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Hul Wim Van

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Canonical Wnt signaling in bone health and disease

2017 Bone Abstracts
- Hul Wim Van
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Common variants in Rspo 1,2 and 3 do not associate with BMD in stratified subpopulations of the Odense Androgen Study and mutations in these genes are not a common cause of craniotubular hyperostosis

2016 Bone Abstracts
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Intronic mutations in the TCIRG1 gene cause human autosomal recessive osteopetrosis

2015
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Search and Functional Evaluation of Rare Variants in RSPO3 Gene

2015
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Genetic Screening of WNT5B in Patients with Monogenic Sclerosing Bone Disorders and Healthy Men with an Extreme Bone Mineral Density

2015
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Rs55710688 in the Kozak sequence of WNT16 increases translation efficiency and is associated with osteoporosis related parameters

2014 Bone Abstracts
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No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders

2013 Bone Abstracts
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Expression analysis of mesenchymal KS483 cells during differentiation towards osteoblasts

2013 Bone Abstracts
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