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The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes.

Journal of molecular and genetic medicine : an international journal of biomedical research

Ferrara F, Molesti E, Böttcher-Friebertshäuser E, Cattoli G, Corti D, Scott SD, Temperton NJ.
PMID: 23577043
J Mol Genet Med. 2012;7:309-14. Epub 2013 Feb 20.

The monomer of influenza haemagglutinin is synthesized as a single polypeptide precursor that during maturation is cleaved by proteases into two active subunits. Other studies have demonstrated that the human Transmembrane Protease Serine 2 (TMPRSS2) can cleave the HA...

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Ferrara F, Molesti E, Böttcher-Friebertshäuser E, et al. The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes. J Mol Genet Med. 2013;7:309-14
Ferrara, F., Molesti, E., Böttcher-Friebertshäuser, E., Cattoli, G., Corti, D., Scott, S. D., & Temperton, N. J. (2012). The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes. Journal of molecular and genetic medicine : an international journal of biomedical research, 7309-14.
Ferrara, Francesca, et al. "The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes." Journal of molecular and genetic medicine : an international journal of biomedical research vol. 7 (2012): 309-14.
Ferrara F, Molesti E, Böttcher-Friebertshäuser E, Cattoli G, Corti D, Scott SD, Temperton NJ. The human Transmembrane Protease Serine 2 is necessary for the production of Group 2 influenza A virus pseudotypes. J Mol Genet Med. 2012;7:309-14. Epub 2013 Feb 20. PMID: 23577043; PMCID: PMC3614188.
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PtI.

Dalton transactions (Cambridge, England : 2003)

Cirri D, Pillozzi S, Gabbiani C, Tricomi J, Bartoli G, Stefanini M, Michelucci E, Arcangeli A, Messori L, Marzo T.
PMID: 28229139
Dalton Trans. 2017 Mar 07;46(10):3311-3317. doi: 10.1039/c6dt03867k.

Colorectal cancer (CRC) is a global health problem being the fourth most common cause of death due to cancer worldwide. Oxaliplatin plays a key role in current CRC treatment but shows serious drawbacks, such as a high systemic toxicity...

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Cirri D, Pillozzi S, Gabbiani C, et al. PtI. Dalton Trans. 2017;46(10):3311-3317doi: 10.1039/c6dt03867k.
Cirri, D., Pillozzi, S., Gabbiani, C., Tricomi, J., Bartoli, G., Stefanini, M., Michelucci, E., Arcangeli, A., Messori, L., & Marzo, T. (2017). PtI. Dalton transactions (Cambridge, England : 2003), 46(10), 3311-3317. https://doi.org/10.1039/c6dt03867k
Cirri, D, et al. "PtI." Dalton transactions (Cambridge, England : 2003) vol. 46,10 (2017): 3311-3317. doi: https://doi.org/10.1039/c6dt03867k
Cirri D, Pillozzi S, Gabbiani C, Tricomi J, Bartoli G, Stefanini M, Michelucci E, Arcangeli A, Messori L, Marzo T. PtI. Dalton Trans. 2017 Mar 07;46(10):3311-3317. doi: 10.1039/c6dt03867k. PMID: 28229139.
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Classification of Healthy Subjects and Alzheimer's Disease Patients with Dementia from Cortical Sources of Resting State EEG Rhythms: A Study Using Artificial Neural Networks.

Frontiers in neuroscience

Triggiani AI, Bevilacqua V, Brunetti A, Lizio R, Tattoli G, Cassano F, Soricelli A, Ferri R, Nobili F, Gesualdo L, Barulli MR, Tortelli R, Cardinali V, Giannini A, Spagnolo P, Armenise S, Stocchi F, Buenza G, Scianatico G, Logroscino G, Lacidogna G, Orzi F, Buttinelli C, Giubilei F, Del Percio C, Frisoni GB, Babiloni C.
PMID: 28184183
Front Neurosci. 2017 Jan 26;10:604. doi: 10.3389/fnins.2016.00604. eCollection 2016.

Previous evidence showed a 75.5% best accuracy in the classification of 120 Alzheimer's disease (AD) patients with dementia and 100 matched normal elderly (Nold) subjects based on cortical source current density and linear lagged connectivity estimated by eLORETA freeware...

