TENCHINI, MARIA LUISA GIUDITTA
 Distribuzione geografica
Continente #
EU - Europa 5.798
NA - Nord America 3.193
AS - Asia 1.204
SA - Sud America 96
Continente sconosciuto - Info sul continente non disponibili 23
OC - Oceania 14
AF - Africa 6
Totale 10.334
Nazione #
US - Stati Uniti d'America 3.105
GB - Regno Unito 2.796
IT - Italia 729
CN - Cina 614
DE - Germania 609
SE - Svezia 481
UA - Ucraina 352
KR - Corea 180
TR - Turchia 174
RU - Federazione Russa 163
EU - Europa 162
IN - India 142
NL - Olanda 134
IE - Irlanda 116
FR - Francia 101
FI - Finlandia 96
CA - Canada 83
CO - Colombia 81
BE - Belgio 75
GR - Grecia 40
SG - Singapore 35
PL - Polonia 30
RO - Romania 16
HK - Hong Kong 15
LU - Lussemburgo 15
AU - Australia 14
IR - Iran 14
BR - Brasile 13
ID - Indonesia 11
DK - Danimarca 10
AT - Austria 4
BA - Bosnia-Erzegovina 4
CZ - Repubblica Ceca 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 10.476
Città #
Southend 2.648
Chandler 346
Jacksonville 324
Seattle 253
Princeton 191
Wilmington 184
Ann Arbor 179
Ashburn 168
Beijing 166
Milan 157
Mountain View 149
Redmond 132
Serra 120
Dublin 115
Nanjing 111
Frankfurt am Main 97
Somerville 90
Sakarya 86
Bogotá 80
Andover 77
Boardman 69
Woodbridge 69
Bengaluru 65
Des Moines 61
Brussels 60
Fairfield 52
Toronto 44
Athens 41
Jinan 40
Dearborn 39
Houston 38
Ottawa 37
Shenyang 36
Redwood City 33
Berlin 31
Hanover 29
Warsaw 29
Medford 24
Shanghai 24
Tianjin 24
Rome 22
Los Angeles 21
Nanchang 21
Hebei 19
Auburn Hills 18
Kunming 17
Verona 17
Bitonto 14
Cambridge 14
Guangzhou 14
San Diego 14
Turin 14
Phoenix 13
Waanrode 13
Changsha 12
Roxbury 12
Seoul 12
Centro 11
Norwalk 11
Helsinki 10
Hong Kong 10
Lanzhou 10
Legnano 10
New York 10
Fuzhou 9
Naples 9
Ningbo 9
Zhengzhou 9
Jiaxing 8
Mumbai 8
São Paulo 8
Washington 8
Hangzhou 7
Chicago 6
Florence 6
Lyon 6
Nürnberg 6
Padova 6
San Francisco 6
Bari 5
Hefei 5
Munich 5
Pskov 5
Saint Petersburg 5
Taiyuan 5
Atlanta 4
Genoa 4
Göteborg 4
Haikou 4
Hamburg 4
Iesi 4
Katy 4
London 4
Napoli 4
Noginsk 4
Palermo 4
Sarajevo 4
Sesto San Giovanni 4
Tehran 4
Vienna 4
Totale 7.058
Nome #
I giovani, la società, la ricerca scientifica : Cus-Mi-Bio, un progetto-ponte università-scuola per la formazione e la diffusione della cultura scientifica 257
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients 243
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 230
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene 183
Non-random retention of protein-coding overlapping genes in Metazoa 176
Teoria per la preparazione agli esami di ammissione e orientamento dei corsi di laurea di Area Scientifica 175
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein 175
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria 171
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione 170
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 166
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 164
ESERCIZI - Prove d’esame ufficiali con soluzione e commento, per la preparazione agli esami di ammissione di Medicina, Odontoiatria, Veterinaria 163
Epilessia notturna del lobo frontale: non solo canalopatia! 163
Teoria per la preparazione agli esami di ammissione in Professioni Sanitarie e Scienze Motorie 160
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP) 159
Alternative splicing and nonsense-mediated decay in the F5 gene 155
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 154
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica 153
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 148
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 147
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 147
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 147
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 147
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 145
CusMiBio : an opportunity for talented young people in biosciences 145
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 143
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population 142
MDR1 C3435T polymorphism and susceptibility to inflammatory bowel disease : lack of association in an italian population 142
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 141
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 141
Uniparental disomy of chromosome 4 including a novel deletion in the FGA gene that causes congenital afibrinogenemia 137
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain 136
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 135
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 134
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 133
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform 133
Congenital hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion 129
The discovery of Mary's mutation 126
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex 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 121
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 121
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 120
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform 119
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 118
Identification of six novel mutations causing coagulation factor V deficiency 115
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 115
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects 114
Inherited defects of coagulation factor V : the hemorrhagic side 114
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 114
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 114
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 113
The molecular basis of quantitative fibrinogen disorders 112
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 112
In-vitro expression and functional characterization of four mutations causing factor XI deficiency 112
Identificazione di 5 nuove mutazioni puntiformi responsabili di carenza di fattore V della coagulazione 112
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions 111
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 110
Hedgehogs, humans and high-school science : the benefits of involving high-school students in university research 109
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione 109
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia 108
Identificazione e caratterizzazione della prima mutazione missense nel gene per la catena Aalpha del fibrinogeno responsabile di afibrinogenemia congenita 108
Molecular genetics of quantitative fibrinogen disorders 108
Coagulopatie ereditarie 107
Severe factor V deficiency : identification and molecular characterization of three novel splicing mutations 106
Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 106
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene 105
Coagulation factor V 104
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 104
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 104
Autosomal dominant nocturnal frontal lobe epilepsy : a critical overview 103
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia 102
The role of the Myocyte Enhancer Factor 2A (MEF2A) gene in the pathogenesis of myocardial infarction 101
Does 9-azaguanine induce or select for chromosome number instability in human cell hybrids? 98
Epilessie idiopatiche e mutazioni nei geni per i canali del sodio 94
IDENTIFICAZIONE E CARATTERIZZAZIONE DI TRE NUOVE MUTAZIONI DI SPLICING RESPONSABILI DI CARENZA GRAVE DI FATTORE V DELLA COAGULAZIONE 94
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation 93
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy 92
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency 91
Reply to: [Factor XI mutation and the origin of Ashkenazi Jews. Haematologica 2008; 93:e59] 91
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome 90
Two new putative susceptibility loci for ADNFLE 88
Expression of transformation markers and suppression of tumorigenicity in human cell hybrids 86
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 83
Frontal lobe epilepsy and mutations of the cortitropin-releasing hormone gene 80
Gene symbol: SCN1A 76
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient 74
Totale 11.022
Categoria #
all - tutte 20.371
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 20.371


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019281 0 0 0 0 0 0 0 0 88 76 65 52
2019/20201.208 139 50 89 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
2022/20231.239 145 126 75 172 150 236 48 91 138 5 34 19
2023/2024574 47 75 34 66 197 77 50 28 0 0 0 0
Totale 11.022