• 417 Citations
  • 11 h-Index
20072015
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Fingerprint Dive into the research topics where Nadia Lo Iacono is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Osteopetrosis Medicine & Life Sciences
Mutation Medicine & Life Sciences
Ectodermal Dysplasia Medicine & Life Sciences
Genes Medicine & Life Sciences
Ectoderm Medicine & Life Sciences
Osteoclasts Medicine & Life Sciences
European Union Medicine & Life Sciences
Extremities Medicine & Life Sciences

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Research Output 2007 2015

  • 417 Citations
  • 11 h-Index
  • 13 Article
4 Citations (Scopus)

IL-10 critically modulates B cell responsiveness in rankl-/- mice

Marrella, V., Lo Iacono, N., Fontana, E., Sobacchi, C., Sic, H., Schena, F., Sereni, L., Castiello, M. C., Poliani, P. L., Vezzoni, P., Cassani, B., Traggiai, E. & Villa, A., May 1 2015, In : Journal of Immunology. 194, 9, p. 4144-4153 10 p.

Research output: Contribution to journalArticle

RANK Ligand
Interleukin-10
B-Lymphocytes
Regulatory B-Lymphocytes
Plasma Cells
17 Citations (Scopus)

DLX5, FGF8 and the Pin1 isomerase control ΔNp63α protein stability during limb development: A regulatory loop at the basis of the SHFM and EEC congenital malformations

Restelli, M., Lopardo, T., Lo Iacono, N., Garaffo, G., Conte, D., Rustighi, A., Napoli, M., Del Sal, G., Perez-Morga, D., Costanzo, A., Merlo, G. R. & Guerrini, L., 2014, In : Human Molecular Genetics. 23, 14, p. 3830-3842 13 p., ddu096.

Research output: Contribution to journalArticle

Isomerases
Protein Stability
European Union
Limb Buds
Foot
17 Citations (Scopus)

RANKL cytokine: From pioneer of the osteoimmunology era to cure for a rare disease

Lo Iacono, N., Pangrazio, A., Abinun, M., Bredius, R., Zecca, M., Blair, H. C., Vezzoni, P., Villa, A. & Sobacchi, C., 2013, In : Clinical and Developmental Immunology. 2013, 412768.

Research output: Contribution to journalArticle

Osteopetrosis
Rare Diseases
Osteoclasts
Cytokines
Bone and Bones
32 Citations (Scopus)

SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity

Pangrazio, A., Fasth, A., Sbardellati, A., Orchard, P. J., Kasow, K. A., Raza, J., Albayrak, C., Albayrak, D., Vanakker, O. M., De Moerloose, B., Vellodi, A., Notarangelo, L. D., Schlack, C., Strauss, G., Kühl, J. S., Caldana, E., Lo Iacono, N., Susani, L., Kornak, U., Schulz, A. & 3 others, Vezzoni, P., Villa, A. & Sobacchi, C., May 2013, In : Journal of Bone and Mineral Research. 28, 5, p. 1041-1049 9 p.

Research output: Contribution to journalArticle

Sorting Nexins
Osteopetrosis
Mutation
Genes
Proton Pumps
17 Citations (Scopus)
Osteopetrosis
Mutation
Genes
Proton Pumps
5' Untranslated Regions