DINDO, MIRCO
 Distribuzione geografica
Continente #
NA - Nord America 653
EU - Europa 591
AS - Asia 413
SA - Sud America 4
OC - Oceania 1
Totale 1.662
Nazione #
US - Stati Uniti d'America 650
CN - Cina 285
GB - Regno Unito 190
IT - Italia 78
SG - Singapore 67
RU - Federazione Russa 56
IE - Irlanda 53
SE - Svezia 52
FR - Francia 47
DE - Germania 41
FI - Finlandia 27
JP - Giappone 27
UA - Ucraina 17
BE - Belgio 13
KR - Corea 10
VN - Vietnam 10
ES - Italia 5
NL - Olanda 4
CA - Canada 2
ID - Indonesia 2
IN - India 2
IR - Iran 2
PT - Portogallo 2
RO - Romania 2
AT - Austria 1
AU - Australia 1
AZ - Azerbaigian 1
BR - Brasile 1
CL - Cile 1
CO - Colombia 1
CR - Costa Rica 1
EE - Estonia 1
HK - Hong Kong 1
IL - Israele 1
IQ - Iraq 1
JO - Giordania 1
LT - Lituania 1
LV - Lettonia 1
PE - Perù 1
PH - Filippine 1
SA - Arabia Saudita 1
TR - Turchia 1
Totale 1.662
Città #
Southend 180
Chandler 146
Singapore 61
Dublin 53
Beijing 51
Ann Arbor 49
Houston 47
Verona 41
Jacksonville 40
Ashburn 38
Jinan 32
Wilmington 26
Woodbridge 26
Nanjing 25
Shenyang 25
Tokyo 23
New York 22
Lawrence 20
Princeton 20
Redwood City 14
Zhengzhou 14
Hebei 13
Taizhou 13
Brussels 11
Falls Church 11
Helsinki 11
Changsha 10
Seoul 10
Kent 9
Ningbo 9
Seattle 8
Tianjin 8
Nanchang 7
Taiyuan 6
Guangzhou 5
Jiaxing 5
Lanzhou 5
Cagliari 4
Dong Ket 4
Haikou 4
Hangzhou 4
Milan 4
Onna 4
Redmond 4
Sindelfingen 4
Boardman 3
Fuzhou 3
Granada 3
Norwalk 3
Perugia 3
Santa Clara 3
Chicago 2
Dallas 2
Groningen 2
Jakarta 2
Kemerovo 2
Los Angeles 2
Novokuznetsk 2
Nürnberg 2
Philadelphia 2
Riva 2
Toronto 2
Waanrode 2
Amman 1
Ardabil 1
Baku 1
Bilbao 1
Bologna 1
Brasov 1
Canary Wharf 1
Charlotte 1
Clearwater 1
Clifton 1
Dearborn 1
Fairfield 1
Falkenstein 1
Haifa 1
Kiev 1
Klyuchik 1
Lancaster 1
Lappeenranta 1
Lima 1
Lincoln 1
Lisbon 1
Luoyang 1
Manila 1
Medellín 1
Moscow 1
Mumbai 1
Nagold 1
Newark 1
Paris 1
Riyadh 1
Rubano 1
Sabz 1
San Diego 1
San Francisco 1
San José 1
Santiago 1
Sydney 1
Totale 1.205
Nome #
The novel R347g pathogenic mutation Of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency 121
Molecular analysis of the dimerization and aggregation processes of human alanine:glyoxylate aminotransferase and effect of mutations leading to Primary Hyperoxaluria Type I 121
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
A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implications 103
Opposite effect of polymorphic mutations on the electrostatic aggregation of human alanine:glyoxylate aminotransferase: implications for the pathogenesis of Primary Hyperoxaluria Type I 99
Folding defects leading to primary hyperoxaluria 90
Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244T 88
Pathogenic variants of human Aromatic L-Amino Acid Decarboxylase: evidences of misfolding in functionally active variants 85
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 85
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I 84
New variants of AADC deficiency expand the knowledge of enzymatic phenotypes 81
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 70
The ILE56 mutation on different genetic backgrounds of alanine: Glyoxylate aminotransferase: Clinical features and biochemical characterization 70
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from Bacillus Subtilis at neutral pH 69
Dimerization drives proper folding of human Alanine:Glyoxylate aminotransferase but is dispensable for peroxisomal targeting 68
Natural and unnatural compounds rescue folding defects of human alanine:glyoxylate aminotransferase leading to Primary Hyperoxaluria Type I 66
Molecular basis of primary hyperoxaluria: clues to innovative treatments 65
Crystal structure of Aspergillus fumigatus AroH, an aromatic amino acid aminotransferase 65
Evolution of chalcone isomerase from a noncatalytic ancestor 63
Totale 1.705
Categoria #
all - tutte 5.693
article - articoli 4.869
book - libri 0
conference - conferenze 261
curatela - curatele 0
other - altro 271
patent - brevetti 0
selected - selezionate 0
volume - volumi 292
Totale 11.386


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020159 0 0 0 0 22 10 26 5 14 15 17 50
2020/2021220 51 46 5 18 34 12 3 3 8 3 26 11
2021/2022245 8 83 40 4 15 6 4 16 11 12 10 36
2022/2023399 23 54 34 69 28 93 8 26 51 1 10 2
2023/2024191 10 10 8 18 15 26 4 18 2 13 53 14
2024/2025169 24 27 7 84 27 0 0 0 0 0 0 0
Totale 1.705