Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mohamed Aguennouz"'
Autor:
Silvana Hrelia, Mohamed Aguennouz, Rosaria Maddalena Ruggeri, Maria Cristina Barbalace, Alfredo Campennì, Marco Malaguti, Cristina Angeloni, Francesco Trimarchi, Salvatore Cannavò, Teresa Manuela Vicchio, Salvatore Giovinazzo, Giuseppe Giuffrida, Mariateresa Cristani, Angela Alibrandi
Background: There is a growing awareness that nutritional habits may influence risk of several inflammatory and immune-mediated disorders, including autoimmune diseases, through various mechanisms. The aim of the present study was to investigate diet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10785a9d3f94bb77faeb57b90ac6e11c
http://hdl.handle.net/11570/3176696
http://hdl.handle.net/11570/3176696
Autor:
Diana Teti, Lucia Altucci, Maria Cucinotta, Mohamed Aguennouz, Saverio Loddo, Maria Visalli, A. Valenti
Publikováno v:
Journal of Biological Chemistry. 283:29760-29769
For a long period of time, the transcription factor CCAAT/enhancer-binding protein homologous protein (CHOP) has been thought to inhibit transcriptional activity for its ability to interact with CCAAT enhancer-binding protein family factors, thus pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d32cee8575c50f119f9400d694a465e
https://doi.org/10.1074/jbc.m803145200
https://doi.org/10.1074/jbc.m803145200
Autor:
Giovanna Spatari, Andrea Alonci, Mohamed Aguennouz, Sabina Russo, Sebastiano Gangemi, Caterina Musolino, Antonio Speciale, Mariateresa Cristani, Alessandro Allegra, Antonino Cannavò, Angela Alibrandi
Publikováno v:
Cancer investigation. 30(1)
The aim of our study was to analyze the serum levels of advanced oxidation protein products (AOPPs) and advanced glycation end products (AGEs), and protein nitrosylation in patients with B-chronic lymphocytic leukemia (B-CLL). AOPPs, AGEs, and S-nitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2a13566a89bdffd6c7ba7732b647f3
https://pubmed.ncbi.nlm.nih.gov/22236186
https://pubmed.ncbi.nlm.nih.gov/22236186
Autor:
Salvatore Saitta, Alessandro Allegra, Andrea Alonci, Sabina Russo, Sebastiano Gangemi, Caterina Musolino, Mohamed Aguennouz, Maria Ferraro
Dear Editor,B-cell chronic lymphocytic leukemia (B-CLL) is characterized by the progressive accumulation of phenotypically mature malignant lymphocytes [1]. B-CLL therapy remains unsatisfactory due...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::382ac113c8b839c38d6742aaa76d55cd
http://hdl.handle.net/11570/1918156
http://hdl.handle.net/11570/1918156
Autor:
Antonino Cannavò, Demetrio Gerace, Angela Alibrandi, Alessia Garufi, Caterina Musolino, Giuseppa Penna, Alessandro Allegra, Mohamed Aguennouz, Andrea Alonci
Patients with B-chronic lymphocytic leukemia present diverse clinical features, genetic abnormalities, variable response to treatment, and heterogeneous prognosis. Novel biological markers such as IgVH mutation, CD38, and ZAP-70 expression have shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d48761bb4206397a25f1d64e71f90ebd
http://hdl.handle.net/11570/1911081
http://hdl.handle.net/11570/1911081
Autor:
Giuseppa Penna, Andrea Alonci, Mohamed Aguennouz, Caterina Musolino, Sabina Russo, Antonino Cannavò, Alessandro Allegra, Angela Granata
Richter's syndrome is defined as the transformation of low-grade lymphoma to a more aggressive high-grade malignant form, usually diffuse large B-cell lymphoma. Hodgkin's lymphoma variant of Richter transformation is relatively rare, and only approxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2c4ad396c57dea6106781ddaef924a2
http://hdl.handle.net/11570/3092853
http://hdl.handle.net/11570/3092853
Autor:
Mohamed Aguennouz, Grazia Annesi, Corrado Messina, Giuseppe M. Campo, Olimpia Musumeci, Antonio Toscano, Carmelo Rodolico, Rita Di Leo, Sonia Messina, Giuseppe Vita
Publikováno v:
Free radical research. 39(7)
Myotonic dystrophy type 1 (DM1) is the most common form of muscular dystrophy affecting adults. The genetic basis of DM1 consists of a mutational expansion of a repetitive trinucleotide sequence (CTG). The number of triplets expansion divides patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18dce9e506399bd38654452a03d9f690
https://pubmed.ncbi.nlm.nih.gov/16036357
https://pubmed.ncbi.nlm.nih.gov/16036357