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FEBS Letters
|
August 22, 1983
Modification of subunit interaction in membrane-bound acid beta-glucosidase from Gaucher disease
A Maret, M Potier, R Salvayre, et al.
Cancer Research
|
January 19, 1999
Cell transformation results in the loss of the density-dependent translational regulation of the expression of fibroblast growth factor 2 isoforms
B Galy, A Maret, A C Prats, et al.
European Journal of Biochemistry
|
February 15, 1985
[Neutral glycosphingolipids of Fabry's disease lymphoblastoid lines established by Epstein-Barr virus transformation]
R Salvayre, A Maret, A Negre, et al.
The International Journal of Biochemistry
|
January 1, 1988
Mechanism of inhibition of beta-hexosaminidase B from human liver by short- and medium-chain monocarboxylic acids
M Hardy, R Salvayre, A Maret, et al.
Biochimica Et Biophysica Acta
|
June 22, 1987
Irreversible inhibition of hexosaminidase C by medium-chain monocarboxylic acids and Triton X-100
M Hardy, R Salvayre, A Maret, et al.
Enzyme
|
January 1, 1990
Acid lability of the mutated glucosylceramide-beta-glucosidase in a lymphoid cell line from type 2 Gaucher disease
A Maret, R Salvayre, M Troly, et al.
Pathologie-Biologie
|
June 1, 1985
[Beta-glucosidases. Molecular bases of Gaucher's disease]
A Maret, R Salvayre, A Negre, et al.
Comptes Rendus Des Seances De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
December 14, 1981
[Comparison of the molecular forms of exonuclease and ribonuclease in normal human spleen]
A Nègre, R Salvayre, A Maret, et al.
Enzyme
|
January 1, 1987
beta-Glucosidase isoenzymes in Epstein-Barr virus-transformed lymphoid cell lines from normal subjects and patients with type 1 Gaucher disease
A Maret, R Salvayre, M Samadi, et al.
Bulletin De L'Academie Nationale De Medecine
|
January 1, 1985
[Value of studying isoenzymes in hereditary lysosomal lipidoses. In particular beta-glucosidase (Gaucher's disease) and acid lipase (Wolman's disease and cholesterol ester storage disease)]
L Douste-Blazy, A Nègre, A Maret, et al.
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of 8
Search research articles
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Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
FEBS Letters
|
August 22, 1983
Modification of subunit interaction in membrane-bound acid beta-glucosidase from Gaucher disease
A Maret, M Potier, R Salvayre, et al.
Cancer Research
|
January 19, 1999
Cell transformation results in the loss of the density-dependent translational regulation of the expression of fibroblast growth factor 2 isoforms
B Galy, A Maret, A C Prats, et al.
European Journal of Biochemistry
|
February 15, 1985
[Neutral glycosphingolipids of Fabry's disease lymphoblastoid lines established by Epstein-Barr virus transformation]
R Salvayre, A Maret, A Negre, et al.
The International Journal of Biochemistry
|
January 1, 1988
Mechanism of inhibition of beta-hexosaminidase B from human liver by short- and medium-chain monocarboxylic acids
M Hardy, R Salvayre, A Maret, et al.
Biochimica Et Biophysica Acta
|
June 22, 1987
Irreversible inhibition of hexosaminidase C by medium-chain monocarboxylic acids and Triton X-100
M Hardy, R Salvayre, A Maret, et al.
Enzyme
|
January 1, 1990
Acid lability of the mutated glucosylceramide-beta-glucosidase in a lymphoid cell line from type 2 Gaucher disease
A Maret, R Salvayre, M Troly, et al.
Pathologie-Biologie
|
June 1, 1985
[Beta-glucosidases. Molecular bases of Gaucher's disease]
A Maret, R Salvayre, A Negre, et al.
Comptes Rendus Des Seances De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
December 14, 1981
[Comparison of the molecular forms of exonuclease and ribonuclease in normal human spleen]
A Nègre, R Salvayre, A Maret, et al.
Enzyme
|
January 1, 1987
beta-Glucosidase isoenzymes in Epstein-Barr virus-transformed lymphoid cell lines from normal subjects and patients with type 1 Gaucher disease
A Maret, R Salvayre, M Samadi, et al.
Bulletin De L'Academie Nationale De Medecine
|
January 1, 1985
[Value of studying isoenzymes in hereditary lysosomal lipidoses. In particular beta-glucosidase (Gaucher's disease) and acid lipase (Wolman's disease and cholesterol ester storage disease)]
L Douste-Blazy, A Nègre, A Maret, et al.
Page
of 8