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W Van Hul

Showing results (71-80 of 89) with videos related to

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Calcified Tissue International|December 7, 2007
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen studyK Brixen, S Beckers, A Peeters, et al.
Calcified Tissue International|May 28, 2004
Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's diseaseG Beyens, E Van Hul, K Van Driessche, et al.
American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.
Human Molecular Genetics|December 14, 2001
Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel geneE Cleiren, O Bénichou, E Van Hul, et al.
The International Journal of Developmental Biology|January 24, 2002
Evidence that the rat osteopetrotic mutation toothless (tl) is not in the TNFSF11 (TRANCE, RANKL, ODF, OPGL) geneP R Odgren, N Kim, L van Wesenbeeck, et al.
American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.
Journal of Medical Genetics|April 4, 2000
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13K Janssens, R Gershoni-Baruch, E Van Hul, et al.
Obesity (Silver Spring, Md.)|March 21, 2013
A gene variant of PNPLA3, but not of APOC3, is associated with histological parameters of NAFLD in an obese populationA Verrijken, S Beckers, S Francque, et al.
Pediatric Obesity|January 18, 2013
Screening for genetic variants in BDNF that contribute to childhood obesityD Zegers, R Hendrickx, A Verrijken, et al.
American Journal of Human Genetics|May 20, 1999
Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21W Balemans, J Van Den Ende, A Freire Paes-Alves, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Calcified Tissue International|December 7, 2007
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with peak bone mass in non-sedentary men: results from the Odense androgen studyK Brixen, S Beckers, A Peeters, et al.
Calcified Tissue International|May 28, 2004
Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's diseaseG Beyens, E Van Hul, K Van Driessche, et al.
American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.
Human Molecular Genetics|December 14, 2001
Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel geneE Cleiren, O Bénichou, E Van Hul, et al.
The International Journal of Developmental Biology|January 24, 2002
Evidence that the rat osteopetrotic mutation toothless (tl) is not in the TNFSF11 (TRANCE, RANKL, ODF, OPGL) geneP R Odgren, N Kim, L van Wesenbeeck, et al.
American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.
Journal of Medical Genetics|April 4, 2000
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13K Janssens, R Gershoni-Baruch, E Van Hul, et al.
Obesity (Silver Spring, Md.)|March 21, 2013
A gene variant of PNPLA3, but not of APOC3, is associated with histological parameters of NAFLD in an obese populationA Verrijken, S Beckers, S Francque, et al.
Pediatric Obesity|January 18, 2013
Screening for genetic variants in BDNF that contribute to childhood obesityD Zegers, R Hendrickx, A Verrijken, et al.
American Journal of Human Genetics|May 20, 1999
Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21W Balemans, J Van Den Ende, A Freire Paes-Alves, et al.
Pageof 9