CATALOGO DEI PRODOTTI DELLA RICERCA

OPPICI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 1.120
EU - Europa 894
AS - Asia 534
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 2.552
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Nazione #
US - Stati Uniti d'America 1.115
CN - Cina 457
GB - Regno Unito 349
IT - Italia 123
SE - Svezia 96
IE - Irlanda 78
FR - Francia 75
DE - Germania 56
FI - Finlandia 52
SG - Singapore 27
BE - Belgio 20
VN - Vietnam 19
UA - Ucraina 18
KR - Corea 14
JP - Giappone 8
ES - Italia 7
RU - Federazione Russa 7
CA - Canada 3
IN - India 3
NL - Olanda 3
AT - Austria 2
AZ - Azerbaigian 2
PT - Portogallo 2
TR - Turchia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AU - Australia 1
BG - Bulgaria 1
DO - Repubblica Dominicana 1
GR - Grecia 1
HK - Hong Kong 1
IR - Iran 1
LT - Lituania 1
LU - Lussemburgo 1
LV - Lettonia 1
MA - Marocco 1
PA - Panama 1
PE - Perù 1
RO - Romania 1
Totale 2.552
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Città #
Southend 313
Chandler 251
Woodbridge 138
Ann Arbor 132
Jacksonville 106
Beijing 100
Dublin 78
Verona 77
Ashburn 56
Jinan 51
Nanjing 38
Houston 35
Lawrence 33
Princeton 33
Shenyang 31
Hebei 30
New York 30
Wilmington 29
Haikou 21
Zhengzhou 19
Brussels 18
Ningbo 18
Seattle 16
Singapore 16
Tianjin 16
Changsha 15
Nanchang 14
Dong Ket 13
Taizhou 13
Lanzhou 12
Seoul 12
Hangzhou 10
Boardman 9
Fuzhou 9
Helsinki 9
Jiaxing 9
Taiyuan 9
Guangzhou 8
Milan 8
Kent 7
Norwalk 7
Tokyo 7
Los Angeles 6
Redwood City 6
Dearborn 5
Redmond 5
Cagliari 4
Lancaster 4
Riva 4
Auburn Hills 3
Caserta 3
Chicago 3
Detroit 3
Falls Church 3
Kemerovo 3
Madrid 3
Qingdao 3
San Francisco 3
Atlanta 2
Baku 2
Clearwater 2
Kirrweiler 2
Mumbai 2
Nagold 2
Novokuznetsk 2
San Diego 2
Sindelfingen 2
Tappahannock 2
Ardabil 1
Barcelona 1
Berlin 1
Bologna 1
Brasov 1
Cambridge 1
Canary Wharf 1
Central District 1
Como 1
Crotone 1
Dongguan 1
Düsseldorf 1
Elora 1
Fairfield 1
Frankfurt am Main 1
Groningen 1
Hefei 1
La Canada Flintridge 1
Lappeenranta 1
Leawood 1
Lima 1
Lincoln 1
Lisbon 1
London 1
Luxembourg 1
Molenbeek-saint-jean 1
Montebelluna 1
Montreal 1
Napoli 1
Nashville 1
Newark 1
Norman 1
Totale 1.969
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Nome #
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase 136
Biochemical and computational approaches to improve the clinical treatment of Dopa decarboxylase-related diseases: an overview 123
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition 108
Molecular and cellular insights into defects of human alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I 103
Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH 100
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine 100
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant. 91
Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications 90
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. 88
Tat-mediated delivery of human alanine:glyoxylate aminotransferase in a cellular model of Primary Hyperoxaluria Type I 86
Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism 86
Gain-of-function mutant p53 enhances mitochondrial ROS through the inhibition of PGC-1α/UCP2 axis in cancer cells 86
A novel pathway for metabolism of the cardiovascular risk factor homoarginine by alanine:glyoxylate aminotransferase 2 85
The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes 83
Folding defects leading to primary hyperoxaluria 83
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview. 82
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I 81
Metastatic breast cancer cells enter into dormant state and express cancer stem cells phenotype under chronic hypoxia 78
S81 L and G170R mutations causing Primary Hyperoxaluria Type I in homozygosis and heterozygosis: an example of positive interallelic complementation. 75
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 75
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I 74
Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I 73
Mutant p53 blocks SESN1/AMPK/PGC-1α/UCP2 axis increasing mitochondrial O2-· production in cancer cells 70
Evolutionary divergent suppressor mutations in conformational diseases 63
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 62
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from Bacillus Subtilis at neutral pH 62
Molecular insights into primary hyperoxaluria Type I pathogenesis. 60
Molecular basis of primary hyperoxaluria: clues to innovative treatments 58
Natural and unnatural compounds rescue folding defects of human alanine:glyoxylate aminotransferase leading to Primary Hyperoxaluria Type I 57
Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I. 55
Dimerization drives proper folding of human Alanine:Glyoxylate aminotransferase but is dispensable for peroxisomal targeting 53
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 43
Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses 42
Totale 2.611
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Categoria #
all - tutte 7.951
article - articoli 7.188
book - libri 0
conference - conferenze 275
curatela - curatele 0
other - altro 248
patent - brevetti 0
selected - selezionate 0
volume - volumi 240
Totale 15.902
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020352 41 2 6 16 35 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
Totale 2.611