Pubblicazioni

Anno

Progetto

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SiMPLOD, a structure-integrated database of collagen lysyl hydroxylase (LH/PLOD) enzyme variants

Scietti L.*, Campioni M.*, Forneris F. (*Equal Contribution)

SiMPLOD, a structure-integrated database of collagen lysyl hydroxylase (LH/PLOD) enzyme variants

Pubblicato in:  Journal of Bone and Mineral Research, 34, 1376-1382 (2019). - DOI 10.1002/jbmr.3692 - PMID 30721533

Structural characterization of the third scavenger receptor cysteine-rich domain of murine Neurotrypsin

Canciani A., Catucci G., Forneris F.

Structural characterization of the third scavenger receptor cysteine-rich domain of murine Neurotrypsin

Pubblicato in:  Protein Science, 28, 746-755 (2019). - DOI 10.1002/pro.3587 - PMID 30748049

A Novel L1 Isoform with Angiogenic Activity Generated by NOVA2-mediated Alternative Splicing

Angiolini F.*, Belloni E.*, Giordano M.*, Campioni M., Forneris F., Paronetto M.P., Lupia M., Brandas C., Pradella D., Di Matteo A., Giampietro C., Jodice G., Luise C., Bertalot G., Freddi S., Malinverno M., Irimia M., Moulton J.D., Summerton J., Chiapparino A., Ghilardi C., Giavazzi R., Nyqvist D., Gabellini D., Dejana E., Cavallaro U., Ghigna C. (*Equal Contribution)

A Novel L1 Isoform with Angiogenic Activity Generated by NOVA2-mediated Alternative Splicing

Pubblicato in:  eLife, 8, e44305 (2019). - DOI 10.7554/eLife.44305 - PMID 30829570

Structural and biochemical evaluation of Ceratitis capitata OBP22 affinity for odorants involved in inter-sex communication

Falchetto M.*, Ciossani G.*, Scolari F., Di Cosimo A., Nenci S., Field L.M., Mattevi A., Zhou J.J., Gasperi G.**, Forneris F.** (*Equal Contribution - **Shared Corresponding Authors)

Structural and biochemical evaluation of Ceratitis capitata OBP22 affinity for odorants involved in inter-sex communication

Pubblicato in:  Insect Molecular Biology, 28, 431-443 (2019). - DOI 10.1111/imb.12559 - PMID 30548711

Molecular architecture of the multifunctional collagen lysyl hydroxylase and glycosyltransferase LH3

Scietti L., Chiapparino A., De Giorgi F., Fumagalli M., Khoriauli L., Nergadze S., Basu S., Olieric V., Cucca L., Banushi B., Profumo A., Giulotto E., Gissen P., Forneris F.

Molecular architecture of the multifunctional collagen lysyl hydroxylase and glycosyltransferase LH3

Pubblicato in:  Nature Communications, 9, 3163 (2018). - DOI 10.1038/s41467-018-05631-5 - PMID 30089812

Investigating the Mechanism of Action of Diketopiperazines Inhibitors of the Burkholderia cenocepacia Quorum Sensing Synthase CepI: A Site-Directed Mutagenesis Study

Buroni S.*, Scoffone V.C.*, Fumagalli M., Makarov V., Cagnone M., Trespidi G., De Rossi E., Forneris F., Riccardi G., Chiarelli L.R. (*Equal Contribution)

Investigating the Mechanism of Action of Diketopiperazines Inhibitors of the Burkholderia cenocepacia Quorum Sensing Synthase CepI: A Site-Directed Mutagenesis Study

Pubblicato in:  Frontiers in Pharmacology, 9, 836 (2018). - DOI 10.3389/fphar.2018.00836 - PMID 30108505

Regulator-dependent mechanisms of C3b processing by factor I allow for differentiation of immune responses

Xue X., Wu J., Ricklin D., Forneris F., Di Crescenzio P., Schmidt C.Q., Granneman J., Sharp T.H., Lambris J.D., Gros P.

Regulator-dependent mechanisms of C3b processing by factor I allow for differentiation of immune responses

Pubblicato in:  Nature Structural and Molecular Biology, 24, 643-651 (2017). - DOI 10.1038/nsmb.3427 - PMID 28671664

Expanding the structural biology toolbox with single-molecule holography

Forneris F.*, Mattevi A.* (*Shared Corresponding Authors)

Expanding the structural biology toolbox with single-molecule holography

Pubblicato in:  Proceedings of the National Academy of Sciences, U.S.A., 114, 1448-1450 (2017). - DOI 10.1073/pnas.1620897114 - PMID 28154136

Autosomal recessive Keratoderma-Ichthyosis-Deafness (ARKID) syndrome is caused by VPS33B mutations affecting Rab protein interaction and collagen modification

Gruber R., Rogerson C., Windpassinger C., Banushi B., Straatman-Iwanowska A., Hanley J., Forneris F., Strohal R., Ulz P., Crumrine D., Menon G.K., Blunder S., Schmuth M., Müller T., Smith H., Mills K., Kroisel P., Janecke A.R., Gissen P.

Autosomal recessive Keratoderma-Ichthyosis-Deafness (ARKID) syndrome is caused by VPS33B mutations affecting Rab protein interaction and collagen modification

Pubblicato in:  Journal of Investigative Dermatology, 137, 32800-32807 (2016). - DOI 10.1016/j.jid.2016.12.010 - PMID 28017832