A deletion polymorphism in the human alpha-2-macroglobulin (A2M) gene.

Por Matthijs, G, Marynen, P
Publicado em 1991

Three RFLPs associated with the human alpha 2-macroglobulin gene (A2M).

Por Marynen, P, Bell, G I, Cavalli-Sforza, L L
Publicado em 1985

Synthesis of a Cys949Tyr alpha 2-macroglobulin thiol ester mutant: co-transfection with wild-type alpha 2-macroglobulin in an episomal expression system.

Por Van Rompaey, L, Van den Berghe, H, Marynen, P
Publicado em 1995

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes.

Por Decorte, R., Wu, R., Marynen, P., Cassiman, J. J.
Publicado em 1994

Inhibition of intracellular proteolytic processing of soluble proproteins by an engineered alpha 2-macroglobulin containing a furin recognition sequence in the bait region.

Por Van Rompaey, L, Ayoubi, T, Van De Ven, W, Marynen, P
Publicado em 1997

Rat hemoglobin interferes with DNA migration in agarose gels.

Por Deichmann, K, Marynen, P, Van den Berghe, H, Cassiman, J J
Publicado em 1988

Design of a new protease inhibitor by the manipulation of the bait region of alpha 2-macroglobulin: inhibition of the tobacco etch virus protease by mutant alpha 2-macroglobulin.

Por Van Rompaey, L, Proost, P, Van den Berghe, H, Marynen, P
Publicado em 1995

Unequal meiotic crossover: a frequent cause of NF1 microdeletions.

Por López Correa, C, Brems, H, Lázaro, C, Marynen, P, Legius, E
Publicado em 2000

Incorporation of dITP or 7-deaza dGTP during PCR improves sequencing of the product.

Por Dierick, H, Stul, M, De Kelver, W, Marynen, P, Cassiman, J J
Publicado em 1993

Relation of internal thioesters to conformational change and receptor-recognition site in alpha 2-macroglobulin complexes.

Por Van Leuven, F, Marynen, P, Cassiman, J J, Van den Berghe, H
Publicado em 1982

Evidence for the existence of a pristanoyl-CoA oxidase gene in man.

Por Vanhooren, J C, Marynen, P, Mannaerts, G P, Van Veldhoven, P P
Publicado em 1997

Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal allele.

Por Guo, C, Van Damme, B, Vanrenterghem, Y, Devriendt, K, Cassiman, J J, Marynen, P
Publicado em 1995

Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene.

Por Legius, E, Wu, R, Eyssen, M, Marynen, P, Fryns, J P, Cassiman, J J
Publicado em 1995

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Por Gu, X X, Decorte, R, Marynen, P, Fryns, J P, Cassiman, J J, Raeymaekers, P
Publicado em 1996

Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS.

Por Ruiz, J C, Cuppens, H, Legius, E, Fryns, J P, Glover, T, Marynen, P, Cassiman, J J
Publicado em 1995

Possible association of CD3 and CD4 polymorphisms with insulin-dependent diabetes mellitus (IDDM).

Por Ghabanbasani, M Z, Buyse, I, Legius, E, Decorte, R, Marynen, P, Bouillon, R, Cassiman, J J
Publicado em 1994

A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephew

Por Cuppens, H, Marynen, P, Berghe, H Van den, Cassiman, J J, Boeck, C De, Eggermont, E, Baets, F De
Publicado em 1990

Genetic heterogeneity in Rieger eye malformation.

Por Legius, E, de Die-Smulders, C E, Verbraak, F, Habex, H, Decorte, R, Marynen, P, Fryns, J P, Cassiman, J J
Publicado em 1994

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Por Devriendt, K, Petit, P, Matthijs, G, Vermeesch, J R, Holvoet, M, De Muelenaere, A, Marynen, P, Cassiman, J J, Fryns, J P
Publicado em 1997

A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded pat...

Por Longo, I, Frints, S, Fryns, J, Meloni, I, Pescucci, C, Ariani, F, Borghgraef, M, Raynaud, M, Marynen, P, Schwartz, C, Renieri, A, Froyen, G
Publicado em 2003