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Novel near-infrared emission from crystal defects in MoS.

Nature communications

Fabbri F, Rotunno E, Cinquanta E, Campi D, Bonnini E, Kaplan D, Lazzarini L, Bernasconi M, Ferrari C, Longo M, Nicotra G, Molle A, Swaminathan V, Salviati G.
PMID: 27698425
Nat Commun. 2016 Oct 04;7:13044. doi: 10.1038/ncomms13044.

The structural defects in two-dimensional transition metal dichalcogenides, including point defects, dislocations and grain boundaries, are scarcely considered regarding their potential to manipulate the electrical and optical properties of this class of materials, notwithstanding the significant advances already made....

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Fabbri F, Rotunno E, Cinquanta E, et al. Novel near-infrared emission from crystal defects in MoS. Nat Commun. 2016;7:13044doi: 10.1038/ncomms13044.
Fabbri, F., Rotunno, E., Cinquanta, E., Campi, D., Bonnini, E., Kaplan, D., Lazzarini, L., Bernasconi, M., Ferrari, C., Longo, M., Nicotra, G., Molle, A., Swaminathan, V., & Salviati, G. (2016). Novel near-infrared emission from crystal defects in MoS. Nature communications, 713044. https://doi.org/10.1038/ncomms13044
Fabbri, F, et al. "Novel near-infrared emission from crystal defects in MoS." Nature communications vol. 7 (2016): 13044. doi: https://doi.org/10.1038/ncomms13044
Fabbri F, Rotunno E, Cinquanta E, Campi D, Bonnini E, Kaplan D, Lazzarini L, Bernasconi M, Ferrari C, Longo M, Nicotra G, Molle A, Swaminathan V, Salviati G. Novel near-infrared emission from crystal defects in MoS. Nat Commun. 2016 Oct 04;7:13044. doi: 10.1038/ncomms13044. PMID: 27698425; PMCID: PMC5059461.
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Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note.

World journal of clinical cases

Marotta N, Landi A, Mancarella C, Rocco P, Pietrantonio A, Galati G, Bolognese A, Delfini R.
PMID: 25610853
World J Clin Cases. 2015 Jan 16;3(1):77-80. doi: 10.12998/wjcc.v3.i1.77.

Xanthogranulomas (XG) are benign proliferative disorder of histiocytes, a non-Langerhans cell histiocytosis. Whose etiology is unknown. The nature of these lesions is controversial and could be either reactive or neoplastic; the presence of monoclonal cells does, however, favor the...

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Marotta N, Landi A, Mancarella C, et al. Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note. World J Clin Cases. 2015;3(1):77-80doi: 10.12998/wjcc.v3.i1.77.
Marotta, N., Landi, A., Mancarella, C., Rocco, P., Pietrantonio, A., Galati, G., Bolognese, A., & Delfini, R. (2015). Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note. World journal of clinical cases, 3(1), 77-80. https://doi.org/10.12998/wjcc.v3.i1.77
Marotta, Nicola, et al. "Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note." World journal of clinical cases vol. 3,1 (2015): 77-80. doi: https://doi.org/10.12998/wjcc.v3.i1.77
Marotta N, Landi A, Mancarella C, Rocco P, Pietrantonio A, Galati G, Bolognese A, Delfini R. Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note. World J Clin Cases. 2015 Jan 16;3(1):77-80. doi: 10.12998/wjcc.v3.i1.77. PMID: 25610853; PMCID: PMC4295222.
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Synthesis of constrained analogues of tryptophan.

Beilstein journal of organic chemistry

Rossi E, Pirovano V, Negrato M, Abbiati G, Dell'Acqua M.
PMID: 26664620
Beilstein J Org Chem. 2015 Oct 27;11:1997-2006. doi: 10.3762/bjoc.11.216. eCollection 2015.

A Lewis acid-catalysed diastereoselective [4 + 2] cycloaddition of vinylindoles and methyl 2-acetamidoacrylate, leading to methyl 3-acetamido-1,2,3,4-tetrahydrocarbazole-3-carboxylate derivatives, is described. Treatment of the obtained cycloadducts under hydrolytic conditions results in the preparation of a small library of compounds bearing...

