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Maria Beatrice Morelli

Researcher at University of Camerino

Publications -  86
Citations -  7811

Maria Beatrice Morelli is an academic researcher from University of Camerino. The author has contributed to research in topics: Transient receptor potential channel & Cancer. The author has an hindex of 28, co-authored 74 publications receiving 6749 citations. Previous affiliations of Maria Beatrice Morelli include Sapienza University of Rome.

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Isofuranodiene synergizes with temozolomide in inducing glioma cells death.

TL;DR: This study demonstrated the glioma selectivity of IFD and its cytotoxic properties suggesting a new strategy for the treatment of GBM in order to overcome the TMZ resistance and to reduce its side effects.
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Axitinib induces senescence-associated cell death and necrosis in glioma cell lines: The proteasome inhibitor, bortezomib, potentiates axitinib-induced cytotoxicity in a p21(Waf/Cip1) dependent manner

TL;DR: It is demonstrated that the TKI axitinib induces DNA damage response (DDR) characterized by γ-H2AX phosphorylation and Chk1 kinase activation leading to G2/M cell cycle arrest and mitotic catastrophe in U87, T98 and U251 glioma cell lines, and p21(Waf1/Cip1) increased levels correlates with induction of ROS and senescence-associated cell death.
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Advances in transient receptor potential vanilloid-2 channel expression and function in tumor growth and progression.

TL;DR: Bladder cancer tumors show loss or reduction of a short TRPV2 variant during cancer progression, with increased malignancy and invasiveness, and high expression of TRpV2 was also observed more frequently in esophageal squamous cell carcinoma patients with advanced pT stage, lymph node metastasis and advanced pathological stage.
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Involvement of the TRPML Mucolipin Channels in Viral Infections and Anti-viral Innate Immune Responses.

TL;DR: TRPML channels might play a double-edged sword in resistance to viral infections: on the other side, by regulating TLR responses in the various immune cells, they contribute to enhance antiviral innate and possibly adaptive immune responses.