IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MALCOVATI, MASSIMO
 Distribuzione geografica
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Continente #
EU - Europa 5.730
NA - Nord America 2.984
AS - Asia 2.499
SA - Sud America 235
AF - Africa 40
Continente sconosciuto - Info sul continente non disponibili 21
OC - Oceania 14
Totale 11.523
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Nazione #
US - Stati Uniti d'America 2.891
IT - Italia 2.162
GB - Regno Unito 1.738
CN - Cina 800
SG - Singapore 787
DE - Germania 376
SE - Svezia 312
RU - Federazione Russa 255
NL - Olanda 232
UA - Ucraina 210
BD - Bangladesh 166
BR - Brasile 161
HK - Hong Kong 155
IN - India 139
FR - Francia 124
VN - Vietnam 120
KR - Corea 107
TR - Turchia 102
EU - Europa 91
FI - Finlandia 79
CA - Canada 70
IE - Irlanda 57
CO - Colombia 49
BE - Belgio 32
GR - Grecia 32
JP - Giappone 25
ES - Italia 16
LU - Lussemburgo 15
AU - Australia 14
RO - Romania 14
ID - Indonesia 13
IQ - Iraq 13
IR - Iran 12
AR - Argentina 10
CZ - Repubblica Ceca 10
DK - Danimarca 10
ZA - Sudafrica 9
AT - Austria 8
MX - Messico 8
PL - Polonia 8
SA - Arabia Saudita 8
CH - Svizzera 7
PK - Pakistan 7
CI - Costa d'Avorio 5
LV - Lettonia 5
MA - Marocco 5
PH - Filippine 5
TH - Thailandia 5
TW - Taiwan 5
UZ - Uzbekistan 5
BA - Bosnia-Erzegovina 4
JM - Giamaica 4
JO - Giordania 4
LT - Lituania 4
ME - Montenegro 4
PT - Portogallo 4
VE - Venezuela 4
A1 - Anonimo 3
AZ - Azerbaigian 3
EC - Ecuador 3
ET - Etiopia 3
IL - Israele 3
MY - Malesia 3
NO - Norvegia 3
NP - Nepal 3
SC - Seychelles 3
CL - Cile 2
DO - Repubblica Dominicana 2
GF - Guiana Francese 2
KE - Kenya 2
KW - Kuwait 2
NI - Nicaragua 2
PE - Perù 2
PR - Porto Rico 2
RS - Serbia 2
SI - Slovenia 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AE - Emirati Arabi Uniti 1
BB - Barbados 1
BJ - Benin 1
BY - Bielorussia 1
CM - Camerun 1
DM - Dominica 1
DZ - Algeria 1
EG - Egitto 1
GE - Georgia 1
GH - Ghana 1
HN - Honduras 1
HU - Ungheria 1
KG - Kirghizistan 1
LB - Libano 1
LK - Sri Lanka 1
MD - Moldavia 1
MG - Madagascar 1
MK - Macedonia 1
MU - Mauritius 1
NG - Nigeria 1
QA - Qatar 1
Totale 11.591
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Città #
Southend 1.607
Singapore 403
Ashburn 322
Milan 288
Chandler 207
Jacksonville 181
Beijing 171
San Jose 159
Hong Kong 148
Seattle 145
Santa Clara 133
Ann Arbor 132
Wilmington 112
Princeton 107
Rome 102
Mountain View 87
Serra 80
Council Bluffs 79
Bengaluru 75
Florence 73
Los Angeles 73
Boardman 70
Nanjing 68
Turin 65
Dallas 63
Redmond 62
Somerville 60
Dublin 55
Hefei 52
Sakarya 46
Andover 44
Bogotá 44
New York 43
Shanghai 42
Woodbridge 42
Naples 41
Ho Chi Minh City 39
Lauterbourg 39
Buffalo 35
Des Moines 34
Verona 34
Moscow 33
Athens 32
Cagliari 31
Fairfield 31
Hanover 30
Frankfurt am Main 28
Hanoi 28
Helsinki 28
Munich 28
Bologna 27
Guangzhou 27
Shenyang 27
Toronto 27
Houston 26
Ottawa 26
Padova 26
Bari 25
Dearborn 24
L’Aquila 24
Brussels 23
Jinan 23
Venice 22
Berlin 20
Brescia 20
Cangzhou 20
Padua 20
Redwood City 20
Tokyo 20
Medford 18
Tianjin 17
Seoul 16
Columbus 15
Hebei 15
Modena 15
Pescara 15
Phoenix 15
Lucca 14
Pavia 14
Bühl 13
Chicago 13
The Dalles 13
Kunming 12
Legnano 12
Ancona 11
Bitonto 11
Fisciano 11
Fuzhou 11
Pisa 11
São Paulo 11
Auburn Hills 10
Centro 10
Hangzhou 10
Nanchang 10
Palermo 10
Quanzhou 10
Sardara 10
Changsha 9
Düsseldorf 9
London 9
Totale 6.758
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Nome #
Molecole, cellule e organismi. Con QR-code 1.859
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients 425
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 393
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene 285
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 269
Teoria per la preparazione agli esami di ammissione in Professioni Sanitarie e Scienze Motorie 265
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 265
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP) 264
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein 260
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione 257
ESERCIZI - Prove d’esame ufficiali con soluzione e commento, per la preparazione agli esami di ammissione di Medicina, Odontoiatria, Veterinaria 247
Teoria per la preparazione agli esami di ammissione e orientamento dei corsi di laurea di Area Scientifica 246
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria 244
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V : broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations 237
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 236
MDR1 C3435T polymorphism and susceptibility to inflammatory bowel disease : lack of association in an italian population 236
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica 227
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects 226
Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the 225
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families 224
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 223
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 216
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 214
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 213
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 212
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 209
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain 206
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 205
Identification of six novel mutations causing coagulation factor V deficiency 201
Uniparental disomy of chromosome 4 including a novel deletion in the FGA gene that causes congenital afibrinogenemia 197
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform 196
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia 192
In-vitro expression and functional characterization of four mutations causing factor XI deficiency 189
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 186
Identificazione di 5 nuove mutazioni puntiformi responsabili di carenza di fattore V della coagulazione 186
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 184
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy 183
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation 180
Identificazione e caratterizzazione della prima mutazione missense nel gene per la catena Aalpha del fibrinogeno responsabile di afibrinogenemia congenita 180
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene 179
IDENTIFICAZIONE E CARATTERIZZAZIONE DI TRE NUOVE MUTAZIONI DI SPLICING RESPONSABILI DI CARENZA GRAVE DI FATTORE V DELLA COAGULAZIONE 179
Severe factor V deficiency : identification and molecular characterization of three novel splicing mutations 178
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione 176
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 173
La qualità ‘possibile’ nella formazione degli operatori sanitari : riflessioni a partire dalla riforma dell’autonomia universitaria 168
Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 163
Two new putative susceptibility loci for ADNFLE 141
Totale 12.019
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Categoria #
all - tutte 25.088
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.088
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022593 43 7 34 12 19 19 71 52 81 94 28 133
2022/2023738 89 81 46 100 96 130 37 49 82 3 16 9
2023/2024440 37 42 15 20 83 39 26 17 14 19 46 82
2024/20252.119 67 148 53 468 225 145 149 201 148 96 127 292
2025/20263.248 333 176 780 289 255 159 241 107 232 246 217 213
2026/2027109 109 0 0 0 0 0 0 0 0 0 0 0
Totale 12.019