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Scientific Data|June 13, 2024
3D atlas of the human fetal chondrocranium in the middle trimesterMarkéta Kaiser, Tomáš Zikmund, Siddharth Vora, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 12, 2013
Dual functions for WNT5A during cartilage development and in diseaseSara Hosseini-Farahabadi, Poongodi Geetha-Loganathan, Katherine Fu, et al.
Human Molecular Genetics|April 30, 2019
Robinow syndrome skeletal phenotypes caused by the WNT5AC83S variant are due to dominant interference with chondrogenesisSarah J Gignac, Sara Hosseini-Farahabadi, Takashi Akazawa, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 31, 2009
The metalloendopeptidase gene Pitrm1 is regulated by hedgehog signaling in the developing mouse limb and is expressed in muscle progenitorsLiam Town, Edwina McGlinn, Salvatore Fiorenza, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 21, 2008
Expression of the NET family member Zfp503 is regulated by hedgehog and BMP signaling in the limbEdwina McGlinn, Joy M Richman, Vicki Metzis, et al.
Development (Cambridge, England)|December 6, 2008
Novel skeletogenic patterning roles for the olfactory pitHeather L Szabo-Rogers, Poongodi Geetha-Loganathan, Cheryl J Whiting, et al.
Frontiers in Physiology|September 16, 2016
MORN5 Expression during Craniofacial Development and Its Interaction with the BMP and TGFβ PathwaysPetra Cela, Marek Hampl, Katherine K Fu, et al.
Orthodontics & Craniofacial Research|May 11, 2019
Analysis of facial skeletal asymmetry during foetal development using μCT imagingMotoki Katsube, Sara M Rolfe, Stephanie R Bortolussi, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 1, 2009
Expression of WNT signalling pathway genes during chicken craniofacial developmentPoongodi Geetha-Loganathan, Suresh Nimmagadda, Laurent Antoni, et al.
Human Molecular Genetics|July 9, 2026
The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypesShruti S Tophkhane, Gamze Akarsu, Sarah J Gignac, et al.
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