IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

RIVA, PAOLA VANDA
 Distribuzione geografica
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Continente #
EU - Europa 7371
NA - Nord America 4754
AS - Asia 3365
SA - Sud America 122
OC - Oceania 35
AF - Africa 21
Continente sconosciuto - Info sul continente non disponibili 15
Totale 15683
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Nazione #
US - Stati Uniti d'America 4568
GB - Regno Unito 3153
CN - Cina 2121
IT - Italia 1501
DE - Germania 876
SE - Svezia 588
TR - Turchia 322
IN - India 308
UA - Ucraina 277
KR - Corea 258
CA - Canada 157
NL - Olanda 136
RU - Federazione Russa 136
FI - Finlandia 122
DK - Danimarca 117
EU - Europa 111
JP - Giappone 102
FR - Francia 99
PL - Polonia 71
GR - Grecia 69
IR - Iran 66
CO - Colombia 61
ES - Italia 52
TW - Taiwan 49
BE - Belgio 47
VN - Vietnam 43
HK - Hong Kong 35
BR - Brasile 33
CH - Svizzera 32
MX - Messico 25
AU - Australia 20
NO - Norvegia 18
NZ - Nuova Zelanda 15
PT - Portogallo 15
IL - Israele 14
RO - Romania 13
CL - Cile 12
ID - Indonesia 12
HU - Ungheria 10
SG - Singapore 8
SC - Seychelles 7
BA - Bosnia-Erzegovina 6
CZ - Repubblica Ceca 6
EG - Egitto 6
MA - Marocco 6
SI - Slovenia 6
MO - Macao, regione amministrativa speciale della Cina 5
AR - Argentina 4
AT - Austria 4
CU - Cuba 4
LU - Lussemburgo 4
MY - Malesia 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
UZ - Uzbekistan 4
EC - Ecuador 3
RS - Serbia 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
FK - Isole Falkland (Malvinas) 2
IE - Irlanda 2
LK - Sri Lanka 2
PE - Perù 2
PH - Filippine 2
PK - Pakistan 2
PY - Paraguay 2
SA - Arabia Saudita 2
A1 - ???statistics.table.value.countryCode.A1??? 1
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BG - Bulgaria 1
HR - Croazia 1
KE - Kenya 1
MD - Moldavia 1
ZA - Sudafrica 1
Totale 15781
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Città #
Southend 2894
Milan 662
Seattle 410
Beijing 379
Hanover 360
Fairfield 319
Wilmington 310
Princeton 264
Ann Arbor 257
Dearborn 254
Woodbridge 218
Houston 214
Nanjing 180
Jacksonville 179
Redwood City 169
Mountain View 152
Redmond 142
Ashburn 133
Shanghai 119
Cambridge 118
Chandler 113
Shenyang 108
Guangzhou 105
Toronto 97
Jinan 93
Changsha 88
Des Moines 88
Hangzhou 87
Sakarya 86
Istanbul 83
Somerville 79
Serra 70
Wuhan 67
Nanchang 66
Andover 61
Zhengzhou 61
Warsaw 57
Athens 55
Bogotá 51
Tianjin 49
Hebei 48
Berlin 44
Kunming 41
Rome 41
Falls Church 38
Hefei 35
Roxbury 35
Chengdu 33
Fuzhou 33
Taipei 32
Ningbo 31
Xian 30
Zogno 29
Medford 28
Tokyo 25
San Diego 24
London 22
Dong Ket 21
Verona 21
Changchun 20
Mumbai 19
Lanzhou 18
Phoenix 18
Auburn Hills 17
Central District 17
Chongqing 17
Jiaxing 17
New York 17
Ottawa 17
Seoul 16
Torino 16
Hamburg 15
Atlanta 14
Chaoyang 14
Hyderabad 14
Kiez 14
Fremont 13
Haikou 13
Monza 13
Rho 13
Taizhou 13
Birmingham 12
Harbin 12
Philadelphia 12
Shenzhen 12
Taiyuan 12
Dallas 11
Jakarta 11
Norwalk 11
Pisa 11
Silver Spring 11
Suri 11
Zurich 11
Bethesda 10
Boston 10
Brussels 10
Lembeek 10
Nanning 10
Paris 10
Renton 10
Totale 10460
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Nome #
The long non-coding RNAs in neurodegenerative diseases : novel mechanisms of pathogenesis 2533
The miR-15/107 Family of microRNA Genes Regulates CDK5R1/p35 with Implications for Alzheimer’s Disease Pathogenesis 535
HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal muscles 477
NIPBL: a new player in myeloid cells differentiation 472
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with nonsyndromic mental retardation 322
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 226
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model? 217
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 197
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies 186
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions 181
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 181
The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration 172
Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2) 170
Mental retardation and cardiovascular malformations are significantly present in NF1-microdeleted patients and point to candidate genes in 17q11.2 168
Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene 167
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases 162
NIPBL a new player with NPMc+ in the onset of acute myeloid leukemia 154
Identification of duplicated genes in 17q11.2 by using FISH on stretched chromosomes and DNA fibers 153
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 151
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression 144
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements 135
Identification and functional characterization of trans-acting factors involved in the post-transcriptional regulation of CDK5R1 134
Monosomia del cromosoma 22 e perdita allelica al locus polimorfico c-sis nel meningioma. 133
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1 132
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability 132
FISH with locus-specific probes on stretched chromosomes : a useful tool for genome organization studies 131
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation 131
Dysregulation of apoptotic pathways in chordoma involving FAS and FASL: implications on notochord regression in zebrafish model 126
NF1 exon 7 skipping by disruption of exonic splice enhancers (ESEs) in neurofibromatosis 1 125
Characterization of breakpoint boundaries in 19 Neurofibromatosis type 1 microdeletions 125
miR-103 and miR-107 are involved in the regulation of CDK5R1/p35 expression 125
FAS/FASL are dysregulated in chordoma and their loss-of-function impairs zebrafish notochord formation 124
null 124
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36 123
19p deletion in recurring leiomyosarcoma lesions from the same patient 123
