Lambert J - Search Results

1

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: lambert j. 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.

2

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: lambert j. 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

3

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

4

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: lambert j. 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.

5

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: lambert j. Pigment Cell Res. 2005 Aug;18(4):285-99. doi: 10.1111/j.1600-0749.2005.00237.x. Pigment Cell Res. 2005. PMID: 16033338

6

Cutis laxa of the autosomal recessive type in a consanguineous family.

de Schepper S, Loeys B, de Paepe A, Lambert J, Naeyaert JM. de Schepper S, et al. Among authors: lambert j. Eur J Dermatol. 2003 Nov-Dec;13(6):529-33. Eur J Dermatol. 2003. PMID: 14721770

7

The quest for the mechanism of melanin transfer.

Van Den Bossche K, Naeyaert JM, Lambert J. Van Den Bossche K, et al. Among authors: lambert j. Traffic. 2006 Jul;7(7):769-78. doi: 10.1111/j.1600-0854.2006.00425.x. Traffic. 2006. PMID: 16787393 Free article. Review.

8

Cytoplasmic dynein colocalizes with melanosomes in normal human melanocytes.

Vancoillie G, Lambert J, Mulder A, Koerten HK, Mommaas AM, Van Oostveldt P, Naeyaert JM. Vancoillie G, et al. Among authors: lambert j. Br J Dermatol. 2000 Aug;143(2):298-306. doi: 10.1046/j.1365-2133.2000.03654.x. Br J Dermatol. 2000. PMID: 10951136

9

Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene.

Leroy JG, Nuytinck L, Lambert J, Naeyaert JM, Mortier GR. Leroy JG, et al. Among authors: lambert j. Am J Med Genet A. 2007 Dec 15;143A(24):3144-9. doi: 10.1002/ajmg.a.31966. Am J Med Genet A. 2007. PMID: 18000903

10

[Motor proteins and pigmentation].

Naeyaert JM, Lambert J, Westbroek W. Naeyaert JM, et al. Among authors: lambert j. Verh K Acad Geneeskd Belg. 2002;64(4):251-7; discussion 258-9. Verh K Acad Geneeskd Belg. 2002. PMID: 12416234 Review. Dutch.

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