IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

TENCHINI, MARIA LUISA GIUDITTA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 6.089
NA - Nord America 3.610
AS - Asia 1.890
SA - Sud America 207
Continente sconosciuto - Info sul continente non disponibili 23
OC - Oceania 18
AF - Africa 11
Totale 11.848
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.516
GB - Regno Unito 2.803
CN - Cina 793
IT - Italia 765
DE - Germania 600
SG - Singapore 498
SE - Svezia 482
UA - Ucraina 354
RU - Federazione Russa 324
NL - Olanda 222
KR - Corea 180
TR - Turchia 177
EU - Europa 162
IN - India 144
BR - Brasile 121
IE - Irlanda 116
FI - Finlandia 113
FR - Francia 107
CA - Canada 84
CO - Colombia 81
BE - Belgio 46
GR - Grecia 41
PL - Polonia 30
HK - Hong Kong 20
AU - Australia 17
ID - Indonesia 17
LU - Lussemburgo 16
RO - Romania 16
IR - Iran 15
DK - Danimarca 11
IQ - Iraq 7
CZ - Repubblica Ceca 6
PK - Pakistan 6
AT - Austria 5
MX - Messico 5
ZA - Sudafrica 5
BA - Bosnia-Erzegovina 4
CH - Svizzera 4
ES - Italia 4
JP - Giappone 4
UZ - Uzbekistan 4
VN - Vietnam 4
A1 - Anonimo 3
AZ - Azerbaigian 3
BD - Bangladesh 3
IL - Israele 3
LV - Lettonia 3
PT - Portogallo 3
TW - Taiwan 3
CI - Costa d'Avorio 2
KW - Kuwait 2
ME - Montenegro 2
MY - Malesia 2
NO - Norvegia 2
PA - Panama 2
RS - Serbia 2
SI - Slovenia 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
BG - Bulgaria 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CL - Cile 1
EC - Ecuador 1
EG - Egitto 1
GP - Guadalupe 1
HU - Ungheria 1
IM - Isola di Man 1
IS - Islanda 1
JM - Giamaica 1
KE - Kenya 1
KG - Kirghizistan 1
KZ - Kazakistan 1
MD - Moldavia 1
NZ - Nuova Zelanda 1
PH - Filippine 1
SN - Senegal 1
TH - Thailandia 1
TN - Tunisia 1
VE - Venezuela 1
Totale 11.990
Salva come PNG Salva come JPEG
Città #
Southend 2.648
Chandler 346
Jacksonville 324
Singapore 318
Seattle 253
Ashburn 208
Princeton 191
Wilmington 184
Ann Arbor 179
Beijing 168
Milan 161
Mountain View 149
Redmond 132
Serra 120
Dublin 115
Council Bluffs 113
Nanjing 113
Santa Clara 112
Somerville 90
Sakarya 86
Bogotá 80
Andover 77
Boardman 69
Woodbridge 69
Bengaluru 65
Des Moines 61
Shanghai 61
Los Angeles 56
Fairfield 52
Toronto 44
Athens 42
Houston 40
Jinan 40
Dearborn 39
Ottawa 37
Shenyang 36
Berlin 34
Redwood City 33
Brussels 31
Hanover 29
Warsaw 29
Rome 28
Helsinki 27
Bühl 25
Tianjin 25
Frankfurt am Main 24
Medford 24
Fuzhou 21
Nanchang 21
Guangzhou 19
Hebei 19
Auburn Hills 18
Kunming 17
Phoenix 17
Verona 17
Hong Kong 15
Bitonto 14
Cambridge 14
San Diego 14
São Paulo 14
Turin 14
Munich 13
Quanzhou 13
Waanrode 13
Changsha 12
Roxbury 12
Seoul 12
Centro 11
Norwalk 11
Lanzhou 10
Legnano 10
New York 10
Hangzhou 9
Naples 9
Ningbo 9
Zhengzhou 9
Eitensheim 8
Florence 8
Jiaxing 8
Mumbai 8
Washington 8
Wuhan 8
Cangzhou 7
Piscataway 7
Belo Horizonte 6
Chicago 6
Hamburg 6
Jakarta 6
Lyon 6
Moscow 6
Nürnberg 6
Padova 6
San Francisco 6
Sittingbourne 6
The Dalles 6
Bari 5
Hefei 5
Kent 5
Pskov 5
Saint Petersburg 5
Totale 7.737
Salva come PNG Salva come JPEG
Nome #
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients 289
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites 279
I giovani, la società, la ricerca scientifica : Cus-Mi-Bio, un progetto-ponte università-scuola per la formazione e la diffusione della cultura scientifica 263
Fibrinogen Mumbai : intracellular retention due to a novel G434D mutation in the Bbeta-chain gene 207
Non-random retention of protein-coding overlapping genes in Metazoa 202
Teoria per la preparazione agli esami di ammissione e orientamento dei corsi di laurea di Area Scientifica 194
Espressione in vitro e caratterizzazione funzionale di 4 mutazioni responsabili di carenza di fattore XI della coagulazione 194
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 190
Congenital afibrinogenemia : intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 188
Editest Teoria per l’ammissione ai Corsi di Laurea in medicina e chirurgia, odontoiatria e protesi dentaria, veterinaria 187
ESERCIZI - Prove d’esame ufficiali con soluzione e commento, per la preparazione agli esami di ammissione di Medicina, Odontoiatria, Veterinaria 187
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency : molecular characterization by expression of the recombinant protein 186
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia 186
Teoria per la preparazione agli esami di ammissione in Professioni Sanitarie e Scienze Motorie 178
A novel Chlamydomonas reinhardtii gene potentially encoding a proline-, glycine- and tyrosine-rich protein (PGYRP) 177
La mutazione tipo II (Glu117stop) causa carenza di fattore XI della coagulazione mediante degradazione allele specifica del corrispondente mRNA 177
Epilessia notturna del lobo frontale: non solo canalopatia! 176
Esercizi per l'ammissione e l'orientamento ai Corsi di Laurea di Area scientifica 174
Alternative splicing and nonsense-mediated decay in the F5 gene 173
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein 167
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 167
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 164
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 163
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 162
Type II mutation (Glu117stop) causes factor XI deficiency by inducing allele specific mRNA degradation 161
MDR1 C3435T polymorphism and susceptibility to inflammatory bowel disease : lack of association in an italian population 160
