CATALOGO DEI PRODOTTI DELLA RICERCA

PRANDINI, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 1.056
EU - Europa 656
AS - Asia 189
OC - Oceania 2
SA - Sud America 2
AN - Antartide 1
Totale 1.906
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Nazione #
US - Stati Uniti d'America 1.053
GB - Regno Unito 229
CN - Cina 178
SE - Svezia 88
FI - Finlandia 63
FR - Francia 62
IE - Irlanda 61
DE - Germania 47
IT - Italia 46
UA - Ucraina 23
BE - Belgio 16
NL - Olanda 9
RU - Federazione Russa 6
KR - Corea 3
MT - Malta 3
MX - Messico 3
AU - Australia 2
ID - Indonesia 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
BR - Brasile 1
CL - Cile 1
EE - Estonia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
IL - Israele 1
IN - India 1
RO - Romania 1
SG - Singapore 1
Totale 1.906
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Città #
Chandler 214
Jacksonville 210
Southend 207
Woodbridge 130
Ann Arbor 85
Houston 79
Dublin 61
New York 50
Lawrence 28
Princeton 28
Ashburn 27
Nanjing 25
Wilmington 25
Jinan 16
Verona 16
Beijing 15
Brussels 14
Hangzhou 14
Helsinki 12
Milan 11
Haikou 10
Tianjin 9
Changsha 8
Jiaxing 8
Shenyang 7
Taizhou 7
Lanzhou 6
Nanchang 6
Ningbo 6
Siegen 6
Florence 5
Guangzhou 5
Hebei 5
Zhengzhou 5
Lancaster 4
Norwalk 4
San Francisco 4
Taiyuan 4
Fairfield 3
Seoul 3
Swansea 3
Ypsilanti 3
Auburn Hills 2
Bekasi 2
Ixtapaluca 2
Los Angeles 2
Mestre 2
Nuremberg 2
Sindelfingen 2
Waanrode 2
Washington 2
Avigliano 1
Bari 1
Boardman 1
Canberra 1
Cleveland 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
Mosta 1
Napoli 1
Nashville 1
Phoenix 1
Redmond 1
Riva 1
Sant'Ambrogio di Valpolicella 1
Seattle 1
Singapore 1
São Paulo 1
Tallinn 1
Vienna 1
Totale 1.436
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Nome #
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 118
Detection of allele-specific gene expression on next generation sequencing data 109
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 77
rs4307059 and rs4141463 study in an Italian cohort with Autism spectrum disorder 77
no association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder 75
Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis. 74
A molecular signature associated with prolonged survival in glioblastoma patients treated with Regorafenib 70
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. 69
Islands of euchromatic-like sequence and expressed genes within the short arm of HSA21: sequence and copy number variability. 69
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 69
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 69
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. 68
Islands of euchromatic-like sequence and expressed genes within the heterochromatic regions: lessons from the initial sequence analysis of 21p. 68
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 68
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology. 67
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 66
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 65
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. 64
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. 63
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. 62
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome 62
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 61
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. 61
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E. 60
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 57
PLCB3 Loss-of-function Reduces P. aeruginosa-dependent IL-8 Release in Cystic Fibrosis 55
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. 55
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance. 49
Totale 1.927
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Categoria #
all - tutte 5.539
article - articoli 3.685
book - libri 0
conference - conferenze 1.854
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.078
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20197 0 0 0 0 0 0 0 0 0 0 3 4
2019/2020210 34 1 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
2023/2024179 7 28 23 18 18 63 2 7 3 7 3 0
Totale 1.927