Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP384749.RAZvJQxSBRhJPYU6LhTRbsJqnupi0yRqtLZ8pVVhCKXWI130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384749.RAZvJQxSBRhJPYU6LhTRbsJqnupi0yRqtLZ8pVVhCKXWI130_provenance.
• NP804732.RAAvEVnC_j1TdRXDMvFgQcbvgL8aOWnw2cKKQ2FPnzyxI130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804732.RAAvEVnC_j1TdRXDMvFgQcbvgL8aOWnw2cKKQ2FPnzyxI130_provenance.
• NP821291.RAB4_LX1s4D5xXFEtnu_gCQax_QiDKDHuC1sNvZa5dNzQ130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821291.RAB4_LX1s4D5xXFEtnu_gCQax_QiDKDHuC1sNvZa5dNzQ130_provenance.
• NP317368.RAoRAn6fSlEJAjKTxPf-gBiw3LkcpB7g2ZdEz_la6sPDo130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317368.RAoRAn6fSlEJAjKTxPf-gBiw3LkcpB7g2ZdEz_la6sPDo130_provenance.
• NP560613.RAO2RplbvIkukLttZ_HU7Tcfw4P5Ze8gaha-FAtSgH-Fk130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560613.RAO2RplbvIkukLttZ_HU7Tcfw4P5Ze8gaha-FAtSgH-Fk130_provenance.
• NP931866.RAGSKK5KnyLXci5GOSSVHkacNYcuEpn2xcPPN5AXr4TOY130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931866.RAGSKK5KnyLXci5GOSSVHkacNYcuEpn2xcPPN5AXr4TOY130_provenance.
• NP723125.RA5Sen5zTmaUJrIs650eNsekE_5l7JjeclbJUCYv7yVuY130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723125.RA5Sen5zTmaUJrIs650eNsekE_5l7JjeclbJUCYv7yVuY130_provenance.
• NP1073704.RA_9XT61kR9s4no89Xqsbtkv3pf1jACe6Z0oh2JxZ308Y130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073704.RA_9XT61kR9s4no89Xqsbtkv3pf1jACe6Z0oh2JxZ308Y130_provenance.
• assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1073705.RAHeSDZYh5oPWW_vGjzmjPb6vwzxGFcpWIzeyY11SKZZ8130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073705.RAHeSDZYh5oPWW_vGjzmjPb6vwzxGFcpWIzeyY11SKZZ8130_provenance.
• NP723228.RAoOsovISSVCuI-u331SANmYdUuYw6evik5DAjSJHW4-Q130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723228.RAoOsovISSVCuI-u331SANmYdUuYw6evik5DAjSJHW4-Q130_provenance.
• NP947276.RAgyzdNhocd3L29YtH9pLS_orWbJKtfwnEH_2Bw9kY_74130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947276.RAgyzdNhocd3L29YtH9pLS_orWbJKtfwnEH_2Bw9kY_74130_provenance.
• NP947362.RAr0KvRK-tg3vv1meUKhdjjA1ZcJbuzsTBoe3LX2M91z0130_assertion description "[Our results demonstrated that TAT-g-CS/siRNA(Sur) nanoparticles not only strongly inhibited the in vitro proliferation of 4T1-Luc tumor cells via inducing cell apoptosis, but also effectively inhibited the in vivo growth and metastasis of malignant breast tumor, which suggested that TAT-g-CS/siRNA nanoparticle was a highly efficient non-viral system for siRNA delivery, especially for anti-tumor therapy based on siRNA therapeutics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947362.RAr0KvRK-tg3vv1meUKhdjjA1ZcJbuzsTBoe3LX2M91z0130_provenance.