http://www.cnr.it/ontology/cnr/individuo/unitaDiPersonaleEsterno/ID4502
EMMANUELE CRESPAN
- Type
- Label
- EMMANUELE CRESPAN (literal)
- EMMANUELE CRESPAN (literal)
- Partecipa a commessa
- Persona in rapporto
- Autore CNR di
- Indolyl-pyrrolone as a new scaffold for Pim1 inhibitors. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Arylthiopyrrole (AThP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors: Synthesis, Structure-Activity Relationships, and Docking Studies (Part 2). (Articolo in rivista) (Prodotto della ricerca)
- Replication protein A and proliferating cell nuclear antigen coordinate DNA polymerase selection in 8-oxo-guanine repair. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Design and synthesis of thiadiazoles and thiazoles targeting the Bcr-Abl T315I mutant: from docking false positives to ATP-noncompetitive inhibitors. (Articolo in rivista) (Prodotto della ricerca)
- 3D QSAR Models Built on Structure-Based Alignments of Abl Tyrosine Kinase Inhibitors. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Dual Src and Abl inhibitors target wild type Abl and the AblT315I Imatinib-resistant mutant with different mechanisms. (Articolo in rivista) (Prodotto della ricerca)
- Crystal Structure of HIV-1 Reverse Transcriptase Bound to a Non-Nucleoside Inhibitor with a Novel Mechanism of Action. (Articolo in rivista) (Prodotto della ricerca)
- Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide. (Articolo in rivista) (Prodotto della ricerca)
- Synthesis, biological evaluation and docking studies of 4-amino substituted 1H-pyrazolo[3,4-d]pyrimidines. (Articolo in rivista) (Prodotto della ricerca)
- Indolyl aryl sulphones as HIV-1 non-nucleoside reverse transcriptase inhibitors: synthesis, biological evaluation and binding mode studies of new derivatives at indole-2-carboxamide. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Slow binding-tight binding interaction between benzimidazol-2-one inhibitors and HIV-1 reverse transcriptase containing the lysine 103 to asparagine mutation. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Error-free bypass of 2-hydroxyadenine by human DNA polymerase lambda with Proliferating Cell Nuclear Antigen and Replication Protein A in different sequence contexts. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Expanding the repertoire of DNA polymerase substrates: template-instructed incorporation of non-nucleoside triphosphate analogues by DNA polymerases beta and lambda. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- N-(thiazol-2-yl)-2-thiophene carboxamide derivatives as Abl inhibitors identified by a pharmacophore-based database screening of commercially available compounds. (Articolo in rivista) (Prodotto della ricerca)
- Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell lines. (Articolo in rivista) (Prodotto della ricerca)
- Discovery and SAR of 1,3,4-thiadiazole derivatives as potent Abl tyrosine kinase inhibitors and cytodifferentiating agents. (Articolo in rivista) (Prodotto della ricerca)
- Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the (Articolo in rivista) (Prodotto della ricerca)
- Overcoming the Drug Resistance Problem with Second-Generation Tyrosine Kinase Inhibitors: From Enzymology to Structural Models. (Articolo in rivista) (Prodotto della ricerca)
- The balance between the rates of incorporation and pyrophosphorolytic removal influences the HIV-1 reverse transcriptase bypass of an abasic site with deoxy-, dideoxy-, and ribonucleotides. (Articolo in rivista) (Prodotto della ricerca)
- 8-oxo-guanine bypass by human DNA polymerases in the presence of auxiliary proteins. (Articolo in rivista) (Prodotto della ricerca)
- Design, Synthesis, Biological Activity, and ADME Properties of Pyrazolo[3,4-d]pyrimidines Active in Hypoxic Human Leukemia Cells: A Lead Optimization Study. (Articolo in rivista) (Prodotto della ricerca)
- Oxidative DNA Damage Bypass in Arabidopsis thaliana Requires DNA Polymerase {lambda} and Proliferating Cell Nuclear Antigen 2. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Slow-, Tight-Binding HIV-1 Reverse Transcriptase Non-Nucleoside Inhibitors Highly Active against Drug-Resistant Mutants. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- DNA polymerase lambda specifically bridges and extends DNA ends containing microhomoloy regions (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Biochemical Approach of PCNA1 and PCNA2 proteins interaction with DNA pol lambda of Arabidopsis thaliana (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Biochemical Approach of PCNA1 and PCNA2 proteins interaction with DNA pol lambda of Arabidopsis thaliana (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- DNA polymerase lambda specifically bridges and extends DNA ends containing microhomoloy regions (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Roles of the human proteins PCNA, RP-A and Fen-1 in avoiding functional redundance between human DNA polymerases b and l in genomic stability safeguarding. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
- DNA polymerases and mutagenesis in human cancers. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The block of DNA polymerase delta strand displacement activity by an abasic site can be rescued by the concerted action of DNA polymerase beta and flap endonuclease 1. (Articolo in rivista) (Prodotto della ricerca)
