IRIS
PERSICHETTI, Francesca
 Distribuzione geografica
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Continente #
EU - Europa 2.228
NA - Nord America 2.108
AS - Asia 1.263
SA - Sud America 165
AF - Africa 28
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.794
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Nazione #
US - Stati Uniti d'America 2.062
RU - Federazione Russa 500
IE - Irlanda 467
SG - Singapore 431
SE - Svezia 376
CN - Cina 276
DE - Germania 226
HK - Hong Kong 192
VN - Vietnam 189
UA - Ucraina 179
IT - Italia 176
BR - Brasile 138
FI - Finlandia 94
FR - Francia 83
GB - Regno Unito 55
IN - India 33
CA - Canada 31
KR - Corea 29
ID - Indonesia 20
JP - Giappone 19
BE - Belgio 17
AR - Argentina 16
BD - Bangladesh 13
AT - Austria 12
NL - Olanda 12
PL - Polonia 12
TR - Turchia 12
ZA - Sudafrica 11
IR - Iran 10
MX - Messico 8
BJ - Benin 7
ES - Italia 7
PK - Pakistan 7
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
PH - Filippine 4
SA - Arabia Saudita 4
EC - Ecuador 3
IQ - Iraq 3
KZ - Kazakistan 3
CH - Svizzera 2
CI - Costa d'Avorio 2
CL - Cile 2
CO - Colombia 2
CZ - Repubblica Ceca 2
EG - Egitto 2
EU - Europa 2
HN - Honduras 2
JO - Giordania 2
LT - Lituania 2
PE - Perù 2
SN - Senegal 2
TH - Thailandia 2
BB - Barbados 1
BN - Brunei Darussalam 1
CR - Costa Rica 1
CU - Cuba 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
HU - Ungheria 1
IL - Israele 1
KE - Kenya 1
KG - Kirghizistan 1
LI - Liechtenstein 1
LV - Lettonia 1
MA - Marocco 1
NP - Nepal 1
PT - Portogallo 1
PY - Paraguay 1
RS - Serbia 1
SV - El Salvador 1
TW - Taiwan 1
VE - Venezuela 1
Totale 5.794
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Città #
Dublin 461
Jacksonville 306
Hong Kong 191
Chandler 163
Dearborn 156
San Jose 149
Singapore 145
Ashburn 114
Beijing 100
Ann Arbor 79
Wilmington 75
Moscow 66
San Mateo 61
Lawrence 55
Los Angeles 55
Princeton 55
Ho Chi Minh City 53
Lauterbourg 52
Council Bluffs 51
Hanoi 43
Piemonte 35
Trieste 33
Buffalo 31
Andover 29
New York 28
Seoul 26
São Paulo 26
Boardman 22
Philadelphia 20
Santa Clara 20
Orem 16
Brussels 15
Bremen 14
Monmouth Junction 12
Munich 12
Toronto 12
Woodbridge 12
Atlanta 11
Brooklyn 11
Dallas 11
Jakarta 11
Montreal 11
Redondo Beach 11
Rome 11
Tokyo 11
Boston 10
Denver 10
Norwalk 10
Novara 10
Chicago 9
Haiphong 9
Milan 9
Poplar 9
Tianjin 9
Vienna 9
Amsterdam 8
Dong Ket 8
Frankfurt am Main 8
Houston 8
Johannesburg 8
Manchester 8
Nuremberg 8
Brasília 7
Cotonou 7
Da Nang 7
Hefei 7
Kocaeli 7
Menlo Park 7
Nanjing 7
Stockholm 7
Warsaw 7
Columbus 6
London 6
Phoenix 6
Sacramento 6
Can Tho 5
Guangzhou 5
Mumbai 5
Thái Bình 5
Hebei 4
Helsinki 4
Hillsboro 4
Kunming 4
Lahore 4
New Delhi 4
Paris 4
Roubaix 4
San Francisco 4
Shanghai 4
Tashkent 4
Turin 4
Vũng Tàu 4
Belo Horizonte 3
Berlin 3
Campinas 3
Chennai 3
Fairfield 3
Falls Church 3
Fuzhou 3
Henderson 3
Totale 3.214
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Nome #
Engineering Translation in Mammalian Cell Factories to Increase Protein Yield: The Unexpected Use of Long Non-Coding SINEUP RNAs 159
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells 140
Differential expression of normal and mutant Huntington’s disease gene alleles 139
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases 139
An Air-well sparging minifermenter system for high-throughput protein production. 130
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia 1 128
CEPH consortium map of chromosome 14 124
SINEUPs: A new class of natural and synthetic antisense long non-coding RNAs that activate translation 124
Specific transcriptional programs differentiate ICOS from CD28 costimulatory signaling in human Naïve CD4+ T cells 123
The RNA-binding protein ILF3 binds to transposable element sequences in SINEUP lncRNAs 122
Autosomal dominant pure cerebellar ataxia 121
Entrapment into liposomes of fusicoccin binding sites 119
An additional HindIII polymorphism at the coagulation factor XIII A locus 115
SINEUPs are modular antisense long non-coding RNAs that increase synthesis of target proteins in cells 115
Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segment 113
The HD mutation does not alter neuronal death in the striatum of HdhQ92 hnock-in mice after mild focal ischemia 112
The gene for spinal cerebellar ataxia 1 (SCA 1) is flanked by two closely linked highly polymorphic microsatellite loci 112
Disequilibrium of multiple DNA markers on the human Y chromosome 112
