IRIS
BAGNI, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 27.288
EU - Europa 2.441
AS - Asia 1.028
Continente sconosciuto - Info sul continente non disponibili 12
SA - Sud America 7
OC - Oceania 6
AF - Africa 1
Totale 30.783
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Nazione #
US - Stati Uniti d'America 27.272
SG - Singapore 646
DE - Germania 426
UA - Ucraina 337
PL - Polonia 329
IE - Irlanda 309
CN - Cina 261
FR - Francia 239
IT - Italia 200
SE - Svezia 182
GB - Regno Unito 173
RU - Federazione Russa 124
FI - Finlandia 70
KR - Corea 69
BE - Belgio 17
IL - Israele 16
CH - Svizzera 15
CA - Canada 13
EU - Europa 10
IN - India 8
JP - Giappone 8
AU - Australia 6
NL - Olanda 6
HK - Hong Kong 5
VN - Vietnam 5
BR - Brasile 3
CL - Cile 3
RO - Romania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AT - Austria 2
CZ - Repubblica Ceca 2
DM - Dominica 2
GR - Grecia 2
IR - Iran 2
AL - Albania 1
AM - Armenia 1
BD - Bangladesh 1
CO - Colombia 1
DK - Danimarca 1
EG - Egitto 1
ES - Italia 1
ID - Indonesia 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
MX - Messico 1
MY - Malesia 1
NO - Norvegia 1
PK - Pakistan 1
RS - Serbia 1
TR - Turchia 1
Totale 30.783
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Città #
Wilmington 7.398
Houston 7.190
Woodbridge 6.908
Fairfield 1.036
Ann Arbor 605
Singapore 569
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 24
Mountain View 24
Norwalk 21
Redwood City 21
London 20
Brussels 17
Verona 11
Hefei 10
Toronto 10
University Park 10
Savignone 9
Seoul 9
Guangzhou 8
Nanjing 8
Nuremberg 8
Phoenix 8
Detroit 7
San Francisco 7
Shanghai 7
Tappahannock 7
Washington 6
Auburn Hills 5
Helsinki 5
Hong Kong 5
Indiana 5
Kilburn 5
Kunming 5
Lappeenranta 5
Leawood 5
Naples 5
Augusta 4
Colorado Springs 4
Hounslow 4
Palermo 4
Palo Alto 4
Prescot 4
Saint Petersburg 4
Tel Aviv 4
Zurich 4
Azzano Decimo 3
Chiswick 3
Hangzhou 3
Ho Chi Minh City 3
Islington 3
Jinan 3
Kemerovo 3
Las Vegas 3
Lausanne 3
Munich 3
Redmond 3
Salerno 3
Shenzhen 3
Amsterdam 2
Brno 2
Catania 2
Chengdu 2
Chennai 2
Chicago 2
Clearwater 2
Council Bluffs 2
Exeter 2
Fuzhou 2
Groningen 2
Hyderabad 2
Langenargen 2
Los Angeles 2
Mcallen 2
Moreno Valley 2
New Bedfont 2
North Hollywood 2
Nürnberg 2
Padova 2
Totale 28.139
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Nome #
Fragile X mental retardation protein control of neuronal mRNA metabolism: Insights into mRNA stability 474
The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at Synapses 472
Structure of Xenopus laevis ribosomal protein L32 and its expression during development 469
Expression of the gene for mitoribosomal protein S12 is controlled in human cells at the levels of transcription, RNA splicing, and translation 465
Abnormal mGlu 5 receptor/endocannabinoid coupling in mice lacking FMRP and BC1 RNA 456
The pyrimidine sequence encompassing the transcription start point of Xenopus laevis ribosomal-protein-encoding genes is not obligatory for activity in oocytes 452
Acetylation of RTN-1C regulates the induction of ER stress by the inhibition of HDAC activity in neuroectodermal tumors. 450
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability 447
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 437
The Fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses 436
Molecular dissection of the events leading to inactivation of the FMR1 gene 436
SnapShot: FMRP mRNA targets and diseases 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 430
Ribosomal protein genes in Xenopus laevis: organization, structure and identification of the cis-element responsible for their translational control 429
Abnormal striatal GABA transmission in the mouse model for the fragile X syndrome 428
Sequence of the gene coding for ribosomal protein S8 of Xenopus laevis 426
Nerve-independence of limb regeneration in larval Xenopus laevis is correlated to the level of fgf-2 mRNA expression in limb tissues. 422
Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome 421
Molecular dynamics simulations show how the FMRP Ile304Asn mutation destabilizes the KH2 domain structure and affects its function 421
The nuclear RNA-binding protein Sam68 translocates to the cytoplasm and associates with the polysomes in mouse spermatocytes 420
Autism Spectrum Disorders: Translating human deficits into mouse behavior 420
Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains 416
BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses 415
SnapShot: FMRP interacting proteins 413
A somatic mutation in the 5 ' UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency 410
Chemical stimulation of synaptosomes modulates alpha-Ca2+/calmodulin-dependent protein kinase II mRNA association to polysomes 410
Role of atrial natriuretic peptide in the suppression of lysophosphatydic acid-induced rat aortic smooth muscle (RASM) cell growth 406
On BC1 RNA and the fragile X mental retardation protein 405
The Drosophila zinc finger transcription factor CF2 is a myogenic marker downstream of MEF2 during muscle development 405
Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS 404
The brain cytoplasmic RNA BC1 regulates dopamine D2 receptor-mediated transmission in the striatum 403
CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic Spine formation 402
