological Chemistry
|
July 14, 2001
Human acid ceramidase: processing, glycosylation, and lysosomal targeting
K 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 sphingolipids
N 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 Europe
S 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 mice
F 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 differentiation
T 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 B
M 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 disease
K Horinouchi, S Erlich, D P Perl, et al.
FEBS Letters
|
July 14, 1997
Bcl-2 antagonizes apoptotic cell death induced by two new ceramide analogues
T Wieder, C C Geilen, T Kolter, et al.
Page
of 26