Zobrazeno 1 - 10 of 20 pro vyhledávání: '"Angela Cassese"'
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Akademický článek
Adenoviral gene transfer of PLD1-D4 enhances insulin sensitivity in mice by disrupting phospholipase D1 interaction with PED/PEA-15.
Autor: Angela Cassese, Gregory A Raciti, Francesca Fiory, Cecilia Nigro, Luca Ulianich, Ilenia Castanò, Vittoria D'Esposito, Daniela Terracciano, Lucio Pastore, Pietro Formisano, Francesco Beguinot, Claudia Miele
Publikováno v: PLoS ONE, Vol 8, Iss 4, p e60555 (2013)
Over-expression of phosphoprotein enriched in diabetes/phosphoprotein enriched in astrocytes (PED/PEA-15) causes insulin resistance by interacting with the D4 domain of phospholipase D1 (PLD1). Indeed, the disruption of this association restores insu
Externí odkaz: https://doaj.org/article/2b1b4ecaf1d24ddeaf20405c6094b3dc
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2
Parkinson-like phenotype in insulin-resistant PED/PEA-15 transgenic mice
Autor: Francesca Fiory, Cecilia Nigro, Giuseppe Perruolo, Claudia Miele, Davide Viggiano, Francesco Beguinot, Antonietta Liotti, Angela Cassese, Pietro Formisano
Publikováno v: Scientific Reports
Scientific reports (Nature Publishing Group) 6 (2016): 29967–29967. doi:10.1038/srep29967
info:cnr-pdr/source/autori:Perruolo, Giuseppe; Viggiano, Davide; Fiory, Francesca; Cassese, Angela; Nigro, Cecilia; Liotti, Antonietta; Miele, Claudia; Beguinot, Francesco; Formisano, Pietro/titolo:Parkinson-like phenotype in insulin-resistant PED%2FPEA-15 transgenic mice/doi:10.1038%2Fsrep29967/rivista:Scientific reports (Nature Publishing Group)/anno:2016/pagina_da:29967/pagina_a:29967/intervallo_pagine:29967–29967/volume:6
Neurological abnormalities, such as Parkinson-like disorders (PlD), are often co-morbidities of Type 2 Diabetic (T2D) patients, although the epidemiological link between these two disorders remains controversial. The PED/PEA-15 protein represents a p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e802599ecdb2cf4bcaa0288b4130b634
https://pubmed.ncbi.nlm.nih.gov/27426254
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3
PED/PEA‐15 controls fibroblast motility and wound closure by ERK1/2‐dependent mechanisms
Autor: Ferdinando Giacco, Claudia Miele, Sergio Caserta, Angela Cassese, Francesco Beguinot, Pietro Formisano, Francesco Oriente, Corrado Garbi, Stefano Guido, Valentina Pagliara, Roberta Buonomo, Angela Vasaturo, Giuseppe Perruolo, Gelsomina Mansueto
Publikováno v: Journal of Cellular Physiology
Journal of Cellular Physiology; Vol 227
Journal of Cellular Physiology, 227, 5, pp. 2106-16
Journal of Cellular Physiology, 227, 2106-16
Journal of cellular physiology
(2012).
info:cnr-pdr/source/autori:Buonomo R, Giacco F, Vasaturo A, Caserta S, Guido S, Pagliara V, Garbi C, Mansueto G, Cassese A, Perruolo G, Oriente F, Miele C, Beguinot F, Formisano P./titolo:PED%2FPEA-15 controls fibroblast motility and wound closure by ERK1%2F2-dependent mechanisms./doi:/rivista:Journal of cellular physiology (Print)/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume
Cell migration is dependent on the control of signaling events that play significant roles in creating contractile force and in contributing to wound closure. We evaluated wound closure in fibroblasts from mice overexpressing (TgPED) or lacking ped/p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f53bb37e451c701138c0da7eae2fda8
https://doi.org/10.1002/jcp.22944
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4
Expression of Concern. Prep1 Controls Insulin Glucoregulatory Function in Liver by Transcriptional Targeting of SHP1 Tyrosine Phosphatase. Diabetes 2011;60:138–147. DOI: 10.2337/db10-0860. PMID: 20864515
Autor: Claudia Miele, Francesco Beguinot, Paola Ungaro, Elena Longobardi, Angela Cassese, Francesco Oriente, Salvatore Iovino, Francesco Blasi, Serena Cabaro, Pietro Formisano
Publikováno v: Diabetes. 67:346-347
On the basis of the recommendation of the American Diabetes Association’s Panel on Ethical Scientific Programs (ESP), the American Diabetes Association, the publisher of Diabetes, is issuing this expression of concern to alert readers to questions
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c9c7fb49543f505dde9d3d7ebda19078
https://doi.org/10.2337/db17-ec2017c
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6
Cytotoxicity of dental resin composites: anin vitroevaluation
Autor: Bruno Di Jeso, Pietro Ausiello, Francesco Beguinot, Angela Cassese, Claudia Miele, Franklin Garcia-Godoy, Luca Ulianich
Publikováno v: Journal of Applied Toxicology. 33:451-457
Resin-based dental restorative materials release residual monomers that may affect the vitality of pulp cells. The purpose of this study was to evaluate the cytotoxic effect of two light-cured restorative materials with and without bis-GMA resin, res
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff5522b00402af3e05384adb17252ff1
https://doi.org/10.1002/jat.1765
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7
Prep1 Controls Insulin Glucoregulatory Function in Liver by Transcriptional Targeting of SHP1 Tyrosine Phosphatase
Autor: Francesco Oriente, Claudia Miele, Salvatore Iovino, Francesco Beguinot, Serena Cabaro, Paola Ungaro, Angela Cassese, Francesco Blasi, Pietro Formisano, Elena Longobardi
Publikováno v: Diabetes (N.Y.N.Y.) 60 (2011): 138–147.
