J-C Deybach - JoVE Visualize

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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.

Journal of Hepatology|July 18, 2000

Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factorsC Andant, H Puy, C Bogard, et al.

Blood|March 9, 1999

Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestationL Gouya, H Puy, J Lamoril, et al.

American Journal of Human Genetics|February 1, 1996

Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase alleleL Gouya, J C Deybach, J Lamoril, et al.

Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009

The molecular genetics of erythropoietic protoporphyriaG H Elder, L Gouya, S D Whatley, et al.

Human Genetics|December 22, 1998

Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyriaH Puy, U Gross, J C Deybach, et al.

Human Genetics|February 1, 1980

Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at riskJ C Deybach, B Grandchamp, M Grelier, et al.

Clinical Chemistry|September 11, 1998

5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-upU Gross, S Sassa, K Jacob, et al.

The Journal of Investigative Dermatology|March 12, 2002

Haplotype analysis in determination of the heredity of erythropoietic protoporphyria among Swiss familiesX Schneider-Yin, U B Rüfenacht, M Hergersberg, et al.

Nucleic Acids Research|August 25, 1989

A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyriaB Grandchamp, C Picat, F de Rooij, et al.

Pageof 9

Showing results (41-50 of 87) with videos related to

Sort By:

Pageof 9

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.

Journal of Hepatology|July 18, 2000

Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factorsC Andant, H Puy, C Bogard, et al.

Blood|March 9, 1999

Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestationL Gouya, H Puy, J Lamoril, et al.

American Journal of Human Genetics|February 1, 1996

Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase alleleL Gouya, J C Deybach, J Lamoril, et al.

Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009

The molecular genetics of erythropoietic protoporphyriaG H Elder, L Gouya, S D Whatley, et al.

Human Genetics|December 22, 1998

Exon 1 donor splice site mutations in the porphobilinogen deaminase gene in the non-erythroid variant form of acute intermittent porphyriaH Puy, U Gross, J C Deybach, et al.

Human Genetics|February 1, 1980

Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at riskJ C Deybach, B Grandchamp, M Grelier, et al.

Clinical Chemistry|September 11, 1998

5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-upU Gross, S Sassa, K Jacob, et al.

The Journal of Investigative Dermatology|March 12, 2002

Haplotype analysis in determination of the heredity of erythropoietic protoporphyria among Swiss familiesX Schneider-Yin, U B Rüfenacht, M Hergersberg, et al.

Nucleic Acids Research|August 25, 1989

A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyriaB Grandchamp, C Picat, F de Rooij, et al.

Pageof 9