DI IORIO, MARIO VINCENZO
 Distribuzione geografica
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Continente #
NA - Nord America 3.326
EU - Europa 477
AS - Asia 285
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
OC - Oceania 1
Totale 4.092
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Nazione #
US - Stati Uniti d'America 3.322
CN - Cina 226
IT - Italia 213
FI - Finlandia 69
SE - Svezia 66
VN - Vietnam 47
DE - Germania 46
FR - Francia 29
GB - Regno Unito 21
NL - Olanda 12
IN - India 7
BE - Belgio 6
IE - Irlanda 5
CA - Canada 4
IR - Iran 4
UA - Ucraina 3
ES - Italia 2
EU - Europa 2
RU - Federazione Russa 2
AU - Australia 1
HU - Ungheria 1
JP - Giappone 1
MA - Marocco 1
PT - Portogallo 1
RO - Romania 1
Totale 4.092
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Città #
Fairfield 699
Woodbridge 415
Ashburn 278
Houston 249
Seattle 243
Cambridge 236
Chandler 217
Wilmington 210
Ann Arbor 174
San Diego 56
Medford 54
Princeton 54
Padova 53
Dong Ket 46
Des Moines 44
Nanjing 41
Beijing 33
Boardman 28
Helsinki 28
Roxbury 25
Shenyang 25
Sarcelles 16
Nanchang 15
Guangzhou 12
Changsha 11
Redmond 10
Tianjin 10
Hebei 9
Jinan 9
Dearborn 8
Hefei 8
Aprilia 7
Haikou 7
Jiaxing 7
London 7
Fort Worth 6
Turin 6
Waanrode 6
Dublin 5
Falls Church 5
Ogden 5
Taizhou 5
New York 4
Norwalk 4
Shanghai 4
Bologna 3
Cutrofiano 3
Detroit 3
Genoa 3
Hangzhou 3
Hounslow 3
Milan 3
Taiyuan 3
Tappahannock 3
Zhengzhou 3
Casamassima 2
Gunzenhausen 2
Kilburn 2
Kunming 2
Lanzhou 2
Leawood 2
Nagold 2
Nürnberg 2
Portland 2
Rockville 2
Sottomarina 2
Abano Terme 1
Brugherio 1
Casalzuigno 1
Costa Mesa 1
Draveil 1
Esslingen am Neckar 1
Frankfurt am Main 1
Freiburg im Breisgau 1
Fuzhou 1
Goito 1
Groningen 1
Ho Chi Minh City 1
Ichihara 1
Indiana 1
Kharkiv 1
Los Angeles 1
Modena 1
Mountain View 1
Ningbo 1
Palermo 1
Perth 1
Phoenix 1
Pratovecchio 1
Prescot 1
Redwood City 1
State College 1
Szeged 1
Timisoara 1
Toronto 1
Trissino 1
Udine 1
Venezia 1
Verona 1
Victoria 1
Totale 3.480
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Nome #
Personalized stem cell therapy to correct corneal defects due to a unique homozygous-heterozygous mosaicism of ectrodactyly-ectodermal dysplasia-clefting syndrome 195
Novel variants of RPGR in X-linked retinitis pigmentosa families and genotype-phenotype correlation 145
New Frontiers of Corneal Gene Therapy 145
Optimized Protocol for Regeneration of the Conjunctival Epithelium Using the Cell Suspension Technique. 144
Cytology of the healthy canine and feline ocular surface: comparison between cytobrush and impression technique 138
Morphological description of limbal epithelium: searching for stem cells crypts in the dog, cat, pig, cow, sheep and horse 136
Generation of a transgene-free human induced pluripotent stem cell line (UNIPDi001-A) from oral mucosa epithelial stem cells 121
Visualization of DNA G-quadruplexes in herpes simplex virus 1-infected cells 118
Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele-Specific Silencing Restores Defective Stem Cell Function 116
Q-FIHC: quantification of fluorescence immunohistochemistry to analyse p63 isoforms and cell cycle phases in human limbal stem cells. 97
Gene transfer of integration defective anti-HSV-1 meganuclease to human corneas ex vivo 94
Advances in corneal surgery and cell therapy: challenges and perspectives for eye banks 92
A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: implications for recurrence risk and prenatal diagnosis 92
Induced pluripotent stem cells line (UNIPDi003-A) from a patient affected by EEC syndrome carrying the R279H mutation in TP63 gene 88
Generation of a transgene-free induced pluripotent stem cells line (UNIPDi002-A) from oral mucosa epithelial stem cells carrying the R304Q mutation in TP63 gene 86
Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted retroviral vectors 85
Recombinant human serum albumin for corneal preservation 85
Identification of novel X-linked gain-of-function RPGR-ORF15 mutation in Italian family with retinitis pigmentosa and pathologic myopia 81
Custom phototherapeutic keratectomy and autologous fibrin-cultured limbal stem cell autografting: a combined approach. 80
A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family. 78
Safety outcomes and long-term effectiveness of ex vivo autologous cultured limbal epithelial transplantation for limbal stem cell deficiency 75