info:cnr-pdr/source/autori:Oriente F, Iovino S, Cabaro S, Cassese A, Longobardi E, Miele C, Ungaro P, Formisano P, Blasi F, Beguinot F./titolo:Prep1 controls insulin glucoregulatory function in liver by transcriptional targeting of SHP1 tyrosine phosphatase./doi:/rivista:Diabetes (N.Y.N.Y.)/anno:2011/pagina_da:138/pagina_a:147/intervallo_pagine:138–147/volume:60
Diabetes; Vol 60
OBJECTIVE We investigated the function of the Prep1 gene in insulin-dependent glucose homeostasis in liver. RESEARCH DESIGN AND METHODS Prep1 action on insulin glucoregulatory function has been analyzed in liver of Prep1-hypomorphic mice (Prep1i/i),
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47b9bc412c5cfb907fbbb464502c41c
https://doi.org/10.2337/db10-0860
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8
Overexpression of the ped/pea-15 Gene Causes Diabetes by Impairing Glucose-Stimulated Insulin Secretion in Addition to Insulin Action
Autor: Francesco Oriente, Francesca Fiory, Francesco Beguinot, Anna Perfetti, Chiara Romano, Giovanni Vigliotta, Giancarlo Troncone, Stefania Santopietro, Giuseppe Portella, Maria Alessandra Maitan, Claudia Miele, Cecilia Tiveron, Angela Cassese, Alessandra Trencia, Pietro Formisano, Laura Tatangelo
Publikováno v: Molecular and cellular biology
24 (2004): 5005–5015.
info:cnr-pdr/source/autori:Vigliotta G; Miele C; Santopietro S; Portella G; Perfetti A; Maitan MA; Cassese A; Oriente F; Trencia A; Fiory F; Romano C; Tiveron C; Tatangelo L; Troncone G; Formisano P; Beguinot F./titolo:Overexpression of the ped%2Fpea-15 gene causes diabetes by impairing glucose-stimulated insulin secretion in addition to insulin action./doi:/rivista:Molecular and cellular biology (Print)/anno:2004/pagina_da:5005/pagina_a:5015/intervallo_pagine:5005–5015/volume:24
Type 2 diabetes is a genetically determined disorder, affecting over 150 million people worldwide (35). The pathogenesis of type 2 diabetes is characterized both by insulin resistance in muscle, fat, and liver and by impaired insulin secretion (10, 1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdc57df33eadd00bc8ac8e5a08d2c045
https://doi.org/10.1128/mcb.24.11.5005-5015.2004
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9
Protein Kinase B/Akt Binds and Phosphorylates PED/PEA-15, Stabilizing Its Antiapoptotic Action
Autor: Francesco Oriente, Anna Perfetti, Gerolama Condorelli, Ferdinando Giacco, Alessandra Trencia, Claudia Miele, Francesco Beguinot, Pietro Formisano, Angela Cassese, Stefania Santopietro, Giovanni Vigliotta
Publikováno v: Molecular and cellular biology
23 (2003): 4511–4521.
info:cnr-pdr/source/autori:Trencia A. 1, Perfetti A. 1, Cassese A. 1, Vigliotta G. 1, Miele C. 1, Oriente F. 1, Santopietro S. 1, Giacco F. 1, Condorelli G. 1, Formisano P. 1, Beguinot F. 1/titolo:Protein kinase B%2FAkt binds and phosphorylates PED%2FPEA-15, stabilizing its antiapoptotic action./doi:/rivista:Molecular and cellular biology (Print)/anno:2003/pagina_da:4511/pagina_a:4521/intervallo_pagine:4511–4521/volume:23
The antiapoptotic protein PED/PEA-15 features an Akt phosphorylation motif upstream from Ser(116). In vitro, recombinant PED/PEA-15 was phosphorylated by Akt with a stoichiometry close to 1. Based on Western blotting with specific phospho-Ser(116) PE
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ebc9f9f37531d4c86d3ae6bf369fb5
https://doi.org/10.1128/mcb.23.13.4511-4521.2003
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10
Cytotoxicity of dental resin composites: an in vitro evaluation
Autor: Pietro, Ausiello, Angela, Cassese, Claudia, Miele, Francesco, Beguinot, Franklin, Garcia-Godoy, Bruno, Di Jeso, Luca, Ulianich
Publikováno v: Journal of applied toxicology : JAT. 33(6)
Resin-based dental restorative materials release residual monomers that may affect the vitality of pulp cells. The purpose of this study was to evaluate the cytotoxic effect of two light-cured restorative materials with and without bis-GMA resin, res
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6889b53748fc9f95866cb00743393298
https://pubmed.ncbi.nlm.nih.gov/22120598
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