OPPICI, Elisa
 Distribuzione geografica
Continente #
NA - Nord America 1.161
EU - Europa 997
AS - Asia 717
SA - Sud America 18
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 2.898
Nazione #
US - Stati Uniti d'America 1.154
CN - Cina 515
GB - Regno Unito 350
SG - Singapore 141
IT - Italia 128
SE - Svezia 96
RU - Federazione Russa 87
IE - Irlanda 78
FR - Francia 75
DE - Germania 58
FI - Finlandia 57
BE - Belgio 22
VN - Vietnam 19
UA - Ucraina 18
BR - Brasile 15
KR - Corea 14
ES - Italia 8
JP - Giappone 8
ID - Indonesia 6
CA - Canada 4
AT - Austria 3
HK - Hong Kong 3
IN - India 3
NL - Olanda 3
AZ - Azerbaigian 2
LT - Lituania 2
MA - Marocco 2
PA - Panama 2
PE - Perù 2
PL - Polonia 2
PT - Portogallo 2
TR - Turchia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AU - Australia 1
BG - Bulgaria 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EC - Ecuador 1
EE - Estonia 1
GR - Grecia 1
IR - Iran 1
LU - Lussemburgo 1
LV - Lettonia 1
MY - Malesia 1
PK - Pakistan 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
Totale 2.898
Città #
Southend 313
Chandler 251
Woodbridge 138
Ann Arbor 132
Jacksonville 106
Singapore 103
Beijing 100
Dublin 78
Verona 77
Ashburn 59
Jinan 51
Nanjing 38
Houston 35
Lawrence 33
Princeton 33
Shenyang 31
Hebei 30
New York 30
Wilmington 29
Haikou 21
Brussels 20
Zhengzhou 20
Ningbo 18
Changsha 16
Seattle 16
Tianjin 16
Helsinki 14
Nanchang 14
Dong Ket 13
Taizhou 13
Lanzhou 12
Seoul 12
Hangzhou 11
Guangzhou 10
Boardman 9
Fuzhou 9
Jiaxing 9
Taiyuan 9
Milan 8
Kent 7
Norwalk 7
Tokyo 7
Los Angeles 6
Redwood City 6
Dearborn 5
Jakarta 5
Redmond 5
Santa Clara 5
Cagliari 4
Lancaster 4
Perugia 4
Qingdao 4
Riva 4
São Paulo 4
Auburn Hills 3
Caserta 3
Chicago 3
Dallas 3
Detroit 3
Falls Church 3
Kemerovo 3
Madrid 3
San Francisco 3
Atlanta 2
Baku 2
Belo Horizonte 2
Berlin 2
Clearwater 2
Frankfurt am Main 2
Hong Kong 2
Kirrweiler 2
Lima 2
Mumbai 2
Nagold 2
Newark 2
Novokuznetsk 2
San Diego 2
Sindelfingen 2
Tappahannock 2
Vienna 2
Achinsk 1
Ardabil 1
Barcelona 1
Bologna 1
Brasov 1
Bratislava 1
Cambridge 1
Canary Wharf 1
Casablanca 1
Central District 1
Changzhou 1
Chongqing 1
Como 1
Conselheiro Lafaiete 1
Crotone 1
Dongguan 1
Düsseldorf 1
Elora 1
Fairfield 1
Groningen 1
Totale 2.095
Nome #
Biochemical and computational approaches to improve the clinical treatment of Dopa decarboxylase-related diseases: an overview 160
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase 148
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition 120
Molecular and cellular insights into defects of human alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I 112
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine 108
Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH 104
Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications 99
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant. 98
Gain-of-function mutant p53 enhances mitochondrial ROS through the inhibition of PGC-1α/UCP2 axis in cancer cells 98
Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I. 97
Tat-mediated delivery of human alanine:glyoxylate aminotransferase in a cellular model of Primary Hyperoxaluria Type I 97
A novel pathway for metabolism of the cardiovascular risk factor homoarginine by alanine:glyoxylate aminotransferase 2 97
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I 92
The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes 92
Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism 92
Folding defects leading to primary hyperoxaluria 91
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview. 90
S81 L and G170R mutations causing Primary Hyperoxaluria Type I in homozygosis and heterozygosis: an example of positive interallelic complementation. 86
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I 85
Metastatic breast cancer cells enter into dormant state and express cancer stem cells phenotype under chronic hypoxia 85
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 85
Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I 83
Mutant p53 blocks SESN1/AMPK/PGC-1α/UCP2 axis increasing mitochondrial O2-· production in cancer cells 82
Evolutionary divergent suppressor mutations in conformational diseases 75
Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B6 71
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from Bacillus Subtilis at neutral pH 70
Natural and unnatural compounds rescue folding defects of human alanine:glyoxylate aminotransferase leading to Primary Hyperoxaluria Type I 68
Dimerization drives proper folding of human Alanine:Glyoxylate aminotransferase but is dispensable for peroxisomal targeting 68
Molecular basis of primary hyperoxaluria: clues to innovative treatments 66
Molecular insights into primary hyperoxaluria Type I pathogenesis. 65
Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I. 64
Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses 55
A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger homeostasis in photoreceptors 54
Totale 2.957
Categoria #
all - tutte 10.066
article - articoli 9.027
book - libri 0
conference - conferenze 429
curatela - curatele 0
other - altro 312
patent - brevetti 0
selected - selezionate 0
volume - volumi 298
Totale 20.132


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020252 0 0 0 0 0 27 43 7 33 44 15 83
2020/2021353 85 72 15 34 39 20 8 10 5 6 35 24
2021/2022339 28 142 28 9 7 3 6 20 16 8 12 60
2022/2023660 40 88 54 118 62 135 15 41 70 1 21 15
2023/2024262 16 13 11 15 30 50 5 35 5 15 48 19
2024/2025346 41 49 22 138 69 27 0 0 0 0 0 0
Totale 2.957