Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_provenance.
• NP286500.RAVThy6T2JyKIV27MquYu3dh_-EyQ7W0wX4dW1FWRPmnw130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286500.RAVThy6T2JyKIV27MquYu3dh_-EyQ7W0wX4dW1FWRPmnw130_provenance.
• NP810367.RAZXc9Uv-9Pp5ibjjRMa-QGcPRh8FeCikn_lXx5BAY-uQ130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810367.RAZXc9Uv-9Pp5ibjjRMa-QGcPRh8FeCikn_lXx5BAY-uQ130_provenance.
• NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_provenance.
• NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
• NP369133.RACZL9zX2Y2nTG-5uDe8prIWpl0TANxDHmSuzffqRup-Q130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369133.RACZL9zX2Y2nTG-5uDe8prIWpl0TANxDHmSuzffqRup-Q130_provenance.
• NP156904.RAr80_zXTenYRJu3wlW8vvQ1HTV-vwGwUlkKP61CtMmc8130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156904.RAr80_zXTenYRJu3wlW8vvQ1HTV-vwGwUlkKP61CtMmc8130_provenance.
• NP297539.RAhihyJgS_ie5ST8DY-TcnQMJbOSSPKBRCB8zY_tVX33g130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297539.RAhihyJgS_ie5ST8DY-TcnQMJbOSSPKBRCB8zY_tVX33g130_provenance.
• NP763959.RAYkwoPyKPgxsTremfHJBRN7ZPEIbc4VCldSEjg5U8PX0130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763959.RAYkwoPyKPgxsTremfHJBRN7ZPEIbc4VCldSEjg5U8PX0130_provenance.
• NP243426.RAyEO8nIzIt5OQ9CccK8m1ZszmS_55UteNtmTG-9UiJdY130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243426.RAyEO8nIzIt5OQ9CccK8m1ZszmS_55UteNtmTG-9UiJdY130_provenance.
• NP790177.RA30VZK426fKm_jQ_G89b9xUThGrB9p71Rhqex81ofq3s130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790177.RA30VZK426fKm_jQ_G89b9xUThGrB9p71Rhqex81ofq3s130_provenance.
• NP274164.RAAw-2RGBYQrgEX_dVGubtXpesxDg4C1BoxuPp3B2fv34130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274164.RAAw-2RGBYQrgEX_dVGubtXpesxDg4C1BoxuPp3B2fv34130_provenance.
• NP274173.RADsdf1um_W_tCBzIV6DEcArbkI6FkJzgMTmwKF_IPzCw130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274173.RADsdf1um_W_tCBzIV6DEcArbkI6FkJzgMTmwKF_IPzCw130_provenance.
• NP274175.RABxem60kG8ablfcdRr2akgYDE2LbxMLvL0VfHmd2jTKA130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274175.RABxem60kG8ablfcdRr2akgYDE2LbxMLvL0VfHmd2jTKA130_provenance.
• NP274176.RADGXzpi-F0kjRMcFA5YSfjqbLKj064JCAyB1Mlpnimh4130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274176.RADGXzpi-F0kjRMcFA5YSfjqbLKj064JCAyB1Mlpnimh4130_provenance.
• NP274159.RAfMnnohT7S__8tknZY7iw_Cmfk9qisEb4uQX3bsqva6A130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274159.RAfMnnohT7S__8tknZY7iw_Cmfk9qisEb4uQX3bsqva6A130_provenance.
• NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
• NP274180.RAXiRdEoN0LWtg63nHJG3lHI9pkQGKkQv1So0KPFX2rls130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274180.RAXiRdEoN0LWtg63nHJG3lHI9pkQGKkQv1So0KPFX2rls130_provenance.
• NP274160.RAtxNsojdrd-rRm5bs243Uzq9i4GsS6SBTBFlwjwx2PBg130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274160.RAtxNsojdrd-rRm5bs243Uzq9i4GsS6SBTBFlwjwx2PBg130_provenance.
• NP274165.RAjhdb3JOrg-Li_pKbUkbog3Y_hhG70yFut-j8jXu8S1A130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274165.RAjhdb3JOrg-Li_pKbUkbog3Y_hhG70yFut-j8jXu8S1A130_provenance.
• NP274181.RAgNtlTQ6uYkQSmPnJOdPQ5CwmHsXIxMCfVYaYO-Tul48130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274181.RAgNtlTQ6uYkQSmPnJOdPQ5CwmHsXIxMCfVYaYO-Tul48130_provenance.
