Matches in Nanopublications for { ?s ?p "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386738.RAa67w0EH31ooUpfItyDj8Dsl_Mg5xM6yRdB0QdXAc0LY130_provenance.
- NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386736.RAEDOM-yFOGVjlboWr3mGZaujDhM12EUkGZDMIX_66ZNg130_provenance.
- NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance.
- NP1386740.RAMTdvJCT6sWkLDseJCQtSSBeQbpDNiWLCBaD81nRKDyE130_assertion description "[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1386740.RAMTdvJCT6sWkLDseJCQtSSBeQbpDNiWLCBaD81nRKDyE130_provenance.