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Showing 1 to 12 of 33 entries
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Electronic Noses for Composites Surface Contamination Detection in Aerospace Industry.

Sensors (Basel, Switzerland)

Vito S, Miglietta ML, Massera E, Fattoruso G, Formisano F, Polichetti T, Salvato M, Alfano B, Esposito E, Francia GD.
PMID: 28368338
Sensors (Basel). 2017 Apr 02;17(4). doi: 10.3390/s17040754.

The full exploitation of Composite Fiber Reinforced Polymers (CFRP) in so-called

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Vito S, Miglietta ML, Massera E, et al. Electronic Noses for Composites Surface Contamination Detection in Aerospace Industry. Sensors (Basel). 2017;17(4)doi: 10.3390/s17040754.
Vito, S., Miglietta, M. L., Massera, E., Fattoruso, G., Formisano, F., Polichetti, T., Salvato, M., Alfano, B., Esposito, E., & Francia, G. D. (2017). Electronic Noses for Composites Surface Contamination Detection in Aerospace Industry. Sensors (Basel, Switzerland), 17(4), . https://doi.org/10.3390/s17040754
Vito, Saverio De, et al. "Electronic Noses for Composites Surface Contamination Detection in Aerospace Industry." Sensors (Basel, Switzerland) vol. 17,4 (2017). doi: https://doi.org/10.3390/s17040754
Vito S, Miglietta ML, Massera E, Fattoruso G, Formisano F, Polichetti T, Salvato M, Alfano B, Esposito E, Francia GD. Electronic Noses for Composites Surface Contamination Detection in Aerospace Industry. Sensors (Basel). 2017 Apr 02;17(4). doi: 10.3390/s17040754. PMID: 28368338; PMCID: PMC5421714.
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Correction to new anticancer agents mimicking protein recognition motifs.

Journal of medicinal chemistry

Persico M, Ramunno A, Maglio V, Franceschelli S, Esposito C, Carotenuto A, Brancaccio D, De Pasquale V, Pavone LM, Varra M, Orteca N, Novellino E, Fattorusso C.
PMID: 25927290
J Med Chem. 2015 May 14;58(9):4088. doi: 10.1021/acs.jmedchem.5b00607. Epub 2015 Apr 30.

No abstract available.

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Persico M, Ramunno A, Maglio V, et al. Correction to new anticancer agents mimicking protein recognition motifs. J Med Chem. 2015;58(9):4088doi: 10.1021/acs.jmedchem.5b00607.
Persico, M., Ramunno, A., Maglio, V., Franceschelli, S., Esposito, C., Carotenuto, A., Brancaccio, D., De Pasquale, V., Pavone, L. M., Varra, M., Orteca, N., Novellino, E., & Fattorusso, C. (2015). Correction to new anticancer agents mimicking protein recognition motifs. Journal of medicinal chemistry, 58(9), 4088. https://doi.org/10.1021/acs.jmedchem.5b00607
Persico, Marco, et al. "Correction to new anticancer agents mimicking protein recognition motifs." Journal of medicinal chemistry vol. 58,9 (2015): 4088. doi: https://doi.org/10.1021/acs.jmedchem.5b00607
Persico M, Ramunno A, Maglio V, Franceschelli S, Esposito C, Carotenuto A, Brancaccio D, De Pasquale V, Pavone LM, Varra M, Orteca N, Novellino E, Fattorusso C. Correction to new anticancer agents mimicking protein recognition motifs. J Med Chem. 2015 May 14;58(9):4088. doi: 10.1021/acs.jmedchem.5b00607. Epub 2015 Apr 30. PMID: 25927290.
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Chemistry of verongida sponges. 9.1 secondary metabolite composition of the caribbean sponge aplysina cauliformis .

Journal of natural products

Ciminiello P, Dell'Aversano C, Fattorusso E, Magno S, Pansini M.
PMID: 10217716
J Nat Prod. 1999 Apr;62(4):590-3. doi: 10.1021/np9805138.

A detailed analysis of the secondary metabolites of the sponge Aplysina cauliformis has been performed. Eight compounds were identified, two of which (13 and 14) are new bromotyrosine derivatives whose structures were determinated from spectroscopic evidence, including 2D NMR....

