CNR Institutional Research Information System

VACCA, MARCELLA
 Distribuzione geografica
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Continente #
AS - Asia 38
EU - Europa 16
NA - Nord America 15
Totale 69
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Nazione #
SG - Singapore 35
US - Stati Uniti d'America 15
IT - Italia 11
DE - Germania 3
CZ - Repubblica Ceca 2
KR - Corea 2
CN - Cina 1
Totale 69
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Città #
Singapore 31
Naples 11
Hanover 3
Broumy 2
Santa Clara 2
Seoul 2
Forest City 1
Guangzhou 1
Totale 53
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Nome #
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 8
Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model 6
Molecular dissection of two human chromatin disease, Rett syndrome and ICF syndrome 6
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 5
The evolutionary history of the second pseudoautosomal region revised 4
X inactivation and reactivation in X-linked diseases 3
Alla ricerca di un "interruttore molecolare" che riattivi la copia dormiente di MECP2 3
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome 3
Longins and their longins domains:regulated SNAREs and multifunctional SNARE regulators 3
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 3
Exogenous Players in Mitochondria-Related CNS Disorders: Viral Pathogens and Unbalanced Microbiota in the Gut-Brain Axis 2
VAMP7j: A Splice Variant of Human VAMP7 That Modulates Neurite Outgrowth by Regulating L1CAM Transport to the Plasma Membrane 2
VAMP subfamilies identified by specific R-SNARE motifs 2
Deep Insights Into Mecp2-Driven Transcriptional (De)Regulation At Embryonic Developmental Stage Through RNA-Seq Data Analysis 2
A novel dual mechanism controlling the localization and function of exocytic v-SNAREs 2
Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling 2
Genetic variability at the second pseudoautosomal region in ancient and modern humans 2
Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms. 2
Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region 2
presentazione progetto AIR2016 1
Sviluppo di nuovi strumenti preclinici per il trattamento della sindrome di Rett, basati sulla riattivazione farmacologica di Mecp2 1
Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia. 1
Nuclear and Cytoplasmatic Players in Mitochondria-Related CNS Disorders: Chromatin Modifications and Subcellular Trafficking 1
Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes. 1
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. 1
Meccanismi epigenetici che regolano l'espressione del gene pseudoautosomale SYBL1 1
Totale 69
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Categoria #
all - tutte 498
article - articoli 306
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 804
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20244 0 0 0 0 0 0 0 0 0 0 3 1
2024/202565 15 0 49 1 0 0 0 0 0 0 0 0
Totale 69