IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

MALCOVATI, MASSIMO
 Distribuzione geografica
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Continente #
EU - Europa 5.651
NA - Nord America 2.822
AS - Asia 2.404
SA - Sud America 232
AF - Africa 40
Continente sconosciuto - Info sul continente non disponibili 21
OC - Oceania 13
Totale 11.183
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Nazione #
US - Stati Uniti d'America 2.736
IT - Italia 2.092
GB - Regno Unito 1.738
CN - Cina 799
SG - Singapore 784
DE - Germania 374
SE - Svezia 312
RU - Federazione Russa 255
NL - Olanda 232
UA - Ucraina 210
BR - Brasile 159
HK - Hong Kong 155
IN - India 139
FR - Francia 123
VN - Vietnam 119
KR - Corea 107
TR - Turchia 102
EU - Europa 91
BD - Bangladesh 79
FI - Finlandia 79
CA - Canada 64
IE - Irlanda 57
CO - Colombia 48
BE - Belgio 32
GR - Grecia 32
JP - Giappone 25
ES - Italia 16
LU - Lussemburgo 15
RO - Romania 14
AU - Australia 13
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
SA - Arabia Saudita 8
CH - Svizzera 7
PK - Pakistan 7
PL - Polonia 7
CI - Costa d'Avorio 5
LV - Lettonia 5
MA - Marocco 5
PH - Filippine 5
TW - Taiwan 5
UZ - Uzbekistan 5
BA - Bosnia-Erzegovina 4
ME - Montenegro 4
PT - Portogallo 4
TH - Thailandia 4
VE - Venezuela 4
A1 - Anonimo 3
AZ - Azerbaigian 3
EC - Ecuador 3
ET - Etiopia 3
IL - Israele 3
JM - Giamaica 3
JO - Giordania 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
SN - Senegal 1
SO - Somalia 1
Totale 11.254
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Città #
Southend 1.607
Singapore 402
Ashburn 295
Milan 282
Chandler 207
Jacksonville 179
Beijing 171
San Jose 157
Hong Kong 148
Seattle 144
Ann Arbor 132
Wilmington 110
Princeton 107
Rome 99
Mountain View 87
Santa Clara 87
Serra 80
Council Bluffs 77
Bengaluru 75
Florence 72
Los Angeles 69
Nanjing 68
Dallas 62
Redmond 62
Somerville 60
Turin 57
Dublin 55
Hefei 52
Sakarya 46
Andover 44
Bogotá 44
Shanghai 42
Woodbridge 42
Lauterbourg 39
Ho Chi Minh City 38
Boardman 37
New York 37
Naples 36
Buffalo 35
Des Moines 34
Moscow 33
Athens 32
Verona 32
Fairfield 31
Hanover 30
Cagliari 29
Frankfurt am Main 28
Hanoi 28
Helsinki 28
Munich 28
Bologna 27
Shenyang 27
Guangzhou 26
Houston 26
Ottawa 26
Padova 26
Toronto 26
Dearborn 24
L’Aquila 24
Brussels 23
Jinan 23
Bari 21
Berlin 20
Cangzhou 20
Padua 20
Redwood City 20
Tokyo 20
Venice 20
Brescia 19
Medford 18
Tianjin 17
Seoul 16
Hebei 15
Pescara 15
Phoenix 15
Columbus 14
Lucca 14
Pavia 14
Bühl 13
Chicago 13
Modena 13
The Dalles 13
Kunming 12
Ancona 11
Bitonto 11
Fisciano 11
Fuzhou 11
Legnano 11
Pisa 11
São Paulo 11
Auburn Hills 10
Centro 10
Hangzhou 10
Nanchang 10
Quanzhou 10
Sardara 10
Changsha 9
London 9
Montesilvano Marina 9
Palermo 9
Totale 6.589
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Nome #
Molecole, cellule e organismi. Con QR-code 1.830
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients 405
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 358
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene 283
Teoria per la preparazione agli esami di ammissione in Professioni Sanitarie e Scienze Motorie 264
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 255
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP) 252
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 251
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione 251
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein 250
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 244
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria 243
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica 227
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 227
MDR1 C3435T polymorphism and susceptibility to inflammatory bowel disease : lack of association in an italian population 226
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 221
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects 217
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 217
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 214
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 211
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 208
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 207
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 205
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 204
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 200
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 199
Identification of six novel mutations causing coagulation factor V deficiency 199
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain 197
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform 193
Uniparental disomy of chromosome 4 including a novel deletion in the FGA gene that causes congenital afibrinogenemia 191
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia 189
In-vitro expression and functional characterization of four mutations causing factor XI deficiency 185
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 183
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 181
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 181
Identificazione di 5 nuove mutazioni puntiformi responsabili di carenza di fattore V della coagulazione 178
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation 177
Severe factor V deficiency : identification and molecular characterization of three novel splicing mutations 177
IDENTIFICAZIONE E CARATTERIZZAZIONE DI TRE NUOVE MUTAZIONI DI SPLICING RESPONSABILI DI CARENZA GRAVE DI FATTORE V DELLA COAGULAZIONE 177
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene 175
Identificazione e caratterizzazione della prima mutazione missense nel gene per la catena Aalpha del fibrinogeno responsabile di afibrinogenemia congenita 175
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione 174
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 171
La qualità ‘possibile’ nella formazione degli operatori sanitari : riflessioni a partire dalla riforma dell’autonomia universitaria 165
Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 157
Two new putative susceptibility loci for ADNFLE 138
Totale 11.679
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Categoria #
all - tutte 23.973
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 23.973
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021319 0 0 0 0 0 0 0 0 0 0 230 89
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
2025/20263.017 333 176 780 289 255 159 241 107 232 246 199 0
Totale 11.679