Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP908417.RAC7Y3shswfX0o-eio7GaJ3ScAAOJc-FHVHAWDRlVm7VA130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908417.RAC7Y3shswfX0o-eio7GaJ3ScAAOJc-FHVHAWDRlVm7VA130_provenance.
• NP348537.RA942tUvtdcc4BItcd1y3vXIubF8NZVRZULCwYgm71hzE130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348537.RA942tUvtdcc4BItcd1y3vXIubF8NZVRZULCwYgm71hzE130_provenance.
• NP807172.RAQ_YSgrH3izDpNO9lc-QE5-H1T5xivvc15W4GWg1BfP4130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807172.RAQ_YSgrH3izDpNO9lc-QE5-H1T5xivvc15W4GWg1BfP4130_provenance.
• assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP233224.RAEKudVQpVwSu19ZysnkRCbCj-bHCiHkTGKToEe1iekCU130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233224.RAEKudVQpVwSu19ZysnkRCbCj-bHCiHkTGKToEe1iekCU130_provenance.
• NP571768.RAeqLliCiCwOwrAGiePnsf_G4_FuFe3z7VAs4Imr7UjwY130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571768.RAeqLliCiCwOwrAGiePnsf_G4_FuFe3z7VAs4Imr7UjwY130_provenance.
• NP762201.RAWggqk3B1vCMAWh5gB_oQllqUGj7y8dqAcTfWXFcNvIc130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762201.RAWggqk3B1vCMAWh5gB_oQllqUGj7y8dqAcTfWXFcNvIc130_provenance.
• NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630226.RAF27ttke8YQMlhq1Xw_AMIjq_dTySKAeF2WmtUMQiKfQ130_provenance.
• NP643530.RAEP4Miq71Cn8DbWFyaDk9De7KUDkrnY7GkH5AQ1QRl30130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643530.RAEP4Miq71Cn8DbWFyaDk9De7KUDkrnY7GkH5AQ1QRl30130_provenance.
• assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP852893.RAAsEx0bvf3bRP8u48ikcZTk-gURKf9HhT5mtqN4yK0v0130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852893.RAAsEx0bvf3bRP8u48ikcZTk-gURKf9HhT5mtqN4yK0v0130_provenance.
• NP852895.RADkRtBc6_BL4GVnp7RprIqbvAAcuNXuMkK9aSzjSUIfk130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852895.RADkRtBc6_BL4GVnp7RprIqbvAAcuNXuMkK9aSzjSUIfk130_provenance.
• NP852896.RAAIORMKgF-2LDgMTqEWynl-oV-vZqMNjPnCzXUi0Zm94130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852896.RAAIORMKgF-2LDgMTqEWynl-oV-vZqMNjPnCzXUi0Zm94130_provenance.
• NP852892.RAUsYqzT4RVYzx76gAE2Mw0N2pZsrMpCDbaCuyAk1YJ8Q130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852892.RAUsYqzT4RVYzx76gAE2Mw0N2pZsrMpCDbaCuyAk1YJ8Q130_provenance.
• NP852897.RAQ-LqIczUilMYpDn6svmcf5xCFOgu5WO3rX-lLWbfQYg130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852897.RAQ-LqIczUilMYpDn6svmcf5xCFOgu5WO3rX-lLWbfQYg130_provenance.
• NP428483.RAhLv-uI9X0qWSCCPkEnFJy-qW-XOCI-gW3WgA4Fv9too130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428483.RAhLv-uI9X0qWSCCPkEnFJy-qW-XOCI-gW3WgA4Fv9too130_provenance.
• NP852890.RAqwKOX-TI4rqrqZ3MymHTckJNTzsI_NE87yKZ1svcSLs130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852890.RAqwKOX-TI4rqrqZ3MymHTckJNTzsI_NE87yKZ1svcSLs130_provenance.
• NP366842.RAHjDZRBTfkFIjPx4lKfO9uXQIeWp2dT3Egz6v5JOzUsI130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366842.RAHjDZRBTfkFIjPx4lKfO9uXQIeWp2dT3Egz6v5JOzUsI130_provenance.
• NP635338.RAJM2gRR7H6M3JT17l_yRVSXTt4iKE2fSlpPRM0pxs5a0130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635338.RAJM2gRR7H6M3JT17l_yRVSXTt4iKE2fSlpPRM0pxs5a0130_provenance.
• NP769049.RAG5aLR_XNF4swNJ5ElBh5ubouRLngAiiqA-Av-Wm_dDw130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769049.RAG5aLR_XNF4swNJ5ElBh5ubouRLngAiiqA-Av-Wm_dDw130_provenance.
• NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852891.RAPUmlJFf9fokjImecs1HQYYK_wcu1bdKCNJqyqrvx2_E130_provenance.
• NP852894.RAHqQGb_8y_fGEc-A7NmPyi1zyH71PwLvqVZkwea4oWTY130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852894.RAHqQGb_8y_fGEc-A7NmPyi1zyH71PwLvqVZkwea4oWTY130_provenance.
• NP940154.RA1DunfysSRYeNBf2-ZJOUlUm1fzVCO-ubrWLWmyxp8D8130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940154.RA1DunfysSRYeNBf2-ZJOUlUm1fzVCO-ubrWLWmyxp8D8130_provenance.
• NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_assertion description "[The most common genetic mutations identified in syndromic craniosynostosis involve the fibroblast growth factor receptor (FGFR) family with other mutations occurring in genes for transcription factors TWIST, MSX2, and GLI3, and other proteins EFNB1, RAB23, RECQL4, and POR, presumed to be involved either upstream or downstream of the FGFR signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907661.RAwekuKzAsabNeoMcbo3av3p20874i4bjtQNpNjhsW9Sg130_provenance.