BAGNI, CLAUDIA
 Distribuzione geografica
Continente #
NA - Nord America 27.329
EU - Europa 2.580
AS - Asia 1.117
SA - Sud America 16
Continente sconosciuto - Info sul continente non disponibili 12
OC - Oceania 8
AF - Africa 1
Totale 31.063
Nazione #
US - Stati Uniti d'America 27.309
SG - Singapore 705
DE - Germania 429
UA - Ucraina 337
PL - Polonia 329
IE - Irlanda 309
CN - Cina 287
FR - Francia 240
RU - Federazione Russa 236
IT - Italia 204
SE - Svezia 182
GB - Regno Unito 178
FI - Finlandia 72
KR - Corea 69
BE - Belgio 17
CA - Canada 16
IL - Israele 16
CH - Svizzera 15
BR - Brasile 12
NL - Olanda 12
EU - Europa 10
IN - India 9
AU - Australia 8
JP - Giappone 8
HK - Hong Kong 5
VN - Vietnam 5
LT - Lituania 4
AT - Austria 3
CL - Cile 3
RO - Romania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BD - Bangladesh 2
CZ - Repubblica Ceca 2
DM - Dominica 2
GR - Grecia 2
IR - Iran 2
MX - Messico 2
TR - Turchia 2
AL - Albania 1
AM - Armenia 1
CO - Colombia 1
DK - Danimarca 1
EG - Egitto 1
ES - Italia 1
ID - Indonesia 1
IQ - Iraq 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
MY - Malesia 1
NO - Norvegia 1
PK - Pakistan 1
PT - Portogallo 1
RS - Serbia 1
Totale 31.063
Città #
Wilmington 7.398
Houston 7.190
Woodbridge 6.908
Fairfield 1.036
Singapore 606
Ann Arbor 605
Chandler 532
Ashburn 492
Seattle 413
Cambridge 347
Kraków 329
Jacksonville 310
Dublin 306
Medford 242
Beijing 167
Santa Clara 146
Dearborn 131
Lawrence 110
Rome 77
Moscow 70
New York 69
Mülheim 58
San Diego 55
Boardman 49
Creede 34
Menlo Park 30
Falls Church 27
San Mateo 27
Milan 26
Mountain View 24
London 22
Norwalk 21
Redwood City 21
Brussels 17
Toronto 11
Verona 11
Hefei 10
University Park 10
Savignone 9
Seoul 9
Council Bluffs 8
Guangzhou 8
Nanjing 8
Nuremberg 8
Phoenix 8
Shanghai 8
Detroit 7
Helsinki 7
San Francisco 7
Tappahannock 7
Washington 7
Auburn Hills 5
Hangzhou 5
Hong Kong 5
Indiana 5
Kilburn 5
Kunming 5
Lappeenranta 5
Leawood 5
Naples 5
Shenzhen 5
Amsterdam 4
Augusta 4
Colorado Springs 4
Hounslow 4
Palermo 4
Palo Alto 4
Prescot 4
Saint Petersburg 4
Tel Aviv 4
Wuxi 4
Zurich 4
Azzano Decimo 3
Chiswick 3
Frankfurt am Main 3
Fuzhou 3
Ho Chi Minh City 3
Islington 3
Jinan 3
Kemerovo 3
Las Vegas 3
Lausanne 3
Munich 3
Redmond 3
Salerno 3
Brno 2
Canberra 2
Catania 2
Changsha 2
Chengdu 2
Chennai 2
Chicago 2
Clearwater 2
Exeter 2
Groningen 2
Hyderabad 2
Langenargen 2
Los Angeles 2
Mcallen 2
Moreno Valley 2
Totale 28.201
Nome #
Expression of the gene for mitoribosomal protein S12 is controlled in human cells at the levels of transcription, RNA splicing, and translation 484
Fragile X mental retardation protein control of neuronal mRNA metabolism: Insights into mRNA stability 475
The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses 474
Structure of Xenopus laevis ribosomal protein L32 and its expression during development 469
Abnormal mGlu 5 receptor/endocannabinoid coupling in mice lacking FMRP and BC1 RNA 460
Acetylation of RTN-1C regulates the induction of ER stress by the inhibition of HDAC activity in neuroectodermal tumors. 454
The pyrimidine sequence encompassing the transcription start point of Xenopus laevis ribosomal-protein-encoding genes is not obligatory for activity in oocytes 453
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability 450
From mRNP trafficking to spine dysmorphogenesis: The roots of fragile X syndrome 442
Atrial natriuretic peptide effects on intracellular pH changes and ROS production in HEPG2 cells: Role of p38 MAPK and phospholipase D 440
Molecular dissection of the events leading to inactivation of the FMR1 gene 437
SnapShot: FMRP mRNA targets and diseases 437
The Fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses 436
Individual variability in the translational regulation of ribosomal protein synthesis in Xenopus laevis 435
Human ribosomal protein L4: cloning and sequencing of the cDNA and primary structure of the protein 431
Abnormal striatal GABA transmission in the mouse model for the fragile X syndrome 431
Ribosomal protein genes in Xenopus laevis: organization, structure and identification of the cis-element responsible for their translational control 430
Sequence of the gene coding for ribosomal protein S8 of Xenopus laevis 426
Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome 424
Nerve-independence of limb regeneration in larval Xenopus laevis is correlated to the level of fgf-2 mRNA expression in limb tissues. 423
The nuclear RNA-binding protein Sam68 translocates to the cytoplasm and associates with the polysomes in mouse spermatocytes 422
Molecular dynamics simulations show how the FMRP Ile304Asn mutation destabilizes the KH2 domain structure and affects its function 422
Autism Spectrum Disorders: Translating human deficits into mouse behavior 421
Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains 418
BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses 417
SnapShot: FMRP interacting proteins 414
A somatic mutation in the 5 ' UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency 413
Chemical stimulation of synaptosomes modulates alpha-Ca2+/calmodulin-dependent protein kinase II mRNA association to polysomes 411
Role of atrial natriuretic peptide in the suppression of lysophosphatydic acid-induced rat aortic smooth muscle (RASM) cell growth 407
The Drosophila zinc finger transcription factor CF2 is a myogenic marker downstream of MEF2 during muscle development 407
On BC1 RNA and the fragile X mental retardation protein 406
The brain cytoplasmic RNA BC1 regulates dopamine D2 receptor-mediated transmission in the striatum 404
CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic Spine formation 404
Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS 404
mRNPs, polysomes or granules: FMRP in neuronal protein synthesis 397
Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: Genotype-phenotype correlation 397
FMRP regulates multipolar to bipolar transition affecting neuronal migration and cortical circuitry 394
Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control 393
The FMRP regulon: From targets to disease convergence 393
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P 392
Isolation and nucleotide sequences of cDNAs for Xenopus laevis ribosomal protein S8: Similarities in the 5' and 3' untranslated regions of mRNAs for various r-proteins 389
Elevated FMR1 mRNA in premutation carriers is due to increased transcription 388
The transcriptional factor CF2 is a mediator of EGF-R-activated dorsoventral patterning in Drosophila oogenesis 388
The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines 386
Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations 381
Gar1p binds to the small nucleolar RNAs snR10 and snR30 in vitro through a nontypical RNA binding element 375
Another view of the role of FMRP in translational regulation 374
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. 373
Cortical and subcortical distribution of ionotropic purinergic receptor subunit type 1 (P2X(1)R) immunoreactive neurons in the rat forebrain 372
Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif 371
Signals, synapses, and synthesis: how new proteins control plasticity 371
Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations 368
Atrial natriuretic peptide induces cell death in human hepatoblastoma (HepG2) through the involvement of NADPH oxidase [2] 368
Altered neuronal network and rescue in a human MECP2 duplication model 358
FMRP and its target RNAs: Fishing for the specificity 355
Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders. 342
Novel RNA-binding motif: The KH module 341
Molecular insights into mental retardation: multiple functions for the Fragile X mental retardation protein? 333
New insights into the metastatic behavior after breast cancer surgery, according to well-established clinicopathological variables and molecular subtypes 320
Disruption of mTOR and MAPK pathways correlates with severity in idiopathic autism 273
Identification of a segment of the small nucleolar ribonucleoprotein-associated protein GAR1 that is sufficient for nucleolar accumulation 271
Differential usage of transcriptional start site and polyadenylation site in FMR1 premutation alleles. 256
Fragile X syndrome: Causes, diagnosis, mechanisms, and therapeutics 202
The autism- and schizophrenia-associated protein CYFIP1 regulates bilateral brain connectivity and behaviour 184
The Fragile X Protein binds mRNAs involved in cancer progression and modulates metastasis formation 168
Alpha2-containing glycine receptors promote neonatal spontaneous activity of striatal medium spiny neurons and support maturation of glutamatergic inputs 167
Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse 162
Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and Intelligence 161
The Fragile X mental retardation protein regulates matrix metalloproteinase 9 mRNA at synapses 153
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes 152
Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: What a fly and mouse model can teach us 151
The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning 151
Molecular and cellular aspects of mental retardation in the Fragile X syndrome: From gene mutation/s to spine dysmorphogenesis 150
The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome 149
Fragile X syndrome: From protein function to therapy 146
MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion 144
A Synaptic Perspective of Fragile X Syndrome and Autism Spectrum Disorders 141
Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis 140
A unique binding mode of the eukaryotic translation initiation factor 4E for guiding the design of novel peptide inhibitors 138
The fragile X mental retardation protein regulates tumor invasiveness-related pathways in melanoma cells 137
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia 136
Cognitive Dysfunctions in Intellectual Disabilities: The Contributions of the Ras-MAPK and PI3K-AKT-mTOR Pathways 134
Fragile X syndrome: From protein function to therapy 133
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene 130
Cooperativity in RNA-protein interactions: The complex is more than the sum of its partners 129
Gender Equality from a European Perspective: Myth and Reality 128
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse 124
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease 124
Makorin ring zinc finger protein 1 (MKRN1), a novel poly(A)-binding protein-interacting protein, stimulates translation in nerve cells 124
Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome 122
FXR2P exerts a positive translational control and is required for the activity-Dependent Increase of PSD95 expression 122
P2X2R purinergic receptor subunit mRNA and protein are expressed by all hypothalamic hypocretin/orexin neurons 121
Synaptopathy - From biology to therapy 120
Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to Synaptic Deficits in Fragile X Syndrome 119
Mitochondrial dysfunction in Autism Spectrum Disorder: clinical features and perspectives 115
Cytoplasmic TERT Associates to RNA Granules in Fully Mature Neurons: Role in the Translational Control of the Cell Cycle Inhibitor p15INK4B 113
Somatosensory map expansion and altered processing of tactile inputs in a mouse model of fragile X syndrome 112
Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice 104
Neurons acetylate their way to migration 101
Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice 100
Totale 30.007
Categoria #
all - tutte 68.792
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 68.792


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205.766 0 0 0 0 595 684 570 569 733 1.151 689 775
2020/20216.703 717 942 748 855 651 702 781 633 134 216 193 131
2021/20221.075 58 82 50 52 25 127 49 39 70 162 37 324
2022/20231.590 134 82 33 214 131 358 104 169 171 37 117 40
2023/2024513 67 20 36 7 76 100 15 34 13 5 9 131
2024/20251.435 83 676 371 196 109 0 0 0 0 0 0 0
Totale 31.482