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Incoming links:
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- Http://www.w3.org/2002/07/owl#sameAs
- Rapporto con persona
- Autore CNR
- Expanding the repertoire of DNA polymerase substrates: template-instructed incorporation of non-nucleoside triphosphate analogues by DNA polymerases beta and lambda. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Error-free bypass of 2-hydroxyadenine by human DNA polymerase lambda with Proliferating Cell Nuclear Antigen and Replication Protein A in different sequence contexts. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- 8-oxo-guanine bypass by human DNA polymerases in the presence of auxiliary proteins. (Articolo in rivista) (Prodotto della ricerca)
- The balance between the rates of incorporation and pyrophosphorolytic removal influences the HIV-1 reverse transcriptase bypass of an abasic site with deoxy-, dideoxy-, and ribonucleotides. (Articolo in rivista) (Prodotto della ricerca)
- Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the (Articolo in rivista) (Prodotto della ricerca)
- Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell lines. (Articolo in rivista) (Prodotto della ricerca)
- Discovery and SAR of 1,3,4-thiadiazole derivatives as potent Abl tyrosine kinase inhibitors and cytodifferentiating agents. (Articolo in rivista) (Prodotto della ricerca)
- N-(thiazol-2-yl)-2-thiophene carboxamide derivatives as Abl inhibitors identified by a pharmacophore-based database screening of commercially available compounds. (Articolo in rivista) (Prodotto della ricerca)
- Synthesis, biological evaluation and docking studies of 4-amino substituted 1H-pyrazolo[3,4-d]pyrimidines. (Articolo in rivista) (Prodotto della ricerca)
- Slow binding-tight binding interaction between benzimidazol-2-one inhibitors and HIV-1 reverse transcriptase containing the lysine 103 to asparagine mutation. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Design and synthesis of thiadiazoles and thiazoles targeting the Bcr-Abl T315I mutant: from docking false positives to ATP-noncompetitive inhibitors. (Articolo in rivista) (Prodotto della ricerca)
- Arylthiopyrrole (AThP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors: Synthesis, Structure-Activity Relationships, and Docking Studies (Part 2). (Articolo in rivista) (Prodotto della ricerca)
- Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide. (Articolo in rivista) (Prodotto della ricerca)
- 3D QSAR Models Built on Structure-Based Alignments of Abl Tyrosine Kinase Inhibitors. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Crystal Structure of HIV-1 Reverse Transcriptase Bound to a Non-Nucleoside Inhibitor with a Novel Mechanism of Action. (Articolo in rivista) (Prodotto della ricerca)
- Dual Src and Abl inhibitors target wild type Abl and the AblT315I Imatinib-resistant mutant with different mechanisms. (Articolo in rivista) (Prodotto della ricerca)
- Oxidative DNA Damage Bypass in Arabidopsis thaliana Requires DNA Polymerase {lambda} and Proliferating Cell Nuclear Antigen 2. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Design, Synthesis, Biological Activity, and ADME Properties of Pyrazolo[3,4-d]pyrimidines Active in Hypoxic Human Leukemia Cells: A Lead Optimization Study. (Articolo in rivista) (Prodotto della ricerca)
- Overcoming the Drug Resistance Problem with Second-Generation Tyrosine Kinase Inhibitors: From Enzymology to Structural Models. (Articolo in rivista) (Prodotto della ricerca)
- Indolyl aryl sulphones as HIV-1 non-nucleoside reverse transcriptase inhibitors: synthesis, biological evaluation and binding mode studies of new derivatives at indole-2-carboxamide. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Replication protein A and proliferating cell nuclear antigen coordinate DNA polymerase selection in 8-oxo-guanine repair. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Indolyl-pyrrolone as a new scaffold for Pim1 inhibitors. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The block of DNA polymerase delta strand displacement activity by an abasic site can be rescued by the concerted action of DNA polymerase beta and flap endonuclease 1. (Articolo in rivista) (Prodotto della ricerca)
- DNA polymerases and mutagenesis in human cancers. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Slow-, Tight-Binding HIV-1 Reverse Transcriptase Non-Nucleoside Inhibitors Highly Active against Drug-Resistant Mutants. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Roles of the human proteins PCNA, RP-A and Fen-1 in avoiding functional redundance between human DNA polymerases b and l in genomic stability safeguarding. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
- DNA polymerase lambda specifically bridges and extends DNA ends containing microhomoloy regions (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Biochemical Approach of PCNA1 and PCNA2 proteins interaction with DNA pol lambda of Arabidopsis thaliana (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- Biochemical Approach of PCNA1 and PCNA2 proteins interaction with DNA pol lambda of Arabidopsis thaliana (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
- DNA polymerase lambda specifically bridges and extends DNA ends containing microhomoloy regions (Abstract/Poster in atti di convegno) (Prodotto della ricerca)