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Transforming growth factor-beta1 to the bone.
Janssens K, ten Dijke P, Janssens S, Van Hul W. Janssens K, et al. Among authors: van hul w. Endocr Rev. 2005 Oct;26(6):743-74. doi: 10.1210/er.2004-0001. Epub 2005 May 18. Endocr Rev. 2005. PMID: 15901668 Review.
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.
Janssens K, Gershoni-Baruch R, Van Hul E, Brik R, Guañabens N, Migone N, Verbruggen LA, Ralston SH, Bonduelle M, Van Maldergem L, Vanhoenacker F, Van Hul W. Janssens K, et al. Among authors: van hul e, van maldergem l, van hul w. J Med Genet. 2000 Apr;37(4):245-9. doi: 10.1136/jmg.37.4.245. J Med Genet. 2000. PMID: 10745041 Free PMC article.
Molecular genetics of too much bone.
Janssens K, Van Hul W. Janssens K, et al. Among authors: van hul w. Hum Mol Genet. 2002 Oct 1;11(20):2385-93. doi: 10.1093/hmg/11.20.2385. Hum Mol Genet. 2002. PMID: 12351574 Review.
Camurati-Engelmann disease. Review of radioclinical features.
Vanhoenacker FM, Janssens K, Van Hul W, Gershoni-Baruch R, Brik R, De Schepper AM. Vanhoenacker FM, et al. Among authors: van hul w. Acta Radiol. 2003 Jul;44(4):430-4. doi: 10.1080/j.1600-0455.2003.00088.x. Acta Radiol. 2003. PMID: 12846694
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.
Hellemans J, Preobrazhenska O, Willaert A, Debeer P, Verdonk PC, Costa T, Janssens K, Menten B, Van Roy N, Vermeulen SJ, Savarirayan R, Van Hul W, Vanhoenacker F, Huylebroeck D, De Paepe A, Naeyaert JM, Vandesompele J, Speleman F, Verschueren K, Coucke PJ, Mortier GR. Hellemans J, et al. Among authors: van roy n, van hul w. Nat Genet. 2004 Nov;36(11):1213-8. doi: 10.1038/ng1453. Epub 2004 Oct 17. Nat Genet. 2004. PMID: 15489854
253 results