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Maria Grazia Narducci

Researcher at University of Ferrara

Publications -  45
Citations -  1796

Maria Grazia Narducci is an academic researcher from University of Ferrara. The author has contributed to research in topics: Cutaneous T-cell lymphoma & Lymphoma. The author has an hindex of 22, co-authored 40 publications receiving 1682 citations.

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Identification of the TCL1 gene involved in T-cell malignancies.

TL;DR: The TCL1 gene sequence, which, to the authors' knowledge, shows no sequence homology with other human genes, is preferentially expressed early in T- and B-lymphocyte differentiation.
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Deregulated expression of TCL1 causes T cell leukemia in mice.

TL;DR: It is demonstrated that transcriptional activation of the TCL1 protooncogene can cause malignant transformation of T lymphocytes, indicating the role of TCL2 in the initiation of malignant transformed T cell neoplasia in T prolymphocytic leukemias and T chronic lymphocyticLeukmias.
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Skin homing of Sézary cells involves SDF-1-CXCR4 signaling and down-regulation of CD26/dipeptidylpeptidase IV

TL;DR: It is reported that SS cells express a functionally active CXCR4 and that its ligand SDF-1 is abundantly produced in the skin, which represents the main destination of SS cell spreading and could play an important role in skin homing of SS through the regulatory activity of CD26.
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MicroRNA profiling reveals that miR-21, miR486 and miR-214 are upregulated and involved in cell survival in Sézary syndrome

TL;DR: This work profiled the expression of 470 microRNAs in a cohort of 22 SS patients, and it identified 45 miRNAs differentially expressed between SS and controls, and defined a signature of 14 mi RNAs, potentially able to discriminate patients with unfavorable and favorable outcome.
Journal Article

Regulation of TCL1 Expression in B- and T-Cell Lymphomas and Reactive Lymphoid Tissues

TL;DR: Analysis of data from a large tumor lymphoma data bank including 194 cases of lymphoproliferative disorders of B- and T-cell origin as well as reactive lymphoid tissues indicates that TCL1 is expressed in more differentiated B cells, under both reactive and neoplastic conditions, from antigen committed B cells and in germinal center B cell cells and is down-regulated in the latest stage ofB-cell differentiation.