Results overview: Found 3 records in 0.02 seconds.
Articles, 3 records found
Articles 3 records found  
1.
19 p, 5.0 MB SIVA-1 regulates apoptosis and synaptic function by modulating XIAP interaction with the death receptor antagonist FAIM-L / Coccia, Elena (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Planells-Ferrer, Laura (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Badillos-Rodríguez, Raquel (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Pascual, Marta (Institut de Neurociències, Universitat de Barcelona. Department of Cell Biology, Physiology and Immunology) ; Segura, Miguel F. (Hospital Universitari Vall d'Hebron. Institut de Recerca Group of Translational Research in Child and Adolescent Cancer, Vall d'Hebron Research Institute (VHIR)-UAB) ; Fernández-Hernández, Rita (Universitat de Lleida, Institut de Recerca Biomèdica de Lleida (IRBLleida)) ; López-Soriano, Joaquin (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Garí, Eloi (Universitat de Lleida. Cell Cycle Laboratory, Institut de Recerca Biomèdica de Lleida (IRBLleida), and Departament de Ciències Mèdiques Bàsiques; Facultat de Medicina) ; Soriano, Eduardo (Institució Catalana de Recerca i Estudis Avançats (ICREA)) ; Barneda-Zahonero, Bruna (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Moubarak, Rana S. (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Pérez-García, M. Jose (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Comella i Carnicé, Joan Xavier (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Universitat Autònoma de Barcelona.Institut de Neurociències
The long isoform of Fas apoptosis inhibitory molecule (FAIM-L) is a neuron-specific death receptor antagonist that modulates apoptotic cell death and mechanisms of neuronal plasticity. FAIM-L exerts its antiapoptotic action by binding to X-linked inhibitor of apoptosis protein (XIAP), an inhibitor of caspases, which are the main effectors of apoptosis. [...]
2020 - 10.1038/s41419-020-2282-x
Cell death and disease, Vol. 11 (february 2020)  
2.
21 p, 6.7 MB Identification and characterization of new isoforms of human fas apoptotic inhibitory molecule (FAIM) / Coccia, Elena (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Calleja Yagüe, Isabel (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Planells Ferrer, Laura (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Sanuy, Blanca (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Sanz, Belen (Cell Division and Cancer Group. Spanish National Cancer Research Centre (CNIO)) ; López Soriano, Joaquin (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Moubarak, Rana S. (Department of Pathology. NYU Langone Medical Center) ; Munell Casadesus, Francina (Hospital Universitari Vall d'Hebron. Institut de Recerca ) ; Barneda Zahonero, Bruna (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Comella i Carnicé, Joan Xavier 1963- (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular) ; Pérez García, María José (Universitat Autònoma de Barcelona. Institut de Neurociències. Departament de Bioquímica i Biologia Molecular)
Fas Apoptosis Inhibitory Molecule (FAIM) is an evolutionarily highly conserved death receptor antagonist, widely expressed and known to participate in physiological and pathological processes. Two FAIM transcript variants have been characterized to date, namely FAIM short (FAIM-S) and FAIM long (FAIM-L). [...]
2017 - 10.1371/journal.pone.0185327
PloS one, Vol. 12 Núm. 10 (october 2017) , p. e0185327  
3.
12 p, 557.9 KB Cathepsin K null mice show reduced adiposity during the rapid accumulation of fat stores / Funicello, Marcella (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; Novelli, Michela (University of Pisa. Department of Experimental Pathology, Medical Biotechnologies, Infectivology and Epidemiology) ; Ragni, Maurizio (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; Vottari, Teresa (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; Cocuzza, Cesare (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; López Soriano, Joaquin (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; Chiellini, Chiara (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; Boschi, Federico (University of Verona (Verona, Itàlia). Department of Morphological-Biomedical Sciences) ; Marzola, Pasquina (University of Verona (Verona, Itàlia). Department of Morphological-Biomedical Sciences) ; Masiello, Pellegrino (University of Pisa. Department of Experimental Pathology, Medical Biotechnologies, Infectivology and Epidemiology) ; Saftig, Paul (Christian-Albrechts University (Kiel, Alemanya). Biochemical Institute) ; Santini, Ferruccio (Christian-Albrechts University (Kiel, Alemanya). Biochemical Institute) ; St-Jacques, René (Merck Frosst Centre for Therapeutic Research (Kirkland, Canadà)) ; Desmarais, Sylvie (Merck Frosst Centre for Therapeutic Research (Kirkland, Canadà)) ; Morin, Nicolas (Merck Frosst Centre for Therapeutic Research (Kirkland, Canadà)) ; Mancini, Joseph (Merck Frosst Centre for Therapeutic Research (Kirkland, Canadà)) ; Percival, M. David (Merck Frosst Centre for Therapeutic Research (Kirkland, Canadà)) ; Pinchera, Aldo (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism) ; Maffei, Margherita (University Hospital of Pisa (Pisa, Itàlia). Department of Endocrinology and Metabolism)
Growing evidences indicate that proteases are implicated in adipogenesis and in the onset of obesity. We previously reported that the cysteine protease cathepsin K (ctsk) is overexpressed in the white adipose tissue (WAT) of obese individuals. [...]
2007 - 10.1371/journal.pone.0000683
PloS one, Vol. 2, Issue 8 (August 2007) , p. e683  

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