What is he best known for?
The fields of study he is best known for:
- Gene
- Cancer
- Internal medicine
His primary scientific interests are in Cell biology, Molecular biology, Internal medicine, Cancer research and Pathology.
His studies deal with areas such as Receptor, Cytotoxic T cell and Immunology as well as Cell biology.
His Molecular biology research incorporates elements of Fibronectin, Epstein–Barr virus, Transcriptional regulation, Transfection and MUC1.
Luigi Frati combines subjects such as Endocrinology, Oncology and Drug resistance with his study of Internal medicine.
His Cancer research research is multidisciplinary, incorporating elements of Apoptosis, Downregulation and upregulation and T cell.
His research in Pathology intersects with topics in Gastroenterology, Cell and Gene expression.
His most cited work include:
- Isolation and Expansion of Adult Cardiac Stem Cells From Human and Murine Heart (1336 citations)
- Constitutive activation of NF‐κB and T‐cell leukemia/lymphoma in Notch3 transgenic mice (376 citations)
- Brain White-Matter Volume Loss and Glucose Hypometabolism Precede the Clinical Symptoms of Huntington's Disease (229 citations)
What are the main themes of his work throughout his whole career to date?
Luigi Frati spends much of his time researching Cell biology, Internal medicine, Molecular biology, Cancer research and Immunology.
The Cell biology study combines topics in areas such as T cell and Cellular differentiation.
His Internal medicine research incorporates themes from Gastroenterology, Endocrinology, Oncology and Pathology.
His Oncology research integrates issues from Breast cancer and Ovarian cancer.
His biological study deals with issues like Antigen, which deal with fields such as Monoclonal antibody.
His Cancer research study combines topics in areas such as Cell culture, Cancer and Apoptosis.
He most often published in these fields:
- Cell biology (24.48%)
- Internal medicine (22.96%)
- Molecular biology (21.44%)
What were the highlights of his more recent work (between 2009-2021)?
- Internal medicine (22.96%)
- Cancer research (18.60%)
- Oncology (9.11%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Internal medicine, Cancer research, Oncology, Pathology and Cell biology.
His study in Internal medicine is interdisciplinary in nature, drawing from both Gastroenterology and Endocrinology.
His Cancer research research incorporates themes from Cell culture, Apoptosis, Programmed cell death, Bortezomib and Receptor.
His Pathology research includes themes of Immunoassay, Radioimmunoassay, Tumor marker and Serum samples.
The concepts of his Cell biology study are interwoven with issues in Molecular biology and Biochemistry.
Luigi Frati combines subjects such as Downregulation and upregulation and Antigen with his study of Molecular biology.
Between 2009 and 2021, his most popular works were:
- HE4: a new potential early biomarker for the recurrence of ovarian cancer (137 citations)
- Circulating tumor cells (CTCs) in metastatic breast cancer (MBC): prognosis, drug resistance and phenotypic characterization (109 citations)
- Human adipose-derived stromal cells for cell-based therapies in the treatment of systemic sclerosis. (81 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Cancer
- Internal medicine
Luigi Frati mainly focuses on Cancer research, Internal medicine, Oncology, Pathology and Downregulation and upregulation.
His Cancer research research incorporates elements of T cell, Apoptosis, Programmed cell death, Bortezomib and Primary effusion lymphoma.
Luigi Frati interconnects Endocrinology and Drug resistance in the investigation of issues within Internal medicine.
His work carried out in the field of Pathology brings together such families of science as Adipose tissue and Hyaluronic acid.
His research in Downregulation and upregulation intersects with topics in Epstein–Barr virus, Receptor, Molecular biology, microRNA and Phosphorylation.
His study on Notch signaling pathway is often connected to HDAC1 as part of broader study in Cell biology.
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