van Hul W - Search Results

1

Missense mutations in LRP5 are not a common cause of idiopathic osteoporosis in adult men.

Crabbe P, Balemans W, Willaert A, van Pottelbergh I, Cleiren E, Coucke PJ, Ai M, Goemaere S, van Hul W, de Paepe A, Kaufman JM. Crabbe P, et al. Among authors: van pottelbergh i, van hul w. J Bone Miner Res. 2005 Nov;20(11):1951-9. doi: 10.1359/JBMR.050705. Epub 2005 Jul 11. J Bone Miner Res. 2005. PMID: 16234968 Free article.

2

Positional cloning of a gene involved in hereditary multiple exostoses.

Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ. Wuyts W, et al. Among authors: van hul ev, van den ouweland am, van hul w. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688

3

Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity.

Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San-Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH. Haslam SI, et al. Among authors: van hul w. J Bone Miner Res. 1998 Jun;13(6):911-7. doi: 10.1359/jbmr.1998.13.6.911. J Bone Miner Res. 1998. PMID: 9626621 Free article.

4

Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

Balemans W, Van Den Ende J, Freire Paes-Alves A, Dikkers FG, Willems PJ, Vanhoenacker F, de Almeida-Melo N, Alves CF, Stratakis CA, Hill SC, Van Hul W. Balemans W, et al. Among authors: van den ende j, van hul w. Am J Hum Genet. 1999 Jun;64(6):1661-9. doi: 10.1086/302416. Am J Hum Genet. 1999. PMID: 10330353 Free PMC article.

5

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).

Wuyts W, Cleiren E, Homfray T, Rasore-Quartino A, Vanhoenacker F, Van Hul W. Wuyts W, et al. Among authors: van hul w. J Med Genet. 2000 Dec;37(12):916-20. doi: 10.1136/jmg.37.12.916. J Med Genet. 2000. PMID: 11106354 Free PMC article.

6

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).

Balemans W, Ebeling M, Patel N, Van Hul E, Olson P, Dioszegi M, Lacza C, Wuyts W, Van Den Ende J, Willems P, Paes-Alves AF, Hill S, Bueno M, Ramos FJ, Tacconi P, Dikkers FG, Stratakis C, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Among authors: van hul e, van den ende j, van hul w. Hum Mol Genet. 2001 Mar 1;10(5):537-43. doi: 10.1093/hmg/10.5.537. Hum Mol Genet. 2001. PMID: 11181578

7

Molecular and radiological diagnosis of sclerosing bone dysplasias.

Van Hul W, Vanhoenacker F, Balemans W, Janssens K, De Schepper AM. Van Hul W, et al. Eur J Radiol. 2001 Dec;40(3):198-207. doi: 10.1016/s0720-048x(01)00400-4. Eur J Radiol. 2001. PMID: 11731208 Review.

8

Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.

Cleiren E, Bénichou O, Van Hul E, Gram J, Bollerslev J, Singer FR, Beaverson K, Aledo A, Whyte MP, Yoneyama T, deVernejoul MC, Van Hul W. Cleiren E, et al. Among authors: van hul e, van hul w. Hum Mol Genet. 2001 Dec 1;10(25):2861-7. doi: 10.1093/hmg/10.25.2861. Hum Mol Genet. 2001. PMID: 11741829

9

Localization of the gene causing autosomal dominant osteopetrosis type I to chromosome 11q12-13.

Van Hul E, Gram J, Bollerslev J, Van Wesenbeeck L, Mathysen D, Andersen PE, Vanhoenacker F, Van Hul W. Van Hul E, et al. Among authors: van wesenbeeck l, van hul w. J Bone Miner Res. 2002 Jun;17(6):1111-7. doi: 10.1359/jbmr.2002.17.6.1111. J Bone Miner Res. 2002. PMID: 12054167 Free article.

10

Extracellular regulation of BMP signaling in vertebrates: a cocktail of modulators.

Balemans W, Van Hul W. Balemans W, et al. Among authors: van hul w. Dev Biol. 2002 Oct 15;250(2):231-50. Dev Biol. 2002. PMID: 12376100 Free article. Review.

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