Identification of post-transcriptional regulatory elements in CDK5R1 3’UTR gene involved in CNS development and functioning 123
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients 123
Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study 122
Functional study of transcription cis-regulatory elements predicted in the CDK5R1 3’UTR 122
The regulation of CDK5R1 gene expression by miRNAs may have a role in Alzheimer’s disease 122
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region 121
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes. Clues to the mechanisms of formation 121
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 121
Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child 121
Centa2 è espresso durante lo sviluppo del cuore ed è un gene candidato per le malformazioni cardiovascolari 121
Expression study of receptor tyrosine kinase targets of Imatinib mesylate in skull base chordomas 120
Centa2 is expressed during heart development and is a candidate gene for CVMs 120
Hyper conserved elements in vertebrate mRNA 3’-UTRs reveal a translational network of RNA-binding proteins controlled by HUR 120
FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure 119
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth 117
Studio comparativo di LOH e di espressione in linee cellulari di cordoma e nei tumori di origine 116
Centaurin-α2 and tubulin interaction increases microtubule stability 114
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells 109
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms 109
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas 108
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 107
IDENTIFICAZIONE DEI GENI TARGET DEL miR-182 NELLA LINEA CELLULARE KASUMI-1, MODELLO DI LEUCEMIA MIELOIDE ACUTA (AML), E NELLE SUE SOTTOPOPOLAZIONI 107
First cytogenetic study of a recurrent familial chordoma of the clivus 106
The human CDK5R1 3'UTR contains distinct subregions affecting transcript stability 105
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 105
The role of p35/CDK5 regulation by miR-15/107 family in Alzheimer’s disease 105
High resolution FISH analysis of NF1 REP and non-REP microdeletions evidences nonhomologous end joining mediated rearrangements 104
Ricerca di interattori molecolari della centaurina-α2 : evidenze di associazione con la tubulina β 103
Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population 103
Identification of a chromosome 21 tandem duplication in a newborn 101
Tandem duplication of the NF1 gene detected by high resolution FISH in 17q11.2 region 99
Update on the Cytogenetics and Molecular Genetics of Chordoma 98
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations 98
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome 95
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome 95
Dysregulation of apoptotic pathway/s in chordoma: searching for prognostic markers and study of fas and fasl involvement in zebrafish model 95
Un metodo rapido e semplice per generare sonde locus-specifiche per l’analisi mediante FISH 94
Ruolo del complesso FAS-FASL nelle alterazioni delle notocorda e nello sviluppo del cordoma 94
Strumento per didattica scientifica 93
Expression of Centa2 and Suz12 during mammalian heart development 93
Morpholino knockdown of the zebrafish CENTA2 orthologue results in cardiovascular defects 93
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases 92
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval 91
Identification of a potential regulatory element forming a hairpin structure within the 3’UTR of CDK5R1 91
Studio di espressione dei recettori tirosin-kinasici target dell’Imatinib mesilato in cordomi della base cranica 91
Studio di LOH e espressione in geni apoptotici in 1p36 : ricerca di marcatori genetico-molecolari prognostici in cordomi della base cranica 89
Search of candidate genes for cardiovascular malformation in NF1 microdeletion syndrome 89
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis 88
Genomic organization study of NF1 duplicon by high resolution FISH 83
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 83
Evidence on microRNA-mediated regulation of CDK5R1 gene expression 82
Searching for centaurin-α2 interacting proteins: evidence of interaction with tubulin-β 81
Dysregulation of apoptotic pathway/s in chordoma : study of fas and fasl role in zebrafish notochord regression 81
Extensive mutational analysis of CDK5 and CDK5R1 in patients with non-syndromic mental retardation reveals novel variants in CDK5R1 3’-UTR 80
Expression study of receptor tyrosine kinase targets of Imatinib mesylate in skull base chordomas 79
Genetica Quantitativa 79
Differential allelic expression of the SOS1 c.755C activating variant in a Noonan syndrome family 79
Evaluation of 1p36 LOH, apoptotic genes’ expression and clinical outcome in a skull base chordoma prospective study 78
Thompson & Thompson : Genetica in medicina 78
Expression of Centa2 during early heart development : a new candidate gene for the onset of cardiovascular malformations 76
Satellite DNA sequences flank amplified DHFR domains in marker chromosomes of mouse fibrosarcoma cells 75
Identification of a new Jnk-activating familial SOS1 and a de novo RAF1 mutations in a Noonan syndrome patient 75
Introduzione 75
Mapping of genes and EST to 17q11.2 to a YAC contig centered on the NF1 gene 74
Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis 72
Totale 15314
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Categoria #
all - tutte 18824
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 18824
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20181498 0120130212 110161 82129 13310724272
2018/20192465 419160152161 101252 244135 168133218322
2019/20203046 348171146220 215351 338171 392377206111
2020/20213119 203281244145 265187 185231 308279549242
2021/20222876 181138232213 249188 230150 356345186408
2022/2023387 3285900 00 00 0000
Totale 16686