Roncador, Alessandro
 Distribuzione geografica
Continente #
NA - Nord America 389
EU - Europa 323
AS - Asia 143
OC - Oceania 1
SA - Sud America 1
Totale 857
Nazione #
US - Stati Uniti d'America 387
GB - Regno Unito 152
CN - Cina 138
IT - Italia 52
FR - Francia 30
SE - Svezia 24
FI - Finlandia 20
IE - Irlanda 15
DE - Germania 13
BE - Belgio 11
CA - Canada 2
KR - Corea 2
UA - Ucraina 2
AU - Australia 1
BG - Bulgaria 1
BR - Brasile 1
ES - Italia 1
IN - India 1
JP - Giappone 1
LV - Lettonia 1
RU - Federazione Russa 1
TR - Turchia 1
Totale 857
Città #
Southend 128
Ann Arbor 89
Chandler 72
Woodbridge 40
Beijing 26
Jacksonville 25
Ashburn 20
Verona 18
Houston 16
Dublin 15
Jinan 13
Brussels 11
Shenyang 11
Hebei 10
Wilmington 10
Lawrence 9
Milan 9
Nanjing 9
Princeton 9
Haikou 8
Nanchang 7
Boardman 6
Seattle 6
Zhengzhou 6
Changsha 5
Hangzhou 5
Taiyuan 5
Cagliari 4
Jiaxing 4
Lanzhou 4
New York 4
Taizhou 4
Falls Church 3
Helsinki 3
Ningbo 3
Qingdao 3
Tianjin 3
Auburn Hills 2
Cambridge 2
Catania 2
Chicago 2
Elora 2
Ficarazzi 2
Guangzhou 2
Norwalk 2
San Diego 2
Tappahannock 2
Trento 2
Turin 2
Woodridge 2
Berlin 1
Birmingham 1
Como 1
Dearborn 1
Fairfield 1
Florianópolis 1
Fuzhou 1
Gambettola 1
Kochi 1
Melbourne 1
Miami 1
Nagold 1
Napoli 1
Nashville 1
Parma 1
Perugia 1
Redwood City 1
Riva 1
Rome 1
San Francisco 1
Sofia 1
Tampa 1
Torino 1
Yicheng 1
Totale 673
Nome #
Allele-specific Characterization of Alanine: Glyoxylate Aminotransferase Variants Associated with Primary Hyperoxaluria 148
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase 135
THE DEFICIT OF ALANINE:GLYOXYLATE AMINOTRANSFERASE LEADS TO PRIMARY HYPEROXALURIA TYPE I: A BIOCHEMICAL STUDY TO UNDERSTAND THE ROLE OF INTERALLELIC COMPLEMENTATION IN COMPOUND HETEROZYGOUS PATIENTS AND TO PROJECT THE DEVELOPMENT OF AN ENZYME ADMINISTRATION THERAPY. 133
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine 96
Tat-mediated delivery of human alanine:glyoxylate aminotransferase in a cellular model of Primary Hyperoxaluria Type I 84
S81 L and G170R mutations causing Primary Hyperoxaluria Type I in homozygosis and heterozygosis: an example of positive interallelic complementation. 74
Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I 72
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 71
Rapid profiling of disease alleles using a tunable reporter of protein misfolding 56
Totale 869
Categoria #
all - tutte 2.220
article - articoli 1.943
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 277
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.440


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201919 0 0 0 0 0 0 0 0 0 5 7 7
2019/2020121 15 1 5 9 12 6 13 3 14 17 9 17
2020/2021101 25 24 4 6 11 6 4 8 1 1 9 2
2021/2022125 11 48 7 2 6 5 5 6 5 3 7 20
2022/2023188 13 28 17 31 18 32 3 12 22 0 7 5
2023/202461 6 5 4 4 11 13 2 14 0 2 0 0
Totale 869