CATALOGO DEI PRODOTTI DELLA RICERCA

DINDO, MIRCO
 Distribuzione geografica
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Continente #
NA - Nord America 605
EU - Europa 529
AS - Asia 289
SA - Sud America 2
OC - Oceania 1
Totale 1.426
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Nazione #
US - Stati Uniti d'America 603
CN - Cina 242
GB - Regno Unito 189
IT - Italia 75
IE - Irlanda 53
SE - Svezia 52
FR - Francia 47
DE - Germania 40
FI - Finlandia 26
JP - Giappone 23
UA - Ucraina 17
BE - Belgio 12
KR - Corea 10
VN - Vietnam 8
RU - Federazione Russa 6
ES - Italia 4
NL - Olanda 4
CA - Canada 2
IN - India 2
IR - Iran 2
RO - Romania 2
AU - Australia 1
BR - Brasile 1
CO - Colombia 1
IQ - Iraq 1
LT - Lituania 1
LV - Lettonia 1
TR - Turchia 1
Totale 1.426
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Città #
Southend 180
Chandler 146
Dublin 53
Ann Arbor 49
Houston 47
Beijing 41
Verona 41
Jacksonville 40
Ashburn 33
Jinan 32
Wilmington 26
Woodbridge 26
Nanjing 25
Shenyang 25
New York 22
Lawrence 20
Princeton 20
Tokyo 19
Redwood City 14
Zhengzhou 14
Hebei 13
Taizhou 13
Falls Church 11
Brussels 10
Changsha 10
Helsinki 10
Seoul 10
Ningbo 9
Seattle 8
Tianjin 8
Nanchang 7
Taiyuan 6
Jiaxing 5
Lanzhou 5
Cagliari 4
Dong Ket 4
Guangzhou 4
Haikou 4
Hangzhou 4
Milan 4
Onna 4
Redmond 4
Sindelfingen 4
Fuzhou 3
Granada 3
Norwalk 3
Boardman 2
Chicago 2
Groningen 2
Kemerovo 2
Los Angeles 2
Novokuznetsk 2
Nürnberg 2
Philadelphia 2
Riva 2
Toronto 2
Waanrode 2
Ardabil 1
Bilbao 1
Bologna 1
Brasov 1
Charlotte 1
Clearwater 1
Dearborn 1
Fairfield 1
Kiev 1
Klyuchik 1
Lancaster 1
Lappeenranta 1
Medellín 1
Mumbai 1
Nagold 1
Paris 1
Rubano 1
Sabz 1
San Diego 1
San Francisco 1
Sydney 1
Vicenza 1
Vilnius 1
Xiangfen 1
Totale 1.089
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Nome #
The novel R347g pathogenic mutation Of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency 111
Molecular analysis of the dimerization and aggregation processes of human alanine:glyoxylate aminotransferase and effect of mutations leading to Primary Hyperoxaluria Type I 109
Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH 97
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine 96
A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implications 93
Opposite effect of polymorphic mutations on the electrostatic aggregation of human alanine:glyoxylate aminotransferase: implications for the pathogenesis of Primary Hyperoxaluria Type I 87
Folding defects leading to primary hyperoxaluria 82
Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244T 77
Pathogenic variants of human Aromatic L-Amino Acid Decarboxylase: evidences of misfolding in functionally active variants 73
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 72
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I 70
New variants of AADC deficiency expand the knowledge of enzymatic phenotypes 68
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 60
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from Bacillus Subtilis at neutral pH 58
The ILE56 mutation on different genetic backgrounds of alanine: Glyoxylate aminotransferase: Clinical features and biochemical characterization 55
Natural and unnatural compounds rescue folding defects of human alanine:glyoxylate aminotransferase leading to Primary Hyperoxaluria Type I 54
Evolution of chalcone isomerase from a noncatalytic ancestor 53
Molecular basis of primary hyperoxaluria: clues to innovative treatments 53
Crystal structure of Aspergillus fumigatus AroH, an aromatic amino acid aminotransferase 51
Dimerization drives proper folding of human Alanine:Glyoxylate aminotransferase but is dispensable for peroxisomal targeting 50
Totale 1.469
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Categoria #
all - tutte 4.265
article - articoli 3.633
book - libri 0
conference - conferenze 187
curatela - curatele 0
other - altro 221
patent - brevetti 0
selected - selezionate 0
volume - volumi 224
Totale 8.530
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20193 0 0 0 0 0 0 0 0 0 0 1 2
2019/2020187 19 5 1 3 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
2023/2024124 10 10 8 18 15 26 4 18 2 13 0 0
Totale 1.469