LANDSBERGER, NICOLETTA
 Distribuzione geografica
Continente #
NA - Nord America 4.328
EU - Europa 3.193
AS - Asia 697
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 2
SA - Sud America 2
Totale 8.227
Nazione #
US - Stati Uniti d'America 4.320
IT - Italia 1.505
UA - Ucraina 674
TR - Turchia 300
SE - Svezia 284
DE - Germania 229
VN - Vietnam 195
CN - Cina 173
FI - Finlandia 172
IE - Irlanda 163
GB - Regno Unito 95
FR - Francia 25
JP - Giappone 21
RU - Federazione Russa 18
BE - Belgio 13
CA - Canada 8
EU - Europa 5
IN - India 4
BG - Bulgaria 3
ES - Italia 3
AU - Australia 2
BR - Brasile 2
DK - Danimarca 2
NL - Olanda 2
AE - Emirati Arabi Uniti 1
BN - Brunei Darussalam 1
CZ - Repubblica Ceca 1
HK - Hong Kong 1
LU - Lussemburgo 1
LV - Lettonia 1
MY - Malesia 1
PL - Polonia 1
PT - Portogallo 1
Totale 8.227
Città #
Milan 1.132
Jacksonville 513
Fairfield 503
Chandler 465
Woodbridge 347
Ashburn 301
Houston 280
Ann Arbor 244
Wilmington 208
Seattle 198
Dearborn 197
Princeton 172
Dublin 163
Cambridge 157
Nyköping 145
Izmir 137
Dong Ket 98
Rome 83
San Mateo 74
Como 53
Beijing 50
New York 41
San Diego 34
Ogden 26
Washington 21
Kocaeli 20
Hefei 18
Nanjing 16
Verona 16
Kunming 15
Norwalk 15
Düsseldorf 14
Tokyo 14
Brussels 13
Auburn Hills 10
Berlin 10
Boardman 10
Los Angeles 10
Guangzhou 7
Helsinki 7
Jinan 7
London 6
Monza 6
Osaka 6
Changsha 5
Ottawa 5
Ponte Lambro 5
Angri 4
Chengdu 4
Frankfurt am Main 4
Naples 4
Pune 4
Siderno 4
Chicago 3
Chiswick 3
Chongqing 3
Detroit 3
Edinburgh 3
Falls Church 3
Fuzhou 3
Madrid 3
Nanchang 3
Zhengzhou 3
Acton 2
Atlanta 2
Baotou 2
Bologna 2
Darmstadt 2
Hangzhou 2
Hebei 2
Hounslow 2
Kilburn 2
Nanning 2
Philadelphia 2
Prescot 2
Quzhou 2
Redmond 2
Shenyang 2
Sofia 2
Torre San Patrizio 2
Turin 2
Villa D'alme 2
Wuhan 2
Andria 1
Bandar Seri Begawan 1
Cattolica 1
Central 1
Cincinnati 1
Dubai 1
Eden Prairie 1
Florence 1
Huzhou 1
Indiana 1
Islington 1
Kuala Lumpur 1
Leawood 1
Lisbon 1
Luxembourg 1
Magenta 1
Markham 1
Totale 5.988
Nome #
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action 187
MeCP2 related studies benefit from the use of CD1 as genetic background 166
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms 159
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex 158
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction 152
DNA methylation directs a time-dependent repression of transcription initiation. 150
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration. 141
Highly repetitive DNA sequence in parthenogenetic Artemia. 140
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 138
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery. 137
Role of chromatin and Xenopus laevis heat shock transcription factor in regulation of transcription from the X. laevis hsp70 promoter in vivo. 136
Molecular mechanisms of gene silencing mediated by DNA methylation 136
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis? 136
A binding protein (p82 protein) recognizes specifically the curved heterochromatic DNA in Artemia franciscana. 131
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties 130
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms 129
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy. 125
Purification and characterization of a proteolytic active fragment of DNA topoisomerase I from the brine shrimp Artemia franciscana (Crustacea Anostraca) 124
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain. 124
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells 123
Chromatin and transcriptional activity in early Xenopus development. 118
Incorporation of mouse zona pellucida proteins into the envelope of Xenopus laevis oocytes. 116
The heat shock response in Xenopus oocytes, embryos and somatic cells: a regulatory role for chromatin. 115
The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA 115
Phylogenetic study of bisexual Artemia using random amplified polymorphic DNA. 112
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation 112
Nucleotide variation and molecular structure of the heterochromatic repetitive AluI DNA in the brine shrimp Artemia franciscana. 111
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis 109
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis 107
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. 106
Oligomerization of RAR and AML1 transcription factors as a novel mechanism of oncogenic activation 105
DNA ricombinante 105
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome 101
