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Rita Perego

Observed name: RITA PEREGO
OpenAlex ID: A5111662991
Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-Met and its complex with the microbial alkaloid K-252a
2003 · Nikolaus Schiering, Stefan Knapp, et al. · Proceedings of the National Academy of Sciences · 162
High-Throughput NMR-Based Screening with Competition Binding Experiments
2002 · Claudio Dalvit, Maria Flocco, et al. · Journal of the American Chemical Society · 158
Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP-1 Inhibitor for Cancer Therapy
2015 · Gianluca Papeo, Helena Posteri, et al. · Journal of Medicinal Chemistry · 150
Identification of 4,5-Dihydro-1H-pyrazolo[4,3-h]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors
2010 · Italo Beria, Dario Ballinari, et al. · Journal of Medicinal Chemistry · 86
Identification of candidate substrates for poly(ADP‐ribose) polymerase‐2 (PARP2) in the absence of DNA damage using high‐density protein microarrays
2011 · Sonia Troiani, Rosita Lupi, et al. · FEBS Journal · 32
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Activation of Zap-70 Tyrosine Kinase Due to a Structural Rearrangement Induced by Tyrosine Phosphorylation and/or ITAM Binding
2000 · Carlo Visco, Giovanni Magistrelli, et al. · Biochemistry · 32
Regulation of the Wild-Type and Y1235D Mutant Met Kinase Activation
2005 · Cinzia Cristiani, Luisa Rusconi, et al. · Biochemistry · 22
Insights into PARP Inhibitors’ Selectivity Using Fluorescence Polarization and Surface Plasmon Resonance Binding Assays
2014 · Gianluca Papeo, Nilla Avanzi, et al. · SLAS DISCOVERY · 20
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Synthesis of the phosphono analogues of α- and β-d-mannopyranosyl phosphate
1984 · Francesco Nicotra, Rita Perego, et al. · Carbohydrate Research · 20
Role of the Src homology 2 domains and interdomain regions in ZAP‐70 phosphorylation and enzymatic activity
1999 · Giovanni Magistrelli, Roberta Bosotti, et al. · European Journal of Biochemistry · 9
Abstract 734: Thienoindoles: New highly promising agents for antibody-drug conjugates generation
2018 · Michele Caruso, Fabio Gasparri, et al. · Cancer Research · 4
Abstract 822: Thienoindoles, a novel class of DNA minor groove alkylating agents highly suited for the generation of novel antibody drug conjugates (ADCs)
2014 · Barbara Valsasina, Fabio Gasparri, et al. · Cancer Research · 2
“Classical” and “non-classical” endothelin analogues
1993 · Roberto de Castiglione, Mauro Galantino, et al. · Springer eBooks · 1
Abstract A149: NMS-P945, a highly active payload for antibody drug conjugates generation
2015 · Fabio Gasparri, Michele Caruso, et al. · Molecular Cancer Therapeutics
Abstract 691: In vitro and in vivo characterization of selective orally available Parp-1 inhibitors with demonstrated antitumor efficacy in BRCA negative cancer models
2010 · Gianluca Papeo, Sonia Rainoldi, et al. · Cancer Research
24 h glycemia variability correlates with arterial structure alteration in type 1 diabetes
2008 · Manuela Carla Colombo, Pierluigi Gamba, et al. · 10th European Congress of Endocrinology
In the metabolic syndrome adrenergic overdrive is independent on the obese state
2008 · Manuela Carla Colombo, Fosca Quarti‐Trevano, et al. · 10th European Congress of Endocrinology
Chemical and enzymatic treatment of endothelin
1995 · RITA PEREGO, LUIGIA GOZZINI, et al. · International journal of peptide & protein research
Works count: 18
Citation count: 698
H-index: 9
I10-index: 9
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