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Ciminiello P, Dell'Aversano C, Fattorusso E, et al. Chemistry of verongida sponges. 9.1 secondary metabolite composition of the caribbean sponge aplysina cauliformis . J Nat Prod. 1999;62(4):590-3doi: 10.1021/np9805138.
Ciminiello, P., Dell'Aversano, C., Fattorusso, E., Magno, S., & Pansini, M. (1999). Chemistry of verongida sponges. 9.1 secondary metabolite composition of the caribbean sponge aplysina cauliformis . Journal of natural products, 62(4), 590-3. https://doi.org/10.1021/np9805138
Ciminiello, et al. "Chemistry of verongida sponges. 9.1 secondary metabolite composition of the caribbean sponge aplysina cauliformis ." Journal of natural products vol. 62,4 (1999): 590-3. doi: https://doi.org/10.1021/np9805138
Ciminiello P, Dell'Aversano C, Fattorusso E, Magno S, Pansini M. Chemistry of verongida sponges. 9.1 secondary metabolite composition of the caribbean sponge aplysina cauliformis . J Nat Prod. 1999 Apr;62(4):590-3. doi: 10.1021/np9805138. PMID: 10217716.
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Co(II) Coordination in Prokaryotic Zinc Finger Domains as Revealed by UV-Vis Spectroscopy.

Bioinorganic chemistry and applications

Sivo V, D'Abrosca G, Russo L, Iacovino R, Pedone PV, Fattorusso R, Isernia C, Malgieri G.
PMID: 29386985
Bioinorg Chem Appl. 2017;2017:1527247. doi: 10.1155/2017/1527247. Epub 2017 Dec 14.

Co(II) electronic configuration allows its use as a spectroscopic probe in UV-Vis experiments to characterize the metal coordination sphere that is an essential component of the functional structure of zinc-binding proteins and to evaluate the metal ion affinities of...

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Sivo V, D'Abrosca G, Russo L, et al. Co(II) Coordination in Prokaryotic Zinc Finger Domains as Revealed by UV-Vis Spectroscopy. Bioinorg Chem Appl. 2017;2017:1527247doi: 10.1155/2017/1527247.
Sivo, V., D'Abrosca, G., Russo, L., Iacovino, R., Pedone, P. V., Fattorusso, R., Isernia, C., & Malgieri, G. (2017). Co(II) Coordination in Prokaryotic Zinc Finger Domains as Revealed by UV-Vis Spectroscopy. Bioinorganic chemistry and applications, 20171527247. https://doi.org/10.1155/2017/1527247
Sivo, Valeria, et al. "Co(II) Coordination in Prokaryotic Zinc Finger Domains as Revealed by UV-Vis Spectroscopy." Bioinorganic chemistry and applications vol. 2017 (2017): 1527247. doi: https://doi.org/10.1155/2017/1527247
Sivo V, D'Abrosca G, Russo L, Iacovino R, Pedone PV, Fattorusso R, Isernia C, Malgieri G. Co(II) Coordination in Prokaryotic Zinc Finger Domains as Revealed by UV-Vis Spectroscopy. Bioinorg Chem Appl. 2017;2017:1527247. doi: 10.1155/2017/1527247. Epub 2017 Dec 14. PMID: 29386985; PMCID: PMC5745721.
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Autism Spectrum Disorders and the Gut Microbiota.

Nutrients

Fattorusso A, Di Genova L, Dell'Isola GB, Mencaroni E, Esposito S.
PMID: 30823414
Nutrients. 2019 Feb 28;11(3). doi: 10.3390/nu11030521.

In recent years, there has been an emerging interest in the possible role of the gut microbiota as a co-factor in the development of autism spectrum disorders (ASDs), as many studies have highlighted the bidirectional communication between the gut...

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Fattorusso A, Di Genova L, Dell'Isola GB, et al. Autism Spectrum Disorders and the Gut Microbiota. Nutrients. 2019;11(3)doi: 10.3390/nu11030521.
Fattorusso, A., Di Genova, L., Dell'Isola, G. B., Mencaroni, E., & Esposito, S. (2019). Autism Spectrum Disorders and the Gut Microbiota. Nutrients, 11(3), . https://doi.org/10.3390/nu11030521
Fattorusso, Antonella, et al. "Autism Spectrum Disorders and the Gut Microbiota." Nutrients vol. 11,3 (2019). doi: https://doi.org/10.3390/nu11030521
Fattorusso A, Di Genova L, Dell'Isola GB, Mencaroni E, Esposito S. Autism Spectrum Disorders and the Gut Microbiota. Nutrients. 2019 Feb 28;11(3). doi: 10.3390/nu11030521. PMID: 30823414; PMCID: PMC6471505.
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Localized herpes zoster infection: a rare cause of syndrome of inappropriate secretion of antidiuretic hormone.

