The lack of transcriptional activation of the v-erbA oncogene is in part due to a mutation present in the DNA binding domain of the protein.

Por de Verneuil, H, Metzger, D
Publicado em 1990

Effects of polychlorinated biphenyl compounds, 2,3,7,8-tetrachlorodibenzo-p-dioxin, phenobarbital and iron on hepatic uroporphyrinogen decarboxylase. Implications for the pathogene...

Por De Verneuil, H, Sassa, S, Kappas, A
Publicado em 1983

Harderoporphyria: a variant hereditary coproporphyria.

Por Nordmann, Y, Grandchamp, B, de Verneuil, H, Phung, L, Cartigny, B, Fontaine, G
Publicado em 1983

Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria.

Por de Verneuil, H, Beaumont, C, Deybach, J C, Nordmann, Y, Sfar, Z, Kastally, R
Publicado em 1984

Identification of a novel alpha1-antitrypsin variant

Por de Seynes, Camille, Ged, C., de Verneuil, H., Chollet, N., Balduyck, M., Raherison, C.
Publicado no Respir Med Case Rep (2016)

Isolation and identification of a cDNA clone coding for rat uroporphyrinogen decarboxylase.

Por Romeo, P H, Dubart, A, Grandchamp, B, de Verneuil, H, Rosa, J, Nordmann, Y, Goossens, M
Publicado em 1984

Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria.

Por de Verneuil, H, Grandchamp, B, Romeo, P H, Raich, N, Beaumont, C, Goossens, M, Nicolas, H, Nordmann, Y
Publicado em 1986

Molecular cloning, sequencing, and functional expression of a cDNA encoding human coproporphyrinogen oxidase.

Por Martasek, P, Camadro, J M, Delfau-Larue, M H, Dumas, J B, Montagne, J J, de Verneuil, H, Labbe, P, Grandchamp, B
Publicado em 1994

Uroporphyrinogen decarboxylase: complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyria.

Por Moran-Jimenez, M. J., Ged, C., Romana, M., Enriquez De Salamanca, R., Taïeb, A., Topi, G., D'Alessandro, L., de Verneuil, H.
Publicado em 1996

Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.

Por Biancalana, V., Taine, L., Bouix, J. C., Finck, S., Chauvin, A., De Verneuil, H., Knight, S. J., Stoll, C., Lacombe, D., Mandel, J. L.
Publicado em 1996