Search Results - "Scarlato, Guglielmo"

Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for Replication by Michikawa, Yuichi, Mazzucchelli, Franca, Bresolin, Nereo, Scarlato, Guglielmo, Attardi, Giuseppe

“…Progressive damage to mitochondrial DNA (mtDNA) during life is thought to contribute to aging processes. However, this idea has been difficult to reconcile…”
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Cognitive Impairment Without Dementia in Older People: Prevalence, Vascular Risk Factors, Impact on Disability. The Italian Longitudinal Study on Aging by Di Carlo, Antonio, Baldereschi, Marzia, Amaducci, Luigi, Maggi, Stefania, Grigoletto, Francesco, Scarlato, Guglielmo, Inzitari, Domenico

“…OBJECTIVES: To investigate prevalence of “cognitive impairment, no dementia” (CIND) in the Italian older population, evaluating the association with…”
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Intraarterial Injection of Muscle-Derived CD34+Sca-1+ Stem Cells Restores Dystrophin in mdx Mice by Torrente, Yuan, Jacques-P. Tremblay, Pisati, Federica, Belicchi, Marzia, Rossi, Barbara, Sironi, Manuela, Fortunato, Franco, El Fahime, Mostafa, D'Angelo, Maria Grazia, Caron, Nicolas J., Constantin, Gabriela, Paulin, Denise, Scarlato, Guglielmo, Bresolin, Nereo

“…Duchenne muscular dystrophy is a lethal recessive disease characterized by widespread muscle damage throughout the body. This increases the difficulty of cell…”
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Induction of IL-10 in rat peritoneal macrophages and dendritic cells by glatiramer acetate by Jung, Stefan, Siglienti, Ines, Grauer, Oliver, Magnus, Tim, Scarlato, Guglielmo, Toyka, Klaus

“…Glatiramer acetate (GLAT) is a mixture of basic polypeptides that have been shown to suppress experimental autoimmune encephalomyelitis (EAE). As Copaxone®,…”
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Decreased Expression of Myotonin-Protein Kinase Messenger RNA and Protein in Adult Form of Myotonic Dystrophy by Fu, Ying-Hui, Friedman, David L., Richards, Stephen, Pearlman, Joel A., Gibbs, Richard A., Pizzuti, Antonio, Ashizawa, Tetsuo, Perryman, M. Benjamin, Scarlato, Guglielmo, Fenwick, Raymond G., Caskey, C. Thomas

“…The myotonic dystrophy mutation has recently been identified; however, the molecular mechanism of the disease is still unknown. The sequence of the…”
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Protein Zero Is Necessary for E-Cadherin-Mediated Adherens Junction Formation in Schwann Cells by Menichella, Daniela Maria, Arroyo, Edgardo J., Awatramani, Rajeshwar, Xu, Theodore, Baron, Pierluigi, Vallat, Jean-Michael, Balsamo, Janne, Lilien, Jack, Scarlato, Guglielmo, Kamholz, John, Scherer, Steven S., Shy, Michael E.

“…Protein Zero (P0), the major structural protein in the peripheral nervous system (PNS) myelin, acts as a homotypic adhesion molecule and is thought to mediate…”
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Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis by Xu, Wenbo, Manichella, Daniela, Jiang, Huiyuan, Vallat, Jean-Michel, Lilien, Jack, Baron, Pierluigi, Scarlato, Guglielmo, Kamholz, John, Shy, Michael E.

“…P0, the major peripheral nervous system (PNS) myelin protein, is a member of the immunoglobulin supergene family of membrane proteins and can mediate homotypic…”
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Aging-dependent Functional Alterations of Mitochondrial DNA (mtDNA) from Human Fibroblasts Transferred into mtDNA-less Cells by Laderman, Kenneth A., Penny, James R., Mazzucchelli, Franca, Bresolin, Nereo, Scarlato, Guglielmo, Attardi, Giuseppe

“…To investigate the role that aging-dependent accumulation of mitochondrial DNA (mtDNA) mutations plays in the senescence processes, mitochondria from…”
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Alternative sources of neurons and glia from somatic stem cells by Torrente, Yvan, Belicchi, Marzia, Pisati, Federica, Pagano, Stefano F, Fortunato, Francesco, Sironi, Manuela, D'Angelo, Maria Grazia, Parati, Eugenio A, Scarlato, Guglielmo, Bresolin, Nereo

“…Stem cell populations have been shown to be extremely versatile: they can generate differentiated cells specific to the tissue in which they reside and…”
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Decrease of nerve Na+,K(+)-ATPase activity in the pathogenesis of human diabetic neuropathy by Scarpini, E, Bianchi, R, Moggio, M, Sciacco, M, Fiori, M G, Scarlato, G

