135 results on '"Bellizzi, M."'
Search Results
2. Daily Life Self-management and Self-treatment of Musculoskeletal Disorders Through SHOULPHY
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Lucchesi, I., Lorussi, F., Bellizzi, M., Carbonaro, N., Casarosa, S., Trotta, L., Tognetti, A., Akan, Ozgur, Series Editor, Bellavista, Paolo, Series Editor, Cao, Jiannong, Series Editor, Coulson, Geoffrey, Series Editor, Dressler, Falko, Series Editor, Ferrari, Domenico, Series Editor, Gerla, Mario, Series Editor, Kobayashi, Hisashi, Series Editor, Palazzo, Sergio, Series Editor, Sahni, Sartaj, Series Editor, Shen, Xuemin (Sherman), Series Editor, Stan, Mircea, Series Editor, Xiaohua, Jia, Series Editor, Zomaya, Albert Y., Series Editor, Perego, Paolo, editor, Rahmani, Amir M., editor, and TaheriNejad, Nima, editor
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- 2018
- Full Text
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3. PAIN MANAGEMENT IN LOWER LIMB MAJOR AMPUTATION: 253
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Bellizzi, M., Cassar, K., and Mifsud, J.
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- 2014
4. Crystal structure of 5,10,15,20-tetrakis(5′-methylthien-2′-yl)porphyrin, C40H30N4S4
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Bellizzi M., Foss P. C. D., Pelto R., Crundwell G., Brückner C., Updegraff J. B., Zeller M., and Hunter A. D.
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Physics ,QC1-999 ,Crystallography ,QD901-999 - Abstract
C40H30N4S4, triclinic, P1̅ (no. 2), a = 6.5126(7) Å, b = 10.499(1) Å, c = 12.635(1) Å, α = 87.818(2)°, β = 79.141(2)°, γ = 86.737(2)°, V = 846.7 Å3, Z = 1, Rgt(F) = 0.057, wRref(F2) = 0.150, T = 100 K.
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- 2004
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5. Crystal structure of 5,1O,15,20-tetrakis(5' -methylthien-2' -yl)porphy rin, C40H30N4S4
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Bellizzi M., Foss P. C. D., Pelto R., Crundwell G., Brückner C., Updegraff J. B., Zeller M., and Hunter A. D.
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Physics ,QC1-999 ,Crystallography ,QD901-999 - Published
- 2004
- Full Text
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6. Nutrition policies in Mediterranean Europe
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Serra-Majem, L., Ferro-Luzzi, A., Bellizzi, M., and Salleras, L.
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Spain -- Social policy ,Italy -- Social policy ,Malta -- Social policy ,Cookery, Mediterranean -- Health aspects ,Nutrition policy -- Europe ,Food/cooking/nutrition - Abstract
Regional nutritional health policy trends in three Mediterranean countries including Malta, Spain, and Italy are presented. Nutritional policies have not historically been a priority in these countries due to the low health risk associated with the Mediterranean diet. However, some changes in this traditionally healthy diet and international trade have prompted these countries to adopt limited regional policies.
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- 1997
7. Nutrition policies in Western Europe: national policies in Belgium, the Netherlands, France, Ireland, and the United Kingdom
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James, W.P.T., Ralph, A., and Bellizzi, M.
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Western Europe -- Social policy ,Nutrition policy -- International aspects ,Food/cooking/nutrition - Abstract
It appears that non-governmental groups have driven many of the dietary policy changes seen in the Netherlands, the United Kingdom, Belgium, France, and Ireland. Efforts aimed at educating the government, the population, food distributors, and food service providers have varied within these countries and have been met with varying success. Some governments have taken a more active role in establishing and implementing dietary policy than others.
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- 1997
8. WALKING ENERGETICS: DO HUMANS HAVE A CHEAP SECRET?
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Weyand, P G., Ty, J M., Patek, E R., Bellizzi, M J., and Wright, S
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- 2003
9. Defect in tracheal tube wall: a novel cause of large leak following tracheal intubation
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Bellizzi, M., primary, Matthews, J., additional, and Pandit, J. J., additional
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- 2019
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10. A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy
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Margoni, M., Soli, F., Sangalli, A., Bellizzi, M., Cecchini, E., and Buganza, M.
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- 2017
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- View/download PDF
11. Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)
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Bonomi, Marco, primary, Vezzoli, Valeria, additional, Krausz, Csilla, additional, Guizzardi, Fabiana, additional, Vezzani, Silvia, additional, Simoni, Manuela, additional, Bassi, Ivan, additional, Duminuco, Paolo, additional, Di Iorgi, Natascia, additional, Giavoli, Claudia, additional, Pizzocaro, Alessandro, additional, Russo, Gianni, additional, Moro, Mirella, additional, Fatti, Letizia, additional, Ferlin, Alberto, additional, Mazzanti, Laura, additional, Zatelli, Maria Chiara, additional, Cannavò, Salvo, additional, Isidori, Andrea M, additional, Pincelli, Angela Ida, additional, Prodam, Flavia, additional, Mancini, Antonio, additional, Limone, Paolo, additional, Tanda, Maria Laura, additional, Gaudino, Rossella, additional, Salerno, Mariacarolina, additional, Francesca, Pregnolato, additional, Maghnie, Mohamad, additional, Maggi, Mario, additional, Persani, Luca, additional, _, _, additional, Aimaretti, G, additional, Altobelli, M, additional, Ambrosio, M R, additional, Andrioli, M, additional, Angeletti, G, additional, Arecco, F, additional, Arnaldi, G, additional, Arosio, M, additional, Balsamo, A, additional, Baldassarri, M, additional, Bartalena, L, additional, Bazzoni, N, additional, Beccaria, L, additional, Beck-Peccoz, P, additional, Bellastella, G, additional, Bellizzi, M, additional, Benedicenti, F, additional, Bernasconi, S, additional, Bizzarri, C, additional, Bona, G, additional, Bonadonna, S, additional, Borretta, G, additional, Boschetti, M, additional, Brunani, A, additional, Brunelli, V, additional, Buzi, F, additional, Cacciatore, C, additional, Cangiano, B, additional, Cappa, M, additional, Casalone, R, additional, Cassio, A, additional, Cavarzere, P, additional, Cherubini, V, additional, Ciampani, T, additional, Cicognani, D, additional, Cignarelli, A, additional, Cisternino, M, additional, Colombo, P, additional, Corbetta, S, additional, Corciulo, N, additional, Corona, G, additional, Cozzi, R, additional, Crivellaro, C, additional, Dalle Mule, I, additional, Danesi, L, additional, D’Elia, A V, additional, degli Uberti, E, additional, De Leo, S, additional, Della Valle, E, additional, De Marchi, M, additional, Di Iorgi, N, additional, Di Mambro, A, additional, Fabbri, A, additional, Foresta, C, additional, Forti, G, additional, Franceschi, A R, additional, Garolla, A, additional, Ghezzi, M, additional, Giacomozzi, C, additional, Giusti, M, additional, Grosso, E, additional, Guabello, G, additional, Guarneri, M P, additional, Grugni, G, additional, Isidori, A M, additional, Lanfranco, F, additional, Lania, A, additional, Lanzi, R, additional, Larizza, L, additional, Lenzi, A, additional, Loche, S, additional, Loli, P, additional, Lombardi, V, additional, Maggio, M C, additional, Mandrile, G, additional, Manieri, C, additional, Mantovani, G, additional, Marelli, S, additional, Marzullo, M, additional, Mencarelli, M A, additional, Migone, N, additional, Motta, G, additional, Neri, G, additional, Padova, G, additional, Parenti, G, additional, Pasquino, B, additional, Pia, A, additional, Piantanida, E, additional, Pignatti, E, additional, Pilotta, A, additional, Pivetta, B, additional, Pollazzon, M, additional, Pontecorvi, A, additional, Porcelli, P, additional, Pozzan, G B, additional, Pozzobon, G, additional, Radetti, G, additional, Razzore, P, additional, Rocchetti, L, additional, Roncoroni, R, additional, Rossi, G, additional, Sala, E, additional, Salvatoni, A, additional, Salvini, F, additional, Secco, A, additional, Segni, M, additional, Selice, R, additional, Sgaramella, P, additional, Sileo, F, additional, Sinisi, A A, additional, Sirchia, F, additional, Spada, A, additional, Tresoldi, A, additional, Vigneri, R, additional, Weber, G, additional, and Zucchini, S, additional
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- 2018
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12. Identification of a novelABCD1 mutation in a family with Adrenoleukodistrophy
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Margoni, M, Buganza, M, Soli, Fiorenza, Sangalli, Antonella, Bellizzi, M, Cecchini, E, and Tranquillini, E.
