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CCN3-mutant mice are distinct from CCN3-null mice
A recent manuscript reported phenotypic alterations associated to the expression of a CCN3 protein deleted for the Von Willebrand type C repeat that is common to the various members of the CCN family of proteins. In this comment, the biological significance of these alterations is briefly discussed.
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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Netherlands
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2443240/ https://ncbi.nlm.nih.gov/pubmed/18523871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12079-008-0020-8 |
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