IRIS
FUSCO, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 583
EU - Europa 447
AS - Asia 124
AF - Africa 22
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
SA - Sud America 1
Totale 1.181
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Nazione #
US - Stati Uniti d'America 570
IT - Italia 257
CN - Cina 81
NL - Olanda 46
IE - Irlanda 30
FI - Finlandia 29
IN - India 23
CI - Costa d'Avorio 22
UA - Ucraina 16
DE - Germania 14
GB - Regno Unito 14
CA - Canada 13
SE - Svezia 13
FR - Francia 10
AL - Albania 8
VN - Vietnam 8
TR - Turchia 6
DK - Danimarca 4
IR - Iran 4
AU - Australia 2
BE - Belgio 2
EU - Europa 2
PL - Polonia 2
BR - Brasile 1
ES - Italia 1
MN - Mongolia 1
SG - Singapore 1
SM - San Marino 1
Totale 1.181
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Città #
Chandler 132
Ashburn 47
Amsterdam 46
Princeton 29
Jacksonville 27
Millbury 27
Nanjing 24
Wilmington 24
Pune 22
Naples 20
Beijing 19
Napoli 16
Boston 13
Como 13
Ottawa 12
Dong Ket 8
Rome 8
Tirana 8
Falls Church 7
Florence 6
Kunming 6
Milan 6
Nanchang 6
Seattle 6
Boardman 5
Jiaxing 5
Kronberg 5
Palermo 5
Woodbridge 5
Ardabil 4
Des Moines 4
Hebei 4
Houston 4
Lanzhou 4
Augusta 3
Cesano Maderno 3
Changchun 3
Dallas 3
Marsala 3
Norwalk 3
Padova 3
Shenyang 3
Tianjin 3
Trieste 3
Ann Arbor 2
Barletta 2
Busto Arsizio 2
Cambridge 2
Capaci 2
Chieti 2
Cigognola 2
Courcelles 2
Dearborn 2
Dublin 2
Fairfield 2
Ferrara 2
Hayward 2
London 2
Magnago 2
Mcallen 2
Mountain View 2
Nanterre 2
Parma 2
Pomarico 2
Puglianello 2
San Giorgio a Cremano 2
San Mateo 2
Sarno 2
Sydney 2
Velletri 2
Anzola Dell'emilia 1
Barcelona 1
Bari 1
Battipaglia 1
Berbenno Di Valtellina 1
Caserta 1
Castellana Grotte 1
Castione Della Presolana 1
Castrovillari 1
Cesena 1
Changsha 1
Cologne 1
Contrada 1
Edinburgh 1
Erba 1
Ercolano 1
Felegara 1
Forlì 1
Giugliano In Campania 1
Grumo Nevano 1
Hangzhou 1
Indiana 1
La Queue-en-brie 1
Leawood 1
Marigliano 1
Mascalucia 1
Montreal 1
Monza 1
Nola 1
Orange 1
Totale 689
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Nome #
La mutazione del gene FOXN1 associata al fenotipo NUDE/SCID previene completamente il differenziamento dei linfociti CD4, ma non dei CD8. 274
Aberrant autophagic vesicles in the lymphocytes from patients affected with Ataxia-Telangiectasia 66
Altered signaling through IL-12 receptor in children with very high serum IgE levels 53
Gamma chain is prominently overexpressed in B-pre acute lymphoblastic leukemia cells 52
Unraveling the link between ectodermal disorders and primary immunodeficiencies 51
Comparazione del blocco ontogenetico T nei due modelli umani di ATIMIA NUDE/SCID e DI GEORGE e allestimento di uno “Scaffold” tridimensionale per la generazione in vitro di cellule T da precursori ematopoietici in assenza di timo. 50
La Sindrome Nude/SCID: dal modello murino al fenotipo umano 50
Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation. 42
Caratterizzazione funzionale della localizzazionemitocondriale di GRK2 40
Abnormal cell-clearance and accumulation of autophagic vesicles in lymphocytes from patients affected with Ataxia-Teleangiectasia 39
From murine to human Nude/SCID: the thymus, T-cell development and the missing link. 35
Betamethasone therapy in Ataxia-Telangiectasia: unraveling the rationale of this serendipitous observation on the basis of the pathogenesis 32
Molecular signature of the T-cell commitment in an in vitro three-dimensional organoid in mimicking the thymic microenvironment 32
Intracardiac injection of AdGRK5-NT reduces left ventricular hypertrophy by inhibiting NF-kappaB-dependent hypertrophic gene expression. 31
Impaired neoangiogenesis in β2-adrenoceptor gene-deficient mice: restoration by intravascular human β2-adrenoceptor gene transfer and role of NFκB and CREB transcription factors. 30
Characterization of the T-cell ontogeny defect in the human athymic models of the Nude/SCID and DiGeorge syndromes. 29
Diagnosi prenatale della sindrome nude-SCID. 29
Diagnosi prenatale della sindrome Nude/SCID 28
GRK2 and GRK5 regulate cardiac hypertrophy: in vitro and in vivo studies 28
Mitochondrial localization unveils a novel role for GRK2 in organelle biogenesis. 27
FOXN1: a master regulator gene of thymic epithelial development program 27
Human clinical phenotype associated with FOXN1 mutations. 23
Gamma chain transducing element: a shared pathway between endocrine and immune system 23
Molecular evidence for a thymus-independent partial T cell development in a FOXN1-/- athymic human fetus 23
Diagnosi prenatale della sindrome Nude/SCID 22
Role of the common γ chain in cell cycle progression of human malignant cell lines 21
Preliminary steps of fibroblasts reprogramming to develop mTECs from control or FOXN1(-/-) fibroblasts 21
Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels 20
Il ruolo del dominio RH di GRK5 nella regolazionedell’ipertrofia cardiaca in vivo 17
Totale 1.215
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Categoria #
all - tutte 3.779
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 3.779
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20196 0 0 0 0 0 0 0 0 0 0 1 5
2019/2020140 37 1 3 1 7 4 4 6 17 12 31 17
2020/2021136 13 11 14 10 6 11 12 4 10 4 17 24
2021/2022206 6 1 6 1 3 5 4 7 33 10 60 70
2022/2023320 31 33 11 20 39 38 11 28 36 50 19 4
2023/2024188 3 34 20 11 13 38 11 53 1 4 0 0
Totale 1.215