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Adrenoleukodistrophy ,splicing ,Adrenoleukodistrophy, ABCD1, splicing ,ABCD1 - Published
- 2016
13. GERMLINE PROKINETICIN RECEPTOR 2 (PROKR2) VARIANTS ASSOCIATED WITH CENTRAL HYPOGONADISM CAUSE DIFFERENTAL MODULATION OF DISTINCT INTRACELLULAR PATHWAYS
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Domenico Vladimiro Libri, Gunnar, Kleinau, Valeria, Vezzoli, Marta, Busnelli, Fabiana, Guizzardi, Antonio Agostino Sinisi, Angela Ida Pincelli, Antonio, Mancini, Gianni, Russo, Paolo Beck Peccoz, Sandro, Loche, Claudio, Crivellaro, Maghnie, Mohamad, Csilla, Krausz, Luca, Persani, Marco, Bonomi, Aimaretti, G., Altobelli, M., Arnaldi, G., Baldi, M., Bartalena, L., Beccaria, L., Bellastella, G., Bellizzi, M., Bona, G., Borretta, G., Buzi, F., Cannavo, S., Cappa, M., Cariboni, A., Ciampani, T., Cicognani, A., Cisternino, M., Corbetta, S., Corciulo, N., Corona, G., Cozzi, R., D'Elia, A. V., Degli Uberti, E., De Marchi, M., Forti, G., Di Iorgi, N., Isidori, Andrea, Fabbri, A., Ferlin, A., Foresta, C., Franceschi, R., Garolla, A., Gaudino, R., Giagulli, V., Grosso, E., Jannini, E., Lanfranco, F., Larizza, L., Lenzi, A., Lombardo, Francesco, Limone, P., Maggi, M., Maggi, R., Maggio, M. C., Mandrile, G., Marino, M., Mencarelli, M. A., Migone, N., Neri, G., Perroni, L., Pignatti, E., Pilotta, A., Pizzocaro, A., Pontecorvi, A., Pozzobon, G., Prodam, F., Radetti, G., Razzore, P., Salerno, M. C., Salvatoni, A., Salvini, F., Secco, A., Segni, Maria, Simoni, M., Vigneri, R., Weber, G., Libri, Dv, Kleinau, G, Vezzoli, V, Busnelli, M, Guizzardi, F, Sinisi, Antonio Agostino, Pincelli, Ai, Mancini, A, Russo, G, Beck Peccoz, P, Loche, S, Crivellaro, C, Maghnie, M, Krausz, C, Persani, L, Bonomi, M., Libri DV, Kleinau G, Vezzoli V, Busnelli M, Guizzardi F, Sinisi AA, Pincelli AI, Mancini A, Russo G, Beck-Peccoz P, Loche S, Crivellaro C, Maghnie M, Krausz C, Persani L, Bonomi M, Maggio MC, et al, Libri, Domenico Vladimiro, Kleinau, Gunnar, Vezzoli, Valeria, Busnelli, Marta, Guizzardi, Fabiana, Pincelli, Angela Ida, Mancini, Antonio, Russo, Gianni, Beck Peccoz, Paolo, Loche, Sandro, Crivellaro, Claudio, Maghnie, Mohamad, Krausz, Csilla, Persani, Luca, Bonomi, Marco, and Salerno, Mariacarolina
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Male ,Kallmann syndrome ,Endocrinology, Diabetes and Metabolism ,Clinical Biochemistry ,Inositol Phosphate ,medicine.disease_cause ,Biochemistry ,Hypogonadotropic hypogonadism ,Germline ,Receptors, G-Protein-Coupled ,Cohort Studies ,Endocrinology ,Settore MED/38 - Pediatria Generale E Specialistica ,Adolescent ,Adult ,Child ,Cyclic AMP ,Female ,Genetic Association Studies ,Humans ,Hypogonadism ,Inositol Phosphates ,Middle Aged ,Mutation, Missense ,Receptors, Peptide ,Signal Transduction ,Young Adult ,Germ-Line Mutation ,Receptors ,mutations ,septo-optic dysplasia ,Missense mutation ,Receptor ,Mutation ,Prokineticin ,Peptide ,Human ,medicine.medical_specialty ,Adolescent, Adult, Child, Cohort Studies, Cyclic AMP ,metabolism, Female, Genetic Association Studies, Germ-Line Mutation, Humans, Hypogonadism ,epidemiology/genetics, Inositol Phosphates ,metabolism, Male, Middle Aged, Missense, Receptors ,G-Protein-Coupled ,genetics, Receptors ,genetics, Signal Transduction ,genetics, Young Adult ,Genetic Association Studie ,Biology ,Germline mutation ,Internal medicine ,medicine ,Biochemistry (medical) ,Prokineticin receptor 2 ,medicine.disease ,PROKR2, hypogonadism, prokineticin ,Missense ,Cohort Studie - Abstract
INTRODUCTION: Defects of prokineticin pathway affect the neuroendocrine control of reproduction, but their role in the pathogenesis of central hypogonadism remains undefined, and the functional impact of the missense PROKR2 variants has been incompletely characterized. MATERIAL AND METHODS: In a series of 246 idiopathic central hypogonadism patients, we found three novel (p.V158I, p.V334M, and p.N15TfsX30) and six already known (p.L173R, p.T260M, p.R268C, p.V274D, p.V331M, and p.H20MfsX23) germline variants in the PROKR2 gene. We evaluated the effects of seven missense alterations on two different prokineticin receptor 2 (PROKR2)-dependent pathways: inositol phosphate-Ca(2+) (Gq coupling) and cAMP (Gs coupling). RESULTS: PROKR2 variants were found in 16 patients (6.5%). Expression levels of variants p.V158I and p.V331M were moderately reduced, whereas they were markedly impaired in the remaining cases, except p.V334M, which was significantly overexpressed. The variants p.T260M, p.R268C, and p.V331M showed no remarkable changes in cAMP response (EC50) whereas the IP signaling appeared more profoundly affected. In contrast, cAMP accumulation cannot be stimulated through the p.L173R and p.V274D, but IP EC50 was similar to wt inp.L173R and increased by 10-fold in p.V274D. The variant p.V334M led to a 3-fold increase of EC50 for both cAMP and IP. CONCLUSION: Our study shows that single PROKR2 missense allelic variants can either affect both signaling pathways differently or selectively. Thus, the integrity of both PROKR2-dependent cAMP and IP signals should be evaluated for a complete functional testing of novel identified allelic variants.
