DI IORIO, MARIO VINCENZO

DI IORIO, MARIO VINCENZO  

Dipartimento di Medicina Molecolare - DMM  

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Risultati 1 - 20 di 59 (tempo di esecuzione: 0.029 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A c.3037G > A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype 2017 Di Iorio, E + INVESTIGACION CLINICA - -
A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family. 2003 DI IORIO, MARIO VINCENZO + EUROPEAN JOURNAL OF HUMAN GENETICS - -
A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: implications for recurrence risk and prenatal diagnosis 2012 CALISTRI, ARIANNAPAROLIN, MARIA CRISTINADI IORIO, MARIO VINCENZO + AMERICAN JOURNAL OF MEDICAL GENETICS. PART A - -
A Simplified Technique for In situ Excision of Cornea and Evisceration of Retinal Tissue from Human Ocular Globe. 2012 DI IORIO, MARIO VINCENZO + JOURNAL OF VISUALIZED EXPERIMENTS - -
Advances in corneal surgery and cell therapy: challenges and perspectives for eye banks 2009 DI IORIO, MARIO VINCENZO + EXPERT REVIEW OF OPHTHALMOLOGY - -
Analysis and pharmacological modulation of senescence in human epithelial stem cells 2022 Alvisi, GualtieroBettio, DanielaSalviati, LeonardoDi Iorio, Enzo + JOURNAL OF CELLULAR AND MOLECULAR MEDICINE - -
C/EBPdelta regulates cell cycle and self-renewal of human limbal stem cells. 2007 DI IORIO, MARIO VINCENZO + THE JOURNAL OF CELL BIOLOGY - -
Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. 2006 DI IORIO, MARIO VINCENZO + NATURE MEDICINE - -
Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted lentiviral vectors. 2008 DI IORIO, MARIO VINCENZO + MOLECULAR THERAPY - -
Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted retroviral vectors 2008 DI IORIO, MARIO VINCENZO + HUMAN GENE THERAPY - HUMAN GENE THERAPY
Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele-Specific Silencing Restores Defective Stem Cell Function 2016 NASTI, ANNAMARIA ASSUNTADEL VECCHIO, CLAUDIAMIGLIORATI, ANGELORAFFA, PAOLONESPECA, PATRIZIAPALU', GIORGIOPAROLIN, MARIA CRISTINADI IORIO, MARIO VINCENZO + STEM CELLS - -
Custom phototherapeutic keratectomy and autologous fibrin-cultured limbal stem cell autografting: a combined approach. 2008 DI IORIO, MARIO VINCENZO + JOURNAL OF REFRACTIVE SURGERY - -
Cytology of the healthy canine and feline ocular surface: comparison between cytobrush and impression technique 2017 PERAZZI, ANNABONSEMBIANTE, FEDERICOGELAIN, MARIA ELENAPATRUNO, MARCO VINCENZODI IORIO, MARIO VINCENZOMIGLIORATI, ANGELOIACOPETTI, ILARIA VETERINARY CLINICAL PATHOLOGY - -
Development of a hemicornea from human primary cell cultures for pharmacotoxicology testing. 2007 DI IORIO, MARIO VINCENZO + CELL BIOLOGY AND TOXICOLOGY - -
Development of an allele-specific real-time PCR assay for discrimination and quantification of p63 R279H mutation in EEC syndrome. 2012 DI IORIO, MARIO VINCENZO + THE JOURNAL OF MOLECULAR DIAGNOSTICS - -
Different expression levels of MUC1 in conjunctiva and cornea for the assessment of ocular surface disorders. 2010 DI IORIO, MARIO VINCENZO + BRITISH JOURNAL OF OPHTHALMOLOGY - -
Dissecting the molecular mechanisms accounting for the Feline Immunodeficiency Virus Envelope Glycoprotein ability to antagonize feline tetherin restriction 2015 CELESTINO, MICHELECALISTRI, ARIANNADI IORIO, MARIO VINCENZOPALU', GIORGIOPAROLIN, MARIA CRISTINA - - Programme and Abstract Book
Evaluation of ocular surface disorders: a new diagnostic tool based on impression cytology and confocal laser scanning microscopy. 2010 DI IORIO, MARIO VINCENZO + BRITISH JOURNAL OF OPHTHALMOLOGY - -
Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing. 2006 DI IORIO, MARIO VINCENZO + INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE - -
Gene editing of patient-specific induced pluripotent stem cells for cell therapy of EEC-syndrome 2018 Marta TrevisanGiulia MasiSilvia RiccettiGualtiero AlvisiEnzo Di Iorio + - - Gene editing of patient-specific induced pluripotent stem cells for cell therapy of EEC-syndrome