Matches in Nanopublications for { ?s ?p "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511350.RAAjAxN1kUNcIko6PxkcIvwssg3_sS6OWDu-OSbgJQ1ac130_provenance.
- NP279337.RAtjIdzURS46JArpxq6Z1TyQxjPpeT6HFO_7cOEknR51s130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279337.RAtjIdzURS46JArpxq6Z1TyQxjPpeT6HFO_7cOEknR51s130_provenance.
- NP754780.RAhHX_MfIkuEYlIyPPpZXpRMOcldLefLm3viT0eABMgmk130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754780.RAhHX_MfIkuEYlIyPPpZXpRMOcldLefLm3viT0eABMgmk130_provenance.
- NP635645.RA6_b_nWBgCMzwWOy2GMXX1ybofGKHrtY4zXQX0YYTtLE130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635645.RA6_b_nWBgCMzwWOy2GMXX1ybofGKHrtY4zXQX0YYTtLE130_provenance.
- NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652899.RAcpDJ7lvQtD56jObjv4Vz2xIN7o5dqT-C8F2u6Uw29PY130_provenance.
- NP788431.RAXtpHC3obtgaDYd1mbvq-ih-_B_J6Tid77Xfbb_rdmoc130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788431.RAXtpHC3obtgaDYd1mbvq-ih-_B_J6Tid77Xfbb_rdmoc130_provenance.
- NP267254.RAVJ-aVEcDOblSArMvr1DFZSID2uOgRjQOcnZvB5nnu9w130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267254.RAVJ-aVEcDOblSArMvr1DFZSID2uOgRjQOcnZvB5nnu9w130_provenance.
- NP267256.RAVIM6KbFopfpemA1aOK8mFtJ2IENZhjyLVYbh_aSEfOo130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267256.RAVIM6KbFopfpemA1aOK8mFtJ2IENZhjyLVYbh_aSEfOo130_provenance.
- NP670548.RAt9bQp2KJ4Gs6xkLXi62ayGVybRiXe0WCEscnYC3GaGw130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670548.RAt9bQp2KJ4Gs6xkLXi62ayGVybRiXe0WCEscnYC3GaGw130_provenance.
- NP392393.RAJPtSV1GDIFFFkSm57BWQeA-h7Vg5m8FMvO9vtW2QmIY130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392393.RAJPtSV1GDIFFFkSm57BWQeA-h7Vg5m8FMvO9vtW2QmIY130_provenance.
- NP267258.RAML7Fjf37U1f5w1VFqC5n5YrZD9_hYSpzxU6da0oYZSw130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267258.RAML7Fjf37U1f5w1VFqC5n5YrZD9_hYSpzxU6da0oYZSw130_provenance.
- NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.