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- 2014
14. Italian Study Group on Idiopathic Central Hypogonadism (ICH). Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways
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Libri, D. V., Kleinau, G., Vezzoli, V., Busnelli, M., Guizzardi, F., Sinisi, A. A., Pincelli, A. I., Mancini, A., Russo, G., Eccoz, P. Beck P., Loche, S., Crivellaro, C., Maghnie, M., Krausz, C., Persani, L., Bonomi, M., Aimaretti, G., Altobelli, M., Arnaldi, G., Baldi, M., Bartalena, Luigi, Beccaria, L., Bellastella, G., Bellizzi, M., Bona, G., Borretta, G., Buzi, F., Cannavò, S., Cappa, M., Cariboni, A., Ciampani, T., Cicognani, A., Cisternino, M., Corbetta, S., Corciulo, N., Corona, G., Cozzi, R., D’Elia, A. V., Degli Uberti, E., De Marchi, M., Forti, G., di Iorgi, N., Isidori, A., Fabbri, A., Ferlin, A., Foresta, C., Franceschi, R., Garolla, A., Gaudino, R., Giagulli, V., Grosso, E., Jannini, E., Lanfranco, F., Larizza, L., Lenzi, A., Lombardo, F., Limone, P., Maggi, M., Maggi, R., Maggio, M. C., Mandrile, G., Marino, M., Mencarelli, M. A., Migone, N., Neri, G., Perroni, L., Pignatti, E., Pilotta, A., Pizzocaro, A., Pontecorvi, A., Pozzobon, G., Prodam, F., Radetti, G., Razzore, P., Salerno, M. C., Salvatoni, Alessandro, Salvini, F., Secco, A., Segni, M., Simoni, M., Vigneri, R., and Weber, G.
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- 2014
15. The Italian National Survey for Prader-Willi syndrome: an epidemiologic study
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Grugni G, Crinò A, Bosio L, Corrias A, Cuttini M, De Toni T, Di Battista E, Gargantini L, Greggio N, Iughetti L, Livieri C, Naselli A, Pagano C, Pozzan G, Ragusa L, Salvatoni A, Trifirò G, Beccaria L, Bellizzi M, Bellone J, Brunani A, Cappa M, Caselli G, Cerioni V, Delvecchio M, Giardino D, Iannì F, Memo L, Pilotta A, Pomara C, Radetti G, Sacco M, Sanzari A, Sartorio A, Tonini G, Vettor R, Zaglia F, Chiumello G, Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology, D.i.a.b.e.t.o.l.o.g.y., FRANZESE, ADRIANA, Grugni, G, Crinò, A, Bosio, L, Corrias, A, Cuttini, M, De Toni, T, Di Battista, E, Franzese, Adriana, Gargantini, L, Greggio, N, Iughetti, L, Livieri, C, Naselli, A, Pagano, C, Pozzan, G, Ragusa, L, Salvatoni, A, Trifirò, G, Beccaria, L, Bellizzi, M, Bellone, J, Brunani, A, Cappa, M, Caselli, G, Cerioni, V, Delvecchio, M, Giardino, D, Iannì, F, Memo, L, Pilotta, A, Pomara, C, Radetti, G, Sacco, M, Sanzari, A, Sartorio, A, Tonini, G, Vettor, R, Zaglia, F, Chiumello, G, Genetic Obesity Study Group of Italian Society of Pediatric, Endocrinology, and D. i. a. b. e. t. o. l. o. g., Y.
- Published
- 2008
16. Timber provisional structures for post-earthquake emergency interventions | L'impiego del legno nelle opere provvisionali urgenti in emergenze sismiche
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Caciolai, M., Bellizzi, M., Bolognese, C., Cavriani, M., D Odorico, A., Maiolo, A., Mannino, E., Munaro, L., Ponticelli, L., Grimaz, S., Moretti, A., Barazza, F., and Petra Malisan
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Abruzzo earthquake ,Firefighters ,Manuale STOP ,Opere provvisionali ,Provisional measures ,Puntellatura di ritegno ,shoring ,Vamecum STOP - Published
- 2013
17. Emerging effects of early environmental factors over genetic background for type 1 diabetes susceptibility: Evidence from a nationwide Italian twin study
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Nisticò, L, Iafusco, D, Galderisi, A, Fagnani, C, Cotichini, R, Toccaceli, V, Stazi, Ma, Study Group on Diabetes of the Italian Society of Pediatric Endocrinology, Collaborators: Cherubini V, D. i. a. b. e. t. o. l. o. g. y., Iannilli, A, Paparusso, Am, Cavallo, L, Zecchino, C, de Filippo, G, Gargantini, L, Salardi, S, Zucchini, S, Maltoni, G, Pasquino, B, Kaufmann, P, Buzi, F, Prandi, E, Gallo, F, Cicchetti, M, Castaldo, E, Citriniti, F, Chiarelli, F, Tumini, S, Di Stefano, A, Sperlì, D, De Marco, R, Banin, P, Toni, S, Lenzi, L, Del Vecchio, M, Lorini, R, D'Annunzio, G, Ingletto, D, Scaramuzza, A, Zuccotti, Gv, Chiumello, G, Meschi, F, Bonfanti, R, Frontino, G, de Luca, F, Lombardo, F, Salzano, G, Iughetti, L, Franzese, A, Buono, P, De Simone, I, Prisco, F, Cocca, A, Cadario, F, Monciotti, Cm, Savio, V, Cardella, F, Vanelli, M, Chiari, G, Errico, K, Iovane, B, Calcaterra, V, Citro, F, Cantoni, S, Marsciani, A, Cappa, M, Patera, Pi, Schiaffini, R, Sulli, N, Spoletini, M, Cerutti, Franco, Rabbone, I, Sicignano, S, Cauvin, V, Bellizzi, M, Tonini, G, Faleschini, E, Salvatoni, A, Pinelli, L, Maffeis, C, Contreas, G., Nisticò, L, Iafusco, D, Galderisi, A, Fagnani, C, Cotichini, R, Toccaceli, V, Stazi, Ma, and the Study Group on Diabetes of the Italian Society of Pediatric Endocrinology and, Diabetology
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Adult ,Male ,Endocrinology, Diabetes and Metabolism ,Biochemistry ,Endocrinology ,Clinical Biochemistry ,Biochemistry (medical) ,medicine.medical_specialty ,Adolescent ,Child ,Child, Preschool ,Diabetes Mellitus, Type 1 ,Environment ,Female ,Humans ,Infant ,Kaplan-Meier Estimate ,Twins, Dizygotic ,Twins, Monozygotic ,Genetic Predisposition to Disease ,type 1 diabetes ,Concordance ,Population ,Twins ,Context (language use) ,Monozygotic ,Internal medicine ,Diabetes mellitus ,Diabetes Mellitus ,Dizygotic ,medicine ,Preschool ,education ,Type 1 diabetes ,education.field_of_study ,business.industry ,medicine.disease ,Twin study ,Zygosity ,Diabetes and Metabolism ,Cohort ,Environmental Exposures ,business ,Type 1 - Abstract
Context:The incidence of type 1 diabetes has been increasing over time.Objective:We estimated the genetic and environmental components of type 1 diabetes susceptibility in a twin cohort of recent-onset cases to explore the sources of changing disease epidemiology.Design:We linked the population-based Italian Twin Registry with 14803 type 1 diabetes records from 36 pediatric diabetes care centers throughout Italy, except Sardinia, and identified 173 diabetic twins. Patients were positive for at least one autoantibody to islet cell, glutamate decarboxylase, tyrosine phosphatase, insulin, or zinc transporter 8 and were insulin dependent since their diagnosis. Zygosity was determined by DNA genotyping or by questionnaire.Outcome Measures:We estimated proband-wise concordance, cotwin recurrence risk with Kaplan-Meier method, and genetic and environmental proportions of susceptibility variance by structural equation models.Results:We recruited 104 diabetic twins (53 males) from 88 pairs (34 monozygotic, 54 dizygotic) and one triplet. The mean age at diagnosis was 8.1 yr (range 1.1-20.5 yr), and the median year of diagnosis was 2002. Proband-wise concordances were 45.5 and 16.4% in monozygotic and dizygotic pairs (P = 0.01). Recurrence risks in monozygotic and dizygotic cotwins were 37 and 12% after 10 yr from the proband's diagnosis (P = 0.005). Genetic contribution to type 1 diabetes susceptibility was 40% (95% confidence interval 8-78), and the shared and individual-specific environmental components were 51% (14-77) and 9% (4-19), respectively.Conclusions:In addition to the moderate genetic effects on type 1 diabetes susceptibility, our results draw attention to the substantial shared environmental effects, suggesting that exposures in fetal or early postnatal life may contribute to the increasing incidence of the disease.
