IRIS
SURACE, Enrico Maria
 Distribuzione geografica
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Continente #
NA - Nord America 997
EU - Europa 592
AS - Asia 159
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 1.758
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Nazione #
US - Stati Uniti d'America 979
IT - Italia 272
CN - Cina 138
UA - Ucraina 78
NL - Olanda 77
FI - Finlandia 59
IE - Irlanda 34
SE - Svezia 32
DE - Germania 19
CA - Canada 16
VN - Vietnam 12
GB - Regno Unito 7
ES - Italia 4
BG - Bulgaria 3
CI - Costa d'Avorio 3
AU - Australia 2
EU - Europa 2
IN - India 2
MX - Messico 2
PL - Polonia 2
SG - Singapore 2
AT - Austria 1
BH - Bahrain 1
CH - Svizzera 1
CY - Cipro 1
FR - Francia 1
JP - Giappone 1
KR - Corea 1
LU - Lussemburgo 1
MA - Marocco 1
PT - Portogallo 1
TN - Tunisia 1
TR - Turchia 1
ZA - Sudafrica 1
Totale 1.758
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Città #
Chandler 277
Naples 95
Amsterdam 76
Millbury 70
Princeton 56
Nanjing 54
Jacksonville 48
Des Moines 38
Ashburn 33
Boston 28
Napoli 26
Wilmington 22
Nanchang 18
Ann Arbor 16
Ottawa 15
Siena 15
Lawrence 13
Shenyang 13
Beijing 12
Dong Ket 12
Jiaxing 12
Hebei 9
Caserta 7
Tianjin 7
Boardman 5
Benevento 4
Enna 4
Falls Church 4
New York 4
Redwood City 4
Rome 4
Zhengzhou 4
Dublin 3
Fairfield 3
Frankfurt am Main 3
Lappeenranta 3
Sofia 3
Trento 3
Guangzhou 2
Hangzhou 2
Los Angeles 2
Milan 2
Norwalk 2
Qualiano 2
San Diego 2
San Jose 2
Seattle 2
Washington 2
Woodbridge 2
Aguascalientes 1
Andover 1
Arzano 1
Battipaglia 1
Changsha 1
Chicago 1
Cieza 1
Cisterna 1
Cologne 1
Como 1
Dearborn 1
Denver 1
Innsbruck 1
Jinan 1
Johannesburg 1
Kronberg 1
Lisbon 1
Madrid 1
Manama 1
Murcia 1
Nabeul 1
New Delhi 1
Nicosia 1
Orange 1
Palermo 1
Parete 1
Paris 1
Poggibonsi 1
Pozzuoli 1
Pune 1
Qingdao 1
Querétaro City 1
Rabat 1
Redmond 1
Rotterdam 1
Salt Lake City 1
San Francisco 1
Santa Clara 1
Sarno 1
Smolec 1
South Bend 1
Stockholm 1
Sydney 1
Taizhou 1
Toronto 1
Verona 1
Warsaw 1
Yellow Springs 1
Zurich 1
Totale 1.094
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Nome #
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance 90
Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum. 67
The centrosomal OFD1 protein interacts with the translation machinery and regulates the synthesis of specific targets. 62
The Ocular Albinism type 1 (OA!) gene controls melanosome maturation and size. 54
AAV-miR-204 Protects from Retinal Degeneration by Attenuation of Microglia Activation and Photoreceptor Cell Death 46
GENE THERAPY FOR LEBER'S CONGENITAL AMAUROSIS IS SAFE AND EFFECTIVE 1.5 YEARS AFTER VECTOR ADMINISTRATION 41
TOWARDS CLINICAL TRIALS FOR AAV-MEDIATED EYE- AND LIVER - DIRECT GENE THERAPY TRANSLATION AAV 36
miR-181a/b downregulation exerts a protective action on mitochondrial disease models 35
Access to cerebrospinal fluid in piglets via the cisterna magna: Optimization and description of the technique 35
Delivery of adeno-associated virus vectors to the fetal retina: impact of viral capsid proteins on retinal neuronal progenitor transduction. 34
AAV vectors efficiently and stably transduce fetal retina. 33
Intein-mediated protein trans-splicing expands adeno-associated virus transfer capacity in the retina 33
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 32
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model 32
Adeno-associated viral vectors for retinal gene transfer. 31
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial. 31
AP20817-inducible activation of chimeric insulin receptor mimics insulin action in hepatocytes transduced with AAV 30
Efficacy of a combined intracerebral and systemic gene delivery approach for the treatment of a severe lysosomal storage disorder. 30
A comprehensive map of CNS transduction by eight recombinant adeno-associated virus serotypes upon cerebrospinal fluid administration in pigs 30
Gene therapy of inherited retinal degenerations: prospects and challenges. 29
The ocular albinism type 1 (OA1) gene controls melanosome maturation and size. 29
Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1 28
Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotides. 28
Molecular and clinical characterization of albinism in a large cohort of Italian patients. 28
Correlation betwen photoreceptor layer integrity and visual function in patients with Stargardt Disease:implication for gene therapy 27
Amelioration of both functional and morphological abnormalities in the retina of a mouse model of ocular albinism following AAV-mediated gene transfer. 27
Müller cell transduction by AAV2 in normal and degenerative retinas. 27