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Triggiani AI, Bevilacqua V, Brunetti A, et al. Classification of Healthy Subjects and Alzheimer's Disease Patients with Dementia from Cortical Sources of Resting State EEG Rhythms: A Study Using Artificial Neural Networks. Front Neurosci. 2017;10:604doi: 10.3389/fnins.2016.00604.
Triggiani, A. I., Bevilacqua, V., Brunetti, A., Lizio, R., Tattoli, G., Cassano, F., Soricelli, A., Ferri, R., Nobili, F., Gesualdo, L., Barulli, M. R., Tortelli, R., Cardinali, V., Giannini, A., Spagnolo, P., Armenise, S., Stocchi, F., Buenza, G., Scianatico, G., Logroscino, G., Lacidogna, G., Orzi, F., Buttinelli, C., Giubilei, F., Del Percio, C., Frisoni, G. B., & Babiloni, C. (2016). Classification of Healthy Subjects and Alzheimer's Disease Patients with Dementia from Cortical Sources of Resting State EEG Rhythms: A Study Using Artificial Neural Networks. Frontiers in neuroscience, 10604. https://doi.org/10.3389/fnins.2016.00604
Triggiani, Antonio I, et al. "Classification of Healthy Subjects and Alzheimer's Disease Patients with Dementia from Cortical Sources of Resting State EEG Rhythms: A Study Using Artificial Neural Networks." Frontiers in neuroscience vol. 10 (2016): 604. doi: https://doi.org/10.3389/fnins.2016.00604
Triggiani AI, Bevilacqua V, Brunetti A, Lizio R, Tattoli G, Cassano F, Soricelli A, Ferri R, Nobili F, Gesualdo L, Barulli MR, Tortelli R, Cardinali V, Giannini A, Spagnolo P, Armenise S, Stocchi F, Buenza G, Scianatico G, Logroscino G, Lacidogna G, Orzi F, Buttinelli C, Giubilei F, Del Percio C, Frisoni GB, Babiloni C. Classification of Healthy Subjects and Alzheimer's Disease Patients with Dementia from Cortical Sources of Resting State EEG Rhythms: A Study Using Artificial Neural Networks. Front Neurosci. 2017 Jan 26;10:604. doi: 10.3389/fnins.2016.00604. eCollection 2016. PMID: 28184183; PMCID: PMC5266711.
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The role of the alpha-stereogenic center in the control of stereoselection in the reduction of alpha-alkyl-beta-hydroxy ketones: a highly diastereoselective protocol for the synthesis of 1,2-syn-2-alkyl-1,3-diols.

Chemistry (Weinheim an der Bergstrasse, Germany)

Bartoli G, Bellucci MC, Bosco M, Dalpozzo R, Marcantoni E, Sambri L.
PMID: 10961404
Chemistry. 2000 Jul 14;6(14):2590-8. doi: 10.1002/1521-3765(20000717)6:14<2590::aid-chem2590>3.0.co;2-x.

Accurate investigations on the role played by an alpha-stereogenic center in controlling the reduction of various classes of beta-hydroxy ketones allowed us to set up a general and highly diastereoselective protocol for the synthesis of 2-alkyl-1,3-diols with 1,2-syn relationship....

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Bartoli G, Bellucci MC, Bosco M, et al. The role of the alpha-stereogenic center in the control of stereoselection in the reduction of alpha-alkyl-beta-hydroxy ketones: a highly diastereoselective protocol for the synthesis of 1,2-syn-2-alkyl-1,3-diols. Chemistry. 2000;6(14):2590-8doi: 10.1002/1521-3765(20000717)6:14<2590::aid-chem2590>3.0.co;2-x.
Bartoli, G., Bellucci, M. C., Bosco, M., Dalpozzo, R., Marcantoni, E., & Sambri, L. (2000). The role of the alpha-stereogenic center in the control of stereoselection in the reduction of alpha-alkyl-beta-hydroxy ketones: a highly diastereoselective protocol for the synthesis of 1,2-syn-2-alkyl-1,3-diols. Chemistry (Weinheim an der Bergstrasse, Germany), 6(14), 2590-8. https://doi.org/10.1002/1521-3765(20000717)6:14<2590::aid-chem2590>3.0.co;2-x
Bartoli, et al. "The role of the alpha-stereogenic center in the control of stereoselection in the reduction of alpha-alkyl-beta-hydroxy ketones: a highly diastereoselective protocol for the synthesis of 1,2-syn-2-alkyl-1,3-diols." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,14 (2000): 2590-8. doi: https://doi.org/10.1002/1521-3765(20000717)6:14<2590::aid-chem2590>3.0.co;2-x
Bartoli G, Bellucci MC, Bosco M, Dalpozzo R, Marcantoni E, Sambri L. The role of the alpha-stereogenic center in the control of stereoselection in the reduction of alpha-alkyl-beta-hydroxy ketones: a highly diastereoselective protocol for the synthesis of 1,2-syn-2-alkyl-1,3-diols. Chemistry. 2000 Jul 14;6(14):2590-8. doi: 10.1002/1521-3765(20000717)6:14<2590::aid-chem2590>3.0.co;2-x. PMID: 10961404.
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A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide.

