De Schepper S - Search Results

1

Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1.

Maertens O, De Schepper S, Vandesompele J, Brems H, Heyns I, Janssens S, Speleman F, Legius E, Messiaen L. Maertens O, et al. Among authors: de schepper s. Am J Hum Genet. 2007 Aug;81(2):243-51. doi: 10.1086/519562. Epub 2007 Jun 20. Am J Hum Genet. 2007. PMID: 17668375 Free PMC article.

2

Multiple myofibromas and an epidermal verrucous nevus in a child with neurofibromatosis type 1.

De Schepper S, Janssens S, Messiaen L, Van den Broecke C, Naeyaert JM. De Schepper S, et al. Dermatology. 2004;209(3):223-7. doi: 10.1159/000079894. Dermatology. 2004. PMID: 15459537

3

Pigment cell-related manifestations in neurofibromatosis type 1: an overview.

De Schepper S, Boucneau J, Lambert J, Messiaen L, Naeyaert JM. De Schepper S, et al. Pigment Cell Res. 2005 Feb;18(1):13-24. doi: 10.1111/j.1600-0749.2004.00206.x. Pigment Cell Res. 2005. PMID: 15649148 Review.

4

Gene expression profiling of cultured human NF1 heterozygous (NF1+/-) melanocytes reveals downregulation of a transcriptional cis-regulatory network mediating activation of the melanocyte-specific dopachrome tautomerase (DCT) gene.

Boucneau J, De Schepper S, Vuylsteke M, Van Hummelen P, Naeyaert JM, Lambert J. Boucneau J, et al. Among authors: de schepper s. Pigment Cell Res. 2005 Aug;18(4):285-99. doi: 10.1111/j.1600-0749.2005.00237.x. Pigment Cell Res. 2005. PMID: 16033338

5

Neurofibromatosis type 1 protein and amyloid precursor protein interact in normal human melanocytes and colocalize with melanosomes.

De Schepper S, Boucneau JM, Westbroek W, Mommaas M, Onderwater J, Messiaen L, Naeyaert JM, Lambert JL. De Schepper S, et al. J Invest Dermatol. 2006 Mar;126(3):653-9. doi: 10.1038/sj.jid.5700087. J Invest Dermatol. 2006. PMID: 16374483 Free article.

6

Café-au-lait spots in neurofibromatosis type 1 and in healthy control individuals: hyperpigmentation of a different kind?

De Schepper S, Boucneau J, Vander Haeghen Y, Messiaen L, Naeyaert JM, Lambert J. De Schepper S, et al. Arch Dermatol Res. 2006 Apr;297(10):439-49. doi: 10.1007/s00403-006-0644-6. Epub 2006 Feb 15. Arch Dermatol Res. 2006. PMID: 16479403

7

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

De Raedt T, Maertens O, Chmara M, Brems H, Heyns I, Sciot R, Majounie E, Upadhyaya M, De Schepper S, Speleman F, Messiaen L, Vermeesch JR, Legius E. De Raedt T, et al. Among authors: de schepper s. Genes Chromosomes Cancer. 2006 Oct;45(10):893-904. doi: 10.1002/gcc.20353. Genes Chromosomes Cancer. 2006. PMID: 16830335

8

Comprehensive NF1 screening on cultured Schwann cells from neurofibromas.

Maertens O, Brems H, Vandesompele J, De Raedt T, Heyns I, Rosenbaum T, De Schepper S, De Paepe A, Mortier G, Janssens S, Speleman F, Legius E, Messiaen L. Maertens O, et al. Among authors: de paepe a, de schepper s, de raedt t. Hum Mutat. 2006 Oct;27(10):1030-40. doi: 10.1002/humu.20389. Hum Mutat. 2006. PMID: 16941471

9

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.

Brems H, Chmara M, Sahbatou M, Denayer E, Taniguchi K, Kato R, Somers R, Messiaen L, De Schepper S, Fryns JP, Cools J, Marynen P, Thomas G, Yoshimura A, Legius E. Brems H, et al. Among authors: de schepper s. Nat Genet. 2007 Sep;39(9):1120-6. doi: 10.1038/ng2113. Epub 2007 Aug 19. Nat Genet. 2007. PMID: 17704776

10

Somatic mutation analysis in NF1 café au lait spots reveals two NF1 hits in the melanocytes.

De Schepper S, Maertens O, Callens T, Naeyaert JM, Lambert J, Messiaen L. De Schepper S, et al. J Invest Dermatol. 2008 Apr;128(4):1050-3. doi: 10.1038/sj.jid.5701095. Epub 2007 Oct 4. J Invest Dermatol. 2008. PMID: 17914445 Free article. No abstract available.

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