CNR Institutional Research Information System

DELLA RAGIONE, FLORIANA
 Distribuzione geografica
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Continente #
NA - Nord America 167
AS - Asia 125
EU - Europa 32
AF - Africa 1
Totale 325
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Nazione #
US - Stati Uniti d'America 167
SG - Singapore 111
IT - Italia 32
CN - Cina 5
KR - Corea 5
JP - Giappone 2
VN - Vietnam 2
DZ - Algeria 1
Totale 325
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Città #
Santa Clara 149
Singapore 77
Naples 13
Aversa 10
Seoul 5
Rome 4
Avellino 3
Guangzhou 2
Hanoi 2
Kyoto 2
Rimini 2
Boca Raton 1
Totale 270
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Nome #
Epigenetic control of hypoxia inducible factor-1?-dependent expression of placental growth factor in hypoxic conditions 18
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 13
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs 11
null 9
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 9
Molecular dissection of two human chromatin disease, Rett syndrome and ICF syndrome 9
Transcriptomic and epigenomic landscape in rett syndrome 7
ZFP57/KAP1 Genomic Association and Targeted Epigenetic Regulation at Imprinted and Not Imprinted Loci 7
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 7
Stroke Causes DNA Methylation at Ncx1 Heart Promoter in the Brain Via DNMT1/MeCP2/REST Epigenetic Complex 6
X inactivation and reactivation in X-linked diseases 6
CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY 6
Non-coding RNAs in chromatin disease involving neurological defects 6
Relationships between MeCP2 and pericentric heterochromatin factors during neural differentiation 6
Glycosphingolipid metabolic reprogramming drives neural differentiation 6
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome 6
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 6
Epigenetic regulation of hypoxia-induced PlGF expression 5
Involvement of HIF-1alfa in hypoxia-induced Placental Growth Factor expression 5
Reduced brain UCP2 expression mediated by microRNA-503 contributes to increased stroke susceptibility in the high-salt fed stroke-prone spontaneously hypertensive rat 5
Glycosphingolipids dependent regulatory circuits controlling gene expression 5
A Multi-Omics approach to get insights into fruit senescence regulatory networks in a tomato landrace with long shelf-life. 5
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome 5
Evaluation of factors involved in the failure of ovum capture in superovulated buffaloes 5
MULTI-OMICS ANALYSIS SHEDS LIGHT ON HOW SHELF-LIFE OF TOMATO FRUIT IS PROLONGED 5
Differential DNA Methylation as a Tool for Non-Invasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies 5
EPITOM: an integrated study of epigenomics in tomato fruit during post-harvest 5
Multi-Omics analysis of tomato fruit senescence 5
INSIGHTS INTO FRUIT SENESCENCE REGULATORY NETWORKS IN A TOMATO LANDRACE WITH LONG SHELF-LIFE 5
MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization 5
Absence of TI-VAMP/Vamp7 Leads to Increased Anxiety in Mice. 5
MeCP2 as a genome-wide modulator: the renewal of an old story. 5
Epigenetic control of hypoxia-induced Placental Growth Factor expression 5
Minimally Invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 4
Role of Mecp2 in the High-Order Chromatin Structure During Neural Differentiation 4
Blood-Brain Barrier Integrity Is Perturbed in a Mecp2-Null Mouse Model of Rett Syndrome 4
Early oxidative damage in Rett mouse brain 4
Epigenetic Factors that Control Pericentric Heterochromatin Organization in Mammals 4
Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 4
The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients 4
Scavenger Receptor B1 oxidative post-translational modifications are responsible for its loss in Rett syndrome 4
Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples 4
Multi-omics data integration provides insights into the post-harvest biology of a long shelf-life tomato landrace 4
Genomic and epigenomic analysis of tomato fruit senescence 4
Analisi molecolare del gene circadiano Period nel lacertide Podarcis sicula 4
GENOME-WIDE ANALYSIS OF HISTONE MODIFICATIONS AND ASSOCIATION WITH RIPENING-RELATED GENES DURING POST-HARVEST IN TOMATO FRUIT 4
Second Human Peudoautosomal Region: Biology, Genes and Implication for the Pathogenesis of Rett Syndrome 4
Subclinical myocardial dysfunction in Rett syndrome 4
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome 4
Meccanismi epigenetici che regolano l'espressione del gene pseudoautosomale SYBL1 4
Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms. 4
Involvement of PGC-1, NRF-1, and NRF-2 in metabolic response by rat liver to hormonal and environmental signals 4
Inflammatory response in repeat breeder buffaloes 3
MECP2, a multi-talented modulator of chromatin architecture 3
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies 3
NPPA/atrial natriuretic peptide is an extracellular modulator of autophagy in the heart 3
Transcriptomic profiles of the ruminal wall in Italian Mediterranean dairy buffaloes fed green forage 3
In vivo studies on possible adverse effects on spermatogenesis and sex steroid receptor mRNA expressions of the fungicide methyl thiophanate in the lizard Podarcis sicula 3
Molecular cloning and characterization of the clock gene period2 in the testis of lizard Podarcis sicula and its expression during seasonal reproductive cycle 2
Progress in the identification and characterization of markers for non invasive diagnosis of X linked aneuploidies 2
MECP2 gene mutation analysis in British and Italian Rett syndrome females 2
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome 2
Exploit Transcriptional Machinery to Develop Therapeutics 2
MeCP2 is required for major satellite forward transcript recruitment at pericentric heterochromatin during neural differentiation 2
Physical mappaing of a retinal-specific trascription factor and the epigenetic mark H3K9me3 correlated to rhodopsin and genome wide retinal loci. 2
DNA methylation, histone modifications and MBD proteins mediate X and Y inactivation of the human gene SYBL1 2
F(4)-neuroprostanes mediate neurological severity in Rett syndrome. 2
MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line 2
Mutation analysis of the MECP2 gene in British and Italian Rett Syndrome females 2
Identification and characterization of markers for NIPD of X linked aneuploidies 1
Identification and characterization of markers for NIPD of X linked aneuploidies 1
SECOND HUMAN PSEUDOAUTOSOMAL REGION: BIOLOGY, GENES AND IMPLICATIONS FOR THE PATHOGENESIS OF RETT SYNDROME 1
The aberrant epigenome of DNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory 1
Totale 338
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Categoria #
all - tutte 1.632
article - articoli 897
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 58
Totale 2.587
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202419 0 0 0 0 0 0 0 0 0 0 19 0
2024/2025319 28 5 98 36 152 0 0 0 0 0 0 0
Totale 338