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease 111
Structural Properties of Polyglutamine Aggregates Investigated via Molecular Dynamics Simulations 111
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins 108
Trinucleotide repeat length: instability and age of onset in Huntington’s disease 106
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum 106
HLA linked spinocerebellar ataxia: a clinical, neuropathologic and genetic study of large Italian kindreds 105
Expression analysis of the long non-coding RNA antisense to Uchl1 (AS Uchl1) during dopaminergic cells' differentiation in vitro and in neurochemical models of Parkinson's disease 105
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington’s disease 103
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number-dependent manner 101
SINEUPs: a novel toolbox for RNA therapeutics 100
Effects of Pin1 loss in HdhQ111 knock-in mice 99
SINEUP non-coding RNAs rescue defective frataxin expression and activity in a cellular model of Friedreich's Ataxia 98
Factors Associated with HD CAG repeat instability in Huntington's disease 94
Recurrent simple tandem repeat mutations during human Y chromosome radiation in Caucasian subpopulation 93
Huntington’s disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains 92
Inactivation of the mouse Huntington’s disease gene homolog (Hdh) 92
The gene for autosomal dominant spinocerebellar ataxia (SCA 1) maps centromeric to D6S89 and shows no recombination in nine large kindreds, with a dinucleotide repeat at the AM10 locus 91
SINEUP non-coding RNA activity depends on specific N6-methyladenosine nucleotides 90
LINE-1 regulates cortical development by acting as long non-coding RNAs 89
The human Y chromosome shows a reduced level of DNA polymorphism 89
The E3 Ubiquitin Ligase TRAF6 Interacts with the Cellular Prion Protein and Modulates Its Solubility and Recruitment to Cytoplasmic p62/SQSTM1-Positive Aggresome-Like Structures 87
Analysis of LINE1 Retrotransposons in Huntington's Disease 86
The mouse Huntington’s disease gene homologue (Hdh) 84
Huntingtin polyQ Mutation Impairs the 17β-Estradiol/Neuroglobin Pathway Devoted to Neuron Survival 83
Mesencephalic dopaminergic neurons express a repertoire of olfactory receptors and respond to odorant-like molecules. 83
Neuronal hemoglobin affects dopaminergic cells' response to stress 83
Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneurons 81
Huntington's disease 81
Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice 81
Genome-wide analysis of mammalian promoter architecture and evolution 81
Tumor necrosis factor receptor-associated factor 6 (TRAF6) associates with huntingtin protein and promotes its atypical ubiquitination to enhance aggregate formation 80
Rrs1 is involved in endoplasmic reticulum stress response in Huntington disease 76
LINE-1 copy number variation in Alzheimer’s disease 73
Ser46 phosphorylation and prolyl-isomerase Pin1-mediated isomerization of p53 are key events in p53-dependent apoptosis induced by mutant huntingtin 72
Spinocerebellar ataxia (SCA 1) in two large Italian kindreds: evidence in favor of a locus position distal to GLO 1 and HLA cluster 71
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles 66
Normal and expanded Huntington’s disease gene alleles produce distinguishable proteins due to translation across the CAG repeat 66
The genetic defect causing Huntington's disease: repeated in other contexts? 66
Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice 64
Neuronal haemoglobin induces loss of dopaminergic neurons in mouse Substantia nigra, cognitive deficits and cleavage of endogenous α-synuclein 59
Transposable element activation promotes neurodegeneration in a Drosophila model of Huntington's disease 54
Internal ribosome entry sites enhance translation in trans in antisense non-coding SINEUP and circular RNAs 39
Totale 5.846
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Categoria #
all - tutte 29.352
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 29.352
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202127 0 0 0 0 0 0 0 0 0 0 0 27
2021/2022522 29 13 120 122 11 4 32 15 31 22 57 66
2022/20231.029 87 42 60 54 88 120 7 62 449 5 36 19
2023/2024235 26 19 27 10 57 2 51 3 0 3 12 25
2024/2025681 17 1 41 13 23 86 48 67 185 65 11 124
2025/20262.114 57 131 158 330 215 174 259 328 141 190 98 33
Totale 5.846