Role of transcriptional regulation and enzyme inactivation in the synthesis of Escherichia coli carbamoylphosphate synthase.

por Piérard, A, Lissens, W, Halleux, P, Cunin, R, Glansdorff, N
Publicado 1980

Characterisation of a cDNA for porcine PDH-E1 alpha and comparison with the human cDNA.

por Sermon, K, De Meirleir, L, Elpers, I, Lissens, W, Liebaers, I
Publicado 1990

Promoter mapping and selection of operator mutants by using insertion of bacteriophage Mu in the argECBH divergent operon of Escherichia coli K-12.

por Beny, G, Boyen, A, Charlier, D, Lissens, W, Feller, A, Glansdorff, N
Publicado 1982

Patterns of polarity in the Escherichia coli car AB gene cluster.

por Gigot, D, Crabeel, M, Feller, A, Charlier, D, Lissens, W, Glansdorff, N, Piérard, A
Publicado 1980

Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTR.

por Lissens, W, Desmyttere, S, Bonduelle, M, Dab, I, Liebaers, I, Mercier, B, Audrezet, M P, Ferec, C
Publicado 1993

Pitfalls in the diagnosis of mtDNA mutations.

por Seneca, S, Lissens, W, Liebaers, I, van den Bergh, P, Nassogne, M C, Benatar, A, de Meirleir, L
Publicado 1998

Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.

por Mercier, B, Verlingue, C, Lissens, W, Silber, S J, Novelli, G, Bonduelle, M, Audrézet, M P, Férec, C
Publicado 1995

Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection.

por Danan, C, Sternberg, D, Van Steirteghem, A, Cazeneuve, C, Duquesnoy, P, Besmond, C, Goossens, M, Lissens, W, Amselem, S
Publicado 1999

Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12

por De Meirleir, L, Seneca, S, Lissens, W, De Clercq, I, Eyskens, F, Gerlo, E, Smet, J, Van Coster, R
Publicado 2004

A pseudodeficiency allele (D152N) of the human beta-glucuronidase gene.

por Vervoort, R, Islam, M R, Sly, W, Chabas, A, Wevers, R, de Jong, J, Liebaers, I, Lissens, W
Publicado 1995

A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations.

por Mercier, B, Lissens, W, Novelli, G, Kalaydjieva, L, de Arce, M, Kapranov, N, Canki Klain, N, Estivill, X, Palacio, A, Cashman, S
Publicado 1994

Molecular analysis of patients with beta-glucuronidase deficiency presenting as hydrops fetalis or as early mucopolysaccharidosis VII.

por Vervoort, R., Islam, M. R., Sly, W. S., Zabot, M. T., Kleijer, W. J., Chabas, A., Fensom, A., Young, E. P., Liebaers, I., Lissens, W.
Publicado 1996

Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11

por Farrall, M., Watson, E., Bates, G., Bell, G., Bell, J., Davies, K. A., Estivill, X., Kruyer, H., Law, H.-Y., Lench, N., Lissens, W., Simon, P., Scambler, P., Stanier, P., Vassart, G., Worrall, C., Williamson, R., Wainwright, B. J.
Publicado 1986