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The Journal of Physical Chemistry Letters|October 3, 2024
Fluorescent Labeling Can Significantly Perturb Measured Binding Affinity and Selectivity of Peptide-Protein InteractionsSara Bobone, Claudia Storti, Chiara Fulci, et al.
The Journal of Biological Chemistry|June 20, 2012
Counteracting effects operating on Src homology 2 domain-containing protein-tyrosine phosphatase 2 (SHP2) function drive selection of the recurrent Y62D and Y63C substitutions in Noonan syndromeSimone Martinelli, Aurelio P Nardozza, Silvia Delle Vigne, et al.
Frontiers in Chemistry|April 16, 2019
Rational Design of Antiangiogenic Helical Oligopeptides Targeting the Vascular Endothelial Growth Factor ReceptorsSimone Zanella, Gianfranco Bocchinfuso, Marta De Zotti, et al.
Journal of Colloid and Interface Science|August 5, 2026
Length-encoded phase transitions in proline-alanine-serine peptides: from nanoaggregates to condensatesHilda Garay-Perez, Marco Savioli, Greta Petrella, et al.
American Journal of Human Genetics|December 17, 2005
Diversity and functional consequences of germline and somatic PTPN11 mutations in human diseaseMarco Tartaglia, Simone Martinelli, Lorenzo Stella, et al.
American Journal of Human Genetics|January 17, 2012
A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndromeViviana Caputo, Luciano Cianetti, Marcello Niceta, et al.
Human Mutation|March 1, 2020
Pathogenic PTPN11 variants involving the poly-glutamine Gln255 -Gln256 -Gln257 stretch highlight the relevance of helix B in SHP2's functional regulationSimone Martinelli, Luca Pannone, Christina Lissewski, et al.
American Journal of Human Genetics|November 20, 2020
A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl-/H+-Exchanger, Causes Early-Onset NeurodegenerationMaya M Polovitskaya, Carlo Barbini, Diego Martinelli, et al.
Nature Genetics|April 28, 2015
Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndromeFanny Kortüm, Viviana Caputo, Christiane K Bauer, et al.
American Journal of Human Genetics|October 6, 2018
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental SyndromeChristiane K Bauer, Paolo Calligari, Francesca Clementina Radio, et al.
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