D. Strina

发表

Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss

S. Mantero, A. Almarza, A. Villa, 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Structural and functional basis for JAK3-deficient severe combined immunodeficiency.

A. Villa, J. Johnston, L. Notarangelo, 1997, Blood.

Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders

S. Mantero, T. Hara, S. Duga, 2020, Molecular therapy. Methods & clinical development.

Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells

C. Recordati, E. Scanziani, A. Villa, 2019, Stem cells.

The genomic organization of the human transcription factor 3 (TFE3) gene.

A. Villa, L. Notarangelo, S. Giliani, 1995, Genomics.

Lymphoid abnormalities in CD40 ligand transgenic mice suggest the need for tight regulation in gene therapy approaches to hyper immunoglobulin M (IgM) syndrome

L. Notarangelo, J. Jonkers, F. Facchetti, 2000, Cancer Gene Therapy.

Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis

M. Ferrari, A. Angius, A. Villa, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis

S. Mantero, J. Barnett, C. Carlo-Stella, 2020, Bone reports.

X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene

L. Notarangelo, P. Macchi, A. Villa, 1995, Nature Genetics.

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

A. Fischer, A. Schulz, A. Durandy, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Targeted Gene Correction in Osteopetrotic-Induced Pluripotent Stem Cells for the Generation of Functional Osteoclasts

C. Recordati, L. Naldini, E. Scanziani, 2015, Stem cell reports.

V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations.

E. Brooks, K. Schwarz, A. Villa, 2001, Blood.

Rapid Isolation of cDNA Clones by

P. Vezzoni, I. Zucchi, D. Strina, 2013 .

Rapid isolation of cDNA clones by aliquot testing via PCR amplification.

A. Di Bacco, P. Vezzoni, I. Zucchi, 1994, PCR methods and applications.

Genome-first approach for the characterization of a complex phenotype with combined NBAS and CUL4B deficiency.

A. Villa, M. Ritelli, M. Colombi, 2020, Bone.

3D Bone Biomimetic Scaffolds for Basic and Translational Studies with Mesenchymal Stem Cells

A. Villa, C. Menale, E. Palagano, 2018, International journal of molecular sciences.

ZNF75: isolation of a cDNA clone of the KRAB zinc finger gene subfamily mapped in YACs 1 Mb telomeric of HPRT.

C. Patrosso, A. Villa, G. Pilia, 1993, Genomics.

Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26.

C. Patrosso, A. Villa, I. Biunno, 1992, Genomics.

Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry.

A. Villa, S. Giliani, P. Macchi, 1995, American journal of human genetics.

Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome

M. van der Burg, H. Wardemann, A. Rolink, 2010, The Journal of experimental medicine.

The ZNF75 zinc finger gene subfamily: isolation and mapping of the four members in humans and great apes.

A. Villa, N. Archidiacono, M. Rocchi, 1996, Genomics.

Type 2 vasopressin receptor gene, the gene responsible nephrogenic diabetes insipidus, maps to Xq28 close to the LICAM gene.

C. Patrosso, A. Villa, P. Vezzoni, 1993, Biochemical and biophysical research communications.

Organization of the human CD40L gene: implications for molecular defects in X chromosome-linked hyper-IgM syndrome and prenatal diagnosis.

C. Patrosso, A. Villa, L. Notarangelo, 1994, Proceedings of the National Academy of Sciences of the United States of America.

C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by Hyper IgM syndrome

A. Villa, S. Giliani, P. Macchi, 1994, Human mutation.

Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived From Structural and Functional Analysis of 14 ClC‐7 Mutants

G. Baynam, A. Kariminejad, A. Rehman, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived from Structural and Functional Analysis of 14 ClC-7 Mutants. Journal of Bone and Mineral Research.

A. Picollo, L. Lagostena, R. Chiesa, 2020 .

Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28.

A. Villa, P. Vezzoni, I. Zucchi, 1994, Genomics.

Partial regression, yet incomplete eradication of mammary tumors in transgenic mice by retrovirally mediated HSVtk transfer 'in vivo'.

G. Finocchiaro, S. Benedetti, P. Macchi, 1996, Gene Therapy.

The exon-intron structure of human LHX1 gene.

A. Villa, P. Vezzoni, D. Strina, 1996, Biochemical and biophysical research communications.

Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency

C. Brombin, G. Crooks, Samuele Ferrari, 2024, Science Translational Medicine.