mRNPs, polysomes or granules: FMRP in neuronal protein synthesis 397
Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: Genotype-phenotype correlation 396
FMRP regulates multipolar to bipolar transition affecting neuronal migration and cortical circuitry 393
Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control 392
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 390
The FMRP regulon: From targets to disease convergence 390
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 388
The transcriptional factor CF2 is a mediator of EGF-R-activated dorsoventral patterning in Drosophila oogenesis 387
Elevated FMR1 mRNA in premutation carriers is due to increased transcription 386
The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines 385
Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations 380
Gar1p binds to the small nucleolar RNAs snR10 and snR30 in vitro through a nontypical RNA binding element 374
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. 372
Cortical and subcortical distribution of ionotropic purinergic receptor subunit type 1 (P2X(1)R) immunoreactive neurons in the rat forebrain 371
Another view of the role of FMRP in translational regulation 371
Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif 370
Signals, synapses, and synthesis: how new proteins control plasticity 370
Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations 367
Atrial natriuretic peptide induces cell death in human hepatoblastoma (HepG2) through the involvement of NADPH oxidase [2] 365
FMRP and its target RNAs: Fishing for the specificity 355
Altered neuronal network and rescue in a human MECP2 duplication model 354
Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders. 341
Novel RNA-binding motif: The KH module 340
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 317
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. 255
Fragile X syndrome: Causes, diagnosis, mechanisms, and therapeutics 198
The autism- and schizophrenia-associated protein CYFIP1 regulates bilateral brain connectivity and behaviour 183
The Fragile X Protein binds mRNAs involved in cancer progression and modulates metastasis formation 166
Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and Intelligence 159
Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse 159
The Fragile X mental retardation protein regulates matrix metalloproteinase 9 mRNA at synapses 152
Alpha2-containing glycine receptors promote neonatal spontaneous activity of striatal medium spiny neurons and support maturation of glutamatergic inputs 151
Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: What a fly and mouse model can teach us 150
The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning 150
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes 149
Molecular and cellular aspects of mental retardation in the Fragile X syndrome: From gene mutation/s to spine dysmorphogenesis 148
The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome 148
Fragile X syndrome: From protein function to therapy 145
Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis 139
MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion 138
A Synaptic Perspective of Fragile X Syndrome and Autism Spectrum Disorders 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
A unique binding mode of the eukaryotic translation initiation factor 4E for guiding the design of novel peptide inhibitors 135
Cognitive Dysfunctions in Intellectual Disabilities: The Contributions of the Ras-MAPK and PI3K-AKT-mTOR Pathways 133
Fragile X syndrome: From protein function to therapy 131
Cooperativity in RNA-protein interactions: The complex is more than the sum of its partners 128
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene 128
Gender Equality from a European Perspective: Myth and Reality 127
SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse 123
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease 123
Makorin ring zinc finger protein 1 (MKRN1), a novel poly(A)-binding protein-interacting protein, stimulates translation in nerve cells 122
FXR2P exerts a positive translational control and is required for the activity-Dependent Increase of PSD95 expression 121
Synaptopathy - From biology to therapy 120
P2X2R purinergic receptor subunit mRNA and protein are expressed by all hypothalamic hypocretin/orexin neurons 119
Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome 119
Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to Synaptic Deficits in Fragile X Syndrome 118
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 111
Somatosensory map expansion and altered processing of tactile inputs in a mouse model of fragile X syndrome 111
Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice 103
Neurons acetylate their way to migration 100
Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice 99
Totale 29.828
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Categoria #
all - tutte 65.465
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 65.465
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206.875 0 0 513 596 595 684 570 569 733 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
2022/20231.595 134 82 33 214 131 358 104 174 171 37 117 40
2023/2024513 67 20 36 7 76 100 15 34 13 5 9 131
2024/20251.124 83 676 365 0 0 0 0 0 0 0 0 0
Totale 31.176