The Journal of organic chemistry

Cappa A, Marcantoni E, Torregiani E, Bartoli G, Bellucci MC, Bosco M, Sambri L.
PMID: 11674643
J Org Chem. 1999 Jul 23;64(15):5696-5699. doi: 10.1021/jo990014r.

No abstract available.

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Cappa A, Marcantoni E, Torregiani E, et al. A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. J Org Chem. 1999;64(15):5696-5699doi: 10.1021/jo990014r.
Cappa, A., Marcantoni, E., Torregiani, E., Bartoli, G., Bellucci, M. C., Bosco, M., & Sambri, L. (1999). A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. The Journal of organic chemistry, 64(15), 5696-5699. https://doi.org/10.1021/jo990014r
Cappa, Anna, et al. "A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide." The Journal of organic chemistry vol. 64,15 (1999): 5696-5699. doi: https://doi.org/10.1021/jo990014r
Cappa A, Marcantoni E, Torregiani E, Bartoli G, Bellucci MC, Bosco M, Sambri L. A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. J Org Chem. 1999 Jul 23;64(15):5696-5699. doi: 10.1021/jo990014r. PMID: 11674643.
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A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide.

The Journal of organic chemistry

Cappa A, Marcantoni E, Torregiani E, Bartoli G, Bellucci MC, Bosco M, Sambri.
PMID: 10968773
J Org Chem. 2000 Jul 28;65(15):4782. doi: 10.1021/jo0040238.

No abstract available.

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Cappa A, Marcantoni E, Torregiani E, et al. A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. J Org Chem. 2000;65(15):4782doi: 10.1021/jo0040238.
Cappa, A., Marcantoni, E., Torregiani, E., Bartoli, G., Bellucci, M. C., Bosco, M., & Sambri. (2000). A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. The Journal of organic chemistry, 65(15), 4782. https://doi.org/10.1021/jo0040238
Cappa, et al. "A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide." The Journal of organic chemistry vol. 65,15 (2000): 4782. doi: https://doi.org/10.1021/jo0040238
Cappa A, Marcantoni E, Torregiani E, Bartoli G, Bellucci MC, Bosco M, Sambri. A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. J Org Chem. 2000 Jul 28;65(15):4782. doi: 10.1021/jo0040238. PMID: 10968773.
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Conformational studies by dynamic NMR. 98. Stereodynamics of bond rotation in beta-hydroxyesters.

The Journal of organic chemistry

Bartoli G, Lunazzi L, Massaccesi M, Mazzanti A.
PMID: 14750810
J Org Chem. 2004 Feb 06;69(3):821-5. doi: 10.1021/jo0355754.

The dynamic processes due to restricted intramolecular motions have been observed in a number of variously substituted beta-hydroxyesters by variable-temperature NMR spectroscopy. The barriers for three such processes (i.e. Ph-C, t-Bu-C, and C(alpha)-C(beta) bond rotation) have been measured.

