Search Results - "Garrè, C"

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families by Ziviello, C, Simonelli, F, Testa, F, Anastasi, M, Marzoli, S B, Falsini, B, Ghiglione, D, Macaluso, C, Manitto, M P, Garrè, C, Ciccodicola, A, Rinaldi, E, Banfi, S

“…Retinitis pigmentosa is the most common form of retinal degeneration and is heterogeneous both clinically and genetically. The autosomal dominant forms (ADRP)…”
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Inflammatory agents partially explain associations between cortical thickness, surface area, and body mass in adolescents and young adulthood by Prats-Soteras, X., Jurado, M. A., Ottino-González, J., García-García, I., Segura, B., Caldú, X., Sánchez-Garre, C., Miró, N., Tor, C., Sender-Palacios, M., Garolera, M.

“…Background/objectives Excessive body mass index (BMI) has been linked to a low-grade chronic inflammation state. Unhealthy BMI has also been related to…”
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Affected connectivity organization of the reward system structure in obesity by Marqués-Iturria, I., Scholtens, L.H., Garolera, M., Pueyo, R., García-García, I., González-Tartiere, P., Segura, B., Junqué, C., Sender-Palacios, M.J., Vernet-Vernet, M., Sánchez-Garre, C., de Reus, M.A., Jurado, M.A., van den Heuvel, M.P.

“…With the prevalence of obesity rapidly increasing worldwide, understanding the processes leading to excessive eating behavior becomes increasingly important…”
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Identification of an import signal for, and the nuclear localization of, human lactoferrin by Penco, Silvana, Scarfi, Sonia, Giovine, Marco, Damonte, Gianluca, Millo, Enrico, Villaggio, Barbara, Passalacqua, Mario, Pozzolini, Marina, Garrè, Cecilia, Benatti, Umberto

“…Many different unique functions have been attributed to lactoferrin (Lf), including DNA and RNA binding, and transport into the nucleus, where Lf binds to…”
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Italian guidelines for molecular analysis in myotonic dystrophies by Botta, A, Bonifazi, E, Vallo, L, Gennarelli, M, Garrè, C, Salehi, L, Iraci, R, Sansone, V, Meola, G, Novelli, G

“…Myotonic dystrophies, the most common form of adult muscular dystrophy, comprise at least two forms, clinically and genetically heterogeneous. Myotonic…”
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Lactoferrin Down-modulates the Activity of the Granulocyte Macrophage Colony-stimulating Factor Promoter in Interleukin-1β-stimulated Cells by Penco, Silvana, Pastorino, Sandra, Bianchi-Scarrà, Giovanna, Garrè, Cecilia

“…The human neutrophil lactoferrin (Lf), a cationic iron-binding glycoprotein, has an inhibitor role on granulocyte macrophage colony-stimulating factor (GM-CSF)…”
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Granulocyte-macrophage colony-stimulating factor activity in cerebrospinal fluid by Leonardi, A., Penco, S., Gramigni, C., Bason, C., Ribizzi, G., Gazzola, P., Mancardi, G.-L., Bianchi-Scarrà, G., Abbruzzese, M., Garrè, C.

“…Objectives ‐ The purpose of this study was to analyse the presence of the granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) in human cerebrospinal…”
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Cytokine expression in human primary and metastatic melanoma cells: analysis in fresh bioptic specimens by Ciotti, P, Rainero, M L, Nicolò, G, Spina, B, Garrè, C, Casabona, F, Santi, P L, Bianchi-Scarrà, G

“…In recent years, several studies have documented that melanoma cell lines produce various cytokine/growth factors and their receptors. Since cell lines can…”
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Terminal erythroid differentiation in the K-562 cell line by 1-β-D-arabinofuranosylcytosine: accompaniment by c-myc messenger RNA decrease by BIANCHI SCARRA, G. L, ROMANI, M, COVIELLO, D. A, GARRE, C, RAVAZZOLO, R, VIDALI, G, AJMAR, F

“…Two erythroid markers, acetylcholinesterase and hemoglobin, can be reversibly induced in the K-562 cell line after sodium butyrate treatment. In the present…”
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A novel mutation in the RDS gene in an Italian family with pattern dystrophy by Testa, F, Marini, V, Rossi, S, Interlandi, E, Nesti, A, Rinaldi, M, Varano, M, Garré, C, Simonelli, F

“…Comment The new mutation, described here, lies very close to the cysteine position 165 and 166 residues that have been suggested to be important for the…”
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A SOD1 gene mutation in a patient with slowly progressing familial ALS by PENCO, S, SCHENONE, A, BORDO, D, BOLOGNESI, M, ABBRUZZESE, M, BUGIANI, O, AJMAR, F, GARRE, C

