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Akademický článek

Diversity of Staphylococcus aureus associated with mastitis from dairy cows in Rwanda

Publikováno v: Journal of Global Antimicrobial Resistance, Vol 36, Iss , Pp 326-335 (2024)

Objectives: The objective of the present study was to examine the diversity of Staphylococcus aureus from mastitis milk samples of cows in Rwanda. Methods: A total of 1080 quarter milk samples from 279 dairy cows were collected in 80 different farms

Externí odkaz: https://doaj.org/article/17a8a4a0475043d8b648a481124e3dfa

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The γ-Secretase Modulator CHF5074 Restores Memory and Hippocampal Synaptic Plasticity in Plaque-Free Tg2576 Mice

Autor: Marina Pizzi, Claudia Balducci, Luciana Giardino, Alessandro Usiello, Arturo R. Viscomi, Gino Villetti, Giuseppe Nisticò, Bruno P. Imbimbo, Annamaria Lanzillotta, Gianluigi Forloni, Luca Lorenzini, Alessandro Giuliani, Ilenia Sarnico, Lydia Mare, Simone Ottonello, Sandra Sivilia, Laura Calzà, Bisan Mehdawy, Robert Nisticò

Publikováno v: Journal of Alzheimer's Disease. 24:799-816

Abnormal amyloid-β (Aβ) production and deposition is believed to represent one of the main causes of Alzheimer's disease (AD). γ-Secretase is the enzymatic complex responsible for Aβ generation from its precursor protein. Inhibition or modulation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c8f1103c9c24466a143010744ae02fb
https://doi.org/10.3233/jad-2011-101839

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Cytogenetic monitoring in Shwachman-Diamond syndrome: a note on clonal progression and a practical warning

Autor: Giuseppe Montalbano, Emanuela Maserati, Barbara Pressato, Francesco Pasquali, Francesco Lo Curto, Roberto Valli, Cristina Marletta, Lydia Mare

Publikováno v: Journal of pediatric hematology/oncology. 37(4)

We analyzed the results of periodic chromosome analyses performed on bone marrow of 22 patients with Shwachman-Diamond syndrome (SDS), 8 directly observed and 14 from the literature, selected because of changes in the cytogenetic picture during the c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43c7b5447bd9f27f99cbb9f47930f5ed
https://pubmed.ncbi.nlm.nih.gov/25887640

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APP1 Transcription Is Regulated by Inositol-phosphorylceramide Synthase 1-Diacylglycerol Pathway and Is Controlled by ATF2 Transcription Factor in Cryptococcus neoformans

Autor: Maurizio Del Poeta, Lydia Mare, Roberta Iatta, Maria Teresa Montagna, Chiara Luberto

Publikováno v: Journal of Biological Chemistry. 280:36055-36064

Inositol-phosphorylceramide synthase 1 (Ipc1) is a fungal-specific enzyme that regulates the level of two bioactive molecules, phytoceramide and diacylglycerol (DAG). In previous studies, we demonstrated that Ipc1 regulates the expression of the anti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20039c7a3de745b8bf31d1dd7f775344
https://doi.org/10.1074/jbc.m507285200

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Suppression of β1,3galactosyltransferase β3Gal-T5 in cancer cells reduces sialyl-Lewis a and enhances poly N-acetyllactosamines and sialyl-Lewis x on O-glycans

Autor: Lydia Mare, Marco Trinchera

Publikováno v: European Journal of Biochemistry. 271:186-194

We investigated the role of β3Gal-T5, a member of the β1,3galactosyltransferase (β1,3Gal-T) family, in cancer-associated glycosylation, focusing on the expression of sialyl-Lewis a (sLea, the epitope of CA19.9 antigen), poly N-acetyllactosamines,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf6b855694a9a415b82259cf10b12e7c
https://doi.org/10.1046/j.1432-1033.2003.03919.x

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CA19.9 antigen circulating in the serum of colon cancer patients: Where is it from?

Autor: Marco Trinchera, Lydia Mare, Anna Caretti, Riccardo Albertini

CA19.9 antigen is a glycoprotein present in human serum and found elevated in various diseases. It is intensively studied since long time as a potential marker for managing cancers of the gastrointestinal tract, but its reliability is widely accepted

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f5ac9080a034de46733646c047d74bc
http://hdl.handle.net/11383/1863118

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Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes

Autor: Lydia Mare, Giuseppe Loffredo, Maria Ester Bernardo, Marco Zecca, Roberto Valli, Alessandra Di Cesare-Merlone, Barbara Pressato, Luciana Vinti, Emanuela Maserati, Giuseppe Montalbano, Cristina Marletta, Franco Locatelli, Giuseppe Menna, Francesco Pasquali, Simona Ferrari, Francesco Lo Curto

Publikováno v: Molecular Cytogenetics, Vol 5, Iss 1, p 39 (2012)
Molecular Cytogenetics

Background Chromosome changes in the bone marrow (BM) of patients with persistent cytopenia are often considered diagnostic for a myelodysplastic syndrome (MDS). Comprehensive cytogenetic evaluations may give evidence of the real pathogenetic role of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de660cac88b5a8840648876e2ccf1e44
https://doi.org/10.1186/1755-8166-5-39

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