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Rossi E, Pirovano V, Negrato M, et al. Synthesis of constrained analogues of tryptophan. Beilstein J Org Chem. 2015;11:1997-2006doi: 10.3762/bjoc.11.216.
Rossi, E., Pirovano, V., Negrato, M., Abbiati, G., & Dell'Acqua, M. (2015). Synthesis of constrained analogues of tryptophan. Beilstein journal of organic chemistry, 111997-2006. https://doi.org/10.3762/bjoc.11.216
Rossi, Elisabetta, et al. "Synthesis of constrained analogues of tryptophan." Beilstein journal of organic chemistry vol. 11 (2015): 1997-2006. doi: https://doi.org/10.3762/bjoc.11.216
Rossi E, Pirovano V, Negrato M, Abbiati G, Dell'Acqua M. Synthesis of constrained analogues of tryptophan. Beilstein J Org Chem. 2015 Oct 27;11:1997-2006. doi: 10.3762/bjoc.11.216. eCollection 2015. PMID: 26664620; PMCID: PMC4661003.
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Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle.

F1000Research

Chaponnier C, Gabbiani G.
PMID: 27335638
F1000Res. 2016 Mar 30;5:416. doi: 10.12688/f1000research.8154.1. eCollection 2016.

Higher vertebrates express six different highly conserved actin isoforms that can be classified in three subgroups: 1) sarcomeric actins, α-skeletal (α-SKA) and α-cardiac (α-CAA), 2) smooth muscle actins (SMAs), α-SMA and γ-SMA, and 3) cytoplasmic actins (CYAs), β-CYA and...

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Chaponnier C, Gabbiani G. Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle. F1000Res. 2016;5:416doi: 10.12688/f1000research.8154.1.
Chaponnier, C., & Gabbiani, G. (2016). Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle. F1000Research, 5416. https://doi.org/10.12688/f1000research.8154.1
Chaponnier, Christine, and Gabbiani, Giulio. "Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle." F1000Research vol. 5 (2016): 416. doi: https://doi.org/10.12688/f1000research.8154.1
Chaponnier C, Gabbiani G. Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle. F1000Res. 2016 Mar 30;5:416. doi: 10.12688/f1000research.8154.1. eCollection 2016. PMID: 27335638; PMCID: PMC4893938.
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Haemorrhoidal disease in severe portal hypertension: a combined approach with transjugular intrahepatic portosystemic shunt (TIPS) and transanal haemorrhoidal dearterialization (THD).

Archives of medical science : AMS

Galati G, De Vincentis A, Ripetti V, La Vaccara V, Vespasiani-Gentilucci U, Mazzarelli C, Gallo P, Luppi G, Grasso RF, Picardi A.
PMID: 24701234
Arch Med Sci. 2014 Feb 24;10(1):195-6. doi: 10.5114/aoms.2014.40746. Epub 2014 Feb 23.

No abstract available.

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Galati G, De Vincentis A, Ripetti V, et al. Haemorrhoidal disease in severe portal hypertension: a combined approach with transjugular intrahepatic portosystemic shunt (TIPS) and transanal haemorrhoidal dearterialization (THD). Arch Med Sci. 2014;10(1):195-6doi: 10.5114/aoms.2014.40746.
Galati, G., De Vincentis, A., Ripetti, V., La Vaccara, V., Vespasiani-Gentilucci, U., Mazzarelli, C., Gallo, P., Luppi, G., Grasso, R. F., & Picardi, A. (2014). Haemorrhoidal disease in severe portal hypertension: a combined approach with transjugular intrahepatic portosystemic shunt (TIPS) and transanal haemorrhoidal dearterialization (THD). Archives of medical science : AMS, 10(1), 195-6. https://doi.org/10.5114/aoms.2014.40746
Galati, Giovanni, et al. "Haemorrhoidal disease in severe portal hypertension: a combined approach with transjugular intrahepatic portosystemic shunt (TIPS) and transanal haemorrhoidal dearterialization (THD)." Archives of medical science : AMS vol. 10,1 (2014): 195-6. doi: https://doi.org/10.5114/aoms.2014.40746
Galati G, De Vincentis A, Ripetti V, La Vaccara V, Vespasiani-Gentilucci U, Mazzarelli C, Gallo P, Luppi G, Grasso RF, Picardi A. Haemorrhoidal disease in severe portal hypertension: a combined approach with transjugular intrahepatic portosystemic shunt (TIPS) and transanal haemorrhoidal dearterialization (THD). Arch Med Sci. 2014 Feb 24;10(1):195-6. doi: 10.5114/aoms.2014.40746. Epub 2014 Feb 23. PMID: 24701234; PMCID: PMC3953988.
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Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle.