Pigment epithelium-derived factor expression in the developing mouse eye. 27
Challenging safety and efficacy of retinal gene therapies by retinogenesis 27
Inclusion of a degron reduces levelsof undesired inteins after AAV-mediated proteintrans-splicing in the retina 27
AAV-mediated Tyrosinase Gene Transfer Restores Melanogenesis and Retinal Function in a Model of Oculo-cutaneous Albinism Type I (OCA1). 26
Safety and efficacy of gene transfer for Leber's congenital amaurosis. 26
SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein associated amino acid transporter family. 25
The long noncoding RNA Vax2os1 controls the cell cycle progression of photoreceptor progenitors in the mouse retina. 25
Mouse embryonic retina delivers information controlling cortical neurogenesis. 25
Corrigendum to: Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum (The EMBO Journal, (2007), 26, 10, (2443-2453), 10.1038/sj.emboj.7601695) 25
MiR-211 is essential for adult cone photoreceptor maintenance and visual function 25
Systemic but not intraocular Epo gene transfer protects the retina from light- and genetic-induced degeneration. 24
Expression pattern of the ocular albinism type 1 (Oa1) gene in the murine retinal pigment epithelium. 24
In utero gene therapy rescues vision in a murine model of congenital blindness. 24
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration. 24
Phenotypic rescue after adeno-associated virus-mediated delivery of 4-sulfatase to the retinal pigment epithelium of feline mucopolysaccharidosis VI. 23
Inhibition of ocular neovascularization by Hedgehog blockade. 22
Gene therapy for Leber congenital amaurosis. 22
The ocular albinism type 1 (OA1) G-protein-coupled receptor functions with MART-1 at early stages of melanogenesis to control melanosome identity and composition. 22
Transdermal spinal catheter placement in piglets: Description and validation of the technique. 22
Combined rod and cone transduction by AAV2/8. 21
The ocular albinism type 1 (OA1) protein, an intracellur G protein-coupled receptor, regulates melanosome transport in pigment cells. 20
Use of compounds that interfere with the hedghehog signaling pathway for the manufacture of a medicament for preventing, inhibiting 20
Systemic but not intraocular Epo gene transfer protects the retina from light-and genetic-induced degeneration. 20
Localization of pigment epithelium derived factor (PEDF) in developing and adult human ocular tissues. 19
Rhodopsin targeted transcriptional silencing by DNA-binding 19
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 18
SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family. 18
The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells. 18
Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1. 17
Therapeutic homology-independent targeted integration in retina and liver 17
Versatility of AAV vectors for retinal gene transfer 16
Novel adeno-associated virus serotypes efficiently transduce murine photoreceptors. 16
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2. 15
The distribution, concentration, and toxicity of enhanced green fluorescent protein in retinal cells after genomic or somatic (virus-mediated) gene transfer. 15
Artificial DNA-binding proteins and uses thereof 15
Recombinant vectors based on porcine adeno-associated viral serotypes transduce the murine and pig retina. 14
Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa 13
Non-erythropoietic erythropoietin derivatives protect from light-induced and genetic photoreceptor degeneration. 13
Erratum: The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells (Human molecular genetics (2008) 17 22 (3487-3501)) 12
miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseases 9
Evaluation of italian patients with Leber Congenital Amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy 9
Targeting and silencing of rhodopsin by ectopic expression of the transcription factor KLF15 9
ECTOPICALLY EXPRESSED TRANSCRIPTION FACTORS AND USES THEREOF 8
Gene replacement therapy provides benefit in an adult mouse model of Leigh syndrome 6
Efficacy, pharmacokinetics, and safety in the mouse and primate retina of dual AAV vectors for Usher syndrome type 1B 4
Totale 1.851
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Categoria #
all - tutte 7.541
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7.541
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201922 0 0 0 0 0 0 0 0 0 0 0 22
2019/2020211 97 0 14 2 13 1 3 4 16 14 25 22
2020/2021173 3 10 21 17 14 20 18 10 21 10 13 16
2021/2022362 8 1 2 8 9 4 23 7 43 40 60 157
2022/2023633 75 50 18 57 85 77 6 54 94 71 38 8
2023/2024264 12 65 102 17 13 22 15 10 3 5 0 0
Totale 1.851