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Bartoli G, Lunazzi L, Massaccesi M, et al. Conformational studies by dynamic NMR. 98. Stereodynamics of bond rotation in beta-hydroxyesters. J Org Chem. 2004;69(3):821-5doi: 10.1021/jo0355754.
Bartoli, G., Lunazzi, L., Massaccesi, M., & Mazzanti, A. (2004). Conformational studies by dynamic NMR. 98. Stereodynamics of bond rotation in beta-hydroxyesters. The Journal of organic chemistry, 69(3), 821-5. https://doi.org/10.1021/jo0355754
Bartoli, Giuseppe, et al. "Conformational studies by dynamic NMR. 98. Stereodynamics of bond rotation in beta-hydroxyesters." The Journal of organic chemistry vol. 69,3 (2004): 821-5. doi: https://doi.org/10.1021/jo0355754
Bartoli G, Lunazzi L, Massaccesi M, Mazzanti A. Conformational studies by dynamic NMR. 98. Stereodynamics of bond rotation in beta-hydroxyesters. J Org Chem. 2004 Feb 06;69(3):821-5. doi: 10.1021/jo0355754. PMID: 14750810.
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Reaction intermediates in the photoreduction of oxygen molecules at the (101) TiO2 (anatase) surface.

Journal of the American Chemical Society

Mattioli G, Filippone F, Amore Bonapasta A.
PMID: 17044705
J Am Chem Soc. 2006 Oct 25;128(42):13772-80. doi: 10.1021/ja062145x.

The structural, electronic, and vibrational properties of intermediates of the O(2) photoreduction at the (101) TiO(2) (anatase) surface have been investigated by performing ab initio density functional calculations. In detail, a recently proposed approach has been used where molecules...

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Mattioli G, Filippone F, Amore Bonapasta A. Reaction intermediates in the photoreduction of oxygen molecules at the (101) TiO2 (anatase) surface. J Am Chem Soc. 2006;128(42):13772-80doi: 10.1021/ja062145x.
Mattioli, G., Filippone, F., & Amore Bonapasta, A. (2006). Reaction intermediates in the photoreduction of oxygen molecules at the (101) TiO2 (anatase) surface. Journal of the American Chemical Society, 128(42), 13772-80. https://doi.org/10.1021/ja062145x
Mattioli, Giuseppe, et al. "Reaction intermediates in the photoreduction of oxygen molecules at the (101) TiO2 (anatase) surface." Journal of the American Chemical Society vol. 128,42 (2006): 13772-80. doi: https://doi.org/10.1021/ja062145x
Mattioli G, Filippone F, Amore Bonapasta A. Reaction intermediates in the photoreduction of oxygen molecules at the (101) TiO2 (anatase) surface. J Am Chem Soc. 2006 Oct 25;128(42):13772-80. doi: 10.1021/ja062145x. PMID: 17044705.
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Organocatalytic asymmetric alpha-halogenation of 1,3-dicarbonyl compounds.

Angewandte Chemie (International ed. in English)

Bartoli G, Bosco M, Carlone A, Locatelli M, Melchiorre P, Sambri L.
PMID: 16136622
Angew Chem Int Ed Engl. 2005 Sep 26;44(38):6219-22. doi: 10.1002/anie.200502134.

No abstract available.

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Bartoli G, Bosco M, Carlone A, et al. Organocatalytic asymmetric alpha-halogenation of 1,3-dicarbonyl compounds. Angew Chem Int Ed Engl. 2005;44(38):6219-22doi: 10.1002/anie.200502134.
Bartoli, G., Bosco, M., Carlone, A., Locatelli, M., Melchiorre, P., & Sambri, L. (2005). Organocatalytic asymmetric alpha-halogenation of 1,3-dicarbonyl compounds. Angewandte Chemie (International ed. in English), 44(38), 6219-22. https://doi.org/10.1002/anie.200502134
Bartoli, Giuseppe, et al. "Organocatalytic asymmetric alpha-halogenation of 1,3-dicarbonyl compounds." Angewandte Chemie (International ed. in English) vol. 44,38 (2005): 6219-22. doi: https://doi.org/10.1002/anie.200502134
Bartoli G, Bosco M, Carlone A, Locatelli M, Melchiorre P, Sambri L. Organocatalytic asymmetric alpha-halogenation of 1,3-dicarbonyl compounds. Angew Chem Int Ed Engl. 2005 Sep 26;44(38):6219-22. doi: 10.1002/anie.200502134. PMID: 16136622.
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H-induced dangling bonds in H-isoelectronic-impurity complexes formed in GaAs1-yNy alloys.

