CATALOGO DEI PRODOTTI DELLA RICERCA

PRANDINI, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 1.091
EU - Europa 707
AS - Asia 241
SA - Sud America 4
OC - Oceania 2
AF - Africa 1
AN - Antartide 1
Totale 2.047
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Nazione #
US - Stati Uniti d'America 1.087
GB - Regno Unito 229
CN - Cina 190
SE - Svezia 88
FI - Finlandia 63
FR - Francia 62
IE - Irlanda 62
IT - Italia 49
RU - Federazione Russa 48
DE - Germania 47
SG - Singapore 33
UA - Ucraina 23
BE - Belgio 16
NL - Olanda 10
JP - Giappone 7
BR - Brasile 3
KR - Corea 3
MT - Malta 3
MX - Messico 3
AT - Austria 2
AU - Australia 2
ID - Indonesia 2
SK - Slovacchia (Repubblica Slovacca) 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
CL - Cile 1
EE - Estonia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
IL - Israele 1
IN - India 1
LK - Sri Lanka 1
LV - Lettonia 1
MA - Marocco 1
PA - Panama 1
RO - Romania 1
Totale 2.047
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Città #
Chandler 214
Jacksonville 210
Southend 207
Woodbridge 130
Ann Arbor 85
Houston 79
Dublin 62
New York 50
Ashburn 33
Lawrence 28
Princeton 28
Nanjing 25
Wilmington 25
Singapore 22
Beijing 21
Jinan 16
Verona 16
Brussels 14
Hangzhou 14
Kent 14
Helsinki 12
Milan 11
Haikou 10
Tianjin 9
Changsha 8
Jiaxing 8
Shenyang 7
Taizhou 7
Tokyo 7
Lanzhou 6
Nanchang 6
Ningbo 6
Siegen 6
Florence 5
Guangzhou 5
Hebei 5
Los Angeles 5
Zhengzhou 5
Lancaster 4
Norwalk 4
San Francisco 4
Taiyuan 4
Boardman 3
Fairfield 3
Seoul 3
Swansea 3
Ypsilanti 3
Auburn Hills 2
Bekasi 2
Bratislava 2
Ixtapaluca 2
Mestre 2
Nuremberg 2
Sindelfingen 2
Sommacampagna 2
São Paulo 2
Vienna 2
Waanrode 2
Washington 2
Williamstown 2
Avigliano 1
Bari 1
Campinas 1
Canberra 1
Cleveland 1
Colombo 1
Dearborn 1
Des Moines 1
Dongguan 1
Dubai 1
Düsseldorf 1
Evanston 1
Frattamaggiore 1
Fuzhou 1
Kemerovo 1
Lappeenranta 1
Mehlingen 1
Melbourne 1
Mexico City 1
Moscow 1
Mosta 1
Napoli 1
Nashville 1
Newark 1
Phoenix 1
Redmond 1
Riga 1
Riva 1
Sant'Ambrogio di Valpolicella 1
Santa Clara 1
Seattle 1
Tallinn 1
Totale 1.510
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Nome #
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 121
Detection of allele-specific gene expression on next generation sequencing data 119
rs4307059 and rs4141463 study in an Italian cohort with Autism spectrum disorder 83
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 82
no association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder 80
A molecular signature associated with prolonged survival in glioblastoma patients treated with Regorafenib 78
Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis. 77
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. 75
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 75
Islands of euchromatic-like sequence and expressed genes within the heterochromatic regions: lessons from the initial sequence analysis of 21p. 74
Islands of euchromatic-like sequence and expressed genes within the short arm of HSA21: sequence and copy number variability. 74
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan. 73
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 73
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology. 72
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 72
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 70
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. 69
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. 68
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. 68
Genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and profiles of clopidogrel-induced antiplatelet effects in type 2 diabetes mellitus patients with coronary artery disease 68
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. 67
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome 67
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E. 66
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 65
Genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and profiles of clopidogrel-induced antiplatelet effects in type 2 diabetes mellitus patients with coronary artery disease 61
PLCB3 Loss-of-function Reduces P. aeruginosa-dependent IL-8 Release in Cystic Fibrosis 60
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. 59
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance. 52
Totale 2.068
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Categoria #
all - tutte 6.571
article - articoli 4.388
book - libri 0
conference - conferenze 2.183
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13.142
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020175 0 0 1 22 8 47 5 25 5 23 9 30
2020/2021227 13 44 18 20 34 24 1 23 19 4 26 1
2021/2022209 22 60 1 22 4 1 4 16 7 1 17 54
2022/2023527 37 82 45 79 61 102 2 31 66 6 11 5
2023/2024237 7 28 23 18 18 63 2 7 3 7 46 15
2024/202583 33 30 20 0 0 0 0 0 0 0 0 0
Totale 2.068