Scientific Commons: L. Messiaen

An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in Exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation (2007)

Upadyaya, M., Huson, S M., Davies, M., Thomas, N., Chuzhanova, N., Giovannini, S., ...

An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in Exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation (2007)

Upadyaya, M., Huson, S M., Davies, M., Thomas, N., Chuzhanova, N., Giovannini, S., ...

An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation (2007)

Upadhyaya, M., Huson, S.M., Davies, M., Thomas, N., Chuzhanova, N., Giovannini, S., ...

Neurofibromatosis type 1 (NF1) is characterized by cafe-au-lait spots, skinfold freckling, and cutaneous neurofibromas. No obvious relationships between small mutations (ACG change of codon 990....

Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1 (2007)

Maertens, Ophélia, DE SCHEPPER, S, Vandesompele, Jo, BRERNS, H, HEYNS, I, JANSSENS, SANDRA, ...

Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients (2006)

Claes, K, Kehrer-Sawatzki, H, Tinschert, S, ...

Neurofibromatosis type 1 (NF1), the most common tumor-predisposing disorder in humans, is caused by defects in the NF1 tumor-suppressor gene. Comprehensive mutation analysis applying RNA-based...

Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH (2006)

Thuresson, A-C, Piotrowski, A, Menzel, U, Grigelionis, G, ...

BACKGROUND: Segmental duplications flanking the neurofibromatosis type 1 (NF1) gene locus on 17q11 mediate most gene deletions in NF1 patients. However, the large size of the gene and the complexity...

Real-time quantitative allele discrimination assay using 3 ' locked nucleic acid primers for detection of low-percentage mosaic mutations (2006)

Maertens, Ophélia, LEGIUS, E, Speleman, Franki, MESSIAEN, L, Vandesompele, Jo

Comprehensive NF1 screening on cultured Schwann cells from neurofibromas (2006)

Maertens, Ophélia, BREMS, H, Vandesompele, Jo, DE RAEDT, T, HEYNS, I, ROSENBAUM, T, ...

Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patients (2006)

DE RAEDT, T, Maertens, Ophélia, CHMARA, M, BREMS, H, HEYNS, I, SCIOT, R, ...

Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients (2006)

Maertens, Ophélia, PRENEN, H, WOZNIAK, A, SCIOT, R, Pauwels, Patrick, DE WEVER, I, ...

An absence of cutaneous neurofibromas associated with a 3-bp in-frame deletion in exon 17 of the NF1 gene (c.2970_2972 deIAAT (2006)

Upadhyaya, M., Huson, S.M., Davies, M., Giovannini, S., Griffiths, S., Consoli, C., ...

Recente moleculaire inzichten in erfelijke borst- en ovariumkanker in België (2005)

Claes, Kathleen, Poppe, Bruce, COENE, ILSE, MESSIAEN, L, De Paepe, Anne

The human FOXL2 mutation database (2004)

Beysen, Diane, Vandesompele, Jo, MESSIAEN, L, De Paepe, Anne, De Baere, Elfride

Multiple myofibromas and an epidermal verrucous nevus in a child with neurofibromatosis type 1 (2004)

De Schepper, Sofie, JANSSENS, S, MESSIAEN, L, Naeyaert, Jean

Multiple myofibromas and an epidermal verrucous nevus in a child with neurofibromatosis type 1 (2004)

De Schepper, S, Janssens, S, Messiaen, L, Naeyaert, JM

Neurofibromatosis type 1 (NF1) is a common neurocutaneous autosomal dominant genetic disorder affecting primarily tissues derived from the embryonic neural crest. Two hallmark features of NF1 are the...

More than 125 FOXL2 mutations and variants in BPES and POF patients in the human FOXL2 allelic variant database. (2003)

Beysen, D, Vandesompele, J, Pattyn, F, De Paepe, A, Messiaen, L, De Baere, E

FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation (2003)

De Baere, E, Beysen, D, Oley, C, Lorenz, B, Cocquet, J, De Sutter, P, ...