Physical review letters

Amore Bonapasta A, Filippone F, Mattioli G.
PMID: 17677720
Phys Rev Lett. 2007 May 18;98(20):206403. doi: 10.1103/PhysRevLett.98.206403. Epub 2007 May 15.

Complexes formed by H and the isoelectronic impurity N in GaAs1-yNy alloys have been widely investigated because the significant effects of N on the GaAs properties and their passivation by H represent a unique tool for a defect engineering...

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Amore Bonapasta A, Filippone F, Mattioli G. H-induced dangling bonds in H-isoelectronic-impurity complexes formed in GaAs1-yNy alloys. Phys Rev Lett. 2007;98(20):206403doi: 10.1103/PhysRevLett.98.206403.
Amore Bonapasta, A., Filippone, F., & Mattioli, G. (2007). H-induced dangling bonds in H-isoelectronic-impurity complexes formed in GaAs1-yNy alloys. Physical review letters, 98(20), 206403. https://doi.org/10.1103/PhysRevLett.98.206403
Amore Bonapasta, A, et al. "H-induced dangling bonds in H-isoelectronic-impurity complexes formed in GaAs1-yNy alloys." Physical review letters vol. 98,20 (2007): 206403. doi: https://doi.org/10.1103/PhysRevLett.98.206403
Amore Bonapasta A, Filippone F, Mattioli G. H-induced dangling bonds in H-isoelectronic-impurity complexes formed in GaAs1-yNy alloys. Phys Rev Lett. 2007 May 18;98(20):206403. doi: 10.1103/PhysRevLett.98.206403. Epub 2007 May 15. PMID: 17677720.
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Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters.

Chemistry (Weinheim an der Bergstrasse, Germany)

Galzerano P, Bencivenni G, Pesciaioli F, Mazzanti A, Giannichi B, Sambri L, Bartoli G, Melchiorre P.
PMID: 19180604
Chemistry. 2009 Aug 10;15(32):7846-9. doi: 10.1002/chem.200802466.

No abstract available.

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Galzerano P, Bencivenni G, Pesciaioli F, et al. Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters. Chemistry. 2009;15(32):7846-9doi: 10.1002/chem.200802466.
Galzerano, P., Bencivenni, G., Pesciaioli, F., Mazzanti, A., Giannichi, B., Sambri, L., Bartoli, G., & Melchiorre, P. (2009). Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters. Chemistry (Weinheim an der Bergstrasse, Germany), 15(32), 7846-9. https://doi.org/10.1002/chem.200802466
Galzerano, Patrizia, et al. "Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 15,32 (2009): 7846-9. doi: https://doi.org/10.1002/chem.200802466
Galzerano P, Bencivenni G, Pesciaioli F, Mazzanti A, Giannichi B, Sambri L, Bartoli G, Melchiorre P. Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters. Chemistry. 2009 Aug 10;15(32):7846-9. doi: 10.1002/chem.200802466. PMID: 19180604.
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Evidence for multistability of light solitons in SF(6) absorption measurements.

Optics letters

Dattoli G, Orsitto FP, Torre A.
PMID: 19749951
Opt Lett. 1989 May 01;14(9):456-8. doi: 10.1364/ol.14.000456.

We report experimental evidence of the multistability of reshaped pulses that are observed when a 1.5-nsec CO(2)-laser pulse interacts with a pure SF(6) absorber. The data demonstrate that the dependence of the reshaped pulse delay on peak power is...

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Dattoli G, Orsitto FP, Torre A. Evidence for multistability of light solitons in SF(6) absorption measurements. Opt Lett. 1989;14(9):456-8doi: 10.1364/ol.14.000456.
Dattoli, G., Orsitto, F. P., & Torre, A. (1989). Evidence for multistability of light solitons in SF(6) absorption measurements. Optics letters, 14(9), 456-8. https://doi.org/10.1364/ol.14.000456
Dattoli, G, et al. "Evidence for multistability of light solitons in SF(6) absorption measurements." Optics letters vol. 14,9 (1989): 456-8. doi: https://doi.org/10.1364/ol.14.000456
Dattoli G, Orsitto FP, Torre A. Evidence for multistability of light solitons in SF(6) absorption measurements. Opt Lett. 1989 May 01;14(9):456-8. doi: 10.1364/ol.14.000456. PMID: 19749951.
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