(FM) Patología, Anatomía y Fisiología
Departamento académico
University of Milan
Milán, ItaliaPublicaciones en colaboración con investigadores/as de University of Milan (12)
2024
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A roadmap for therapeutic discovery in pulmonary hypertension associated with left heart failure. A scientific statement of the Heart Failure Association (HFA) of the ESC and the ESC Working Group on Pulmonary Circulation & Right Ventricular Function
European Journal of Heart Failure, Vol. 26, Núm. 4, pp. 707-729
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Tracking dynamic evolution of low- and intermediate-risk differentiated thyroid cancer: Identification of individuals at risk of recurrence
Clinical Endocrinology, Vol. 101, Núm. 3, pp. 286-294
2022
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miRNome profiling of lung cancer metastases revealed a key role for miRNA-PD-L1 axis in the modulation of chemotherapy response
Journal of Hematology and Oncology, Vol. 15, Núm. 1
2021
2019
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Experimental models to unravel the molecular pathogenesis, cell of origin and stem cell properties of cholangiocarcinoma
Liver International, Vol. 39, Núm. S1, pp. 79-97
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Identification of mutations associated with acquired resistance to sunitinib in renal cell cancer
International Journal of Cancer, Vol. 145, Núm. 7, pp. 1991-2001
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P65BTK is a novel potential actionable target in KRAS-mutated/EGFR-wild type lung adenocarcinoma
Journal of Experimental and Clinical Cancer Research, Vol. 38, Núm. 1
2017
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Dual modulation of MCL-1 and mTOR determines the response to sunitinib
Journal of Clinical Investigation, Vol. 127, Núm. 1, pp. 153-168
2014
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Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33
Human Molecular Genetics, Vol. 23, Núm. 24, pp. 6616-6633
2013
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The histone methyltransferase MMSET/WHSC1 activates TWIST1 to promote an epithelial-mesenchymal transition and invasive properties of prostate cancer
Oncogene, Vol. 32, Núm. 23, pp. 2882-2890
1999
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Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene
Thrombosis and Haemostasis, Vol. 82, Núm. 6, pp. 1634-1638
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The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: Prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels
Thrombosis Research, Vol. 93, Núm. 1, pp. 1-8