IRIS
PERSICHETTI, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 2.303
EU - Europa 2.236
AS - Asia 1.279
SA - Sud America 172
Continente sconosciuto - Info sul continente non disponibili 55
AF - Africa 29
Totale 6.074
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Nazione #
US - Stati Uniti d'America 2.245
RU - Federazione Russa 500
IE - Irlanda 467
SG - Singapore 438
SE - Svezia 376
CN - Cina 279
DE - Germania 226
HK - Hong Kong 193
VN - Vietnam 189
IT - Italia 182
UA - Ucraina 179
BR - Brasile 140
FI - Finlandia 94
FR - Francia 85
GB - Regno Unito 55
CA - Canada 39
IN - India 34
KR - Corea 29
ID - Indonesia 21
JP - Giappone 19
AR - Argentina 17
BE - Belgio 17
BD - Bangladesh 14
AT - Austria 12
NL - Olanda 12
PL - Polonia 12
TR - Turchia 12
ZA - Sudafrica 11
IR - Iran 10
MX - Messico 8
PK - Pakistan 8
BJ - Benin 7
ES - Italia 7
AE - Emirati Arabi Uniti 5
CO - Colombia 5
UZ - Uzbekistan 5
PH - Filippine 4
SA - Arabia Saudita 4
CL - Cile 3
EC - Ecuador 3
IQ - Iraq 3
KZ - Kazakistan 3
CH - Svizzera 2
CI - Costa d'Avorio 2
CR - Costa Rica 2
CU - Cuba 2
CZ - Repubblica Ceca 2
EG - Egitto 2
EU - Europa 2
HN - Honduras 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
LT - Lituania 2
PE - Perù 2
SN - Senegal 2
TH - Thailandia 2
BB - Barbados 1
BN - Brunei Darussalam 1
CW - ???statistics.table.value.countryCode.CW??? 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
HU - Ungheria 1
IL - Israele 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 6.022
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Città #
Dublin 461
Jacksonville 306
Hong Kong 192
Chandler 163
Dearborn 156
San Jose 152
Singapore 149
Council Bluffs 127
Ashburn 120
Beijing 102
Ann Arbor 79
Wilmington 75
Moscow 66
San Mateo 61
Los Angeles 58
Lawrence 55
Princeton 55
Ho Chi Minh City 53
Lauterbourg 52
Hanoi 43
Columbus 41
Piemonte 35
Trieste 33
Buffalo 32
Andover 29
New York 28
Seoul 26
São Paulo 26
Santa Clara 25
Boardman 22
Philadelphia 21
Orem 16
Brussels 15
Bremen 14
Dallas 13
Toronto 13
Monmouth Junction 12
Montreal 12
Munich 12
Rome 12
Woodbridge 12
Atlanta 11
Brooklyn 11
Chicago 11
Jakarta 11
Redondo Beach 11
Tokyo 11
Boston 10
Denver 10
Milan 10
Norwalk 10
Novara 10
Haiphong 9
Phoenix 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
London 6
Sacramento 6
Can Tho 5
Guangzhou 5
Mumbai 5
Paris 5
Shanghai 5
Thái Bình 5
Hebei 4
Helsinki 4
Hillsboro 4
Kunming 4
Lahore 4
New Delhi 4
Roubaix 4
San Diego 4
San Francisco 4
Tashkent 4
Turin 4
Virginia Beach 4
Vũng Tàu 4
Belo Horizonte 3
Berlin 3
Campinas 3
Chennai 3
Dhaka 3
Fairfield 3
Totale 3.366
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Nome #
Engineering Translation in Mammalian Cell Factories to Increase Protein Yield: The Unexpected Use of Long Non-Coding SINEUP RNAs 166
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases 149
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells 146
Differential expression of normal and mutant Huntington’s disease gene alleles 141
An Air-well sparging minifermenter system for high-throughput protein production. 133
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia 1 131
Specific transcriptional programs differentiate ICOS from CD28 costimulatory signaling in human Naïve CD4+ T cells 129
CEPH consortium map of chromosome 14 129
SINEUPs: A new class of natural and synthetic antisense long non-coding RNAs that activate translation 129
The RNA-binding protein ILF3 binds to transposable element sequences in SINEUP lncRNAs 128
Autosomal dominant pure cerebellar ataxia 124
Entrapment into liposomes of fusicoccin binding sites 124
SINEUPs are modular antisense long non-coding RNAs that increase synthesis of target proteins in cells 119
An additional HindIII polymorphism at the coagulation factor XIII A locus 118
The gene for spinal cerebellar ataxia 1 (SCA 1) is flanked by two closely linked highly polymorphic microsatellite loci 116
Disequilibrium of multiple DNA markers on the human Y chromosome 116
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease 115
Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segment 115
The HD mutation does not alter neuronal death in the striatum of HdhQ92 hnock-in mice after mild focal ischemia 113
Structural Properties of Polyglutamine Aggregates Investigated via Molecular Dynamics Simulations 112
Trinucleotide repeat length: instability and age of onset in Huntington’s disease 111
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum 111
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins 110
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 108
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number-dependent manner 107
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington’s disease 106
HLA linked spinocerebellar ataxia: a clinical, neuropathologic and genetic study of large Italian kindreds 106
SINEUPs: a novel toolbox for RNA therapeutics 106
Effects of Pin1 loss in HdhQ111 knock-in mice 103
SINEUP non-coding RNAs rescue defective frataxin expression and activity in a cellular model of Friedreich's Ataxia 103
LINE-1 regulates cortical development by acting as long non-coding RNAs 99
Inactivation of the mouse Huntington’s disease gene homolog (Hdh) 98
Factors Associated with HD CAG repeat instability in Huntington's disease 96
SINEUP non-coding RNA activity depends on specific N6-methyladenosine nucleotides 95
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 95
Recurrent simple tandem repeat mutations during human Y chromosome radiation in Caucasian subpopulation 94
Huntington’s disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains 93
The human Y chromosome shows a reduced level of DNA polymorphism 93
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 93
Analysis of LINE1 Retrotransposons in Huntington's Disease 90
Neuronal hemoglobin affects dopaminergic cells' response to stress 88
Mesencephalic dopaminergic neurons express a repertoire of olfactory receptors and respond to odorant-like molecules. 87
Genome-wide analysis of mammalian promoter architecture and evolution 87
The mouse Huntington’s disease gene homologue (Hdh) 86
Huntingtin polyQ Mutation Impairs the 17β-Estradiol/Neuroglobin Pathway Devoted to Neuron Survival 86
Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice 83
Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneurons 82
Huntington's disease 82
Tumor necrosis factor receptor-associated factor 6 (TRAF6) associates with huntingtin protein and promotes its atypical ubiquitination to enhance aggregate formation 81
Rrs1 is involved in endoplasmic reticulum stress response in Huntington disease 79
LINE-1 copy number variation in Alzheimer’s disease 75
Ser46 phosphorylation and prolyl-isomerase Pin1-mediated isomerization of p53 are key events in p53-dependent apoptosis induced by mutant huntingtin 75
Spinocerebellar ataxia (SCA 1) in two large Italian kindreds: evidence in favor of a locus position distal to GLO 1 and HLA cluster 72
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles 68
Normal and expanded Huntington’s disease gene alleles produce distinguishable proteins due to translation across the CAG repeat 68
The genetic defect causing Huntington's disease: repeated in other contexts? 67
Neuronal haemoglobin induces loss of dopaminergic neurons in mouse Substantia nigra, cognitive deficits and cleavage of endogenous α-synuclein 66
Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice 66
Transposable element activation promotes neurodegeneration in a Drosophila model of Huntington's disease 60
Internal ribosome entry sites enhance translation in trans in antisense non-coding SINEUP and circular RNAs 46
Totale 6.074
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Categoria #
all - tutte 30.806
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 30.806
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022493 0 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
2025/20262.119 57 131 158 330 215 174 259 328 141 190 98 38
2026/2027223 86 137 0 0 0 0 0 0 0 0 0 0
Totale 6.074