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Carlo M. Croce

Researcher at Ohio State University

Publications -  1156
Citations -  199822

Carlo M. Croce is an academic researcher from Ohio State University. The author has contributed to research in topics: microRNA & Cancer. The author has an hindex of 198, co-authored 1135 publications receiving 189007 citations. Previous affiliations of Carlo M. Croce include University of Nebraska Medical Center & University of California, Los Angeles.

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Fhit tumor suppressor: guardian of the preneoplastic genome.

TL;DR: Fhit interacts with and stabilizes ferrodoxin reductase (Fdxr), a mitochondrial flavoprotein that transfers electrons from NADPH to cytochrome P450, suggesting a role for Fhit in the modulation of reactive oxygen species production and of genomic damage.
Patent

Methods and compositions for the diagnosis and treatment of esphageal adenocarcinomas

TL;DR: In this article, methods and compositions for the diagnosis, prognosis and/or treatment of esophageal adenocarcinoma and Barrett's esophagus associated carcinoma are disclosed.
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Loss of p53 and altered miR15-a/16-1→MCL-1 pathway in CLL: insights from TCL1-Tg:p53−/− mouse model and primary human leukemia cells

TL;DR: In this article, a mouse model with TCL1-Tg:p53(-/-) genotype was generated to investigate the underlying mechanisms for the highly malignant phenotype of 17p-CLL and to facilitate in vivo evaluation of potential drugs against CLL with p53 deletion.
Journal Article

Characterization of t(11;14) translocation in mantle cell lymphoma by fluorescent in situ hybridization.

TL;DR: This study detected BCL-1 translocations in eight of eight patients with clinical and immunological features of mantle cell lymphoma, suggesting that the t(11;14) translocation is a critical event in the pathogenesis of MCL and may be a primary element for the diagnosis.
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Identification of the Genes Up- and Down-Regulated by the High Mobility Group A1 (HMGA1) Proteins: Tissue Specificity of the HMGA1-Dependent Gene Regulation

TL;DR: High mobility group A (HMGA) proteins are chromatinic proteins that do not have transcriptional activity per se, however, by interacting with the transcription machinery, they regulate, negatively or positively, the expression of several genes.