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Publications by Paolo Vezzoni

Analysis of Mutations From SCID and Omenn Syndrome Patients Reveals the Central Role of the Rag2 PHD Domain in Regulating V(D)J Recombination

Journal of Clinical Investigation
Medicine
2010English

As Little as Needed: The Extraordinary Case of a Mild Recessive Osteopetrosis Owing to a Novel Splicing Hypomorphic Mutation in theTCIRG1Gene

Journal of Bone and Mineral Research
EndocrinologyOrthopedicsSports MedicineMetabolismDiabetes
2014English

RANK-dependent Autosomal Recessive Osteopetrosis: Characterization of Five New Cases With Novel Mutations

Journal of Bone and Mineral Research
EndocrinologyOrthopedicsSports MedicineMetabolismDiabetes
2012English

A Pre-Screening FISH-based Method to Detect CRISPR/Cas9 Off-Targets in Mouse Embryonic Stem Cells

Scientific Reports
Multidisciplinary
2015English

A Hypomorphic R229Q Rag2 Mouse Mutant Recapitulates Human Omenn Syndrome

Journal of Clinical Investigation
Medicine
2007English

Lymphoid Abnormalities in CD40 Ligand Transgenic Mice Suggest the Need for Tight Regulation in Gene Therapy Approaches to Hyper Immunoglobulin M (IgM) Syndrome

Cancer Gene Therapy
Cancer ResearchMolecular MedicineMolecular Biology
2000English

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