• 11 Citations
  • 1 h-Index
20172019
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Fingerprint Dive into the research topics where Luca Pannone is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Noonan Syndrome Medicine & Life Sciences
Mutation Medicine & Life Sciences
Premature Aging Medicine & Life Sciences
Cell Aging Medicine & Life Sciences
Histones Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Codon Medicine & Life Sciences
Germ-Line Mutation Medicine & Life Sciences

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Research Output 2017 2019

  • 11 Citations
  • 1 h-Index
  • 3 Article

Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging

Flex, E., Martinelli, S., Van Dijck, A., Ciolfi, A., Cecchetti, S., Coluzzi, E., Pannone, L., Andreoli, C., Radio, F. C., Pizzi, S., Carpentieri, G., Bruselles, A., Catanzaro, G., Pedace, L., Miele, E., Carcarino, E., Ge, X., Chijiwa, C., Lewis, M. E. S., Meuwissen, M. & 40 others, Kenis, S., Van der Aa, N., Larson, A., Brown, K., Wasserstein, M. P., Skotko, B. G., Begtrup, A., Person, R., Karayiorgou, M., Roos, J. L., Van Gassen, K. L., Koopmans, M., Bijlsma, E. K., Santen, G. W. E., Barge-Schaapveld, D. Q. C. M., Ruivenkamp, C. A. L., Hoffer, M. J. V., Lalani, S. R., Streff, H., Craigen, W. J., Graham, B. H., van den Elzen, A. P. M., Kamphuis, D. J., Õunap, K., Reinson, K., Pajusalu, S., Wojcik, M. H., Viberti, C., Di Gaetano, C., Bertini, E., Petrucci, S., De Luca, A., Rota, R., Ferretti, E., Matullo, G., Dallapiccola, B., Sgura, A., Walkiewicz, M., Kooy, R. F. & Tartaglia, M., Sep 5 2019, In : American Journal of Human Genetics. 105, 3, p. 493-508 16 p.

Research output: Contribution to journalArticle

Premature Aging
Cell Aging
Histones
Chromatin
DNA Packaging

Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes

University of Washington Center for Mendelian Genomics, Feb 1 2018, In : American Journal of Human Genetics. 102, 2, p. 309-320 12 p.

Research output: Contribution to journalArticle

Phenotype
Mutation
Noonan Syndrome
Exome
Monomeric GTP-Binding Proteins
11 Citations (Scopus)

Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome

Pannone, L., Bocchinfuso, G., Flex, E., Rossi, C., Baldassarre, G., Lissewski, C., Pantaleoni, F., Consoli, F., Lepri, F., Magliozzi, M., Anselmi, M., Delle Vigne, S., Sorge, G., Karaer, K., Cuturilo, G., Sartorio, A., Tinschert, S., Accadia, M., Digilio, M. C., Zampino, G. & 9 others, De Luca, A., Cavé, H., Zenker, M., Gelb, B. D., Dallapiccola, B., Stella, L., Ferrero, G. B., Martinelli, S. & Tartaglia, M., Apr 2017, In : Human Mutation. 38, 4, p. 451-459 9 p.

Research output: Contribution to journalArticle

Noonan Syndrome
Codon
Mutation
SH2 Domain-Containing Protein Tyrosine Phosphatases
Protein Tyrosine Phosphatases