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Fingerprint Dive into the research topics where Riccardo Valli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Neoplasms Medicine & Life Sciences
Bone Marrow Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Lymphoma, Large B-Cell, Diffuse Medicine & Life Sciences
Gastrointestinal Stromal Tumors Medicine & Life Sciences
Chromosomes, Human, Pair 20 Medicine & Life Sciences
Differential Diagnosis Medicine & Life Sciences
B-Cell Lymphoma Medicine & Life Sciences

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Research Output 2002 2020

Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype

Khan, A. W., Minelli, A., Frattini, A., Montalbano, G., Bogni, A., Fabbri, M., Porta, G., Acquati, F., Pinto, R. M., Bergami, E., Mura, R., Pegoraro, A., Cesaro, S., Cipolli, M., Zecca, M., Danesino, C., Locatelli, F., Maserati, E., Pasquali, F. & Valli, R., Jan 2 2020, In : Molecular Cytogenetics. 13, 1, 1.

Research output: Contribution to journalArticle

Open Access
Chromosomes, Human, Pair 20
Diamond
Microarrays
Chromosomes
Karyotype

A cell-autonomous oncosuppressive role of human RNASET2 affecting ECM-mediated oncogenic signaling

Roggiani, F., Riva, C., Raspagliesi, F., Porta, G., Valli, R., Taramelli, R., Acquati, F., Mezzanzanica, D. & Tomassetti, A., Feb 2019, In : Cancers. 11, 2, 255.

Research output: Contribution to journalArticle

Open Access
Extracellular Matrix
Phenotype
Neoplasms
Drug Delivery Systems
Ribonucleases

A tricky and rare cause of pulmonary eosinophilia: Myeloid/lymphoid neoplasm with eosinophilia and rearrangement of PDGFRA

Zanelli, M., Smith, M., Zizzo, M., Carloni, A., Valli, R., De Marco, L., Foroni, M., Palicelli, A., Martino, G. & Ascani, S., Nov 19 2019, In : BMC Pulmonary Medicine. 19, 1, 216.

Research output: Contribution to journalArticle

Open Access
Pulmonary Eosinophilia
Eosinophilia
Neoplasms
Lung
Platelet-Derived Growth Factor beta Receptor

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

Valli, R., Vinti, L., Frattini, A., Fabbri, M., Montalbano, G., Olivieri, C., Minelli, A., Locatelli, F., Pasquali, F. & Maserati, E., 2018, In : Molecular Cytogenetics. 11, 1

Research output: Contribution to journalArticle

Chromosomes
Bone
Aplastic Anemia
Genes
Bone Marrow

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

Valli, R., Vinti, L., Frattini, A., Fabbri, M., Montalbano, G., Olivieri, C., Minelli, A., Locatelli, F., Pasquali, F. & Maserati, E., 2018, In : Molecular Cytogenetics. 11, p. 2 9 p.

Research output: Contribution to journalArticle

Chromosomes
Bone
Aplastic Anemia
Genes
Bone Marrow