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H de Verneuil

Showing results (11-20 of 89) with videos related to

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Human Genetics|January 1, 1985
Hereditary hepatic porphyria with delta aminolevulinate dehydrase deficiency: immunologic characterization of the non-catalytic enzymeH de Verneuil, M Doss, N Brusco, et al.
Science (New York, N.Y.)|November 7, 1986
Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyriaH de Verneuil, B Grandchamp, C Beaumont, et al.
Biochimica Et Biophysica Acta|July 16, 1986
Porphobilinogen deaminase is unstable in the absence of its substrateC Beaumont, B Grandchamp, M Bogard, et al.
Archives Francaises De Pediatrie|January 1, 1981
[Late cutaneous porphyria in a child with Down's syndrome (author's transl)]R Mariani, H de Verneuil, M Albertini, et al.
Blood|March 15, 1995
Metabolic correction of congenital erythropoietic porphyria by retrovirus-mediated gene transfer into Epstein-Barr virus-transformed B-cell linesF Moreau-Gaudry, F Mazurier, M Bensidhoum, et al.
Blood|May 1, 1990
Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease)J C Deybach, H de Verneuil, S Boulechfar, et al.
Biochimica Et Biophysica Acta|May 22, 1980
Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyriaB Grandchamp, J C Deybach, M Grelier, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Genetic alterations in colorectal cancer, comparative analysis of deletion events, and point mutationsH el Sebaï, C Ged, F Bonichon, et al.
Cancer Gene Therapy|January 19, 2008
Catalase overexpression reduces UVB-induced apoptosis in a human xeroderma pigmentosum reconstructed epidermisH R Rezvani, C Ged, B Bouadjar, et al.
European Journal of Biochemistry|January 2, 1987
Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single geneB Grandchamp, H De Verneuil, C Beaumont, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Human Genetics|January 1, 1985
Hereditary hepatic porphyria with delta aminolevulinate dehydrase deficiency: immunologic characterization of the non-catalytic enzymeH de Verneuil, M Doss, N Brusco, et al.
Science (New York, N.Y.)|November 7, 1986
Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyriaH de Verneuil, B Grandchamp, C Beaumont, et al.
Biochimica Et Biophysica Acta|July 16, 1986
Porphobilinogen deaminase is unstable in the absence of its substrateC Beaumont, B Grandchamp, M Bogard, et al.
Archives Francaises De Pediatrie|January 1, 1981
[Late cutaneous porphyria in a child with Down's syndrome (author's transl)]R Mariani, H de Verneuil, M Albertini, et al.
Blood|March 15, 1995
Metabolic correction of congenital erythropoietic porphyria by retrovirus-mediated gene transfer into Epstein-Barr virus-transformed B-cell linesF Moreau-Gaudry, F Mazurier, M Bensidhoum, et al.
Blood|May 1, 1990
Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease)J C Deybach, H de Verneuil, S Boulechfar, et al.
Biochimica Et Biophysica Acta|May 22, 1980
Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyriaB Grandchamp, J C Deybach, M Grelier, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Genetic alterations in colorectal cancer, comparative analysis of deletion events, and point mutationsH el Sebaï, C Ged, F Bonichon, et al.
Cancer Gene Therapy|January 19, 2008
Catalase overexpression reduces UVB-induced apoptosis in a human xeroderma pigmentosum reconstructed epidermisH R Rezvani, C Ged, B Bouadjar, et al.
European Journal of Biochemistry|January 2, 1987
Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single geneB Grandchamp, H De Verneuil, C Beaumont, et al.
Pageof 9