“…We report a new missense mutation (Gly12Arg) [corrected] in exon 1 of the Cu/Zn superoxide dismutase (SOD1) gene in a 67-year-old patient with familial ALS…”
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Hepatic angiosarcoma. Presentation of two cases by Egea Valenzuela, J, López Poveda, M J, Pérez Fuenzalida, F J, Garre Sánchez, C, Martínez Barba, E, Carballo Alvarez, F

“…Hepatic angiosarcoma is a rare primary tumor of the liver with a mesenchymal origin. Diagnosis is difficult because clinical manifestations and imaging studies…”
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Presentation of two cases of Crouzon syndrome: allelic cranio-stenotic conditions of FGFR genes by Vidal Sanahuja, R, Gean Molins, E, Sánchez Garré, C, Quilis Esquerra, J, García Fructuoso, G, Costa Clara, J M

“…Craniosynostosis is an abnormal and premature fusion of any cranial suture. Twenty per cent of them involve any specific syndrome with Mendelian transmission;…”
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Can we expand the indications for liver transplantation among hepatocellular carcinoma patients with increased tumor size? by Fernández, J.A, Robles, R, Marin, C, Sánchez-Bueno, F, Ramirez, P, Pons, J.A, Garre, M.C, Pérez, D, Parrilla, A, Navalón, J.C, Parrilla, P

“…Due to the scarcity of donors and the fact that size is the main prognostic factor, Milan criteria have been used since 1996 to select hepatocellular carcinoma…”
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Isolation and characterization of a K562 cell line resistant to 1-beta-D-arabinofuranosylcytosine-mediated erythroid induction by Biancha Scarrà, G, Fiorentini, P, Gambari, R, Nastruzzi, C, Barbieri, R, Sessarego, M, Ravazzolo, R, Garrè, C

“…The isolation of a K562 cell line, K562(S)R, resistant to 1-beta-D-arabinofuranosylcytosine (ara-C)-mediated erythroid induction, is described. Ara-C (10-50…”
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Síndrome de Crouzon: a propósito de 2 casos. Entidades craneoestenóticas alélicas de los genes FGFR by Vidal Sanahuja, R, Gean Molins, E, Sánchez Garré, C, Quilis Esquerra, J, García Fructuoso, G, Costa Clara, J.M

“…Resumen Introducción La craneosinostosis consiste en una fusión patológica precoz de una o varias suturas craneales. El 20% de los casos corresponde a formas…”
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SOD1 mutations in amyotrophic lateral sclerosis : Results from a multicenter Italian study by BATTISTINI, Stefania, GIANNINI, Fabio, CAPONNETTO, Claudia, ORIGONE, Paola, MAROCCHI, Alessandro, DEL CORONA, Alberto, SICILIANO, Gabriele, CARRERA, Paola, MASCIA, Vincenzo, GIAGHEDDU, Marcello, CARCASSI, Carlo, ORRU, Sandro, GRECO, Giuseppe, GARRE, Cecilia, PENCO, Silvana, BIBBO, Giuseppe, FERRERA, Loretta, MARINI, Valeria, CAUSARANO, Renzo, CASULA, Michela, LANDO, Giuliana, PATROSSO, Maria Cristina

“…Amyotrophic Lateral Sclerosis (ALS), the most common form among motoneuron diseases, is characterized by a progressive neurodegenerative process involving…”
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Lactoferrin binding sites and nuclear localization in K562(S) cells by Garré, C, Bianchi-Scarrá, G, Sirito, M, Musso, M, Ravazzolo, R

“…Lactoferrin, a single chain cationic glycoprotein, present in the secondary granules of neutrophils, acts as a negative feedback regulator of myelopoiesis…”
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Expression of erythroid acetylcholinesterase in the K-562 leukemia cell line by Ajmar, F, Garrè, C, Sessarego, M, Ravazzolo, R, Barresi, R, Scarrà, G B, Lituania, M

“…Differentiation-dependent expression of enzyme loci was evaluated in two human leukemic cell lines, the pluripotent leukemia cell line K-562 and the…”
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Regulation of acetylcholinesterase expression in the K-562 cell line by GARRE, C, RAVAZZOLO, R, BIANCHI SCARRA, G, SESSAREGO, M, BARRESI, R, AJMAR, F

“…Acetylcholinesterase, an erythroid marker constitutively expressed in K-562 cells, can be further induced by sodium butyrate. The highest level of…”
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