IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

TENCHINI, MARIA LUISA GIUDITTA
 Distribuzione geografica
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Continente #
EU - Europa 5.911
NA - Nord America 3.284
AS - Asia 1.636
SA - Sud America 96
Continente sconosciuto - Info sul continente non disponibili 23
OC - Oceania 15
AF - Africa 6
Totale 10.971
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Nazione #
US - Stati Uniti d'America 3.196
GB - Regno Unito 2.802
CN - Cina 764
IT - Italia 751
DE - Germania 592
SE - Svezia 481
UA - Ucraina 352
SG - Singapore 314
RU - Federazione Russa 277
KR - Corea 180
TR - Turchia 174
EU - Europa 162
IN - India 142
NL - Olanda 134
IE - Irlanda 116
FI - Finlandia 109
FR - Francia 105
CA - Canada 83
CO - Colombia 81
BE - Belgio 45
GR - Grecia 40
PL - Polonia 30
RO - Romania 16
AU - Australia 15
HK - Hong Kong 15
LU - Lussemburgo 15
ID - Indonesia 14
IR - Iran 14
BR - Brasile 13
DK - Danimarca 10
CZ - Repubblica Ceca 5
AT - Austria 4
BA - Bosnia-Erzegovina 4
ES - Italia 4
JP - Giappone 4
A1 - Anonimo 3
MX - Messico 3
PT - Portogallo 3
VN - Vietnam 3
ZA - Sudafrica 3
CH - Svizzera 2
CI - Costa d'Avorio 2
IL - Israele 2
KW - Kuwait 2
LV - Lettonia 2
ME - Montenegro 2
MY - Malesia 2
NO - Norvegia 2
SI - Slovenia 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
BG - Bulgaria 1
BY - Bielorussia 1
BZ - Belize 1
CL - Cile 1
EC - Ecuador 1
EG - Egitto 1
GP - Guadalupe 1
IM - Isola di Man 1
IS - Islanda 1
MD - Moldavia 1
PH - Filippine 1
RS - Serbia 1
UZ - Uzbekistan 1
Totale 11.113
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Città #
Southend 2.648
Chandler 346
Jacksonville 324
Seattle 253
Princeton 191
Singapore 191
Ashburn 184
Wilmington 184
Ann Arbor 179
Beijing 166
Milan 160
Mountain View 149
Redmond 132
Serra 120
Dublin 115
Nanjing 112
Somerville 90
Sakarya 86
Bogotá 80
Andover 77
Boardman 69
Woodbridge 69
Bengaluru 65
Des Moines 61
Shanghai 60
Fairfield 52
Los Angeles 51
Toronto 44
Athens 41
Houston 40
Jinan 40
Dearborn 39
Ottawa 37
Shenyang 36
Berlin 34
Redwood City 33
Brussels 30
Hanover 29
Warsaw 29
Rome 27
Bühl 25
Frankfurt am Main 24
Medford 24
Tianjin 24
Helsinki 23
Fuzhou 21
Nanchang 21
Hebei 19
Auburn Hills 18
Guangzhou 17
Kunming 17
Verona 17
Phoenix 15
Bitonto 14
Cambridge 14
San Diego 14
Turin 14
Munich 13
Quanzhou 13
Waanrode 13
Changsha 12
Roxbury 12
Seoul 12
Centro 11
Norwalk 11
Hong Kong 10
Lanzhou 10
Legnano 10
New York 10
Santa Clara 10
Hangzhou 9
Naples 9
Ningbo 9
Zhengzhou 9
Eitensheim 8
Jiaxing 8
Mumbai 8
São Paulo 8
Washington 8
Wuhan 7
Chicago 6
Florence 6
Hamburg 6
Lyon 6
Nürnberg 6
Padova 6
San Francisco 6
Sittingbourne 6
Bari 5
Hefei 5
Kent 5
Pskov 5
Saint Petersburg 5
Taiyuan 5
Xiamen 5
Atlanta 4
Genoa 4
Göteborg 4
Haikou 4
Iesi 4
Totale 7.327
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Nome #
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients 266
I giovani, la società, la ricerca scientifica : Cus-Mi-Bio, un progetto-ponte università-scuola per la formazione e la diffusione della cultura scientifica 254
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 253
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene 197
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione 184
Non-random retention of protein-coding overlapping genes in Metazoa 181
Teoria per la preparazione agli esami di ammissione e orientamento dei corsi di laurea di Area Scientifica 180
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 180
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein 179
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 179
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria 175
ESERCIZI - Prove d’esame ufficiali con soluzione e commento, per la preparazione agli esami di ammissione di Medicina, Odontoiatria, Veterinaria 174
Epilessia notturna del lobo frontale: non solo canalopatia! 172
Teoria per la preparazione agli esami di ammissione in Professioni Sanitarie e Scienze Motorie 166
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 166
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP) 162
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica 159
Alternative splicing and nonsense-mediated decay in the F5 gene 159
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 158
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 156
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 154
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 153
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 153
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 152
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 150
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 150
