IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

TENCHINI, MARIA LUISA GIUDITTA
 Distribuzione geografica
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Continente #
EU - Europa 6.686
NA - Nord America 4.942
AS - Asia 4.135
SA - Sud America 413
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 25
OC - Oceania 20
Totale 16.283
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Nazione #
US - Stati Uniti d'America 4.770
GB - Regno Unito 2.845
CN - Cina 1.332
SG - Singapore 1.316
IT - Italia 882
DE - Germania 686
SE - Svezia 482
RU - Federazione Russa 477
UA - Ucraina 357
HK - Hong Kong 315
BR - Brasile 272
IN - India 244
NL - Olanda 233
VN - Vietnam 207
FR - Francia 206
KR - Corea 189
TR - Turchia 188
EU - Europa 162
BD - Bangladesh 133
FI - Finlandia 128
IE - Irlanda 119
CA - Canada 117
CO - Colombia 86
BE - Belgio 47
PL - Polonia 43
GR - Grecia 41
JP - Giappone 40
ID - Indonesia 28
IQ - Iraq 23
AR - Argentina 19
AU - Australia 19
LU - Lussemburgo 18
RO - Romania 17
AT - Austria 16
MX - Messico 16
ZA - Sudafrica 16
IR - Iran 15
CZ - Repubblica Ceca 13
ES - Italia 13
DK - Danimarca 11
PK - Pakistan 11
SA - Arabia Saudita 11
TW - Taiwan 9
UZ - Uzbekistan 9
CH - Svizzera 8
EC - Ecuador 8
PH - Filippine 8
AZ - Azerbaigian 7
CL - Cile 7
MY - Malesia 7
TH - Thailandia 7
ET - Etiopia 6
KE - Kenya 6
NP - Nepal 6
VE - Venezuela 6
CI - Costa d'Avorio 5
IL - Israele 5
JM - Giamaica 5
LV - Lettonia 5
MA - Marocco 5
NI - Nicaragua 5
TT - Trinidad e Tobago 5
AE - Emirati Arabi Uniti 4
BA - Bosnia-Erzegovina 4
BG - Bulgaria 4
KG - Kirghizistan 4
ME - Montenegro 4
NO - Norvegia 4
PE - Perù 4
PY - Paraguay 4
A1 - Anonimo 3
BB - Barbados 3
BS - Bahamas 3
BY - Bielorussia 3
DO - Repubblica Dominicana 3
JO - Giordania 3
KW - Kuwait 3
PA - Panama 3
PT - Portogallo 3
RS - Serbia 3
SC - Seychelles 3
TN - Tunisia 3
UY - Uruguay 3
AL - Albania 2
AM - Armenia 2
BJ - Benin 2
BZ - Belize 2
DZ - Algeria 2
EG - Egitto 2
GF - Guiana Francese 2
GT - Guatemala 2
HN - Honduras 2
HU - Ungheria 2
IS - Islanda 2
KZ - Kazakistan 2
LB - Libano 2
LT - Lituania 2
NG - Nigeria 2
PR - Porto Rico 2
SI - Slovenia 2
Totale 16.397
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Città #
Southend 2.648
Singapore 680
Ashburn 514
Chandler 346
Jacksonville 326
Beijing 316
Hong Kong 300
San Jose 281
Seattle 256
Milan 192
Princeton 191
Wilmington 185
Ann Arbor 179
Mountain View 149
Santa Clara 148
Bengaluru 132
Los Angeles 132
Redmond 132
Council Bluffs 122
Serra 121
Dublin 117
Nanjing 114
Dallas 109
Somerville 90
Sakarya 86
Bogotá 80
Andover 77
Moscow 75
Lauterbourg 71
Boardman 69
Woodbridge 69
Hefei 68
Shanghai 67
Ho Chi Minh City 65
Des Moines 63
Buffalo 61
Frankfurt am Main 60
New York 57
Fairfield 52
Hanoi 51
Toronto 50
Houston 43
Athens 42
Guangzhou 42
Jinan 41
Dearborn 39
Munich 38
Ottawa 37
Shenyang 37
Berlin 36
Helsinki 36
Rome 35
Tianjin 35
Redwood City 33
Tokyo 33
Warsaw 33
Brussels 31
Cangzhou 30
Hanover 29
Bühl 25
Phoenix 25
São Paulo 25
Medford 24
Columbus 22
The Dalles 22
Fuzhou 21
Nanchang 21
Seoul 21
Hebei 19
Auburn Hills 18
Verona 18
Kunming 17
Mumbai 16
San Diego 15
Turin 15
Bitonto 14
Cambridge 14
Changsha 14
Hangzhou 14
Chicago 13
Florence 13
Naples 13
Quanzhou 13
Waanrode 13
Roxbury 12
Wuhan 12
Centro 11
Jakarta 11
Legnano 11
Norwalk 11
Rio de Janeiro 11
Amsterdam 10
Baghdad 10
Lanzhou 10
London 10
Vienna 10
Washington 10
Bari 9
Haiphong 9
Montreal 9
Totale 10.162
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Nome #
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
Non-random retention of protein-coding overlapping genes in Metazoa 335
I giovani, la società, la ricerca scientifica : Cus-Mi-Bio, un progetto-ponte università-scuola per la formazione e la diffusione della cultura scientifica 318
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
Alternative splicing and nonsense-mediated decay in the F5 gene 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
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 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