Blepharophimosis syndrome (BPES), an autosomal dominant syndrome in which an eyelid malformation is associated (type I) or not (type II) with premature ovarian failure (POF), has recently been...

FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation (2003)

Baere, E. De, Beysen, D., Oley, C., Lorenz, B., Cocquet, J., Sutter, P. De, ...

Independent NF1 mutations in two large families with spinal neurofibromatosis (2003)

MESSIAEN, L, RICCARDI, V, PELTONEN, J, Maertens, Ophélia, CALLENS, T, KARVONEN, SL, ...

Complex splicing pattern generates great diversity in human NF1 transcripts (2002)

Vandenbroucke, I, Callens, T, De Paepe, A, Messiaen, L

Background: Mutation analysis of the neurofibromatosis type 1 (NF1) gene has shown that about 30% of NF1 patients carry a splice mutation resulting in the production of one or several shortened...

Investigation of tumour-invasion mechanisms. (2002)

MAREEL, MARCUS, Van Roy, Frans, MESSIAEN, L, Bracke, Marc, BOGHAERT, E, COOPMAN, P

Spontaneous and oncogene-mediated acquisition of the invasive phenotype by cells in culture. (2002)

MAREEL, MARCUS, COOPMAN, P, DRAGONETTI, C, Fiers, Walther, GAO, J, MESSIAEN, L, ...

Correlates of malignancy in cultured cells (2002)

MAREEL, MARCUS, Van Roy, Frans, MESSIAEN, L, Van Larebeke, Nicolas, BOGHAERT, E

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation (2001)

Dixon, M J, Small, K W, Jabs, E W, Leroy, B P, ...

Mutations in FOXL2, a forkhead transcription factor gene, have recently been shown to cause blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) types I and II, a rare genetic disorder. In...

Genetisch advies bij het familiaal voorkomen van borstkanker (2001)

Poppe, Bruce, MEIRE, I, DELVAUX, I, Claes, Kathleen, MESSIAEN, L, De Paepe, Anne

Occurrence of scleroderma in monozygotic twins. (2000)

DE KEYSER, F, PEENE, I, JOOS, R, Naeyaert, Jean, MESSIAEN, L, VEYS, EM

Association between the Cys282Tyr missense mutation and the haptoglobin phenotype polymorphism in patients with chronic hepatitis C. (2000)

Van Vlierberghe, Hans, MESSIAEN, L, DE PAEPE, A, Delanghe, Joris, Praet, Marleen, DE VOS, M, ...

Identification and characterisation of a founder mutation in the Belgian breast/ovarian cancer population (2000)

Claes, Kathleen, Poppe, Bruce, SCHEIR, PETRA, DE VOS, M, DELVEAUX, I, COENE, ILSE, ...

Genetics in ophthalmology (1999)

Messiaen, L, Speleman, F, Van Maldergem, L, ...

The Netherlands Ophthalmic Research Institute, Amsterdam, The Netherlands.

Molecular analysis of Ip36 breakpoints in two Merkel cell carcinomas (1998)

Gele, M. Van, Roy, N. Van, Ronan, S.G., Messiaen, L., Vandesompele, J., Geerts, M.L., ...

Identification of two novel mutations in the protein S active gene using a non-isotopic scanning and sequencing method (1997)

MESSIAEN, L, CALLENS, T, Vanbrabandt, Bart, BAELE, G

UNE NOUVELLE VISION DES BRUITS DE CIRCULATION AVEC LES P.A.I.S. (1992)

Maurin, M., Messiaen, L.

Nous explorons les ressources d'une nouvelle modélisation des niveaux de bruit routier, les mesures à proximité des voies routières chargées montrent un accord satisfaisant.

UNE NOUVELLE VISION DES BRUITS DE CIRCULATION AVEC LES P.A.I.S. (1992)

Maurin, M., Messiaen, L.

Nous explorons les ressources d'une nouvelle modélisation des niveaux de bruit routier, les mesures à proximité des voies routières chargées montrent un accord satisfaisant.

UNE NOUVELLE VISION DES BRUITS DE CIRCULATION AVEC LES P.A.I.S. (1992)

Maurin, M., Messiaen, L.