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- 2012
18. Permanent diabetes during the first year of life: multiple gene screening in 54 patients
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Russo, L, Iafusco, D, Brescianini, S, Nocerino, V, Bizzarri, C, Toni, S, Cerutti, F, Monciotti, C, Pesavento, R, Iughetti, L, Bernanrdini, L, Bonfanti, R, Gargantini, L, Vanelli, M, AGUILAR BRYAN, L, Stazi, Ma, Grasso, V, Colombo, C, Barbetti, F, the EARLY DIABETES STUDY GROUP LERA, R, Cherubini, V, Fifi, Ar, Torelli, C, Frezza, E, Cavallo, L, Zucchini, S, Pasquino, B, Kaufmann, P, Frongia, P, Zedda, N, Ripoli, C, LA LOGGIA, A, LO PRESTI, D, Pocecco, M, Chiarelli, F, Tumini, S, DEL DONNO, M, DE MARCO MR, Lenzi, L, Lorini, R, D'Annunzio, G, Lombardo, F, Meschi, F, Franzese, A, Buono, P, Prisco, F, Cadario, F, Cardella, F, Calcaterra, V, DE GIORGI, G, Federico, Giovanni, Cappa, M, Sulli, N, MANCA BITTI ML, Delvecchio, M, Cotellessa, M, Rabbone, I, Cauvin, V, Bellizzi, M, Tonini, G, Salvatoni, A, and Pinelli, L.
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- 2011
19. The Italian National Survey for Prader-Willi syndrome: an epidemiologic study
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Grugni, G, Crinò, A, Bosio, L, Corrias, A, Cuttini, M, DE TONI, T, DI BATTISTA, E, Franzese, A, Gargantini, L, Greggio, N, Iughetti, Lorenzo, Livieri, C, Naselli, A, Pagano, C, Pozzan, G, Ragusa, L, Salvatoni, A, Trifirò, G, Beccaria, L, Bellizzi, M, Bellone, J, Brunani, A, Cappa, M, Caselli, G, Cerioni, V, Delvecchio, M, Giardino, D, Iannì, F, Memo, L, Pilotta, A, Pomara, C, Radetti, G, Sacco, M, Sanzari, A, Sartorio, A, Tonini, G, Vettor, R, Zaglia, F, Chiumello, G, and GENETIC OBESITY STUDY GROUP OF ITALIAN SOCIETY OF PEDIATRIC ENDOCRINOLOGY AND DIABETOLOGY ISPED
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Adult ,Male ,obesity ,congenital, hereditary, and neonatal diseases and abnormalities ,medicine.medical_specialty ,Pediatrics ,Epidemiologic study ,Adolescent ,Body Mass Index ,Chromosome 15 ,death ,Internal medicine ,Epidemiology ,Genetics ,medicine ,Humans ,Obesity ,Child ,Genetics (clinical) ,In Situ Hybridization, Fluorescence ,Cause of death ,Chromosomes, Human, Pair 15 ,business.industry ,Mortality rate ,Prader-Willi syndrome ,GH therapy ,nutritional and metabolic diseases ,Respiratory infection ,Infant ,Middle Aged ,medicine.disease ,Death ,Endocrinology ,Italy ,Child, Preschool ,Growth Hormone ,Female ,Risk of death ,business ,Prader-Willi Syndrome ,Prader-Willi syndrome, obesity, GH therapy, death - Abstract
Twenty-five medical centers and the Prader–Willi Syndrome (PWS) Association collaborated on a study which attempted to identify all people with genetically confirmed diagnosis of PWS living in Italy. Investigators of the participating centers contacted PWS subjects and/or their family, filled in a specially developed form with the required data and forwarded this information by email. The study identified 425 subjects (209 males and 216 females, between the ages of 0.4–46.7). Two hundred thirty-eight patients had del15, 104 had UPD15, 4 demonstrated a translocation affecting chromosome 15 and 79 showed a positive methylation test. There were fewer subjects found over the age of 35, probably due to the low rate of identification of older PWS patients as well as the high mortality rate. There were a greater number of male children and adolescents with PWS whilst, amongst adults, there were more females. As expected, the majority of subjects with PWS were obese, especially in adult life. Nevertheless, it is noteworthy that 26% of patients aged between 6 and 17 were normal weight. A total of 212 subjects had received GH treatment, of which 141 were still receiving therapy, while the remaining 71 had stopped. In children and adolescents (233 cases), 89 subjects had never undergone GH therapy. Eighteen PWS patients had died in the past 20 years. Obesity-related cardiovascular and respiratory diseases were the cause of death, both during childhood and after 18 years of age. Three children died suddenly whilst undergoing GH therapy. Respiratory infection and cardiac illness were the causes of death in two cases. There was no definitive cause of death found in the third case. Overall, there was no increase in number of deaths during GH treatment, suggesting that GH administration in patients with PWS, as a group, does not increase the risk of death. © 2008 Wiley-Liss, Inc.
- Published
- 2008
20. Mortalità e fattori di rischio nella sindrome di Prader-Willi
- Author
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Grugni, G, Crin, A, Bosio, L, Cappa, M, Corrias, A, Cuttini, M, Detoni, T, Dibattista, E, Franzese, A, Gargantini, L, Greggio, N, Iughetti, L, Livieri, C, Naselli, A, Pagano, C, Pilotta, A, Pozzan, G, Radetti, G, Ragusa, L, Salvatoni, Alessandro, Sartorio, A, Tonini, G, Trifir, G, Beccaria, L, Bellizzi, M, Caselli, G, Cerioni, V, DEL VECCHIO, M, Jann, F, Memo, L, Pomara, C, Sanzari, A, Sacco, M, Vettor, R, Zaglia, F, and Chiumello, G.
- Published
- 2007
21. Memory Impairment and Painful Side
- Author
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Puca, F. M., primary, Antonaci, F., additional, Savarese, M., additional, Covelli, V., additional, Tarascio, G., additional, Bellizzi, M., additional, Lamorgese, C., additional, Musmeci, G. M., additional, and Sorrento, G., additional
- Full Text
- View/download PDF
22. Attenuation of Microglial Activation Protects Hippocampal Synapses in Experimental Autoimmune Encephalomyelitis (P05.112)
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Bellizzi, M., primary and Gelbard, H., additional
- Published
- 2012
- Full Text
- View/download PDF
23. Nutrition Policies in Western Europe: National Policies in Belgium, the Netherlands, France, Ireland, and the United Kingdom
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James, W.P.T., primary, Ralph, A., additional, and Bellizzi, M., additional
- Published
- 2009
- Full Text
- View/download PDF
24. Nutrition Policies in Mediterranean Europe
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Serra-Majem, L., primary, Ferro-Luzzi, A., additional, Bellizzi, M., additional, and Salleras, L., additional
- Published
- 2009
- Full Text
- View/download PDF
25. PO.22 VALUE OF PSYCHOMETRIC AND NEUROPHYSIOLOGICAL TESTS FOR THE DETECTION OF MINIMAL HEPATIC ENCEPHALOPATHY IN CIRRHOTICS
- Author
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Antonicelli, D., primary, Francavilla, T., additional, Difruscolo, O., additional, Bellizzi, G., additional, Barone, M., additional, Rendina, M., additional, Bucci, A., additional, Bellizzi, M., additional, DiLeo, A., additional, and Francavilla, A., additional
- Published
- 2008
- Full Text
- View/download PDF
26. Obesità essenziale Proposta di cartella clinica in età pediatrica
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Cerutti, M., De Simone, M., Monetti, N., Corrias, A., Rusconi, R., Gastaldi, R., Salvatoni, Alessandro, Vido, L., Maffeis, C., Peverelli, P., Crinò, A., Tonini, G., Degiorgi, G., Iughetti, L., Grassi, R., Balsamo, A., Livieri, C., Gobio Casali, L., Brambilla, P., Uasone, R., Cuccarolo, G., De Toni, T., Riganti, G., Antonello, I., Pinelli, L., Sposito, M., Bernasconi, S., Bellizzi, M., Lorini, R., Fontana, F., and Chiumello, G.
