CATALOGO DEI PRODOTTI DELLA RICERCA

PRANDINI, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 1.403
EU - Europa 1.312
AS - Asia 790
SA - Sud America 169
AF - Africa 9
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
AN - Antartide 1
Totale 3.688
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Nazione #
US - Stati Uniti d'America 1.385
RU - Federazione Russa 562
SG - Singapore 316
CN - Cina 263
GB - Regno Unito 243
BR - Brasile 144
SE - Svezia 90
DE - Germania 82
HK - Hong Kong 80
FI - Finlandia 73
FR - Francia 65
IE - Irlanda 62
VN - Vietnam 60
IT - Italia 56
UA - Ucraina 25
KR - Corea 21
BE - Belgio 16
NL - Olanda 13
IN - India 9
JP - Giappone 8
AR - Argentina 7
CA - Canada 6
CO - Colombia 6
ZA - Sudafrica 6
AT - Austria 5
ID - Indonesia 5
MX - Messico 5
BD - Bangladesh 4
LT - Lituania 4
TR - Turchia 4
UZ - Uzbekistan 4
EC - Ecuador 3
IQ - Iraq 3
MT - Malta 3
PA - Panama 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
BA - Bosnia-Erzegovina 2
BO - Bolivia 2
CL - Cile 2
HN - Honduras 2
KE - Kenya 2
KZ - Kazakistan 2
PH - Filippine 2
PL - Polonia 2
PY - Paraguay 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
XK - ???statistics.table.value.countryCode.XK??? 2
AZ - Azerbaigian 1
BG - Bulgaria 1
EE - Estonia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
IL - Israele 1
IR - Iran 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MA - Marocco 1
PE - Perù 1
PK - Pakistan 1
RS - Serbia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
VE - Venezuela 1
Totale 3.688
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Città #
Chandler 214
Jacksonville 210
Southend 207
Moscow 194
Dallas 132
Woodbridge 130
Singapore 118
Ann Arbor 85
Hong Kong 80
Houston 79
Ashburn 69
Dublin 62
New York 52
Beijing 30
Lawrence 28
Princeton 28
Ho Chi Minh City 26
Nanjing 25
Wilmington 25
Munich 23
Los Angeles 22
Helsinki 17
Jinan 16
Verona 16
Brussels 14
Hangzhou 14
Kent 14
Milan 12
São Paulo 12
The Dalles 11
Tianjin 11
Haikou 10
Buffalo 9
Hanoi 9
Redondo Beach 9
Brasília 8
Changsha 8
Jiaxing 8
San Francisco 8
Taizhou 8
Tokyo 8
Lanzhou 7
Rio de Janeiro 7
Shenyang 7
Guangzhou 6
London 6
Nanchang 6
Ningbo 6
Nuremberg 6
Santa Clara 6
Siegen 6
Columbus 5
Florence 5
Hebei 5
Phoenix 5
Turku 5
Zhengzhou 5
Chennai 4
Goiânia 4
Johannesburg 4
Lancaster 4
Norwalk 4
Taiyuan 4
Tashkent 4
Amsterdam 3
Boardman 3
Fairfield 3
Falkenstein 3
Guarulhos 3
Haiphong 3
Montreal 3
Poplar 3
Seoul 3
Swansea 3
Vienna 3
Ypsilanti 3
Auburn Hills 2
Bekasi 2
Biên Hòa 2
Bogotá 2
Boston 2
Bratislava 2
Brooklyn 2
Cachoeirinha 2
Campinas 2
Chicago 2
Conselheiro Lafaiete 2
Cuenca 2
Da Nang 2
Denver 2
Frankfurt am Main 2
Ixtapaluca 2
Manchester 2
Mestre 2
Mexico City 2
Nairobi 2
Niterói 2
Nova Odessa 2
Orem 2
Ponta Grossa 2
Totale 2.266
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Nome #
Detection of allele-specific gene expression on next generation sequencing data 204
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 188
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 176
A molecular signature associated with prolonged survival in glioblastoma patients treated with Regorafenib 156
PLCB3 Loss-of-function Reduces P. aeruginosa-dependent IL-8 Release in Cystic Fibrosis 150
Islands of euchromatic-like sequence and expressed genes within the short arm of HSA21: sequence and copy number variability. 140
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 139
Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis. 139
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 135
rs4307059 and rs4141463 study in an Italian cohort with Autism spectrum disorder 134
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. 132
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. 132
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 125
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. 125
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. 122
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 122
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 120
no association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder 120
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. 120
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 119
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome 119
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology. 118
Islands of euchromatic-like sequence and expressed genes within the heterochromatic regions: lessons from the initial sequence analysis of 21p. 118
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E. 117
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 117
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. 113
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. 112
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance. 98
Totale 3.710
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Categoria #
all - tutte 11.555
article - articoli 7.735
book - libri 0
conference - conferenze 3.820
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 23.110
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021132 0 0 0 0 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
2024/2025650 33 30 27 110 22 27 73 19 129 30 39 111
2025/20261.075 118 125 118 318 396 0 0 0 0 0 0 0
Totale 3.710