Multidrug resistance 1 gene polymorphism and susceptibility to inflammatory bowel disease 158
Congenital afibrinogenemia : two novel fibrinogen gene mutations identified in two patients from Iran 157
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 156
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform 153
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population 152
Uniparental disomy of chromosome 4 including a novel deletion in the FGA gene that causes congenital afibrinogenemia 151
Severe factor V deficiency : exon skipping in the factor V gene causing a partial deletion of the C1 domain 150
CusMiBio : an opportunity for talented young people in biosciences 149
The DNA pooling technique applied to the mutational screening of human congenital afibrinogenemia : identification of 3 novel mutations 149
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 144
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs 142
cDNA cloning and expression of the flavoprotein D-aspartate oxidase from bovine kidney cortex 142
The discovery of Mary's mutation 139
A type mutation II (Glu117stop), induction of allele-specific mRNA degradation and FXI deficiency 139
Mutational screening of six afibrinogenemic patients : identification and characterization of four novel molecular defects 138
Identification of six novel mutations causing coagulation factor V deficiency 138
Congenital hypofibrinogenemia : characterization of two missense mutations affecting fibrinogen assembly and secretion 138
In-vitro expression and functional characterization of four mutations causing factor XI deficiency 137
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 136
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 135
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 134
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform 134
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 133
Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 133
Identificazione e caratterizzazione del pattern di splicing alternativo del gene F11 e di una nuova isoforma FXI della coagulazione 132
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern 131
Inherited defects of coagulation factor V : the hemorrhagic side 130
Molecular genetics of quantitative fibrinogen disorders 130
Autosomal dominant nocturnal frontal lobe epilepsy : a critical overview 129
Shedding light on the dark side of the genome : overlapping genes in higher eukaryotes 129
Identificazione di 5 nuove mutazioni puntiformi responsabili di carenza di fattore V della coagulazione 128
Identificazione e caratterizzazione della prima mutazione missense nel gene per la catena Aalpha del fibrinogeno responsabile di afibrinogenemia congenita 127
Hedgehogs, humans and high-school science : the benefits of involving high-school students in university research 127
The DNA-pooling technique allowed for the identification of three novel mutations responsible for afibrinogenemia 126
Coagulation factor V gene analysis in five Indian patients : identification of three novel small deletions 126
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 126
The molecular basis of quantitative fibrinogen disorders 125
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 125
Severe factor V deficiency : identification and molecular characterization of three novel splicing mutations 125
Fibrinogen Mumbai: impaired secretion due to a novel missense mutation in the Bbeta-chain gene 123
Exploring the intracellular fate of coagulation factor V carrying the R2074C mutation 122
IDENTIFICAZIONE E CARATTERIZZAZIONE DI TRE NUOVE MUTAZIONI DI SPLICING RESPONSABILI DI CARENZA GRAVE DI FATTORE V DELLA COAGULAZIONE 121
Coagulopatie ereditarie 117
Coagulation factor V 116
Molecular characterization of two novel mutations causing factor XI deficiency : a splicing defect and a missense mutation responsible for a CRM+ defect 116
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia 115
The role of the Myocyte Enhancer Factor 2A (MEF2A) gene in the pathogenesis of myocardial infarction 114
Epilessie idiopatiche e mutazioni nei geni per i canali del sodio 110
The role of the Protein Kinase C Alpha (PRKCA) gene in the predisposition to multiple sclerosis in the Italian population 110
Does 9-azaguanine induce or select for chromosome number instability in human cell hybrids? 108
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome 107
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency 103
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy 103
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 100
Two new putative susceptibility loci for ADNFLE 98
Reply to: [Factor XI mutation and the origin of Ashkenazi Jews. Haematologica 2008; 93:e59] 98
Expression of transformation markers and suppression of tumorigenicity in human cell hybrids 94
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient 88
Frontal lobe epilepsy and mutations of the cortitropin-releasing hormone gene 86
Gene symbol: SCN1A 83
Totale 12.536
Salva come PNG Salva come JPEG
Categoria #
all - tutte 28.994
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 28.994
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020241 0 0 0 0 0 0 0 0 0 124 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
2024/20251.381 91 212 40 249 195 102 58 186 126 122 0 0
Totale 12.536