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H de Verneuil

Showing results (31-40 of 89) with videos related to

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American Journal of Human Genetics|May 1, 1984
Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyriaH de Verneuil, C Beaumont, J C Deybach, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 8, 1998
Expression, purification, crystallization and preliminary X-ray diffraction analysis of human uroporphyrinogen decarboxylaseM Laterrière, B L d'Estaintot, A Dautant, et al.
Gastroenterology|June 1, 1987
Porphyria cutanea tarda and HLA-linked hemochromatosis. Evidence against a systematic associationC Beaumont, R Fauchet, L N Phung, et al.
The Journal of Laboratory and Clinical Medicine|April 1, 1981
Congenital erythropoietic porphyria (Günther's disease): enzymatic studies on two cases of late onsetJ C Deybach, H de Verneuil, N Phung, et al.
Respiratory Medicine Case Reports|January 6, 2017
Identification of a novel alpha1-antitrypsin variantCamille de Seynes, C Ged, H de Verneuil, et al.
Human Genetics|January 1, 1992
Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyriaS Boulechfar, V Da Silva, J C Deybach, et al.
The Journal of Gene Medicine|May 16, 2000
Control of transgene expression using local hyperthermia in combination with a heat-sensitive promoterA Vekris, C Maurange, C Moonen, et al.
The Journal of Pediatrics|September 1, 1996
Correction of congenital erythropoietic porphyria by bone marrow transplantationC Thomas, C Ged, Y Nordmann, et al.
Experimental Cell Research|October 1, 1984
Effects of succinylacetone on dimethylsulfoxide-mediated induction of heme pathway enzymes in mouse friend virus-transformed erythroleukemia cellsC Beaumont, J C Deybach, B Grandchamp, et al.
American Journal of Medical Genetics|June 13, 1997
Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese familyN Takamura, I Hombrados, K Tanigawa, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|May 1, 1984
Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyriaH de Verneuil, C Beaumont, J C Deybach, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 8, 1998
Expression, purification, crystallization and preliminary X-ray diffraction analysis of human uroporphyrinogen decarboxylaseM Laterrière, B L d'Estaintot, A Dautant, et al.
Gastroenterology|June 1, 1987
Porphyria cutanea tarda and HLA-linked hemochromatosis. Evidence against a systematic associationC Beaumont, R Fauchet, L N Phung, et al.
The Journal of Laboratory and Clinical Medicine|April 1, 1981
Congenital erythropoietic porphyria (Günther's disease): enzymatic studies on two cases of late onsetJ C Deybach, H de Verneuil, N Phung, et al.
Respiratory Medicine Case Reports|January 6, 2017
Identification of a novel alpha1-antitrypsin variantCamille de Seynes, C Ged, H de Verneuil, et al.
Human Genetics|January 1, 1992
Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyriaS Boulechfar, V Da Silva, J C Deybach, et al.
The Journal of Gene Medicine|May 16, 2000
Control of transgene expression using local hyperthermia in combination with a heat-sensitive promoterA Vekris, C Maurange, C Moonen, et al.
The Journal of Pediatrics|September 1, 1996
Correction of congenital erythropoietic porphyria by bone marrow transplantationC Thomas, C Ged, Y Nordmann, et al.
Experimental Cell Research|October 1, 1984
Effects of succinylacetone on dimethylsulfoxide-mediated induction of heme pathway enzymes in mouse friend virus-transformed erythroleukemia cellsC Beaumont, J C Deybach, B Grandchamp, et al.
American Journal of Medical Genetics|June 13, 1997
Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese familyN Takamura, I Hombrados, K Tanigawa, et al.
Pageof 9