Oral mucosa-derived induced pluripotent stem cells from patients with ectrodactyly-ectodermal dysplasia-clefting syndrome 75
Towards xeno-free cultures of human limbal stem cells for ocular surface reconstruction 74
Laser Scanning Confocal Microscopy: Application in Manufacturing and Research of Corneal Stem Cells 73
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. 72
Techniques for culture and assessment of limbal stem cell grafts. 72
Evaluation of ocular surface disorders: a new diagnostic tool based on impression cytology and confocal laser scanning microscopy. 72
Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. 71
Localization and expression of CHST6 and keratan sulfate proteoglycans in the human cornea. 70
Targeting corneal disorders using gene therapy 70
Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations. 68
Hearing loss: frequency and functional studies of the most common connexin26 alleles. 68
Development of a hemicornea from human primary cell cultures for pharmacotoxicology testing. 67
Multimodal imaging quality control of epithelia regenerated with cultured human donor corneal limbal epithelial stem cells 65
A Simplified Technique for In situ Excision of Cornea and Evisceration of Retinal Tissue from Human Ocular Globe. 64
Retinitis pigmentosa: genes and disease mechanisms. 63
Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted lentiviral vectors. 63
Long-term effectiveness of autologous cultured limbal stem cell grafts in patients with limbal stem cell deficiency due to chemical burns. 61
Development of an allele-specific real-time PCR assay for discrimination and quantification of p63 R279H mutation in EEC syndrome. 61
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. 61
Nuclear Akt2 opposes limbal keratinocyte stem cell self-renewal by repressing a FOXO-mTORC1 signaling pathway. 61
On The Mechanism Of Tumor Cell Entry Of Aloe-Emodin, A Natural Compound Endowed With Anticancer Activity 60
Gene Therapy approaches for corneal diseases 55
Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing. 45
C/EBPdelta regulates cell cycle and self-renewal of human limbal stem cells. 44
Dissecting the molecular mechanisms accounting for the Feline Immunodeficiency Virus Envelope Glycoprotein ability to antagonize feline tetherin restriction 40
Different expression levels of MUC1 in conjunctiva and cornea for the assessment of ocular surface disorders. 36
USE OF SYNTHETIC AND NATURAL SCAFFOLDS TO DEVELOP NEW CLINICAL APPLICATIONS FOR CORNEAL EPITHELIAL STEM CELLS 35
Sordità. Malattie genetiche. Molecole e geni. Diagnosi, prevenzione e terapia. 32
Gene editing of patient-specific induced pluripotent stem cells for cell therapy of EEC-syndrome 31
Reconstruction of a human hemicornea through natural scaffolds compatible with the growth of corneal epithelial stem cells and stromal keratocytes. 29
Isoforms of DeltaNp63 and the migration of ocular limbal cells in human corneal regeneration. 27
A c.3037G > A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype 24
In Vivo Confocal Microscopy 1 Year after Autologous Cultured Limbal Stem Cell Grafts 24
Analysis and pharmacological modulation of senescence in human epithelial stem cells 17
Innovative Therapeutic Approaches for the Treatment of the Ocular Morbidities in Patients with EEC Syndrome 13
Structural determinants of phosphorylation-dependent nuclear transport of HCMV DNA polymerase processivity factor UL44 4
Structural and functional characterization of siadenovirus core protein VII nuclear localization demonstrates the existence of multiple nuclear transport pathways 4
Ocular Manifestations in Patients Affected by p63-Associated Disorders: Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) and Ankyloblepharon-Ectodermal Defects-Cleft Lip Palate (AEC) Syndromes 1
Totale 4.163
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Categoria #
all - tutte 13.223
article - articoli 12.347
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 441
Totale 26.011
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019454 0 0 0 0 0 0 0 0 0 115 186 153
2019/2020966 144 36 11 47 109 76 120 118 115 120 47 23
2020/2021647 22 30 14 28 71 24 9 51 107 108 100 83
2021/2022892 20 96 213 43 69 31 37 87 36 23 67 170
2022/2023484 88 34 7 57 93 62 1 35 59 9 31 8
2023/2024169 5 35 46 26 13 10 15 6 8 5 0 0
Totale 4.163