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 218
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects 217
Epilessia notturna del lobo frontale: non solo canalopatia! 215
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 214
CusMiBio : an opportunity for talented young people in biosciences 212
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 211
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 210
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
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population 203
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians 202
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 200
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 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
Congenital hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion 199
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex 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
Hedgehogs, humans and high-school science : the benefits of involving high-school students in university research 190
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia 189
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 189
The molecular basis of quantitative fibrinogen disorders 188
Molecular genetics of quantitative fibrinogen disorders 188
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform 188
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 188
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
Activation of NF-kappaB by IL-1beta blocks IL-6-induced sustained STAT3 activation and STAT3-dependent gene expression of the human gamma-fibrinogen gene 182
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
The discovery of Mary's mutation 178
Identificazione di 5 nuove mutazioni puntiformi responsabili di carenza di fattore V della coagulazione 178
Inherited defects of coagulation factor V : the hemorrhagic side 177
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
The role of the Myocyte Enhancer Factor 2A (MEF2A) gene in the pathogenesis of myocardial infarction 173
Cryptic splice site usage in exon 7 of the human fibrinogen Bbeta-chain gene is regulated by a naturally silent SF2/ASF binding site within this exon 171
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 171
Autosomal dominant nocturnal frontal lobe epilepsy : a critical overview 169
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 167
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 166
Coagulation factor V 165
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions 164
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome 162
Reply to: [Factor XI mutation and the origin of Ashkenazi Jews. Haematologica 2008; 93:e59] 158
Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 157
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia 151
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy 150
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency 148
Coagulopatie ereditarie 147
Epilessie idiopatiche e mutazioni nei geni per i canali del sodio 146
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 144
Two new putative susceptibility loci for ADNFLE 138
Does 9-azaguanine induce or select for chromosome number instability in human cell hybrids? 134
Frontal lobe epilepsy and mutations of the cortitropin-releasing hormone gene 127
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient 126
Expression of transformation markers and suppression of tumorigenicity in human cell hybrids 123
Gene symbol: SCN1A 117
Totale 17.124
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Categoria #
all - tutte 38.726
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 38.726
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021487 0 0 0 0 0 0 0 0 0 0 354 133
2021/2022952 65 16 38 16 32 30 107 83 126 160 43 236
2022/20231.220 145 126 75 172 150 236 48 89 129 5 30 15
2023/2024726 45 72 28 36 150 77 50 28 17 40 79 104
2024/20252.067 91 212 40 249 195 102 58 186 126 163 166 479
2025/20263.902 538 234 401 246 400 277 454 179 382 398 393 0
Totale 17.124