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TitoloData di pubblicazioneAutoriTipoAbstract
IMPACT OF KILLER-CELL IMMUNOGLOBULIN-LIKE RECEPTORS ON PROGRESSION OF HEPATOCELLULAR CARCINOMA2019CHESSA, LUCHINO  ; PERRA, ANDREA  ; LAI, SARA  ; SERRA, MANUELA  ; LOI, VALENTINA  ; RAGATZU, PAOLA  ; CONGEDDU, ELENA  ; ALBA, FRANCESCA  ; FIGORILLI, FRANCESCO  ; ONALI, SIMONA  ; CASALE, MICHELE  ; BARCA, LUCIA  ; ORRU, SANDRO  ; CARCASSI, CARLO  1 Contributo su Rivista::1.5 Abstract in rivista-
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients2017MERKOURI PAPADIMA, ELENI  ; ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients2017SANTORU, MARIA LAURA  ; PIRAS, CRISTINA  ; MURGIA, ANTONIO  ; PALMAS, VANESSA  ; CAMBONI, TANIA  ; LIGGI, SONIA  ; IBBA, IVAN  ; ORRU, SANDRO  ; USAI, PAOLO  ; CABONI, PIERLUIGI  ; ATZORI, LUIGI  ; MANZIN, ALDO  1 Contributo su Rivista::1.1 Articolo in rivista
HLA-G molecules and clinical outcome in Chronic Myeloid Leukemia2017CAOCCI, GIOVANNI  ; ORRU, SANDRO  ; CARCASSI, CARLO  ; LA NASA, GIORGIO  1 Contributo su Rivista::1.1 Articolo in rivista
Cross sectional evaluation of the gut-microbiome metabolome axis in an Italian cohort of IBD patients2017PALMAS, VANESSA  ; SANTORU, MARIA LAURA  ; PIRAS, CRISTINA  ; MURGIA, ANTONIO  ; CAMBONI, TANIA  ; LIGGI, SONIA  ; IBBA, IVAN  ; ORRU, SANDRO  ; USAI, PAOLO  ; CABONI, PIERLUIGI  ; ATZORI, LUIGI  ; MANZIN, ALDO  4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno-
KIR and their HLA Class I ligands: Two more pieces towards completing the puzzle of chronic rejection and graft loss in kidney transplantation2017ORRU, SANDRO  ; LA NASA, GIORGIO  ; CAOCCI, GIOVANNI  ; CARCASSI, CARLO  1 Contributo su Rivista::1.1 Articolo in rivista
Reduced stress granule formation and cell death in fibroblasts with the A382T mutation of TARDBP gene: evidence for loss of TDP-43 nuclear function.2016ORRU, SANDRO  ; CONI, PAOLA  ; FLORIS, ANDREA  ; CARCASSI, CARLO  ; SOGOS, VALERIA  ; BRANCIA, CARLA  1 Contributo su Rivista::1.1 Articolo in rivista
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis2016ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
What unrelated hematopoietic stem cell transplantation in thalassemia taught us about transplant immunogenetics2016LA NASA, GIORGIO  ; ORRU, SANDRO  ; CARCASSI, CARLO  ; CAOCCI, GIOVANNI  1 Contributo su Rivista::1.1 Articolo in rivista
GUT MICROBIAL PROFILE IN WEIGHT CYCLING PATIENTS WITH OBESITY2016DELEDDA, ANDREA  ; BOI, ALESSANDRO  ; SCANO, SIMONA  ; PISANU, SILVIA  ; LOVISELLI, ANDREA  ; PALMAS, VANESSA  ; CAMBONI, TANIA  ; ORRU, SANDRO  ; MANZIN, ALDO  ; VELLUZZI, FERNANDA  4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno
VGF protein and its C-terminal derived peptides in amyotrophic lateral sclerosis: Human and animal model studies2016BRANCIA, CARLA  ; NOLI, BARBARA  ; MARROSU, FRANCESCO  ; ORRU, SANDRO  ; MANCONI, BARBARA  ; D'AMATO, FILOMENA  ; MESSANA, IRENE  ; FERRI, GIAN LUCA  ; COCCO, CRISTINA  1 Contributo su Rivista::1.1 Articolo in rivista
Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis2016CHESSA, LUCHINO  ; ONALI, SIMONA  ; FIGORILLI, FRANCESCO  ; LA NASA, GIORGIO  ; CAOCCI, GIOVANNI  ; CASALE, MICHELE  ; CASU, STEFANIA  ; BARCA, LUCIA  ; MATTA, LAURA  ; SCIOSCIA, ROSETTA  ; FAA, GAVINO  ; ORRU, SANDRO  ; CARCASSI, CARLO  1 Contributo su Rivista::1.1 Articolo in rivista
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male2015ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome2015ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista-
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases2015ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia2015ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature2014ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report2014ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
ALTERED STRESS GRANULE ASSEMBLY IN CULTURED FIBROBLASTS FROM ALS PATIENTS CARRYING A TARDBP MUTATION2014SOGOS, VALERIA  ; BRANCIA, CARLA  ; ORRU, SANDRO  4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno-
A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics2014ORRU, SANDRO  ; 1 Contributo su Rivista::1.1 Articolo in rivista
   
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