F1000Research

Chaponnier C, Gabbiani G.
PMID: 27335638
F1000Res. 2016 Mar 30;5:416. doi: 10.12688/f1000research.8154.2. eCollection 2016.

Higher vertebrates (mammals and birds) express six different highly conserved actin isoforms that can be classified in three subgroups: 1) sarcomeric actins, α-skeletal (α-SKA) and α-cardiac (α-CAA), 2) smooth muscle actins (SMAs), α-SMA and γ-SMA, and 3) cytoplasmic actins...

Cite
Chaponnier C, Gabbiani G. Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle. F1000Res. 2016;5:416doi: 10.12688/f1000research.8154.2.
Chaponnier, C., & Gabbiani, G. (2016). Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle. F1000Research, 5416. https://doi.org/10.12688/f1000research.8154.2
Chaponnier, Christine, and Gabbiani, Giulio. "Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle." F1000Research vol. 5 (2016): 416. doi: https://doi.org/10.12688/f1000research.8154.2
Chaponnier C, Gabbiani G. Monoclonal antibodies against muscle actin isoforms: epitope identification and analysis of isoform expression by immunoblot and immunostaining in normal and regenerating skeletal muscle. F1000Res. 2016 Mar 30;5:416. doi: 10.12688/f1000research.8154.2. eCollection 2016. PMID: 27335638; PMCID: PMC4893938.
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PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro.

Frontiers in neuroscience

Cellot G, Lagonegro P, Tarabella G, Scaini D, Fabbri F, Iannotta S, Prato M, Salviati G, Ballerini L.
PMID: 26834546
Front Neurosci. 2016 Jan 14;9:521. doi: 10.3389/fnins.2015.00521. eCollection 2015.

UNLABELLED: The design of electrodes based on conductive polymers in brain-machine interface technology offers the opportunity to exploit variably manufactured materials to reduce gliosis, indeed the most common brain response to chronically implanted neural electrodes. In fact, the use...

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Cellot G, Lagonegro P, Tarabella G, et al. PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro. Front Neurosci. 2016;9:521doi: 10.3389/fnins.2015.00521.
Cellot, G., Lagonegro, P., Tarabella, G., Scaini, D., Fabbri, F., Iannotta, S., Prato, M., Salviati, G., & Ballerini, L. (2015). PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro. Frontiers in neuroscience, 9521. https://doi.org/10.3389/fnins.2015.00521
Cellot, Giada, et al. "PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro." Frontiers in neuroscience vol. 9 (2015): 521. doi: https://doi.org/10.3389/fnins.2015.00521
Cellot G, Lagonegro P, Tarabella G, Scaini D, Fabbri F, Iannotta S, Prato M, Salviati G, Ballerini L. PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro. Front Neurosci. 2016 Jan 14;9:521. doi: 10.3389/fnins.2015.00521. eCollection 2015. PMID: 26834546; PMCID: PMC4712304.
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Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: a new one-pot approach to functionalized pyridines.

The Journal of organic chemistry

Abbiati G, Arcadi A, Bianchi G, Di Giuseppe S, Marinelli F, Rossi E.
PMID: 12946136
J Org Chem. 2003 Sep 05;68(18):6959-66. doi: 10.1021/jo0347260.

A general one-pot synthesis of pyridines 4a-t from the reaction of dialkyl acyclic/cyclic ketones 1a-i, methyl, aryl/heteroaryl ketones 1m-r, and aldehydes bearing alpha-hydrogens 1s,t with propargylamine 2 is described. Gold and copper salts are efficient catalysts for the reaction...