Nous explorons les ressources d'une nouvelle modélisation des niveaux de bruit routier, les mesures à proximité des voies routières chargées montrent un accord satisfaisant.

SPONTANEOUS ACQUISITION OF TUMORIGENICITY AND INVASIVENESS BY MOUSE LENS EXPLANT CELLS DURING CULTURE INVITRO. (1991)

MESSIAEN, L, QIAN, S, DEBRUYNE, G, BOGHAERT, E, MOENS, T, RABAEY, M, ...

Pathology of tumours produced in syngeneic Fischer rats by fibroblast-like cells before and after transfections with oncogenes. (1987)

GAO, J, Van Roy, Frans, MESSIAEN, L, COSAERT, J, LIEBAUT, G, COOPMAN, P, ...

Invasiveness and metastatic capability of rat fibroblast-like cells before and after transfection with immortalizing and transforming genes. (1986)

Van Roy, Frans, MESSIAEN, L, LIEBAUT, G, JIN, G, DRAGONETTI, CH, FIERS, WC, ...

An Absence of Cutaneous Neurofibromas Associated with a 3-bp Inframe Deletion in Exon 17 of the NF1 Gene (c.2970-2972 delAAT): Evidence of a Clinically Significant NF1 Genotype-Phenotype Correlation

Upadhyaya, M., Huson, S. M., Davies, M., Thomas, N., Chuzhanova, N., Giovannini, S., ...

Neurofibromatosis type 1 (NF1) is characterized by café-au-lait spots, skinfold freckling, and cutaneous neurofibromas. No obvious relationships between small mutations (

FOXL2 mutation screening in a large panel of POF patients and XX males

De Baere, E, Lemercier, B, Christin-Maitre, S, Durval, D, Messiaen, L, Fellous, M, ...

Independent NF1 mutations in two large families with spinal neurofibromatosis

Messiaen, L, Riccardi, V, Peltonen, J, Maertens, O, Callens, T, Karvonen, S, ...

Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts

Sharp, A, Messiaen, L, Page, G, Antignac, C, Gubler, M, Onuchic, L, ...

Evolution and expression of FOXL2

Cocquet, J, Pailhoux, E, Jaubert, F, Servel, N, Xia, X, Pannetier, M, ...

Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1

Messiaen, L, Wimmer, K

Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array‐CGH

Mantripragada, K K, Thuresson, A‐C, Piotrowski, A, De Ståhl, T Díaz, Menzel, U, Grigelionis, G, ...

Identification of two novel mutations in the active protein S gene using a non-isotopic scanning and sequencing method. Thromb. Haemost. Suppl. 1997, PS-1716.

MESSIAEN, L, CALLENS, T, VANBRABANDT, B, Baele, Gaston

Experience with the APC resistance test without and with F V deficient plasma. Thromb. Haemost. Suppl. 1997, PS-95.

VAN ACKER, J, MESSIAEN, L, Baele, Gaston

APC resistance and associated F II variant or C677T homozygosity. Haemostasis, 28, 1998, 408.

Baele, Gaston, MESSIAEN, L

Myosin V produces different transcripts in a tissue-specific manner. PigmentCellRes.il, 1998.

Lambert, Jo, Naeyaert, Jean, CALLENS, T, DE PAEPE, A, MESSIAEN, L

Human Myosin V Gene Produces Different Transcripts in a Cell Type-Specific Manner. Biochemical and Biophysical Research Communications, 252, 1998, 329- 333.

Lambert, Jo, Naeyaert, Jean, CALLENS, T, DE PAEPE, A, MESSIAEN, L

Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition

Baeyens, A, Thierens, H, Claes, K, Poppe, B, Messiaen, L, De Ridder, L, ...

The chromosomal radiosensitivity of breast cancer patients with a known or putative genetic predisposition was investigated and compared to a group of healthy women. The chromosomal radiosensitivity...

BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families

Claes, K, Poppe, B, Coene, I, Paepe, A De, Messiaen, L

L. Messiaen

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