- Published
- 1992
27. Synaptic activity becomes excitotoxic in neurons exposed to elevated levels of platelet-activating factor
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Bellizzi, M. J., primary
- Published
- 2005
- Full Text
- View/download PDF
28. WALKING ENERGETICS
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Weyand, P G., primary, Ty, J M., additional, Patek, E R., additional, Bellizzi, M J., additional, and Wright, S, additional
- Published
- 2003
- Full Text
- View/download PDF
29. Angular correlations and internal conversion coefficients of γ-ray transitions in104Pd
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Bellizzi, M. E., primary, Giannatiempo, A., additional, Nannini, A., additional, Perego, A., additional, and Sona, P., additional
- Published
- 2001
- Full Text
- View/download PDF
30. Effects of antioxidants on vascular health
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Duthie, G. G, primary and Bellizzi, M. C, additional
- Published
- 1999
- Full Text
- View/download PDF
31. Manuale Opere provvisionali. L'intervento tecnico urgente in emergenza sismica
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Stefano Grimaz, Barazza, Fausto, Bellizzi, M., Bolognese, C., Cavriani, M., Caciolai, M., D Odorico, A., Maiolo, A., Petra Malisan, Mannino, E., Moretti, A., Munaro, L., and Ponticelli, L.
32. Vademecum STOP. Schede tecniche delle opere provvisionali per la messa in sicurezza post-sisma da parte dei Vigili del Fuoco
- Author
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Stefano Grimaz, Barazza, Fausto, Bellizzi, M., Bolognese, C., Cavriani, M., Caciolai, M., D Odorico, A., Maiolo, A., Petra Malisan, Mannino, E., Moretti, A., Munaro, L., and Ponticelli, L.
33. Establishing a standard definition for child overweight and obesity worldwide: International survey
- Author
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Cole, T. J., Bellizzi, M. C., Katherine Flegal, and Dietz, W. H.
- Subjects
GeneralLiterature_MISCELLANEOUS ,Science & Technology, Life Sciences & Biomedicine, Medicine, General & Internal, General & Internal Medicine, BODY-MASS INDEX, CARDIOVASCULAR RISK, YOUNG-ADULTS, ADOLESCENTS
34. Different short term effects of a short and a long acting LHRH analogue. Endocrinological and ultrasonographic study | CONFRONTO A BREVE TERMINE DEL TRATTAMENTO DELLA PUBERTA PRECOCE CON DUE DIVERSI ANTAGONISTI DELL'LHRH (BUSERELIN E TRIPTORELINA A CESSIONE PROTRATTA). STUDIO ENDOCRINOLOGICO ED ECOGRAFICO
- Author
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Cicognani, A., Cacciari, E., Antonio Balsamo, Cassio, A., Papasodero, A., Bellizzi, M., Guacci, P., and Zappulla, F.
35. Clinical and Brain Imaging Findings in a Child with Vitamin B12 Deficiency
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Francesca Incandela, Maria Bellizzi, Roberto Franceschi, Paola Feraco, Cesare Gagliardo, Feraco, Paola, Incandela, Francesca, Franceschi, Roberto, Gagliardo, Cesare, Bellizzi, Maria, Feraco P., Incandela F., Franceschi R., Gagliardo C., and Bellizzi M.
- Subjects
Pediatrics ,medicine.medical_specialty ,Malabsorption ,magnetic resonance imaging (MRI) ,business.industry ,Settore MED/37 - Neuroradiologia ,nutritional and metabolic diseases ,Case Report ,Vegan Diet ,vitamin B12 ,medicine.disease ,RJ1-570 ,Atrophy ,Neuroimaging ,Failure to thrive ,Medicine ,Brain magnetic resonance imaging ,Vitamin B12 ,medicine.symptom ,business ,After treatment ,brain atrophy - Abstract
Vitamin B12 (Vit-B12) deficiency is a rare and treatable cause of failure to thrive and delayed development in infants who are exclusively breastfed. Apart from genetic causes, it can be related to a malabsorption syndrome or when the mother follows a strict vegetarian or vegan diet, causing a low hepatic storage of Vit-B12 in the infant at birth. As the neurological symptoms are nonspecific, a brain magnetic resonance imaging (MRI) exam is usually performed to rule out primary causes of neurodevelopmental delay. Findings related to brain atrophy are usually observed. A favorable response is achieved with Vit-B12 therapy, and neurological symptoms dramatically improve within a few days after the treatment. We present the case of an infant with severe Vit-B12 deficiency, exclusively breastfed by his young vegan mother, and whose clinical symptoms together with MRI findings improved after treatment. Brain atrophy recovery after Vit-B12 therapy has been seldom documented.
- Published
- 2021
36. A young boy with ventricular arrhythmias and thyroid dysgenesis: two genes are not enough?
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Franceschi R, Maines E, Bellizzi M, Rivieri F, Bacca A, Filippi A, Valente EM, Plumari M, Soffiati M, Vincenzi M, Teofoli F, and Camilot M
- Subjects
- Male, Humans, Phenotype, Arrhythmias, Cardiac, Mutation, Intellectual Disability, Congenital Hypothyroidism diagnosis, Thyroid Dysgenesis genetics
- Abstract
Congenital hypothyroidism (CH) may be caused by biallelic variants in the TSHR gene. CH due to thyroid dysgenesis has also been linked to pathogenic variants of the nucleotide kinase 2, homeobox 5 (NKX2-5) gene, which can also cause sudden cardiac death from ventricular arrhythmia. In particular, the NKX2-5 p.Arg25Cys missense variant has been repeatedly reported in patients with congenital heart defects and, more rarely, with hypogonadism. We report the case of a 7 year old boy with ventricular arrhythmias, thyroid dysgenesis and intellectual disability, born from consanguineous Tunisian parents. Exome sequencing and segregation analysis revealed two potentially relevant variants: the NKX2-5 p.Arg25Cys variant (maternally inherited), as well as a single heterozygous TSHR p.Gln90Pro variant (paternally inherited). Of note, a male sibling of the proband, presenting with intellectual disability only, carried the same two variants. No other TSHR variants, or other potentially relevant variants were identified. In this proband, despite the identification of variants in two genes potentially correlated to the phenotype, a definite genetic diagnosis could not be reached. This case report highlights the complexity of exome data interpretation, especially when dealing with families presenting complex phenotypes and variable expression of clinical traits.
- Published
- 2023
- Full Text
- View/download PDF
37. Seronegative phenotype in a pediatric population with Hashimoto's thyroiditis.
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Rizzardi C, Franceschi R, Cauvin V, Bellizzi M, Liguori A, Longhi S, Lupi F, Soffiati M, and Radetti G
- Subjects
- Adolescent, Child, Humans, Overweight, Phenotype, Thyrotropin, Hashimoto Disease diagnosis, Hashimoto Disease epidemiology, Hypothyroidism, Pediatric Obesity
- Abstract
Purpose: The aim was to verify in a pediatric population with Hashimoto's thyroiditis whether there is a relationship between antithyroid antibodies and inflammatory status on thyroid ultrasound and thyroid function., Subjects and Methods: A total of 154 children and adolescents, aged 4 to 18 years, diagnosed with Hashimoto's thyroiditis with normal body weight were followed up for 1 year., Results: Patients with only antiperoxidase antibodies presented with higher TSH levels than subjects with only antithyroglobulin antibodies (p 0.027) but with similar FT4 levels and thyroid score. Prevalence of seronegative Hashimoto's thyroiditis in this cohort was 12.3% (19/154). At diagnosis, the seronegative group presented with lower prevalence of overt hypothyroidism, symptoms of hypothyroidism, and thyroid score, meaning less severe thyroid involvement. In contrast, similar TSH and FT4 values were found at diagnosis and during follow-up in both the seronegative and seropositive groups. A comparison between patients with seronegative Hashimoto's thyroiditis and an overweight/obese antibody-negative population, who presented superimposable altered parenchymal pattern on thyroid ultrasound without circulating antithyroid antibodies, presented similar clinical data., Conclusion: We report for the first time in the literature that seronegative Hashimoto's thyroiditis in the pediatric age group has a less severe pattern. The seronegative group presents similar characteristics to those of overweight/obese children and adolescents with ultrasound changes, but, according to the established knowledge, the latter condition is reversible and does not need follow-up examinations., (© 2022. Hellenic Endocrine Society.)