“…A decrease in Na+,K(+)-ATPase activity is claimed to play a central role in the pathogenesis of electrophysiological and morphological abnormalities that…”
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Glial activation in Alzheimer’s disease: the role of Aβ and its associated proteins by Meda, Lucia, Baron, Pierluigi, Scarlato, Guglielmo

“…A common feature of Alzheimer’s disease (AD) pathology is the abundance of reactive astrocytes and activated microglia in close proximity to neuritic plaques…”
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Lumbosacral root and facial nerve enhancement in Miller Fisher syndrome by Pedotti, R, Carpo, M, Lucchi, S, Righini, A, Scarlato, G, Nobile-Orazio, E

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In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: evidence of programmed cell death after muscle cell transplantation by Del Bo, R, Torrente, Y, Corti, S, D'Angelo, M G, Comi, G P, Fagiolari, G, Salani, S, Cova, A, Pisati, F, Moggio, M, Ausenda, C, Scarlato, G, Bresolin, N

“…Ex vivo gene therapy of Duchenne muscular dystrophy based on autologous transplantation of genetically modified myoblasts is limited by their premature…”
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Reversible Cognitive Frailty, Dementia, and All-Cause Mortality. The Italian Longitudinal Study on Aging by Solfrizzi, Vincenzo, MD, PhD, Scafato, Emanuele, MD, Seripa, Davide, PhD, Lozupone, Madia, MD, Imbimbo, Bruno P., PhD, D'Amato, Angela, MD, Tortelli, Rosanna, MD, Schilardi, Andrea, MD, Galluzzo, Lucia, MD, Gandin, Claudia, MD, Baldereschi, Marzia, MD, Di Carlo, Antonio, MD, Inzitari, Domenico, MD, Daniele, Antonio, MD, PhD, Sabbà, Carlo, MD, Logroscino, Giancarlo, MD, PhD, Panza, Francesco, MD, PhD

“…Abstract Objectives Cognitive frailty, a condition describing the simultaneous presence of physical frailty and mild cognitive impairment, has been recently…”
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Expression of the low-affinity NGF receptor during human muscle development, regeneration, and in tissue culture by Baron, P, Scarpini, E, Meola, G, Santilli, I, Conti, G, Pleasure, D, Scarlato, G

“…The expression of the low-affinity NGF receptor (LNGFR) during human muscle development, regeneration, and in tissue culture was analyzed using a murine…”
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Incidence of Dementia, Alzheimer's Disease, and Vascular Dementia in Italy. The ILSA Study by Di Carlo, Antonio, Baldereschi, Marzia, Amaducci, Luigi, Lepore, Vito, Bracco, Laura, Maggi, Stefania, Bonaiuto, Salvatore, Perissinotto, Egle, Scarlato, Guglielmo, Farchi, Gino, Inzitari, Domenico, For The ILSA Working Group

“…OBJECTIVES: To estimate the incidence of dementia, Alzheimer's disease (AD), and vascular dementia (VaD) in older Italians and evaluate the relationship of…”
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Central nervous system trans-synaptic effects of acute axonal injury: a 1H magnetic resonance spectroscopy study by Rango, M, Spagnoli, D, Tomei, G, Bamonti, F, Scarlato, G, Zetta, L

“…N-acetylaspartate (NAA) has previously been proposed as a neuronal marker. 1H magnetic resonance spectroscopy (MRS) is able to detect NAA in brain, and…”
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IP-10 and MCP-1 levels in CSF and serum from multiple sclerosis patients with different clinical subtypes of the disease by Scarpini, Elio, Galimberti, Daniela, Baron, Pierluigi, Clerici, Raffaella, Ronzoni, Marco, Conti, Giancarlo, Scarlato, Guglielmo

“…Interferon-γ–inducible Protein-10 (IP-10) and Monocyte Chemotactic Protein-1 (MCP-1) levels were measured by enzyme-linked immunosorbent assay (ELISA) in the…”
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A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance by PIZZUTI, A, FRITTITTA, L, TASSI, V, TRISCHITTA, V, ARGIOLAS, A, BARATTA, R, GOLDFINE, I. D, BOZZALI, M, ERCOLINO, T, SCARLATO, G, IACOVIELLO, L, VIGNERI, R

“…A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance. A Pizzuti , L Frittitta , A Argiolas ,…”
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β-enolase deficiency, a new metabolic myopathy of distal glycolysis by Comi, Giacomo P., Fortunato, Francesco, Lucchiari, Sabrina, Bordoni, Andreina, Prelle, Alessandro, Jann, Stefano, Keller, Angélica, Ciscato, Patrizia, Galbiati, Sara, Chiveri, Luca, Torrente, Yvan, Scarlato, Guglielmo, Bresolin, Nereo

“…A severe muscle enolase deficiency, with 5% of residual activity, was detected in a 47‐year‐old man affected with exercise intolerance and myalgias. No rise of…”
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