CATALOGO DEI PRODOTTI DELLA RICERCA

PRANDINI, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 1.653
EU - Europa 1.417
AS - Asia 994
SA - Sud America 187
AF - Africa 27
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
AN - Antartide 1
Totale 4.284
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Nazione #
US - Stati Uniti d'America 1.629
RU - Federazione Russa 620
SG - Singapore 419
CN - Cina 280
GB - Regno Unito 246
BR - Brasile 155
VN - Vietnam 110
SE - Svezia 90
DE - Germania 86
IT - Italia 86
HK - Hong Kong 83
FI - Finlandia 73
FR - Francia 68
IE - Irlanda 62
UA - Ucraina 29
KR - Corea 27
IN - India 17
BE - Belgio 16
NL - Olanda 13
AR - Argentina 11
NG - Nigeria 10
CA - Canada 9
ZA - Sudafrica 9
JP - Giappone 8
BD - Bangladesh 7
MX - Messico 7
CO - Colombia 6
IQ - Iraq 6
AT - Austria 5
ID - Indonesia 5
TR - Turchia 5
UZ - Uzbekistan 5
LT - Lituania 4
PK - Pakistan 4
AE - Emirati Arabi Uniti 3
AU - Australia 3
BO - Bolivia 3
EC - Ecuador 3
HN - Honduras 3
KE - Kenya 3
MT - Malta 3
PA - Panama 3
PL - Polonia 3
BA - Bosnia-Erzegovina 2
CL - Cile 2
ET - Etiopia 2
IL - Israele 2
KZ - Kazakistan 2
MA - Marocco 2
PE - Perù 2
PH - Filippine 2
PY - Paraguay 2
RO - Romania 2
SK - Slovacchia (Repubblica Slovacca) 2
VE - Venezuela 2
XK - ???statistics.table.value.countryCode.XK??? 2
AZ - Azerbaigian 1
BG - Bulgaria 1
EE - Estonia 1
EG - Egitto 1
ES - Italia 1
GS - Georgia del Sud e Isole Sandwich Australi 1
HU - Ungheria 1
IR - Iran 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
KW - Kuwait 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LV - Lettonia 1
MY - Malesia 1
NP - Nepal 1
RS - Serbia 1
SA - Arabia Saudita 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
Totale 4.284
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Città #
Chandler 214
Jacksonville 210
Southend 207
Moscow 205
Singapore 198
Dallas 133
Woodbridge 130
Ashburn 124
San Jose 117
Ann Arbor 85
Hong Kong 82
Houston 79
Dublin 62
New York 52
Ho Chi Minh City 45
The Dalles 44
Verona 44
Beijing 31
Lawrence 28
Princeton 28
Los Angeles 25
Nanjing 25
Wilmington 25
Munich 23
Hanoi 18
Helsinki 17
Jinan 16
Brussels 14
Hangzhou 14
Kent 14
Milan 12
São Paulo 12
Buffalo 11
Tianjin 11
Abuja 10
Haikou 10
Redondo Beach 9
Brasília 8
Changsha 8
Jiaxing 8
San Francisco 8
Taizhou 8
Tokyo 8
Chennai 7
Guangzhou 7
Haiphong 7
Lanzhou 7
Orem 7
Rio de Janeiro 7
Santa Clara 7
Shenyang 7
Da Nang 6
London 6
Nanchang 6
Ningbo 6
Nuremberg 6
Siegen 6
Columbus 5
Florence 5
Frankfurt am Main 5
Hebei 5
Johannesburg 5
Phoenix 5
Tashkent 5
Turku 5
Zhengzhou 5
Goiânia 4
Guarulhos 4
Lancaster 4
Montreal 4
Norwalk 4
Poplar 4
Taiyuan 4
Amsterdam 3
Biên Hòa 3
Boardman 3
Can Tho 3
Fairfield 3
Falkenstein 3
Nairobi 3
Porto Alegre 3
Seoul 3
Swansea 3
Vienna 3
Washington 3
Ypsilanti 3
Atlanta 2
Auburn Hills 2
Baghdad 2
Bekasi 2
Bogotá 2
Boston 2
Bratislava 2
Brooklyn 2
Cachoeirinha 2
Campinas 2
Chicago 2
Conselheiro Lafaiete 2
Cuenca 2
Denver 2
Totale 2.664
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Nome #
Detection of allele-specific gene expression on next generation sequencing data 231
A novel synonymous substitution in the GCK gene causes aberrant splicing in an Italian patient with GCK-MODY phenotype 219
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families 201
PLCB3 Loss-of-function Reduces P. aeruginosa-dependent IL-8 Release in Cystic Fibrosis 194
A molecular signature associated with prolonged survival in glioblastoma patients treated with Regorafenib 188
Association between genetic polymorphisms of the insulin receptor substrate-1 (IRS1) gene and cardiovascular events in type 2 diabetes mellitus patients 168
Islands of euchromatic-like sequence and expressed genes within the short arm of HSA21: sequence and copy number variability. 160
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs. 157
Impact of insulin receptor substrate-1 genotypes on platelet reactivity and cardiovascular outcomes in patients with type 2 diabetes mellitus and coronary artery disease 156
Transient Receptor Potential Ankyrin 1 Channels Modulate Inflammatory Response in Respiratory Cells from Patients with Cystic Fibrosis. 156
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. 154
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 150
rs4307059 and rs4141463 study in an Italian cohort with Autism spectrum disorder 150
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 148
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. 144
Role of the C1236T (rs1128503) polymorphism of the MDR-1 gene on clopidogrel responsiveness 141
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 141
no association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder 140
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology. 137
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency. 137
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. 137
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome 135
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy. 134
Islands of euchromatic-like sequence and expressed genes within the heterochromatic regions: lessons from the initial sequence analysis of 21p. 133
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E. 129
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. 128
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I. 127
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance. 111
Totale 4.306
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Categoria #
all - tutte 12.752
article - articoli 8.511
book - libri 0
conference - conferenze 4.241
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.504
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202131 0 0 0 0 0 0 0 0 0 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
2025/20261.671 118 125 118 318 459 107 130 80 108 108 0 0
Totale 4.306