Cuppens H - Search Results

1

Art meets science: The Cosmopolitan Chicken Research Project.

Stinckens A, Vereijken A, Ons E, Konings P, Van As P, Cuppens H, Moreau Y, Sakai R, Aerts J, Goddeeris B, Buys N, Vanmechelen K, Cassiman JJ. Stinckens A, et al. Among authors: cuppens h. Facts Views Vis Obgyn. 2015;7(3):163-72. Facts Views Vis Obgyn. 2015. PMID: 26977265 Free PMC article. Review.

2

A quality control study of CFTR mutation screening in 40 different European laboratories. The European Concerted Action on Cystic Fibrosis.

Cuppens H, Cassiman JJ. Cuppens H, et al. Eur J Hum Genet. 1995;3(4):235-45. doi: 10.1159/000472304. Eur J Hum Genet. 1995. PMID: 8528672

3

Solid phase fluorescent sequencing of the CFTR gene.

Cuppens H, Cassiman JJ. Cuppens H, et al. Methods Mol Biol. 2001;167:63-88. doi: 10.1385/1-59259-113-2:063. Methods Mol Biol. 2001. PMID: 11265322 Review. No abstract available.

4

Cystic fibrosis.

Cuppens H, Dequeker E, Cassiman JJ. Cuppens H, et al. Methods Mol Med. 2004;92:221-44. doi: 10.1385/1-59259-432-8:221. Methods Mol Med. 2004. PMID: 14733315 No abstract available.

5

CFTR mutations and polymorphisms in male infertility.

Cuppens H, Cassiman JJ. Cuppens H, et al. Int J Androl. 2004 Oct;27(5):251-6. doi: 10.1111/j.1365-2605.2004.00485.x. Int J Androl. 2004. PMID: 15379964 Review.

6

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. 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.

7

Rapid detection of hypervariable regions by the polymerase chain reaction technique.

Decorte R, Cuppens H, Marynen P, Cassiman JJ. Decorte R, et al. Among authors: cuppens h. DNA Cell Biol. 1990 Jul-Aug;9(6):461-9. doi: 10.1089/dna.1990.9.461. DNA Cell Biol. 1990. PMID: 2206402

8

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. Genomics. 1993 Dec;18(3):693-7. doi: 10.1016/s0888-7543(05)80376-3. Genomics. 1993. PMID: 7508414

9

Identification of seven rather infrequent and one novel CFTR mutation in the Belgian population.

Teng H, Cuppens H, De Boeck C, Cassiman JJ. Teng H, et al. Among authors: cuppens h. Hum Mol Genet. 1994 Dec;3(12):2249-50. doi: 10.1093/hmg/3.12.2249. Hum Mol Genet. 1994. PMID: 7881429 No abstract available.

10

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. Mol Cell Probes. 1992 Feb;6(1):33-9. doi: 10.1016/0890-8508(92)90069-a. Mol Cell Probes. 1992. PMID: 1372093

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