• NP274183.RAopQSiSoLJx94WL_WxgXNvUyjFQHGLBDv8Ji9Sxs5D8w130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274183.RAopQSiSoLJx94WL_WxgXNvUyjFQHGLBDv8Ji9Sxs5D8w130_provenance.
• NP274163.RAJEnMAjIqkw90gu2hWuNxq4trPFiyeletwfif1qLopX8130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274163.RAJEnMAjIqkw90gu2hWuNxq4trPFiyeletwfif1qLopX8130_provenance.
• NP274167.RAMXTTCyEgsrTpKTFrDzIub990XxXmpN_6kJ15u50-kec130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274167.RAMXTTCyEgsrTpKTFrDzIub990XxXmpN_6kJ15u50-kec130_provenance.
• NP274170.RAMKCfrPcSpavvteMJVuU2dp0vHoCPWRoKMMgwEC13GTg130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274170.RAMKCfrPcSpavvteMJVuU2dp0vHoCPWRoKMMgwEC13GTg130_provenance.
• NP274171.RAJ1uokqSB0Iw8sTKzt1_Q9FRrFzNMs06KNdNAnrAgVas130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274171.RAJ1uokqSB0Iw8sTKzt1_Q9FRrFzNMs06KNdNAnrAgVas130_provenance.
• NP274174.RAEki2NrzO3UFtvOLkNGZ3hqB-dXN0LQmlHL0AIgrEm8o130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274174.RAEki2NrzO3UFtvOLkNGZ3hqB-dXN0LQmlHL0AIgrEm8o130_provenance.
• NP274177.RAItRIv_cfg_z2AFDj7edxZACk6XpuB8Mv-LvGRFtTCu8130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274177.RAItRIv_cfg_z2AFDj7edxZACk6XpuB8Mv-LvGRFtTCu8130_provenance.
• NP274184.RAKeDTUtJdpw5bwu47jxwqRFf2GFmEVKXtgQrpHbSE80w130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274184.RAKeDTUtJdpw5bwu47jxwqRFf2GFmEVKXtgQrpHbSE80w130_provenance.
• NP274185.RAPD3YtIQBKmYXmxAgBU-RlkGidKLUTqekL3u-fUhCZuw130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274185.RAPD3YtIQBKmYXmxAgBU-RlkGidKLUTqekL3u-fUhCZuw130_provenance.
• NP274162.RAxDpMP9GbgAX03LhllfHRAI6h6o6LMzcOmLwMMG7HB1I130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274162.RAxDpMP9GbgAX03LhllfHRAI6h6o6LMzcOmLwMMG7HB1I130_provenance.
• NP274166.RA7a6mYDM40ZBp2fd7QY1omN30ojonuM4hVSptujsUAN0130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274166.RA7a6mYDM40ZBp2fd7QY1omN30ojonuM4hVSptujsUAN0130_provenance.
• NP274168.RA1RECqkSLTGbldYIs__viRcgFQVfMKvTwItDhAdy9lEA130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274168.RA1RECqkSLTGbldYIs__viRcgFQVfMKvTwItDhAdy9lEA130_provenance.
• NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_provenance.
• NP274172.RA0Cc5r-tv_9xbxZAihk8fBRwlE5JCj8fPMOAfa7u8wdo130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274172.RA0Cc5r-tv_9xbxZAihk8fBRwlE5JCj8fPMOAfa7u8wdo130_provenance.
• NP274178.RAyM7sT1Xq69Ggg9ksMP3Ep0-oUI9LhV7ukn0MI-LUiaY130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274178.RAyM7sT1Xq69Ggg9ksMP3Ep0-oUI9LhV7ukn0MI-LUiaY130_provenance.
• NP274179.RAzrzkXJ2m6j7ccykOU8Ipb2Cdr0bu1MlAdbmD5IAvgpg130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274179.RAzrzkXJ2m6j7ccykOU8Ipb2Cdr0bu1MlAdbmD5IAvgpg130_provenance.
• NP274182.RAxaO1DtO-XXr7ecViBACwmNW0EsxjWV7Ik03C8Erh-rw130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274182.RAxaO1DtO-XXr7ecViBACwmNW0EsxjWV7Ik03C8Erh-rw130_provenance.