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Abbiati G, Arcadi A, Bianchi G, et al. Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: a new one-pot approach to functionalized pyridines. J Org Chem. 2003;68(18):6959-66doi: 10.1021/jo0347260.
Abbiati, G., Arcadi, A., Bianchi, G., Di Giuseppe, S., Marinelli, F., & Rossi, E. (2003). Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: a new one-pot approach to functionalized pyridines. The Journal of organic chemistry, 68(18), 6959-66. https://doi.org/10.1021/jo0347260
Abbiati, Giorgio, et al. "Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: a new one-pot approach to functionalized pyridines." The Journal of organic chemistry vol. 68,18 (2003): 6959-66. doi: https://doi.org/10.1021/jo0347260
Abbiati G, Arcadi A, Bianchi G, Di Giuseppe S, Marinelli F, Rossi E. Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: a new one-pot approach to functionalized pyridines. J Org Chem. 2003 Sep 05;68(18):6959-66. doi: 10.1021/jo0347260. PMID: 12946136.
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Regioselectivity on the palladium-catalyzed intramolecular cyclization of indole derivatives.

The Journal of organic chemistry

Abbiati G, Beccalli EM, Broggini G, Zoni C.
PMID: 14510534
J Org Chem. 2003 Oct 03;68(20):7625-8. doi: 10.1021/jo034636v.

Indole 2-carboxamide derivatives 4 underwent palladium-catalyzed intramolecular cyclization reactions to afford beta-carbolinones or pyrazino[1,2-a]indoles according to different reaction pathways. The complete regioselectivity of the reactions was obtained in different reaction conditions.

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Abbiati G, Beccalli EM, Broggini G, et al. Regioselectivity on the palladium-catalyzed intramolecular cyclization of indole derivatives. J Org Chem. 2003;68(20):7625-8doi: 10.1021/jo034636v.
Abbiati, G., Beccalli, E. M., Broggini, G., & Zoni, C. (2003). Regioselectivity on the palladium-catalyzed intramolecular cyclization of indole derivatives. The Journal of organic chemistry, 68(20), 7625-8. https://doi.org/10.1021/jo034636v
Abbiati, Giorgio, et al. "Regioselectivity on the palladium-catalyzed intramolecular cyclization of indole derivatives." The Journal of organic chemistry vol. 68,20 (2003): 7625-8. doi: https://doi.org/10.1021/jo034636v
Abbiati G, Beccalli EM, Broggini G, Zoni C. Regioselectivity on the palladium-catalyzed intramolecular cyclization of indole derivatives. J Org Chem. 2003 Oct 03;68(20):7625-8. doi: 10.1021/jo034636v. PMID: 14510534.
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Covering by a flap induces apoptosis of granulation tissue myofibroblasts and vascular cells.

Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society

Garbin S, Pittet B, Montandon D, Gabbiani G, Desmoulière A.
PMID: 17177821
Wound Repair Regen. 1996 Apr-Jun;4(2):244-51. doi: 10.1046/j.1524-475X.1996.40213.x.

It has recently been shown that during the healing of an open wound, apoptosis mediates the decrease in cellularity during the transition between granulation tissue and scar. Because reduced contraction and a decrease in the number of fibroblastic cells...

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Garbin S, Pittet B, Montandon D, et al. Covering by a flap induces apoptosis of granulation tissue myofibroblasts and vascular cells. Wound Repair Regen. 1996;4(2):244-51doi: 10.1046/j.1524-475X.1996.40213.x.
Garbin, S., Pittet, B., Montandon, D., Gabbiani, G., & Desmoulière, A. (1996). Covering by a flap induces apoptosis of granulation tissue myofibroblasts and vascular cells. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society, 4(2), 244-51. https://doi.org/10.1046/j.1524-475X.1996.40213.x
Garbin, S, et al. "Covering by a flap induces apoptosis of granulation tissue myofibroblasts and vascular cells." Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society vol. 4,2 (1996): 244-51. doi: https://doi.org/10.1046/j.1524-475X.1996.40213.x
Garbin S, Pittet B, Montandon D, Gabbiani G, Desmoulière A. Covering by a flap induces apoptosis of granulation tissue myofibroblasts and vascular cells. Wound Repair Regen. 1996 Apr-Jun;4(2):244-51. doi: 10.1046/j.1524-475X.1996.40213.x. PMID: 17177821.
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Enhancement of the core near-band-edge emission induced by an amorphous shell in coaxial one-dimensional nanostructure: the case of SiC/SiO2 core/shell self-organized nanowires.

