Search Results - "Mancinelli, E."

Motibot: the Virtual Coach for healthy coping intervention in diabetes by Bassi, G., Giuliano, C., Perinelli, A., Forti, S., Gabrielli, S., Mancinelli, E., Salcuni, S.

“…Introduction Virtual coaches (VCs) can support people with Diabetes Mellitus (DM) by motivating them to better manage their health. Few VCs were aimed at…”
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TM4SF18 is aberrantly expressed in pancreatic cancer and regulates cell growth by Singhal, Megha, Khatibeghdami, Mahsa, Principe, Daniel R, Mancinelli, Georgina E, Schachtschneider, Kyle M, Schook, Lawrence B, Grippo, Paul J, Grimaldo, Sam R

“…Current therapies for pancreatic ductal adenocarcinoma (PDAC) only modestly impact survival and can be highly toxic. A greater understanding of the molecules…”
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The probiotic strain Bacillus subtilis CU1 primes antimicrobial innate immune response and reduces low-grade inflammation: a clinical study by Mourey, F, Scholtens, P, Jeanne, J-F, Rodriguez, B, Decherf, A, Machuron, F, Kardinaal, A, Scheithauer, T, Porbahaie, M, Narni-Mancinelli, E, Crinier, A

“…LifeinU™ Bacillus subtilis CU1 (BSCU1) has been previously shown to be effective in stimulating mucosal immune responses and supporting resistance to common…”
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Husbandry risk factors associated with hock pododermatitis in UK pet rabbits (Oryctolagus cuniculus) by Mancinelli, E., Keeble, E., Richardson, J., Hedley, J.

“…Pododermatitis, often called ‘sore hocks’, is a chronic, granulomatous, ulcerative dermatitis which most commonly affects the plantar aspect of the caudal…”
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Increased apoptosis, huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects by Ciammola, A, Sassone, J, Alberti, L, Meola, G, Mancinelli, E, Russo, M A, Squitieri, F, Silani, V

“…Mutated huntingtin (htt) is ubiquitously expressed in tissues of Huntington's disease (HD) patients. In the brain, the mutated protein leads to neuronal cell…”
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γ-Glutamyl-transferase (GGT) activity in the urine of clinically healthy domestic rabbits (Oryctolagus cuniculus) by Mancinelli, E., Shaw, D. J., Meredith, A. L.

“…Free-catch urine samples were collected from forty-one clinically normal domestic rabbits of various ages, breeds and both sexes. The Test γ GT…”
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Use of arterial blood gas analysis as a superior method for evaluating respiratory function in pet rabbits (Oryctolagus cuniculus) by Eatwell, K., Mancinelli, E., Hedley, J., Benato, L., Shaw, D. J., Self, I., Meredith, A.

“…A retrospective study compared invasive (arterial blood gas analysis) and non-invasive (capnography and pulse oximetry) methods of monitoring respiratory…”
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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 by Vihola, A, Bassez, G, Meola, G, Zhang, S, Haapasalo, H, Paetau, A, Mancinelli, E, Rouche, A, Hogrel, J Y, Laforêt, P, Maisonobe, T, Pellissier, J F, Krahe, R, Eymard, B, Udd, B

“…Muscle biopsy findings in DM2 have been reported to be similar to those in DM1. The authors used myosin heavy chain immunohistochemistry and enzyme…”
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Partial ear canal ablation and lateral bulla osteotomy in rabbits by Eatwell, K., Mancinelli, E., Hedley, J., Keeble, E., Kovalik, M., Yool, D. A.

“…Six lop rabbits were presented with clinical signs of otitis media or externa. The presence of disease was confirmed by computerized tomography examination,…”
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Acetazolamide prevents vacuolar myopathy in skeletal muscle of K+‐depleted rats by Tricarico, D, Lovaglio, S, Mele, A, Rotondo, G, Mancinelli, E, Meola, G, Camerino, D C

“…Background and purpose: Acetazolamide and dichlorphenamide are carbonic anhydrase (CA) inhibitors effective in the clinical condition of hypokalemic periodic…”
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Severe Necrotizing Myocarditis caused by Serratia marcescens Infection in an Axolotl ( Ambystoma mexicanum) by Del-Pozo, J., Girling, S., Pizzi, R., Mancinelli, E., Else, R.W.

“…This report provides the first account of the pathological changes associated with infection by Serratia marcescens in an adult male axolotl. The infection…”
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RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study by Malatesta, M., Cardani, R., Giagnacovo, M., Mancinelli, E., Meola, G., Pellicciari, C.

“…Myotonic dystrophy type 2 (DM2) is a dominantly inherited autosomal disease with multi-systemic clinical features and it is caused by expansion of a CCTG…”
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RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study by Perdoni, F, Malatesta, M, Cardani, R, Giagnacovo, M, Mancinelli, E, Meola, G, Pellicciari, C

“…Myotonic dystrophy type 2 (DM2) is a dominantly inherited autosomal disease with multi-systemic clinical features and it is caused by expansion of a CCTG…”
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A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1 by Cardani, R, Mancinelli, E, Saino, G, Bonavina, L, Meola, G

“…Abstract Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder caused by expansion of unstable trinucleotide (CTG) repeats at 3′…”
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Effects of Flight on Gene Expression and Aging in the Honey Bee Brain and Flight Muscle by Margotta, Joseph W, Mancinelli, Georgina E, Benito, Azucena A, Ammons, Andrew, Roberts, Stephen P, Elekonich, Michelle M

“…Honey bees move through a series of in-hive tasks (e.g., "nursing") to outside tasks (e.g., "foraging") that are coincident with physiological changes and…”
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Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies by Cardani, R, Mancinelli, E, Giagnacovo, M, Sansone, V, Meola, G

“…Myotonic dystrophy type 2 (DM2) is a dominantly inherited disorder caused by a CCTG repeat expansion in intron 1 of ZNF9 gene. The size and the somatic…”
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D.P.4.06 No correlation of increase in size of ribonuclear inclusions to type II fibre atrophy in myotonic dystrophy type 2 over time by Cardani, R, Perbellini, R, Mancinelli, E, Meola, G

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Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy by Cardani, R, Mancinelli, E, Sansone, V, Rotondo, G, Meola, G

“…Myotonic dystrophy type 2 (DM2) is a dominantly inherited disorder with multisystemic clinical features, caused by a CCTG repeat expansion in intron 1 of the…”
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Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2 by Cardani, R, Mancinelli, E, Rotondo, G, Sansone, V, Meola, G

“…Myotonic dystrophies (DM) are repeat expansion diseases in which expanded CTG (DM1) and CCTG (DM2) repeats cause the disease. Mutant transcripts containing…”
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Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion by Lucchiari, S, Pagliarani, S, Corti, S, Mancinelli, E, Servida, M, Fruguglietti, E, Sansone, V, Moggio, M, Bresolin, N, Comi, G.P, Meola, G

“…Abstract Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder caused by a CCTG repeat expansion in intron 1 of the zinc finger…”
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