The cDNA encoding Xenopus laevis heat-shock factor 1 (XHSF1): nucleotide and deduced amino-acid sequences, and properties of the encoded protein. 98
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells 98
Biologia molecolare del gene 98
Biologia molecolare del gene 91
Heterochromatic bent DNA influences the topology and the compaction of a structural DNA domain 90
A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome. 90
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS. 89
In vitro reconstitution of Artemia satellite chromatin 89
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins 89
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome 89
2nd European Working Group on Rett Syndrome 88
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome 87
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms. 87
Caratterizzazione funzionale di CDKL5, un nuovo gene coinvolto nella sindrome di Rett 87
Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte. EMBO J. 16, 4361-4373. 86
Characterization of a novel MeCP2 interacting protein 85
Molecular pathology and functional interactions of the CDKL5 and MECP2 genes: molecular bases and clinical consequences of an altered neurobiological network. 85
Sequence-directed curvature of repetitive AluI DNA in constitutive heterochromatin of Artemia franciscana. 84
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity 83
Regulatory roles for chromatin. 81
A novel interaction between MeCP2 and HIPK2: characterization of its role in cell proliferation and apoptosis 81
DNA ricombinante Geni e genomi 80
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis. 78
Topoisomerase I action on the heterochromatic DNA from the brine shrimp Artemia franciscana: studies in vivo and in vitro 78
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 78
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome. 77
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 77
Caratterizzazione di nuovi interattori di MeCP2 e loro coinvolgimento nella sindrome di Rett 77
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 76
Molecular pathologies and functional interactions of the X-linked MECP2 and CDKL5 genes. 75
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology 75
Xenopus NF-Y pre-sets chromatin to potentiate p300 and acetylation-responsive transcription from the Xenopus hsp70 promoter in vivo. 72
MeCP2 phopshorylation and related kinases in Rett syndrome and early infantile epileptic encephalopathy 72
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized 71
MOLECULAR AND FUNCTIONAL CHARACTERIZATION OF THE NEWLY IDENTIFIED INTERACTION BETWEEN RETT SYNDROME ASSOCIATED FACTOR MECP2 AND THE PRO-APOPTOTIC FACTOR HIPK2 71
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 70
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 68
Struttura della cromatina e controllo dell'espressione genica 68
MeCP2 phopshorylation and related kinases in rett syndrome. 66
Proteomic approaches for the molecula characterization of CDKL5, a novel protein invoved in severe forms of mental retardation associated with infantile spasms. 65
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome 63
Identification and characterization of proteins that, by interacting with MeCp2, could be involved in Rett synrome 63
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett syndrome 63
DNA methylation and Rett Syndrome 62
Characterization of four proteins that, by interacting with MeCP2, could be involved in Rett syndrome 61
European Working Group on Rett Syndrome 60
alpha test 2 59
Chromatin structure modifications induced by the oncogenic protein PML-RAR 58
Role of the methyl-binding protein 2, MeCP2, and its target genes in prostate cancer. 58
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins 54
Molecular mechanisms of gene silencing by DNA methylation 50
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome 47
Cromatina e controllo dell'espressione genica 46
Totale 8.247
Categoria #
all - tutte 25.317
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 25.317


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019257 0 0 0 0 0 0 0 0 0 0 0 257
2019/20201.561 65 46 59 280 85 191 253 195 102 148 20 117
2020/20211.119 15 132 16 122 34 126 40 99 200 54 107 174
2021/2022774 86 85 82 35 33 27 23 37 56 124 76 110
2022/20231.180 111 78 70 127 87 260 0 178 168 35 30 36
2023/20241.829 297 272 304 353 344 157 11 18 42 7 10 14
Totale 8.247