Messiaen L - Search Results

1

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. Among authors: messiaen l. J Invest Dermatol. 2006 Mar;126(3):653-9. doi: 10.1038/sj.jid.5700087. J Invest Dermatol. 2006. PMID: 16374483 Free article.

2

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. Among authors: messiaen l. 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.

3

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. Among authors: messiaen l. 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

4

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: messiaen l. 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.

5

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. Among authors: messiaen l. 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.

6

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. Among authors: messiaen l. Dermatology. 2004;209(3):223-7. doi: 10.1159/000079894. Dermatology. 2004. PMID: 15459537

7

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 Free article.

8

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

9

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: messiaen l. Hum Mutat. 2006 Oct;27(10):1030-40. doi: 10.1002/humu.20389. Hum Mutat. 2006. PMID: 16941471

10

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: messiaen l. Nat Genet. 2007 Sep;39(9):1120-6. doi: 10.1038/ng2113. Epub 2007 Aug 19. Nat Genet. 2007. PMID: 17704776

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