GL
Giovanna Lattanzi
CNR Instiute of Molecular Genetics, CNR Institute of Molecular Genetics, National Research Council, University of Bologna, IRCCS Istituto Ortopedico Rizzoli
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Nuclear Structure and Function · Muscle Physiology and Disorders · Genomics and Rare Diseases
Employment
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CNR Instiute of Molecular Genetics Research director2020 - Present
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CNR Institute of Molecular Genetics Director2013 - Present
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CNR Institute of Molecular Genetics First Researcher2007 - Present
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IRCCS Istituto Ortopedico Rizzoli1998 - Present
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CNR ITOI Researcher1996 - 2007
Education
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National Research Council CNR Fellowship1990 - 1991
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University of Bologna AIRC Fellowship1986 - 1988
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University of Bologna Degree in Biological Sciences1981 - 1985
Projects & Funding
Projects & funding information is unavailable.
Publications (156)
- Collaborating with AIProSaB—A researcher's perspective on patient advocacy for progeria Save
- Sammy Basso, his life and message, and the importance of progeria research Save
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts Save
- Aging research from bench to bedside and beyond: What we learned from Sammy Basso Save
- Desmin and Plectin Recruitment to the Nucleus and Nuclei Orientation Are Lost in Emery-Dreifuss Muscular Dystrophy Myoblasts Subjected to Mechanical Stimulation Save
- Mineralocorticoid Receptor Antagonism Prevents Type 2 Familial Partial Lipodystrophy Brown Adipocyte Dysfunction Save
- Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome Save
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies Save
- Clinical Profile, Arrhythmias, and Adverse Cardiac Outcomes in Emery–Dreifuss Muscular Dystrophies: A Systematic Review of the Literature Save
- Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues Save
- Epigenomic signature of the progeroid Cockayne syndrome exposes distinct and common features with physiological ageing Save
- Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins Save
- Genomic loci mispositioning in Tmem120a knockout mice yields latent lipodystrophy Save
- Ectopic Expression of Ankrd2 Affects Proliferation, Motility and Clonogenic Potential of Human Osteosarcoma Cells Save
- Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice. Save
- Joining European Scientific Forces to Face Pandemics. Save
- PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation Save
- Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin–BAF Interaction and BAF Nuclear Localization Save
- Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction Save
- Lamin A involvement in ageing processes. Save