RR
Rosa Romano
Research areas: Immunology and Microbiology · Immunology · T-cell and B-cell Immunology · Immunodeficiency and Autoimmune Disorders · Virus-based gene therapy research
0000-0002-1206-5165
Employment
Employment history is unavailable.
Education
Education history is unavailable.
Projects & Funding
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CRISPR/Cas9-based genome editing for very early onset inflammatory bowel disease. Crohn's & Colitis Foundation2020 - 2021
Publications (20)
- Gene therapy for primary immunodeficiency Save
- Highly Efficient and Marker-free Genome Editing of Human Pluripotent Stem Cells by CRISPR-Cas9 RNP and AAV6 Donor-Mediated Homologous Recombination Save
- Identification of preexisting adaptive immunity to Cas9 proteins in humans Save
- Combined immunodeficiency and Epstein-Barr virus- induced B cell malignancy in humans with inherited CD70 deficiency Save
- NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion Save
- FOXN1 in organ development and human diseases Save
- In this issue: FOX genes and the immune response Save
- Alterations of the autoimmune regulator transcription factor and failure of central tolerance: APECED as a model Save
- Betamethasone therapy in ataxia telangiectasia: Unraveling the rationale of this serendipitous observation on the basis of the pathogenesis Save
- FOXN1: A master regulator gene of thymic epithelial development program Save
- Human skin-derived keratinocytes and fibroblasts co-cultured on 3D poly ε-caprolactone scaffold support in vitro HSC differentiation into T-lineage committed cells Save
- Molecular evidence for a thymus-independent partial T cell development in a FOXN1-/- athymic human fetus Save
- Networking between γc and GH-R signaling in the control of cell growth Save
- The R156H variation in IL-12Rβ1 is not a mutation Save
- De novo 13q12.3-q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia, and cerebellar hypoplasia, mimicking an A-T like phenotype Save
- From murine to human Nude/SCID: The thymus, T-Cell development and the missing link Save
- Genetic basis of altered central tolerance and autoimmune diseases: A lesson from AIRE mutations Save
- Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels Save
- Role of the common γ chain in cell cycle progression of human malignant cell lines Save
- SCID-like phenotype associated with an inhibitory autoreactive immunoglobulin Save