Arama Sonuçları - Sabrina Prudente

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  1. 1
    Role of insulin resistance in kidney dysfunction: insights into the mechanism and epidemiological evidence

    Role of insulin resistance in kidney dysfunction: insights into the mechanism and epidemiological evidence Yazar: Salvatore De Cosmo, Claudia Menzaghi, Sabrina Prudente, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2012
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  2. 2
    The Mammalian Tribbles Homolog TRIB3, Glucose Homeostasis, and Cardiovascular Diseases

    The Mammalian Tribbles Homolog TRIB3, Glucose Homeostasis, and Cardiovascular Diseases Yazar: Sabrina Prudente, Giorgio Sesti, Assunta Pandolfi, Francesco Andreozzi, Agostino Consoli, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2012
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  3. 3
    The Common −866G/A Polymorphism in the Promoter Region of the UCP-2 Gene Is Associated with Reduced Risk of Type 2 Diabetes in Caucasians from Italy

    The Common −866G/A Polymorphism in the Promoter Region of the UCP-2 Gene Is Associated with Reduced Risk of Type 2 Diabetes in Caucasians from Italy Yazar: Angela Bulotta, Ornella Ludovico, Angelo Coco, Rosa Di Paola, Alessandro Quattrone, Massimo Carella, Fabio Pellegrini, Sabrina Prudente, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2005
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  4. 4
    The Functional Q84R Polymorphism of Mammalian <i>Tribbles</i> Homolog <i>TRB3</i> Is Associated With Insulin Resistance and Related Cardiovascular Risk in Caucasians From Italy

    The Functional Q84R Polymorphism of Mammalian <i>Tribbles</i> Homolog <i>TRB3</i> Is Associated With Insulin Resistance and Related Cardiovascular Risk in Caucasians From Italy Yazar: Sabrina Prudente, Marta Letizia Hribal, Elisabetta Flex, Federica Turchi, Eleonora Morini, Salvatore De Cosmo, Simonetta Bacci, Vittorio Tassi, Marina Cardellini, Renato Lauro, Giorgio Sesti, Bruno Dallapiccola, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2005
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  5. 5
    A Functional Variant of the Adipocyte Glycerol Channel Aquaporin 7 Gene Is Associated With Obesity and Related Metabolic Abnormalities

    A Functional Variant of the Adipocyte Glycerol Channel Aquaporin 7 Gene Is Associated With Obesity and Related Metabolic Abnormalities Yazar: Sabrina Prudente, Elisabetta Flex, Eleonora Morini, Federica Turchi, Daria Capponi, Salvatore De Cosmo, Vittorio Tassi, Valentina Guida, Angelo Avogaro, Franco Folli, Francesca Maiani, Lucia Frittitta, Bruno Dallapiccola, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2007
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  6. 6
    The<i>TRIB3</i>Q84R Polymorphism and Risk of Early-Onset Type 2 Diabetes

    The<i>TRIB3</i>Q84R Polymorphism and Risk of Early-Onset Type 2 Diabetes Yazar: Sabrina Prudente, Daniela Scarpelli, Manisha Chandalia, Yuanyuan Zhang, Eleonora Morini, S Del Guerra, Francesco Perticone, Rong Li, Christine Powers, Francesco Andreozzi, Piero Marchetti, Bruno Dallapiccola, Nicola Abate, Alessandro Doria, Giorgio Sesti, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2008
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  7. 7
    The K121Q Polymorphism of the <i>ENPP1/PC-1</i> Gene Is Associated With Insulin Resistance/Atherogenic Phenotypes, Including Earlier Onset of Type 2 Diabetes and Myocardial Infarction

    The K121Q Polymorphism of the <i>ENPP1/PC-1</i> Gene Is Associated With Insulin Resistance/Atherogenic Phenotypes, Including Earlier Onset of Type 2 Diabetes and Myocardial Infarct... Yazar: Simonetta Bacci, Ornella Ludovico, Sabrina Prudente, Yuanyuan Zhang, Rosa Di Paola, Davide Mangiacotti, Anna Rauseo, David Nolan, Jill Duffy, G. Fini, Lucia Salvemini, Cesare Amico, Carlo Vigna, Fabio Pellegrini, Claudia Menzaghi, Alessandro Doria, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2005
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  8. 8
    Serum Resistin, Cardiovascular Disease and All-Cause Mortality in Patients with Type 2 Diabetes

