Marynen P - Search Results

1

Simultaneous screening for 11 mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex amplification and reverse dot-blot.

Cuppens H, Buyse I, Baens M, Marynen P, Cassiman JJ. Cuppens H, et al. Among authors: marynen p. Mol Cell Probes. 1992 Feb;6(1):33-9. doi: 10.1016/0890-8508(92)90069-a. Mol Cell Probes. 1992. PMID: 1372093

2

An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptoms.

Loumi O, Cuppens H, Bakour R, Benabadji M, Baghriche M, Marynen P, Cassiman JJ. Loumi O, et al. Among authors: marynen p. Genet Couns. 1992;3(4):205-7. Genet Couns. 1992. PMID: 1282016

3

Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian population.

Cuppens H, Loumi O, Marynen P, Cassiman JJ. Cuppens H, et al. Among authors: marynen p. Hum Mol Genet. 1992 Jul;1(4):283-4. doi: 10.1093/hmg/1.4.283. Hum Mol Genet. 1992. PMID: 1284627 No abstract available.

4

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

Cuppens H, Marynen P, De Boeck C, De Baets F, Eggermont E, Van den Berghe H, Cassiman JJ. Cuppens H, et al. Among authors: marynen p. J Med Genet. 1990 Nov;27(11):717-9. doi: 10.1136/jmg.27.11.717. J Med Genet. 1990. PMID: 2135388 Free PMC article.

5

Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR gene.

Cuppens H, Marynen P, De Boeck C, Cassiman JJ. Cuppens H, et al. Among authors: marynen p. Genomics. 1993 Dec;18(3):693-7. doi: 10.1016/s0888-7543(05)80376-3. Genomics. 1993. PMID: 7508414

6

Co-amplification of the cystic fibrosis delta F508 mutation with the HLA DQA1 sequence in single cell PCR: implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosis.

Wu R, Cuppens H, Buyse I, Decorte R, Marynen P, Gordts S, Cassiman JJ. Wu R, et al. Among authors: marynen p. Prenat Diagn. 1993 Dec;13(12):1111-22. doi: 10.1002/pd.1970131206. Prenat Diagn. 1993. PMID: 7513888

7

Rapid DNA typing of class II HLA antigens using the polymerase chain reaction and reverse dot blot hybridization.

Buyse I, Decorte R, Baens M, Cuppens H, Semana G, Emonds MP, Marynen P, Cassiman JJ. Buyse I, et al. Among authors: marynen p. Tissue Antigens. 1993 Jan;41(1):1-14. doi: 10.1111/j.1399-0039.1993.tb01970.x. Tissue Antigens. 1993. PMID: 8456438

8

Detection of bacterial and mycoplasma contamination in cell cultures by polymerase chain reaction.

Spaepen M, Angulo AF, Marynen P, Cassiman JJ. Spaepen M, et al. Among authors: marynen p. FEMS Microbiol Lett. 1992 Nov 15;78(1):89-94. doi: 10.1016/0378-1097(92)90293-w. FEMS Microbiol Lett. 1992. PMID: 1468621

9

A genetic polymorphism in a functional domain of human pregnancy zone protein: the bait region. Genomic structure of the bait domains of human pregnancy zone protein and alpha 2 macroglobulin.

Marynen P, Devriendt K, Van den Berghe H, Cassiman JJ. Marynen P, et al. FEBS Lett. 1990 Mar 26;262(2):349-52. doi: 10.1016/0014-5793(90)80226-9. FEBS Lett. 1990. PMID: 1692292 Free article.

10

Localization of the gene encoding the alpha 2 subunit of the human VLA-2 receptor to chromosome 5q23-31.

Jaspers M, Marynen P, Aly MS, Cuppens H, Hilliker C, Cassiman JJ. Jaspers M, et al. Among authors: marynen p. Somat Cell Mol Genet. 1991 Sep;17(5):505-11. doi: 10.1007/BF01233174. Somat Cell Mol Genet. 1991. PMID: 1763388

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