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IFT80 is essential for chondrocyte differentiation by regulating hedgehog and Wnt signaling pathways
Partial mutation of intraflagellar transport 80 (IFT80) in humans causes Jeune asphyxiating thoracic dystrophy (JATD) and short-rib polydactyly (SRP) syndrome type III. These diseases are autosomal recessive chondrodysplasias that share clinical similarities, including shortened long bones and const...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2013
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3908790/ https://ncbi.nlm.nih.gov/pubmed/23333501 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2012.12.028 |
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