Matches in Nanopublications for { ?s ?p "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_assertion description "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293702.RADOfHE6abUYtBlKI3SpudwiAuJmHzGWB3aQykIFzYUQ4130_provenance.
- NP1293703.RADGNkGOcaCa0ZZpiwExGka_wLXPuwxVu6xK6408mclfw130_assertion description "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293703.RADGNkGOcaCa0ZZpiwExGka_wLXPuwxVu6xK6408mclfw130_provenance.
- NP1293700.RAiUL96mjNYXSm0OWls-Qdwh1sK1T3aDLMGs6aA9lZdPQ130_assertion description "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293700.RAiUL96mjNYXSm0OWls-Qdwh1sK1T3aDLMGs6aA9lZdPQ130_provenance.
- NP1293701.RAoEUuiyr9Y1YWqPnY57ftgv-TIi_llGCzjJnC1rxFV9E130_assertion description "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293701.RAoEUuiyr9Y1YWqPnY57ftgv-TIi_llGCzjJnC1rxFV9E130_provenance.
- NP1293704.RAtnJlxxxKg9wv6PZpRwhPTi4QO5XgRJ4p2FprVl-HWWs130_assertion description "[We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293704.RAtnJlxxxKg9wv6PZpRwhPTi4QO5XgRJ4p2FprVl-HWWs130_provenance.