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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 Review.
Characterization and genomic localization of the mouse Extl2 gene.
Wuyts W, Van Hul W. Wuyts W, et al. Among authors: van hul w. Cytogenet Cell Genet. 2000;89(3-4):185-8. doi: 10.1159/000015609. Cytogenet Cell Genet. 2000. PMID: 10965119
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease.
Janssens K, Gershoni-Baruch R, GuaƱabens N, Migone N, Ralston S, Bonduelle M, Lissens W, Van Maldergem L, Vanhoenacker F, Verbruggen L, Van Hul W. Janssens K, et al. Among authors: van maldergem l, van hul w. Nat Genet. 2000 Nov;26(3):273-5. doi: 10.1038/81563. Nat Genet. 2000. PMID: 11062463
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.
Evaluation of the role of RANK and OPG genes in Paget's disease of bone.
Wuyts W, Van Wesenbeeck L, Morales-Piga A, Ralston S, Hocking L, Vanhoenacker F, Westhovens R, Verbruggen L, Anderson D, Hughes A, Van Hul W. Wuyts W, et al. Among authors: van wesenbeeck l, van hul w. Bone. 2001 Jan;28(1):104-7. doi: 10.1016/s8756-3282(00)00411-7. Bone. 2001. PMID: 11165949
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
Evidence that the rat osteopetrotic mutation toothless (tl) is not in the TNFSF11 (TRANCE, RANKL, ODF, OPGL) gene.
Odgren PR, Kim N, van Wesenbeeck L, MacKay C, Mason-Savas A, Safadi FF, Popoff SN, Lengner C, van-Hul W, Choi Y, Marks SC Jr. Odgren PR, et al. Among authors: van wesenbeeck l, van hul w. Int J Dev Biol. 2001 Dec;45(8):853-9. Int J Dev Biol. 2001. PMID: 11804028
Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.
Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JB, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Among authors: van hul e, van hul w. J Med Genet. 2002 Feb;39(2):91-7. doi: 10.1136/jmg.39.2.91. J Med Genet. 2002. PMID: 11836356 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.
The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: Evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondral ossification.
Van Wesenbeeck L, Odgren PR, MacKay CA, D'Angelo M, Safadi FF, Popoff SN, Van Hul W, Marks SC Jr. Van Wesenbeeck L, et al. Among authors: van hul w. Proc Natl Acad Sci U S A. 2002 Oct 29;99(22):14303-8. doi: 10.1073/pnas.202332999. Epub 2002 Oct 11. Proc Natl Acad Sci U S A. 2002. PMID: 12379742 Free PMC article.
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