    Serum Resistin, Cardiovascular Disease and All-Cause Mortality in Patients with Type 2 Diabetes Yazar: Claudia Menzaghi, Simonetta Bacci, Lucia Salvemini, Christine Mendonça, Giuseppe Palladino, Andrea Fontana, Concetta De Bonis, Antonella Marucci, Elizabeth Goheen, Sabrina Prudente, Eleonora Morini, Stefano Rizza, Alyssa Kanagaki, G. Fini, Davide Mangiacotti, Massimo Federici, Salvatore De Cosmo, Fabio Pellegrini, Alessandro Doria, Vincenzo Trischitta

    Baskı/Yayın Bilgisi 2013
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  9. 9
    Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes

    Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes Yazar: Ernesto Maddaloni, Lucia Coraggio, Rocco Amendolara, Marco Giorgio Baroni, Maria Gisella Cavallo, Massimiliano Copetti, Efisio Cossu, Paola D’Angelo, Luca D’Onofrio, Salvatore De Cosmo, Frida Leonetti, Susanna Morano, Lelio Morviducci, Nicola Napoli, Sabrina Prudente, Giuseppe Pugliese, Kyoungmin Park, Rury R. Holman, Vincenzo Trischitta, Raffaella Buzzetti

    Baskı/Yayın Bilgisi 2023
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  10. 10
    Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus

    Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus Yazar: Sabrina Prudente, Prapaporn Jungtrakoon, Antonella Marucci, Ornella Ludovico, Patinut Buranasupkajorn, Tommaso Mazza, Timothy Hastings, Teresa Milano, Eleonora Morini, Luana Mercuri, Diego Bailetti, Christine Mendonça, Federica Alberico, Giorgio Basile, Marta Romani, Elide Miccinilli, Antonio Pizzuti, Massimo Carella, Fabrizio Barbetti, Stefano Pascarella, Piero Marchetti, Vincenzo Trischitta, Rosa Di Paola, Alessandro Doria

    Baskı/Yayın Bilgisi 2015
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  11. 11
    Association Between a Genetic Variant Related to Glutamic Acid Metabolism and Coronary Heart Disease in Individuals With Type 2 Diabetes

    Association Between a Genetic Variant Related to Glutamic Acid Metabolism and Coronary Heart Disease in Individuals With Type 2 Diabetes Yazar: Lu Qi, Qibin Qi, Sabrina Prudente, Christine Mendonça, Francesco Andreozzi, Natalia Di Pietro, Mariella Sturma, Valeria Novelli, Gaia Chiara Mannino, Gloria Formoso, Ernest V. Gervino, Thomas H. Hauser, Jochen D. Muehlschlegel, Monika A. Niewczas, Andrzej S. Królewski, Gianni Biolo, Assunta Pandolfi, Eric B. Rimm, Giorgio Sesti, Vincenzo Trischitta, Frank B. Hu, Alessandro Doria

    Baskı/Yayın Bilgisi 2013
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  12. 12
    Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies

    Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies Yazar: Marcello Niceta, Emilia Stellacci, Karen W. Gripp, Giuseppe Zampino, Maria Kousi, Massimiliano Anselmi, Alice Traversa, Andrea Ciolfi, Deborah L. Stabley, Alessandro Bruselles, Viviana Caputo, Serena Cecchetti, Sabrina Prudente, Maria Teresa Fiorenza, Carla Boitani, Nicole Philip, Dmitriy Niyazov, Chiara Leoni, Takaya Nakane, Kim M. Keppler‐Noreuil, Stephen R. Braddock, Gabriele Gillessen‐Kaesbach, Antonio Palleschi, Philippe M. Campeau, Brendan Lee, Célio Pouponnot, Lorenzo Stella, Gianfranco Bocchinfuso, Nicholas Katsanis, Katia Sol‐Church, Marco Tartaglia

    Baskı/Yayın Bilgisi 2015
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