Matches in Nanopublications for { ?s ?p "[Contrary to previous studies in patients with Charcot-Marie-Tooth disease type 2A, fibroblasts carrying the MFN2 mutation present with a respiratory chain deficiency, a fragmentation of the mitochondrial network and a significant reduction of MFN2 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP845234.RAwcaZaoh23ehK6X92WrsoEOgrl3MBgtmrXOjsNu9c1kg130_assertion description "[Contrary to previous studies in patients with Charcot-Marie-Tooth disease type 2A, fibroblasts carrying the MFN2 mutation present with a respiratory chain deficiency, a fragmentation of the mitochondrial network and a significant reduction of MFN2 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845234.RAwcaZaoh23ehK6X92WrsoEOgrl3MBgtmrXOjsNu9c1kg130_provenance.
- NP644381.RAKEzNZKOYDy73z7_cK2IY6_EXxOzNQSP7TtLS0NUe6FU130_assertion description "[Contrary to previous studies in patients with Charcot-Marie-Tooth disease type 2A, fibroblasts carrying the MFN2 mutation present with a respiratory chain deficiency, a fragmentation of the mitochondrial network and a significant reduction of MFN2 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644381.RAKEzNZKOYDy73z7_cK2IY6_EXxOzNQSP7TtLS0NUe6FU130_provenance.
- assertion description "[Contrary to previous studies in patients with Charcot-Marie-Tooth disease type 2A, fibroblasts carrying the MFN2 mutation present with a respiratory chain deficiency, a fragmentation of the mitochondrial network and a significant reduction of MFN2 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP948471.RAZpH1ZWu62Fn7u1rX0Oh-Hxj-1-Yn6CIO2Dv-0Xs2Iwg130_assertion description "[Contrary to previous studies in patients with Charcot-Marie-Tooth disease type 2A, fibroblasts carrying the MFN2 mutation present with a respiratory chain deficiency, a fragmentation of the mitochondrial network and a significant reduction of MFN2 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948471.RAZpH1ZWu62Fn7u1rX0Oh-Hxj-1-Yn6CIO2Dv-0Xs2Iwg130_provenance.
- NP832586.RAqGfrYloW1cUewg51iY-xVW1i9Zt_DoxXej5JXOxI9Oo130_assertion description "[Contrary to previous studies in patients with Charcot-Marie-Tooth disease type 2A, fibroblasts carrying the MFN2 mutation present with a respiratory chain deficiency, a fragmentation of the mitochondrial network and a significant reduction of MFN2 protein expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP832586.RAqGfrYloW1cUewg51iY-xVW1i9Zt_DoxXej5JXOxI9Oo130_provenance.