- Published
- 2022
- Full Text
- View/download PDF
38. Clinical and Brain Imaging Findings in a Child with Vitamin B12 Deficiency.
- Author
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Feraco P, Incandela F, Franceschi R, Gagliardo C, and Bellizzi M
- Abstract
Vitamin B12 (Vit-B12) deficiency is a rare and treatable cause of failure to thrive and delayed development in infants who are exclusively breastfed. Apart from genetic causes, it can be related to a malabsorption syndrome or when the mother follows a strict vegetarian or vegan diet, causing a low hepatic storage of Vit-B12 in the infant at birth. As the neurological symptoms are nonspecific, a brain magnetic resonance imaging (MRI) exam is usually performed to rule out primary causes of neurodevelopmental delay. Findings related to brain atrophy are usually observed. A favorable response is achieved with Vit-B12 therapy, and neurological symptoms dramatically improve within a few days after the treatment. We present the case of an infant with severe Vit-B12 deficiency, exclusively breastfed by his young vegan mother, and whose clinical symptoms together with MRI findings improved after treatment. Brain atrophy recovery after Vit-B12 therapy has been seldom documented.
- Published
- 2021
- Full Text
- View/download PDF
39. Generalized Arterial Calcification of Infancy Type 1 (GACI1): Identification of a Novel Pathogenic Variant (c.1715T>C (p.Leu572Ser)).
- Author
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Bulfamante GP, Carpenito L, Bragantini E, Graziani S, Bellizzi M, Bagowski CP, Shoukier M, Rivieri F, Soffiati M, and Barbareschi M
- Abstract
Generalized Arterial Calcification of Infancy (GACI) is a rare disease inherited in a recessive manner, with severe and diffuse early onset of calcifications along the internal elastic lamina in large and medium size arteries. The diagnosis results are from clinical manifestations, imaging, histopathologic exams, and genetic tests. GACI is predominantly caused by biallelic pathogenic variant in the ENPP1 gene (GACI1, OMIM#208000) and, to a lesser extent, by pathogenic variants in the ABCC6 gene (GACI2, OMIM#614473). We present a novel variation in the ENPP1 gene identified in a patient clinically diagnosed with GACI and confirmed by genetic investigation and autopsy as GACI type 1. The sequence analysis of the patient's ENPP1 gene detected two heterozygous variants c.1412A>G (p.Tyr471Cys) and c.1715T>C (p.Leu572Ser). The variant c.1715T>C (p.Leu572Ser) has not been described yet in the literature and in mutation databases. A genetic analysis was also carried out for the parents of the newborn; the heterozygous pathogenic variant c.1412A>G (p.Tyr471Cys) was detected in the mother's ENPP1 gene, and a sequence analysis of the father's ENPP1 gene revealed the novel heterozygous variant c.1715T>C (p.Leu572Ser) . Our results showed that the variant c.1715T>C (p.Leu572Ser) may have a pathogenic role in the development of GACI type1 (GACI1, OMIM#208000), at least when associated with the pathogenic c.1412A>G (p.Tyr471Cys) variant. The identification of novel mutations potentially enabled genotype/phenotype associations that will ultimately have an impact on clinical management and prognosis for the disease.
- Published
- 2021
- Full Text
- View/download PDF
40. Two VOZ transcription factors link an E3 ligase and an NLR immune receptor to modulate immunity in rice.
- Author
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Wang J, Wang R, Fang H, Zhang C, Zhang F, Hao Z, You X, Shi X, Park CH, Hua K, He F, Bellizzi M, Xuan Vo KT, Jeon JS, Ning Y, and Wang GL
- Subjects
- Gene Expression Regulation, Plant, Gene Silencing, Magnaporthe physiology, Models, Biological, Oryza genetics, Oryza microbiology, Plant Diseases microbiology, Protein Binding, Proteolysis, Repressor Proteins metabolism, Trans-Activators metabolism, NLR Proteins metabolism, Oryza immunology, Plant Immunity, Plant Proteins metabolism, Receptors, Immunologic metabolism, Transcription Factors metabolism, Ubiquitin-Protein Ligases metabolism
- Abstract
Nucleotide-binding leucine-rich repeat (NLR) proteins play critical roles in plant immunity. However, how NLRs are regulated and activate defense signaling is not fully understood. The rice (Oryza sativa) NLR receptor Piz-t confers broad-spectrum resistance to the fungal pathogen Magnaporthe oryzae and the RING-type E3 ligase AVRPIZ-T INTERACTING PROTEIN 10 (APIP10) negatively regulates Piz-t accumulation. In this study, we found that APIP10 interacts with two rice transcription factors, VASCULAR PLANT ONE-ZINC FINGER 1 (OsVOZ1) and OsVOZ2, and promotes their degradation through the 26S proteasome pathway. OsVOZ1 displays transcriptional repression activity while OsVOZ2 confers transcriptional activation activity in planta. The osvoz1 and osvoz2 single mutants display modest but opposite M. oryzae resistance in the non-Piz-t background. However, the osvoz1 osvoz2 double mutant exhibits strong dwarfism and cell death, and silencing of both genes via RNA interference also leads to dwarfism, mild cell death, and enhanced resistance to M. oryzae in the non-Piz-t background. Both OsVOZ1 and OsVOZ2 interact with Piz-t. Double silencing of OsVOZ1 and OsVOZ2 in the Piz-t background decreases Piz-t protein accumulation and transcription, reactive oxygen species-dependent cell death, and resistance to M. oryzae containing AvrPiz-t. Taken together, these results indicate that OsVOZ1 and OsVOZ2 negatively regulate basal defense but contribute positively to Piz-t-mediated immunity., (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2021
- Full Text
- View/download PDF
41. A fungal effector and a rice NLR protein have antagonistic effects on a Bowman-Birk trypsin inhibitor.
- Author
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Zhang C, Fang H, Shi X, He F, Wang R, Fan J, Bai P, Wang J, Park CH, Bellizzi M, Zhou X, Wang GL, and Ning Y
- Subjects
- NLR Proteins, Plant Diseases, Plant Proteins genetics, Trypsin Inhibitors, Magnaporthe, Oryza genetics
- Abstract
Bowman-Birk trypsin inhibitors (BBIs) play important roles in animal and plant immunity, but how these protease inhibitors are involved in the immune system remains unclear. Here, we show that the rice (Oryza sativa) BBI protein APIP4 is a common target of a fungal effector and an NLR receptor for innate immunity. APIP4 exhibited trypsin inhibitor activity in vitro and in vivo. Knockout of APIP4 in rice enhanced susceptibility, and overexpression of APIP4 increased resistance to the fungal pathogen Magnaporthe oryzae. The M. oryzae effector AvrPiz-t interacted with APIP4 and suppressed APIP4 trypsin inhibitor activity. By contrast, the rice NLR protein Piz-t interacted with APIP4, enhancing APIP4 transcript and protein levels, and protease inhibitor activity. Our findings reveal a novel host defence mechanism in which a host protease inhibitor targeted by a fungal pathogen is protected by an NLR receptor., (© 2020 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.)