Nanotechnology

Fabbri F, Rossi F, Attolini G, Salviati G, Iannotta S, Aversa L, Verucchi R, Nardi M, Fukata N, Dierre B, Sekiguchi T.
PMID: 20683139
Nanotechnology. 2010 Aug 27;21(34):345702. doi: 10.1088/0957-4484/21/34/345702. Epub 2010 Aug 04.

We report the influence of the native amorphous SiO(2) shell on the cathodoluminescence emission of 3C-SiC/SiO(2) core/shell nanowires. A shell-induced enhancement of the SiC near-band-edge emission is observed and studied as a function of the silicon dioxide thickness. Since...

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Fabbri F, Rossi F, Attolini G, et al. Enhancement of the core near-band-edge emission induced by an amorphous shell in coaxial one-dimensional nanostructure: the case of SiC/SiO2 core/shell self-organized nanowires. Nanotechnology. 2010;21(34):345702doi: 10.1088/0957-4484/21/34/345702.
Fabbri, F., Rossi, F., Attolini, G., Salviati, G., Iannotta, S., Aversa, L., Verucchi, R., Nardi, M., Fukata, N., Dierre, B., & Sekiguchi, T. (2010). Enhancement of the core near-band-edge emission induced by an amorphous shell in coaxial one-dimensional nanostructure: the case of SiC/SiO2 core/shell self-organized nanowires. Nanotechnology, 21(34), 345702. https://doi.org/10.1088/0957-4484/21/34/345702
Fabbri, Filippo, et al. "Enhancement of the core near-band-edge emission induced by an amorphous shell in coaxial one-dimensional nanostructure: the case of SiC/SiO2 core/shell self-organized nanowires." Nanotechnology vol. 21,34 (2010): 345702. doi: https://doi.org/10.1088/0957-4484/21/34/345702
Fabbri F, Rossi F, Attolini G, Salviati G, Iannotta S, Aversa L, Verucchi R, Nardi M, Fukata N, Dierre B, Sekiguchi T. Enhancement of the core near-band-edge emission induced by an amorphous shell in coaxial one-dimensional nanostructure: the case of SiC/SiO2 core/shell self-organized nanowires. Nanotechnology. 2010 Aug 27;21(34):345702. doi: 10.1088/0957-4484/21/34/345702. Epub 2010 Aug 04. PMID: 20683139.
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Integration of water stress response: Cell expansion and cuticle deposition in Arabidopsis thaliana.

Plant signaling & behavior

Cominelli E, Galbiati M, Tonelli C.
PMID: 19704466
Plant Signal Behav. 2008 Aug;3(8):556-7. doi: 10.4161/psb.3.8.5699.

Inhibition of cell expansion and modification in the accumulation of cuticle components are two important processes that plants adopted to respond to water deficit. In our recent publication in The Plant Journal we characterized an Arabidopsis thaliana transcription factor,...

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Cominelli E, Galbiati M, Tonelli C. Integration of water stress response: Cell expansion and cuticle deposition in Arabidopsis thaliana. Plant Signal Behav. 2008;3(8):556-7doi: 10.4161/psb.3.8.5699.
Cominelli, E., Galbiati, M., & Tonelli, C. (2008). Integration of water stress response: Cell expansion and cuticle deposition in Arabidopsis thaliana. Plant signaling & behavior, 3(8), 556-7. https://doi.org/10.4161/psb.3.8.5699
Cominelli, Eleonora, et al. "Integration of water stress response: Cell expansion and cuticle deposition in Arabidopsis thaliana." Plant signaling & behavior vol. 3,8 (2008): 556-7. doi: https://doi.org/10.4161/psb.3.8.5699
Cominelli E, Galbiati M, Tonelli C. Integration of water stress response: Cell expansion and cuticle deposition in Arabidopsis thaliana. Plant Signal Behav. 2008 Aug;3(8):556-7. doi: 10.4161/psb.3.8.5699. PMID: 19704466; PMCID: PMC2634494.
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