Oxford medical case reports

Bassi V, Fattoruso O, Santinelli C.
PMID: 29230301
Oxf Med Case Reports. 2017 Nov 13;2017(11):omx065. doi: 10.1093/omcr/omx065. eCollection 2017 Nov.

Hyponatremia is the most common electrolyte abnormality observed in clinical practice and syndrome of inappropriate secretion of antidiuretic hormone (SIADH) is diagnosed in nearly 40% of the hospitalized hyponatremic patients. We present a case report of herpes zoster infection...

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Bassi V, Fattoruso O, Santinelli C. Localized herpes zoster infection: a rare cause of syndrome of inappropriate secretion of antidiuretic hormone. Oxf Med Case Reports. 2017;2017(11):omx065doi: 10.1093/omcr/omx065.
Bassi, V., Fattoruso, O., & Santinelli, C. (2017). Localized herpes zoster infection: a rare cause of syndrome of inappropriate secretion of antidiuretic hormone. Oxford medical case reports, 2017(11), omx065. https://doi.org/10.1093/omcr/omx065
Bassi, V, et al. "Localized herpes zoster infection: a rare cause of syndrome of inappropriate secretion of antidiuretic hormone." Oxford medical case reports vol. 2017,11 (2017): omx065. doi: https://doi.org/10.1093/omcr/omx065
Bassi V, Fattoruso O, Santinelli C. Localized herpes zoster infection: a rare cause of syndrome of inappropriate secretion of antidiuretic hormone. Oxf Med Case Reports. 2017 Nov 13;2017(11):omx065. doi: 10.1093/omcr/omx065. eCollection 2017 Nov. PMID: 29230301; PMCID: PMC5691395.
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The Pharmacoresistant Epilepsy: An Overview on Existant and New Emerging Therapies.

Frontiers in neurology

Fattorusso A, Matricardi S, Mencaroni E, Dell'Isola GB, Di Cara G, Striano P, Verrotti A.
PMID: 34239494
Front Neurol. 2021 Jun 22;12:674483. doi: 10.3389/fneur.2021.674483. eCollection 2021.

Epilepsy is one of the most common neurological chronic disorders, with an estimated prevalence of 0. 5 - 1%. Currently, treatment options for epilepsy are predominantly based on the administration of symptomatic therapy. Most patients are able to achieve...

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Fattorusso A, Matricardi S, Mencaroni E, et al. The Pharmacoresistant Epilepsy: An Overview on Existant and New Emerging Therapies. Front Neurol. 2021;12:674483doi: 10.3389/fneur.2021.674483.
Fattorusso, A., Matricardi, S., Mencaroni, E., Dell'Isola, G. B., Di Cara, G., Striano, P., & Verrotti, A. (2021). The Pharmacoresistant Epilepsy: An Overview on Existant and New Emerging Therapies. Frontiers in neurology, 12674483. https://doi.org/10.3389/fneur.2021.674483
Fattorusso, Antonella, et al. "The Pharmacoresistant Epilepsy: An Overview on Existant and New Emerging Therapies." Frontiers in neurology vol. 12 (2021): 674483. doi: https://doi.org/10.3389/fneur.2021.674483
Fattorusso A, Matricardi S, Mencaroni E, Dell'Isola GB, Di Cara G, Striano P, Verrotti A. The Pharmacoresistant Epilepsy: An Overview on Existant and New Emerging Therapies. Front Neurol. 2021 Jun 22;12:674483. doi: 10.3389/fneur.2021.674483. eCollection 2021. PMID: 34239494; PMCID: PMC8258148.
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Ubiquitin binds the amyloid β peptide and interferes with its clearance pathways.

Chemical science

Bellia F, Lanza V, García-Viñuales S, Ahmed IMM, Pietropaolo A, Iacobucci C, Malgieri G, D'Abrosca G, Fattorusso R, Nicoletti VG, Sbardella D, Tundo GR, Coletta M, Pirone L, Pedone E, Calcagno D, Grasso G, Milardi D.
PMID: 30996991
Chem Sci. 2019 Jan 10;10(9):2732-2742. doi: 10.1039/c8sc03394c. eCollection 2019 Mar 07.

Several lines of evidence point to a compromised proteostasis associated with a reduction of the Ubiquitin Proteasome System (UPS) activity in patients affected by Alzheimer's Disease (AD) and suggest that the amyloid β peptide (Aβ) is an important player...

