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Bioorganic Chemistry|August 6, 2022
Novel pyrazolo[3,4-d]pyrimidines as dual Src/Bcr-Abl kinase inhibitors: Synthesis and biological evaluation for chronic myeloid leukemia treatmentSalvatore Di Maria, Francesca Picarazzi, Mattia Mori, et al.Journal of Cellular Physiology|September 2, 2018
Apoptosis-associated speck-like protein containing a caspase-1 recruitment domain (ASC) contributes to osteoblast differentiation and osteogenesisSuelen Sartoretto, Sara Gemini-Piperni, Rodrigo A da Silva, et al.Journal of Medicinal Chemistry|June 27, 2017
Prodrugs of Pyrazolo[3,4-d]pyrimidines: From Library Synthesis to Evaluation as Potential Anticancer Agents in an Orthotopic Glioblastoma ModelGiulia Vignaroli, Giulia Iovenitti, Claudio Zamperini, et al.Journal of Medicinal Chemistry|October 13, 2007
Identification of a novel pyrazolo[3,4-d]pyrimidine able to inhibit cell proliferation of a human osteogenic sarcoma in vitro and in a xenograft model in miceFabrizio Manetti, Annalisa Santucci, Giada A Locatelli, et al.Ebiomedicine|June 2, 2019
Paradoxical effects of JZL184, an inhibitor of monoacylglycerol lipase, on bone remodelling in healthy and cancer-bearing miceSilvia Marino, Daniëlle de Ridder, Ryan T Bishop, et al.Arthritis Research & Therapy|August 15, 2021
Blocking Jak/STAT signalling using tofacitinib inhibits angiogenesis in experimental arthritisPaola Di Benedetto, Piero Ruscitti, Onorina Berardicurti, et al.Journal of Cell Science|July 27, 2007
Osteopenia, decreased bone formation and impaired osteoblast development in Sox4 heterozygous miceLise Sofie Haug Nissen-Meyer, Rune Jemtland, Vigdis T Gautvik, et al.Cancer Research|August 5, 2008
A six-gene signature predicting breast cancer lung metastasisThomas Landemaine, Amanda Jackson, Akeila Bellahcène, et al.Cancers|November 13, 2021
Targeting DDX3X Helicase Activity with BA103 Shows Promising Therapeutic Effects in Preclinical Glioblastoma ModelsAnnalaura Brai, Valentina Riva, Letizia Clementi, et al.Journal of Medicinal Chemistry|April 30, 2015
Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and TumorsCristina Tintori, Giuseppina La Sala, Giulia Vignaroli, et al.Pageof 18