- Published
- 2020
- Full Text
- View/download PDF
42. A CRISPR/dCas9 toolkit for functional analysis of maize genes.
- Author
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Gentzel IN, Park CH, Bellizzi M, Xiao G, Gadhave KR, Murphree C, Yang Q, LaMantia J, Redinbaugh MG, Balint-Kurti P, Sit TL, and Wang GL
- Abstract
Background: The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 system has become a powerful tool for functional genomics in plants. The RNA-guided nuclease can be used to not only generate precise genomic mutations, but also to manipulate gene expression when present as a deactivated protein (dCas9)., Results: In this study, we describe a vector toolkit for analyzing dCas9-mediated activation (CRISPRa) or inactivation (CRISPRi) of gene expression in maize protoplasts. An improved maize protoplast isolation and transfection method is presented, as well as a description of dCas9 vectors to enhance or repress maize gene expression., Conclusions: We anticipate that this maize protoplast toolkit will streamline the analysis of gRNA candidates and facilitate genetic studies of important trait genes in this transformation-recalcitrant plant., Competing Interests: Competing interestsThe authors declare that they have no competing interests., (© The Author(s) 2020.)
- Published
- 2020
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- View/download PDF
43. Role of lysine residues of the Magnaporthe oryzae effector AvrPiz-t in effector- and PAMP-triggered immunity.
- Author
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Bai P, Park CH, Shirsekar G, Songkumarn P, Bellizzi M, and Wang GL
- Subjects
- Disease Resistance immunology, Fungal Proteins chemistry, Fungal Proteins immunology, Magnaporthe metabolism, Oryza immunology, Plant Diseases microbiology, Plant Immunity immunology, Plant Proteins genetics, Plant Proteins immunology, Plant Proteins metabolism, Fungal Proteins metabolism, Lysine chemistry, Magnaporthe immunology, Magnaporthe pathogenicity, Oryza metabolism, Oryza microbiology
- Abstract
Magnaporthe oryzae is an important fungal pathogen of both rice and wheat. However, how M. oryzae effectors modulate plant immunity is not fully understood. Previous studies have shown that the M. oryzae effector AvrPiz-t targets the host ubiquitin-proteasome system to manipulate plant defence. In return, two rice ubiquitin E3 ligases, APIP6 and APIP10, ubiquitinate AvrPiz-t for degradation. To determine how lysine residues contribute to the stability and function of AvrPiz-t, we generated double (K1,2R-AvrPiz-t), triple (K1,2,3R-AvrPiz-t) and lysine-free (LF-AvrPiz-t) mutants by mutating lysines into arginines in AvrPiz-t. LF-AvrPiz-t showed the highest protein accumulation when transiently expressed in rice protoplasts. When co-expressed with APIP10 in Nicotiana benthamiana, LF-AvrPiz-t was more stable than AvrPiz-t and was less able to degrade APIP10. The avirulence of LF-AvrPiz-t on Piz-t:HA plants was less than that of AvrPiz-t, which led to resistance reduction and lower accumulation of the Piz-t:HA protein after inoculation with the LF-AvrPiz-t-carrying isolate. Chitin- and flg22-induced production of reactive oxygen species (ROS) was higher in LF-AvrPiz-t than in AvrPiz-t transgenic plants. In addition, LF-AvrPiz-t transgenic plants were less susceptible than AvrPiz-t transgenic plants to a virulent isolate. Furthermore, both AvrPiz-t and LF-AvrPiz-t interacted with OsRac1, but the suppression of OsRac1-mediated ROS generation by LF-AvrPiz-t was significantly lower than that by AvrPiz-t. Together, these results suggest that the lysine residues of AvrPiz-t are required for its avirulence and virulence functions in rice., (© 2018 The Authors. Molecular Plant Pathology Published by BSPP and John Wiley & Sons Ltd.)
- Published
- 2019
- Full Text
- View/download PDF
44. The Monocot-Specific Receptor-like Kinase SDS2 Controls Cell Death and Immunity in Rice.
- Author
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Fan J, Bai P, Ning Y, Wang J, Shi X, Xiong Y, Zhang K, He F, Zhang C, Wang R, Meng X, Zhou J, Wang M, Shirsekar G, Park CH, Bellizzi M, Liu W, Jeon JS, Xia Y, Shan L, and Wang GL
- Subjects
- Gene Expression Regulation, Plant, Gene Regulatory Networks, Apoptosis, Magnaporthe immunology, Oryza physiology, Plant Diseases immunology, Plant Immunity, Protein Kinases metabolism
- Abstract
Programmed cell death (PCD) plays critical roles in plant immunity but must be regulated to prevent excessive damage. The E3 ubiquitin ligase SPL11 negatively regulates PCD and immunity in plants. We show that SPL11 cell-death suppressor 2 (SDS2), an S-domain receptor-like kinase, positively regulates PCD and immunity in rice by engaging and regulating SPL11 and related kinases controlling defense responses. An sds2 mutant shows reduced immune responses and enhanced susceptibility to the blast fungus Magnaporthe oryzae. Conversely, SDS2 over-expression induces constitutive PCD accompanied by elevated immune responses and enhanced resistance to M. oryzae. SDS2 interacts with and phosphorylates SPL11, which in turn ubiquitinates SDS2, leading to its degradation. In addition, SDS2 interacts with related receptor-like cytoplasmic kinases, OsRLCK118/176, that positively regulate immunity by phosphorylating the NADPH oxidase OsRbohB to stimulate ROS production. Thus, a plasma membrane-resident protein complex consisting of SDS2, SPL11, and OsRLCK118/176 controls PCD and immunity in rice., (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
45. Mild Encephalitis/Encephalopathy with Reversible Splenial Lesion (MERS) due to Cytomegalovirus: Case Report and Review of the Literature.
- Author
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Feraco P, Porretti G, Marchiò G, Bellizzi M, and Recla M
- Subjects
- Anticonvulsants therapeutic use, Antiviral Agents therapeutic use, Brain Diseases diagnostic imaging, Brain Diseases drug therapy, Brain Diseases virology, Corpus Callosum diagnostic imaging, Corpus Callosum drug effects, Corpus Callosum virology, Cytomegalovirus Infections diagnostic imaging, Cytomegalovirus Infections drug therapy, Electroencephalography, Encephalitis diagnostic imaging, Encephalitis drug therapy, Encephalitis virology, Humans, Infant, Magnetic Resonance Imaging, Male, Brain Diseases etiology, Corpus Callosum pathology, Cytomegalovirus pathogenicity, Cytomegalovirus Infections complications, Encephalitis etiology
- Abstract
Mild encephalopathy with a reversible splenial lesion (MERS) is a clinico-radiological syndrome characterized by a transient mild encephalopathy and MRI findings of a reversible lesion in the splenium of corpus callosum (SCC). It is classified in MERS type I and MERS type II, depending on the involvement of SCC alone or also other white matter areas. The syndrome mainly affects children and young adults; the prognosis is favorable with complete or nearly complete neurological and radiological resolution within days or weeks. The vast majority of the cases described in the literature involve Asian and Australian children. The exact pathophysiology is unknown; however, infectious-related MERS (in particular virus associated MERS) remains the most common cause of reversible splenial lesions in childhood. To the best of our knowledge, there is only one published case of MERS associated with cytomegalovirus (CMV) infection involving an Australian child. We present here the first case of a CMV-related MERS in a European Caucasian child., Competing Interests: Conflict of Interest: No conflict of interest is declared by all authors., (Georg Thieme Verlag KG Stuttgart · New York.)
- Published
- 2018
- Full Text
- View/download PDF
46. Genotyping-by-Sequencing-Based Genetic Analysis of African Rice Cultivars and Association Mapping of Blast Resistance Genes Against Magnaporthe oryzae Populations in Africa.