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Bellia F, Lanza V, García-Viñuales S, et al. Ubiquitin binds the amyloid β peptide and interferes with its clearance pathways. Chem Sci. 2019;10(9):2732-2742doi: 10.1039/c8sc03394c.
Bellia, F., Lanza, V., García-Viñuales, S., Ahmed, I. M. M., Pietropaolo, A., Iacobucci, C., Malgieri, G., D'Abrosca, G., Fattorusso, R., Nicoletti, V. G., Sbardella, D., Tundo, G. R., Coletta, M., Pirone, L., Pedone, E., Calcagno, D., Grasso, G., & Milardi, D. (2019). Ubiquitin binds the amyloid β peptide and interferes with its clearance pathways. Chemical science, 10(9), 2732-2742. https://doi.org/10.1039/c8sc03394c
Bellia, F, et al. "Ubiquitin binds the amyloid β peptide and interferes with its clearance pathways." Chemical science vol. 10,9 (2019): 2732-2742. doi: https://doi.org/10.1039/c8sc03394c
Bellia F, Lanza V, García-Viñuales S, Ahmed IMM, Pietropaolo A, Iacobucci C, Malgieri G, D'Abrosca G, Fattorusso R, Nicoletti VG, Sbardella D, Tundo GR, Coletta M, Pirone L, Pedone E, Calcagno D, Grasso G, Milardi D. Ubiquitin binds the amyloid β peptide and interferes with its clearance pathways. Chem Sci. 2019 Jan 10;10(9):2732-2742. doi: 10.1039/c8sc03394c. eCollection 2019 Mar 07. PMID: 30996991; PMCID: PMC6419943.
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Covalent Inhibitors of .

ACS medicinal chemistry letters

Cullia G, Bruno S, Parapini S, Margiotta M, Tamborini L, Pinto A, Galbiati A, Mozzarelli A, Persico M, Paladino A, Fattorusso C, Taramelli D, Conti P.
PMID: 30996801
ACS Med Chem Lett. 2019 Feb 20;10(4):590-595. doi: 10.1021/acsmedchemlett.8b00592. eCollection 2019 Apr 11.

Covalent inhibitors of

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Cullia G, Bruno S, Parapini S, et al. Covalent Inhibitors of . ACS Med Chem Lett. 2019;10(4):590-595doi: 10.1021/acsmedchemlett.8b00592.
Cullia, G., Bruno, S., Parapini, S., Margiotta, M., Tamborini, L., Pinto, A., Galbiati, A., Mozzarelli, A., Persico, M., Paladino, A., Fattorusso, C., Taramelli, D., & Conti, P. (2019). Covalent Inhibitors of . ACS medicinal chemistry letters, 10(4), 590-595. https://doi.org/10.1021/acsmedchemlett.8b00592
Cullia, Gregorio, et al. "Covalent Inhibitors of ." ACS medicinal chemistry letters vol. 10,4 (2019): 590-595. doi: https://doi.org/10.1021/acsmedchemlett.8b00592
Cullia G, Bruno S, Parapini S, Margiotta M, Tamborini L, Pinto A, Galbiati A, Mozzarelli A, Persico M, Paladino A, Fattorusso C, Taramelli D, Conti P. Covalent Inhibitors of . ACS Med Chem Lett. 2019 Feb 20;10(4):590-595. doi: 10.1021/acsmedchemlett.8b00592. eCollection 2019 Apr 11. PMID: 30996801; PMCID: PMC6466836.
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Folding mechanisms steer the amyloid fibril formation propensity of highly homologous proteins.

Chemical science

Malgieri G, D'Abrosca G, Pirone L, Toto A, Palmieri M, Russo L, Sciacca MFM, Tatè R, Sivo V, Baglivo I, Majewska R, Coletta M, Pedone PV, Isernia C, De Stefano M, Gianni S, Pedone EM, Milardi D, Fattorusso R.
PMID: 29780459
Chem Sci. 2018 Mar 01;9(13):3290-3298. doi: 10.1039/c8sc00166a. eCollection 2018 Apr 07.

Significant advances in the understanding of the molecular determinants of fibrillogenesis can be expected from comparative studies of the aggregation propensities of proteins with highly homologous structures but different folding pathways. Here, we fully characterize, by means of stopped-flow,...

