IRIS
PERSICHETTI, Francesca
 Distribuzione geografica
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Continente #
EU - Europa 1.483
NA - Nord America 1.341
AS - Asia 194
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 1
Totale 3.021
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Nazione #
US - Stati Uniti d'America 1.331
IE - Irlanda 466
SE - Svezia 369
DE - Germania 188
UA - Ucraina 171
IT - Italia 147
FI - Finlandia 93
CN - Cina 77
HK - Hong Kong 48
SG - Singapore 30
GB - Regno Unito 21
BE - Belgio 16
CA - Canada 9
IN - India 9
IR - Iran 9
VN - Vietnam 8
TR - Turchia 7
FR - Francia 5
NL - Olanda 4
EU - Europa 2
JP - Giappone 2
PK - Pakistan 2
BD - Bangladesh 1
CL - Cile 1
CU - Cuba 1
ES - Italia 1
KR - Corea 1
LI - Liechtenstein 1
RU - Federazione Russa 1
Totale 3.021
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Città #
Dublin 460
Jacksonville 305
Chandler 163
Dearborn 156
Ann Arbor 79
Wilmington 75
San Mateo 61
Lawrence 55
Princeton 55
Hong Kong 48
Beijing 35
Piemonte 35
Trieste 30
Andover 29
Boardman 22
Philadelphia 20
Ashburn 14
Bremen 14
Brussels 14
Singapore 14
Monmouth Junction 12
Woodbridge 12
Norwalk 10
Rome 10
Dong Ket 8
Kocaeli 7
Menlo Park 7
Toronto 7
Milan 6
Nanjing 6
Sacramento 6
Hefei 5
Hebei 4
Kunming 4
Berlin 3
Dallas 3
Fairfield 3
Falls Church 3
Fuzhou 3
Guangzhou 3
Helsinki 3
Henderson 3
Houston 3
Nanchang 3
Phoenix 3
Scuola 3
Turin 3
Zanjan 3
Alessandria 2
Amsterdam 2
Ardabil 2
Borgomanero 2
Castelnuovo Bormida 2
Des Moines 2
Gunzenhausen 2
Lahore 2
Leawood 2
Minatomirai 2
Munich 2
Novara 2
Paris 2
Pozzuolo del Friuli 2
Priocca 2
Romainville 2
Rozzano 2
Waanrode 2
Winnipeg 2
Zhengzhou 2
Baotou 1
Bolzaneto 1
Caserta 1
Cassano Magnago 1
Changsha 1
Cividale Del Friuli 1
Dhaka 1
Dreieich 1
Eboli 1
Grafing 1
Havana 1
Jinan 1
Kashan 1
Los Angeles 1
Moruzzo 1
Mülheim 1
Nanning 1
Padova 1
Portland 1
San Diego 1
Sant'arpino 1
Seattle 1
Seodaemun-gu 1
Shenyang 1
Simi Valley 1
Solna 1
Taiyuan 1
Tarzo 1
Torino 1
Totale 1.899
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Nome #
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells 87
Engineering Translation in Mammalian Cell Factories to Increase Protein Yield: The Unexpected Use of Long Non-Coding SINEUP RNAs 85
Differential expression of normal and mutant Huntington’s disease gene alleles 81
The HD mutation does not alter neuronal death in the striatum of HdhQ92 hnock-in mice after mild focal ischemia 80
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease 79
Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segment 79
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia 1 72
Trinucleotide repeat length: instability and age of onset in Huntington’s disease 69
Disequilibrium of multiple DNA markers on the human Y chromosome 67
Huntington’s disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains 66
Autosomal dominant pure cerebellar ataxia 66
An Air-well sparging minifermenter system for high-throughput protein production. 65
HLA linked spinocerebellar ataxia: a clinical, neuropathologic and genetic study of large Italian kindreds 64
Inactivation of the mouse Huntington’s disease gene homolog (Hdh) 62
CEPH consortium map of chromosome 14 62
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington’s disease 61
The mouse Huntington’s disease gene homologue (Hdh) 60
Recurrent simple tandem repeat mutations during human Y chromosome radiation in Caucasian subpopulation 60
The RNA-binding protein ILF3 binds to transposable element sequences in SINEUP lncRNAs 60
SINEUPs are modular antisense long non-coding RNAs that increase synthesis of target proteins in cells 59
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 59
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases 59
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins 58
SINEUPs: A new class of natural and synthetic antisense long non-coding RNAs that activate translation 58
An additional HindIII polymorphism at the coagulation factor XIII A locus 56
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 55
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum 55
Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneurons 54
Tumor necrosis factor receptor-associated factor 6 (TRAF6) associates with huntingtin protein and promotes its atypical ubiquitination to enhance aggregate formation 54
The gene for spinal cerebellar ataxia 1 (SCA 1) is flanked by two closely linked highly polymorphic microsatellite loci 54
SINEUPs: a novel toolbox for RNA therapeutics 54
Structural Properties of Polyglutamine Aggregates Investigated via Molecular Dynamics Simulations 52
Huntington's disease 52
Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice 52
Spinocerebellar ataxia (SCA 1) in two large Italian kindreds: evidence in favor of a locus position distal to GLO 1 and HLA cluster 49
Entrapment into liposomes of fusicoccin binding sites 48
Factors Associated with HD CAG repeat instability in Huntington's disease 48
Neuronal hemoglobin affects dopaminergic cells' response to stress 47
Effects of Pin1 loss in HdhQ111 knock-in mice 46
LINE-1 copy number variation in Alzheimer’s disease 45
SINEUP non-coding RNAs rescue defective frataxin expression and activity in a cellular model of Friedreich's Ataxia 45
The human Y chromosome shows a reduced level of DNA polymorphism 43
Mesencephalic dopaminergic neurons express a repertoire of olfactory receptors and respond to odorant-like molecules. 43
Ser46 phosphorylation and prolyl-isomerase Pin1-mediated isomerization of p53 are key events in p53-dependent apoptosis induced by mutant huntingtin 43
Rrs1 is involved in endoplasmic reticulum stress response in Huntington disease 42
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles 42
Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice 40
Huntingtin polyQ Mutation Impairs the 17β-Estradiol/Neuroglobin Pathway Devoted to Neuron Survival 38
Normal and expanded Huntington’s disease gene alleles produce distinguishable proteins due to translation across the CAG repeat 38
Genome-wide analysis of mammalian promoter architecture and evolution 38
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number-dependent manner 36
The genetic defect causing Huntington's disease: repeated in other contexts? 32
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 31
Specific transcriptional programs differentiate ICOS from CD28 costimulatory signaling in human Naïve CD4+ T cells 30
Analysis of LINE1 Retrotransposons in Huntington's Disease 26
SINEUP non-coding RNA activity depends on specific N6-methyladenosine nucleotides 20
Transposable element activation promotes neurodegeneration in a Drosophila model of Huntington's disease 18
LINE-1 regulates cortical development by acting as long non-coding RNAs 15
Neuronal haemoglobin induces loss of dopaminergic neurons in mouse Substantia nigra, cognitive deficits and cleavage of endogenous α-synuclein 9
Totale 3.068
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Categoria #
all - tutte 16.025
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 16.025
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020517 0 1 50 9 95 100 109 25 53 14 61 0
2020/2021420 58 1 51 6 52 8 56 11 63 14 73 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
2024/202517 17 0 0 0 0 0 0 0 0 0 0 0
Totale 3.068