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M T Zabot

Showing results (11-20 of 54) with videos related to

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Human Mutation|February 6, 1998
The molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in French families; report of two novel mutationsG Liu, B Aral, M T Zabot, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Unreliable verification of prenatal diagnosis of Canavan disease: aspartoacylase activity in deficient and normal fetal skin fibroblastsM O Rolland, G Mandon, A Bernard, et al.
Presse Medicale (Paris, France : 1983)|January 22, 1983
[Treatment of cystinosis with cysteamine]J J Louis, P Guibaud, R Dumoulin, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Four novel mutations at the cystathionine beta-synthase locus causing homocystinuriaM Coudé, J Aupetit, M T Zabot, et al.
Biochimica Et Biophysica Acta|January 22, 1993
Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblastsC Bertrand, C Largillière, M T Zabot, et al.
Journal De Genetique Humaine|March 1, 1979
[Mucopolysaccharidesis Type VII resulting from beta-glucuronidase deficiency. Report of one family]P Guibaud, I Maire, R Goddon, et al.
Annales De Biologie Clinique|January 1, 1978
[Organization and computerization of a cell bank (proceedings)]M T Zabot, S Boyer, J Genoud, et al.
American Journal of Human Genetics|March 3, 1999
Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type BJ Reiss, C Dorche, B Stallmeyer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 3, 2001
Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotypeD S Roe, C Vianey-Saban, S Sharma, et al.
Pathologie-Biologie|January 1, 1989
[Lysosomal enzyme deficiency: in vitro correlation of deficient cells using a conditioned medium or by co-culturing with non-deficient cells]P Veyron, R el Habib, M T Zabot, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Human Mutation|February 6, 1998
The molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in French families; report of two novel mutationsG Liu, B Aral, M T Zabot, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Unreliable verification of prenatal diagnosis of Canavan disease: aspartoacylase activity in deficient and normal fetal skin fibroblastsM O Rolland, G Mandon, A Bernard, et al.
Presse Medicale (Paris, France : 1983)|January 22, 1983
[Treatment of cystinosis with cysteamine]J J Louis, P Guibaud, R Dumoulin, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Four novel mutations at the cystathionine beta-synthase locus causing homocystinuriaM Coudé, J Aupetit, M T Zabot, et al.
Biochimica Et Biophysica Acta|January 22, 1993
Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblastsC Bertrand, C Largillière, M T Zabot, et al.
Journal De Genetique Humaine|March 1, 1979
[Mucopolysaccharidesis Type VII resulting from beta-glucuronidase deficiency. Report of one family]P Guibaud, I Maire, R Goddon, et al.
Annales De Biologie Clinique|January 1, 1978
[Organization and computerization of a cell bank (proceedings)]M T Zabot, S Boyer, J Genoud, et al.
American Journal of Human Genetics|March 3, 1999
Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type BJ Reiss, C Dorche, B Stallmeyer, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 3, 2001
Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotypeD S Roe, C Vianey-Saban, S Sharma, et al.
Pathologie-Biologie|January 1, 1989
[Lysosomal enzyme deficiency: in vitro correlation of deficient cells using a conditioned medium or by co-culturing with non-deficient cells]P Veyron, R el Habib, M T Zabot, et al.
Pageof 6