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Malgieri G, D'Abrosca G, Pirone L, et al. Folding mechanisms steer the amyloid fibril formation propensity of highly homologous proteins. Chem Sci. 2018;9(13):3290-3298doi: 10.1039/c8sc00166a.
Malgieri, G., D'Abrosca, G., Pirone, L., Toto, A., Palmieri, M., Russo, L., Sciacca, M. F. M., Tatè, R., Sivo, V., Baglivo, I., Majewska, R., Coletta, M., Pedone, P. V., Isernia, C., De Stefano, M., Gianni, S., Pedone, E. M., Milardi, D., & Fattorusso, R. (2018). Folding mechanisms steer the amyloid fibril formation propensity of highly homologous proteins. Chemical science, 9(13), 3290-3298. https://doi.org/10.1039/c8sc00166a
Malgieri, Gaetano, et al. "Folding mechanisms steer the amyloid fibril formation propensity of highly homologous proteins." Chemical science vol. 9,13 (2018): 3290-3298. doi: https://doi.org/10.1039/c8sc00166a
Malgieri G, D'Abrosca G, Pirone L, Toto A, Palmieri M, Russo L, Sciacca MFM, Tatè R, Sivo V, Baglivo I, Majewska R, Coletta M, Pedone PV, Isernia C, De Stefano M, Gianni S, Pedone EM, Milardi D, Fattorusso R. Folding mechanisms steer the amyloid fibril formation propensity of highly homologous proteins. Chem Sci. 2018 Mar 01;9(13):3290-3298. doi: 10.1039/c8sc00166a. eCollection 2018 Apr 07. PMID: 29780459; PMCID: PMC5933289.
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3β, 5α-Dihydroxy-6β-Methoxycholest-7-enes from the Marine Sponge Spongia agaricina.

Journal of natural products

Aiello A, Ciminiello P, Fattorusso E, Magno S.
PMID: 21401194
J Nat Prod. 1988 Sep;51(5):999-1002. doi: 10.1021/np50059a036.

No abstract available.

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Aiello A, Ciminiello P, Fattorusso E, et al. 3β, 5α-Dihydroxy-6β-Methoxycholest-7-enes from the Marine Sponge Spongia agaricina. J Nat Prod. 1988;51(5):999-1002doi: 10.1021/np50059a036.
Aiello, A., Ciminiello, P., Fattorusso, E., & Magno, S. (1988). 3β, 5α-Dihydroxy-6β-Methoxycholest-7-enes from the Marine Sponge Spongia agaricina. Journal of natural products, 51(5), 999-1002. https://doi.org/10.1021/np50059a036
Aiello, A, et al. "3β, 5α-Dihydroxy-6β-Methoxycholest-7-enes from the Marine Sponge Spongia agaricina." Journal of natural products vol. 51,5 (1988): 999-1002. doi: https://doi.org/10.1021/np50059a036
Aiello A, Ciminiello P, Fattorusso E, Magno S. 3β, 5α-Dihydroxy-6β-Methoxycholest-7-enes from the Marine Sponge Spongia agaricina. J Nat Prod. 1988 Sep;51(5):999-1002. doi: 10.1021/np50059a036. PMID: 21401194.
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The Role of Fractional Excretion of Uric Acid in the Differential Diagnosis of Hypotonic Hyponatraemia in Patients with Diuretic Therapy.

Cureus

Bassi V, Fattoruso O.
PMID: 32455079
Cureus. 2020 Apr 21;12(4):e7762. doi: 10.7759/cureus.7762.

Hyponatraemia is the most common electrolyte imbalance found in hospital population and worldwide thiazide and loop-diuretics are among the most widely used drugs. Syndrome of inappropriate antidiuresis diagnosis (SIAD) is complicated in the presence of diuretic therapy due to...

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Bassi V, Fattoruso O. The Role of Fractional Excretion of Uric Acid in the Differential Diagnosis of Hypotonic Hyponatraemia in Patients with Diuretic Therapy. Cureus. 2020;12(4):e7762doi: 10.7759/cureus.7762.
Bassi, V., & Fattoruso, O. (2020). The Role of Fractional Excretion of Uric Acid in the Differential Diagnosis of Hypotonic Hyponatraemia in Patients with Diuretic Therapy. Cureus, 12(4), e7762. https://doi.org/10.7759/cureus.7762
Bassi, Vincenzo, and Fattoruso, Olimpia. "The Role of Fractional Excretion of Uric Acid in the Differential Diagnosis of Hypotonic Hyponatraemia in Patients with Diuretic Therapy." Cureus vol. 12,4 (2020): e7762. doi: https://doi.org/10.7759/cureus.7762
Bassi V, Fattoruso O. The Role of Fractional Excretion of Uric Acid in the Differential Diagnosis of Hypotonic Hyponatraemia in Patients with Diuretic Therapy. Cureus. 2020 Apr 21;12(4):e7762. doi: 10.7759/cureus.7762. PMID: 32455079; PMCID: PMC7243088.
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Showing 1 to 12 of 33 entries