- Author
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Mgonja EM, Park CH, Kang H, Balimponya EG, Opiyo S, Bellizzi M, Mutiga SK, Rotich F, Ganeshan VD, Mabagala R, Sneller C, Correll J, Zhou B, Talbot NJ, Mitchell TK, and Wang GL
- Subjects
- Africa, Phylogeny, Quantitative Trait Loci, Genotype, Magnaporthe physiology, Oryza genetics, Oryza immunology, Plant Diseases immunology, Plant Diseases microbiology
- Abstract
Understanding the genetic diversity of rice germplasm is important for the sustainable use of genetic materials in rice breeding and production. Africa is rich in rice genetic resources that can be utilized to boost rice productivity on the continent. A major constraint to rice production in Africa is rice blast, caused by the hemibiotrophic fungal pathogen Magnaporthe oryzae. In this report, we present the results of a genotyping-by-sequencing (GBS)-based diversity analysis of 190 African rice cultivars and an association mapping of blast resistance (R) genes and quantitative trait loci (QTLs). The 190 African cultivars were clustered into three groups based on the 184K single nucleotide polymorphisms generated by GBS. We inoculated the rice cultivars with six African M. oryzae isolates. Association mapping identified 25 genomic regions associated with blast resistance (RABRs) in the rice genome. Moreover, PCR analysis indicated that RABR_23 is associated with the Pi-ta gene on chromosome 12. Our study demonstrates that the combination of GBS-based genetic diversity population analysis and association mapping is effective in identifying rice blast R genes/QTLs that contribute to resistance against African populations of M. oryzae. The identified markers linked to the RABRs and 14 highly resistant cultivars in this study will be useful for rice breeding in Africa.
- Published
- 2017
- Full Text
- View/download PDF
47. A Chemical-Induced, Seed-Soaking Activation Procedure for Regulated Gene Expression in Rice.
- Author
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Chen Z, Cheng Q, Hu C, Guo X, Chen Z, Lin Y, Hu T, Bellizzi M, Lu G, Wang GL, Wang Z, Chen S, and Wang F
- Abstract
Inducible gene expression has emerged as a powerful tool for plant functional genomics. The estrogen receptor-based, chemical-inducible system XVE has been used in many plant species, but the limited systemic movement of inducer β-estradiol in transgenic rice plants has prohibited a wide use of the XVE system in this important food crop. Here, we constructed an improved chemical-regulated, site-specific recombination system by employing the XVE transactivator in combination with a Cre/ loxP -FRT system, and optimized a seed-soaking procedure for XVE induction in rice. By using a gus gene and an hpRNAi cassette targeted for OsPDS as reporters, we demonstrated that soaking transgenic seeds with estradiol solution could induce highly efficient site-specific recombination in germinating embryos, resulting in constitutive and high-level expression of target gene or RNAi cassette in intact rice plants from induced seeds. The strategy reported here thereby provides a useful gene activation approach for effectively regulating gene expression in rice.
- Published
- 2017
- Full Text
- View/download PDF
48. Genome-Wide Association Mapping of Rice Resistance Genes Against Magnaporthe oryzae Isolates from Four African Countries.
- Author
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Mgonja EM, Balimponya EG, Kang H, Bellizzi M, Park CH, Li Y, Mabagala R, Sneller C, Correll J, Opiyo S, Talbot NJ, Mitchell T, and Wang GL
- Subjects
- Africa, Breeding, Chromosome Mapping, Genotype, Oryza immunology, Oryza microbiology, Plant Diseases microbiology, Disease Resistance genetics, Genome-Wide Association Study, Magnaporthe physiology, Oryza genetics, Plant Diseases immunology, Quantitative Trait Loci genetics
- Abstract
Rice blast disease is emerging as a major constraint to rice production in Africa. Although a traditional gene-tagging strategy using biparental crosses can effectively identify resistance (R) genes or quantitative trait loci (QTL) against Magnaporthe oryzae, the mapping procedure required is time consuming and requires many populations to investigate the genetics of resistance. In this report, we conducted a genome-wide association study (GWAS) to rapidly map rice genes conferring resistance against eight M. oryzae isolates from four African countries. We inoculated 162 rice cultivars, which were part of the rice diversity panel 1 (RDP1) and were previously genotyped with the 44,000 single-nucleotide polymorphism (SNP) chip, with the eight isolates. The GWAS identified 31 genomic regions associated with blast resistance (RABR) in the rice genome. In addition, we used polymerase chain reaction analysis to confirm the association between the Pish gene and a major RABR on chromosome 1 that was associated with resistance to four M. oryzae isolates. Our study has demonstrated the power of GWAS for the rapid identification of rice blast R or QTL genes that are effective against African populations of M. oryzae. The identified SNP markers associated with RABR can be used in breeding for resistance against rice blast in Africa.
- Published
- 2016
- Full Text
- View/download PDF
49. Immunity to Rice Blast Disease by Suppression of Effector-Triggered Necrosis.
- Author
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Wang R, Ning Y, Shi X, He F, Zhang C, Fan J, Jiang N, Zhang Y, Zhang T, Hu Y, Bellizzi M, and Wang GL
- Subjects
- Cell Death, Fungal Proteins metabolism, Gene Silencing, Host-Pathogen Interactions, Magnaporthe genetics, Oryza microbiology, Plant Proteins metabolism, Plant Roots growth & development, Plant Roots microbiology, Plant Roots physiology, Fungal Proteins genetics, Magnaporthe physiology, Oryza immunology, Plant Diseases microbiology, Plant Immunity, Plant Proteins genetics
- Abstract
Hemibiotrophic pathogens are some of the most destructive plant pathogens, causing huge economic losses and threatening global food security. Infection with these organisms often involves an initial biotrophic infection phase, during which the pathogen spreads in host tissue asymptomatically, followed by a necrotrophic phase, during which host-cell death is induced. How hemibiotrophic pathogens trigger host necrosis and how plants inhibit the transition from the biotrophic stage to the necrotrophic stage in disease symptom expression are mainly unknown. The rice blast fungus Magnaporthe oryzae spreads in rice biotrophically early during infection, but this biotrophic stage is followed by a pronounced switch to cell death and lesion formation. Here, we show that the M. oryzae effector AvrPiz-t interacts with the bZIP-type transcription factor APIP5 in the cytoplasm and suppresses its transcriptional activity and protein accumulation at the necrotrophic stage. Silencing of APIP5 in transgenic rice leads to cell death, and the phenotype is enhanced by the expression of AvrPiz-t. Conversely, Piz-t interacts with and stabilizes APIP5 to prevent necrosis at the necrotrophic stage. At the same time, APIP5 is essential for Piz-t stability. These results demonstrate a novel mechanism for the suppression of effector-triggered necrosis at the necrotrophic stage by an NLR receptor in plants., (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
50. The E3 Ligase APIP10 Connects the Effector AvrPiz-t to the NLR Receptor Piz-t in Rice.
- Author
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Park CH, Shirsekar G, Bellizzi M, Chen S, Songkumarn P, Xie X, Shi X, Ning Y, Zhou B, Suttiviriya P, Wang M, Umemura K, and Wang GL
- Subjects
- Magnaporthe, Oryza enzymology, Ubiquitination immunology, Oryza microbiology, Plant Diseases microbiology, Ubiquitin-Protein Ligases metabolism
- Abstract
Although nucleotide-binding domain, leucine-rich repeat (NLR) proteins are the major immune receptors in plants, the mechanism that controls their activation and immune signaling remains elusive. Here, we report that the avirulence effector AvrPiz-t from Magnaporthe oryzae targets the rice E3 ligase APIP10 for degradation, but that APIP10, in return, ubiquitinates AvrPiz-t and thereby causes its degradation. Silencing of APIP10 in the non-Piz-t background compromises the basal defense against M. oryzae. Conversely, silencing of APIP10 in the Piz-t background causes cell death, significant accumulation of Piz-t, and enhanced resistance to M. oryzae, suggesting that APIP10 is a negative regulator of Piz-t. We show that APIP10 promotes degradation of Piz-t via the 26S proteasome system. Furthermore, we demonstrate that AvrPiz-t stabilizes Piz-t during M. oryzae infection. Together, our results show that APIP10 is a novel E3 ligase that functionally connects the fungal effector AvrPiz-t to its NLR receptor Piz-t in rice.
- Published
- 2016
- Full Text
- View/download PDF
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