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 150
MDR1 C3435T polymorphism and susceptibility to inflammatory bowel disease : lack of association in an italian population 148
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population 146
Uniparental disomy of chromosome 4 including a novel deletion in the FGA gene that causes congenital afibrinogenemia 145
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain 143
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 143
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 143
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform 142
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 141
CusMiBio : an opportunity for talented young people in biosciences 138
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 134
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 133
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex 133
The discovery of Mary's mutation 132
Congenital hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion 129
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects 128
Identification of six novel mutations causing coagulation factor V deficiency 127
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform 127
Inherited defects of coagulation factor V : the hemorrhagic side 126
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 126
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 125
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 125
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 124
Identificazione di 5 nuove mutazioni puntiformi responsabili di carenza di fattore V della coagulazione 122
In-vitro expression and functional characterization of four mutations causing factor XI deficiency 121
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 121
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 121
The molecular basis of quantitative fibrinogen disorders 120
Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 120
Identificazione e caratterizzazione della prima mutazione missense nel gene per la catena Aalpha del fibrinogeno responsabile di afibrinogenemia congenita 119
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia 117
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione 117
Hedgehogs, humans and high-school science : the benefits of involving high-school students in university research 116
Molecular genetics of quantitative fibrinogen disorders 116
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions 115
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 115
Severe factor V deficiency : identification and molecular characterization of three novel splicing mutations 115
Autosomal dominant nocturnal frontal lobe epilepsy : a critical overview 114
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene 113
Coagulopatie ereditarie 113
Coagulation factor V 110
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 109
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 108
The role of the Myocyte Enhancer Factor 2A (MEF2A) gene in the pathogenesis of myocardial infarction 107
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation 106
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia 106
Epilessie idiopatiche e mutazioni nei geni per i canali del sodio 104
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 103
IDENTIFICAZIONE E CARATTERIZZAZIONE DI TRE NUOVE MUTAZIONI DI SPLICING RESPONSABILI DI CARENZA GRAVE DI FATTORE V DELLA COAGULAZIONE 103
Does 9-azaguanine induce or select for chromosome number instability in human cell hybrids? 102
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy 97
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome 95
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency 93
Two new putative susceptibility loci for ADNFLE 92
Reply to: [Factor XI mutation and the origin of Ashkenazi Jews. Haematologica 2008; 93:e59] 92
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 90
Expression of transformation markers and suppression of tumorigenicity in human cell hybrids 88
Frontal lobe epilepsy and mutations of the cortitropin-releasing hormone gene 82
Gene symbol: SCN1A 80
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient 77
Totale 11.659
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Categoria #
all - tutte 25.467
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 25.467
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020930 0 0 0 32 83 102 106 119 247 124 92 25
2020/20211.657 44 216 147 6 139 95 194 51 138 140 354 133
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
2024/2025504 91 212 40 161 0 0 0 0 0 0 0 0
Totale 11.659