Messiaen L - Search Results

1

Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2.

Claes K, Poppe B, Machackova E, Coene I, Foretova L, De Paepe A, Messiaen L. Claes K, et al. Among authors: messiaen l. Genes Chromosomes Cancer. 2003 Jul;37(3):314-20. doi: 10.1002/gcc.10221. Genes Chromosomes Cancer. 2003. PMID: 12759930

2

Lack of independence between five DNA polymorphisms in the NF1 gene.

Messiaen L, De Bie S, Moens T, Van den Enden A, Leroy J. Messiaen L, et al. Hum Mol Genet. 1993 Apr;2(4):485. doi: 10.1093/hmg/2.4.485. Hum Mol Genet. 1993. PMID: 8504312 No abstract available.

3

Characterisation of two different nonsense mutations, C6792A and C6792G, causing skipping of exon 37 in the NF1 gene.

Messiaen L, Callens T, De Paepe A, Craen M, Mortier G. Messiaen L, et al. Hum Genet. 1997 Nov;101(1):75-80. doi: 10.1007/s004390050590. Hum Genet. 1997. PMID: 9385374

4

Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing method.

Messiaen L, Callens T, Baele G. Messiaen L, et al. Haemostasis. 1997 Sep-Oct;27(5):228-36. doi: 10.1159/000217461. Haemostasis. 1997. PMID: 9690481

5

Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.

Van Gele M, Van Roy N, Ronan SG, Messiaen L, Vandesompele J, Geerts ML, Naeyaert JM, Blennow E, Bar-Am I, Das Gupta TK, van der Drift P, Versteeg R, Leonard JH, Speleman F. Van Gele M, et al. Among authors: messiaen l. Genes Chromosomes Cancer. 1998 Sep;23(1):67-71. doi: 10.1002/(sici)1098-2264(199809)23:1<67::aid-gcc10>3.0.co;2-b. Genes Chromosomes Cancer. 1998. PMID: 9713999

6

Human myosin V gene produces different transcripts in a cell type-specific manner.

Lambert J, Naeyaert JM, Callens T, De Paepe A, Messiaen L. Lambert J, et al. Among authors: messiaen l. Biochem Biophys Res Commun. 1998 Nov 18;252(2):329-33. doi: 10.1006/bbrc.1998.9644. Biochem Biophys Res Commun. 1998. PMID: 9826529

7

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online.

Claes K, Machackova E, De Vos M, Mortier G, De Paepe A, Messiaen L. Claes K, et al. Among authors: messiaen l. Hum Mutat. 1999;13(3):256. doi: 10.1002/(SICI)1098-1004(1999)13:3<256::AID-HUMU12>3.0.CO;2-M. Hum Mutat. 1999. PMID: 10090482

8

Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G.

Claes K, Machackova E, De Vos M, Poppe B, De Paepe A, Messiaen L. Claes K, et al. Among authors: messiaen l. Dis Markers. 1999 Oct;15(1-3):69-73. doi: 10.1155/1999/241046. Dis Markers. 1999. PMID: 10595255 Free PMC article.

9

Genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approach.

De Vos M, Poppe B, Delvaux I, Mortier G, Claes K, Messiaen L, De Paepe A. De Vos M, et al. Among authors: messiaen l. Dis Markers. 1999 Oct;15(1-3):191-5. doi: 10.1155/1999/809125. Dis Markers. 1999. PMID: 10595277 Free PMC article.

10

arg-cys substitution at codon 1246 of the human myosin Va gene is not associated with Griscelli syndrome.

Lambert J, Naeyaert JM, De Paepe A, Van Coster R, Ferster A, Song M, Messiaen L. Lambert J, et al. Among authors: messiaen l. J Invest Dermatol. 2000 Apr;114(4):731-3. doi: 10.1046/j.1523-1747.2000.00933.x. J Invest Dermatol. 2000. PMID: 10733681

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