Matches in Nanopublications for { ?s ?p "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_provenance.
- assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP662357.RAOcjuwElujm3L9R_yFiY8zh_Jrp8_FcRTOznRmZ80Jxo130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662357.RAOcjuwElujm3L9R_yFiY8zh_Jrp8_FcRTOznRmZ80Jxo130_provenance.
- assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_provenance.
- NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- NP530270.RA74nY-evE7on28yvzgHIDPJvz4G-8lGBGDZJArisH1zc130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530270.RA74nY-evE7on28yvzgHIDPJvz4G-8lGBGDZJArisH1zc130_provenance.
- NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.