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		<title>Faulty Connexin 43 Gene Reveals Hidden Signaling Switch Behind Rare Bone Disorder</title>
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		<category><![CDATA[c-MYC]]></category>
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		<category><![CDATA[connexin 43]]></category>
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		<category><![CDATA[mesenchymal stromal cells]]></category>
		<category><![CDATA[MMP3]]></category>
		<category><![CDATA[NF-κB]]></category>
		<category><![CDATA[oculodentodigital dysplasia]]></category>
		<category><![CDATA[osteogenic differentiation]]></category>
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					<description><![CDATA[A new study shows that GJA1 mutations in oculodentodigital dysplasia suppress Wnt/c-MYC signaling, driving a paradoxical inflammatory imbalance and excessive matrix degradation in patient-derived cells.]]></description>
		
		
		
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