LANDSBERGER, NICOLETTA
 Distribuzione geografica
Continente #
NA - Nord America 4.132
EU - Europa 2.530
AS - Asia 663
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 2
OC - Oceania 1
Totale 7.333
Nazione #
US - Stati Uniti d'America 4.124
IT - Italia 930
UA - Ucraina 674
TR - Turchia 300
SE - Svezia 284
VN - Vietnam 195
DE - Germania 191
FI - Finlandia 172
CN - Cina 163
IE - Irlanda 107
GB - Regno Unito 87
BE - Belgio 28
FR - Francia 24
RU - Federazione Russa 18
CA - Canada 8
EU - Europa 5
BG - Bulgaria 3
ES - Italia 3
BR - Brasile 2
DK - Danimarca 2
NL - Olanda 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
BN - Brunei Darussalam 1
CZ - Repubblica Ceca 1
HK - Hong Kong 1
JP - Giappone 1
LU - Lussemburgo 1
LV - Lettonia 1
MY - Malesia 1
PL - Polonia 1
PT - Portogallo 1
Totale 7.333
Città #
Milan 767
Jacksonville 513
Fairfield 503
Chandler 465
Woodbridge 347
Houston 280
Ann Arbor 244
Ashburn 208
Wilmington 208
Dearborn 197
Seattle 190
Princeton 172
Cambridge 157
Nyköping 145
Izmir 137
Dublin 107
Dong Ket 98
San Mateo 74
Como 51
Beijing 50
Rome 49
San Diego 34
Brussels 28
Washington 21
Kocaeli 20
Hefei 18
Nanjing 16
Verona 16
Kunming 15
Norwalk 15
Düsseldorf 14
Auburn Hills 10
Boardman 10
Philadelphia 10
Guangzhou 7
Helsinki 7
Jinan 7
London 6
Monza 6
Changsha 5
Los Angeles 5
Ottawa 5
Ponte Lambro 5
Angri 4
Chengdu 4
Naples 4
Siderno 4
Chicago 3
Chiswick 3
Chongqing 3
Detroit 3
Edinburgh 3
Falls Church 3
Fuzhou 3
Madrid 3
Nanchang 3
Zhengzhou 3
Atlanta 2
Baotou 2
Bologna 2
Hangzhou 2
Hebei 2
Islington 2
Nanning 2
New York 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
Frankfurt am Main 1
Huzhou 1
Indiana 1
Kuala Lumpur 1
Leawood 1
Lisbon 1
Luxembourg 1
Magenta 1
Markham 1
Melbourne 1
Melfi 1
Miami 1
Mountain View 1
New Bedfont 1
Orvieto 1
Padova 1
Palermo 1
Piemonte 1
Prague 1
Totale 5.347
Nome #
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action 175
MeCP2 related studies benefit from the use of CD1 as genetic background 150
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms 149
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex 144
DNA methylation directs a time-dependent repression of transcription initiation. 142
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction 140
Molecular mechanisms of gene silencing mediated by DNA methylation 134
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties 131
Role of chromatin and Xenopus laevis heat shock transcription factor in regulation of transcription from the X. laevis hsp70 promoter in vivo. 125
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration. 125
Highly repetitive DNA sequence in parthenogenetic Artemia. 123
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 123
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells 122
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery. 122
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis? 122
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms 120
A binding protein (p82 protein) recognizes specifically the curved heterochromatic DNA in Artemia franciscana. 114
Purification and characterization of a proteolytic active fragment of DNA topoisomerase I from the brine shrimp Artemia franciscana (Crustacea Anostraca) 112
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy. 111
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation 109
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain. 108
The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA 105
Chromatin and transcriptional activity in early Xenopus development. 105
The heat shock response in Xenopus oocytes, embryos and somatic cells: a regulatory role for chromatin. 104
Incorporation of mouse zona pellucida proteins into the envelope of Xenopus laevis oocytes. 104
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis 103
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis 102
Oligomerization of RAR and AML1 transcription factors as a novel mechanism of oncogenic activation 101
Nucleotide variation and molecular structure of the heterochromatic repetitive AluI DNA in the brine shrimp Artemia franciscana. 99
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. 98
The cDNA encoding Xenopus laevis heat-shock factor 1 (XHSF1): nucleotide and deduced amino-acid sequences, and properties of the encoded protein. 98
Phylogenetic study of bisexual Artemia using random amplified polymorphic DNA. 98
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells 97
DNA ricombinante 88
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms. 86
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome 85
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome 84
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS. 83
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome 82
Characterization of a novel MeCP2 interacting protein 82
Biologia molecolare del gene 82
Heterochromatic bent DNA influences the topology and the compaction of a structural DNA domain 78
Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte. EMBO J. 16, 4361-4373. 76
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis. 75
Biologia molecolare del gene 75
2nd European Working Group on Rett Syndrome 74
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins 74
Molecular pathology and functional interactions of the CDKL5 and MECP2 genes: molecular bases and clinical consequences of an altered neurobiological network. 73
In vitro reconstitution of Artemia satellite chromatin 72
Regulatory roles for chromatin. 71
Caratterizzazione funzionale di CDKL5, un nuovo gene coinvolto nella sindrome di Rett 71
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. 71
Sequence-directed curvature of repetitive AluI DNA in constitutive heterochromatin of Artemia franciscana. 70
DNA ricombinante Geni e genomi 70
Topoisomerase I action on the heterochromatic DNA from the brine shrimp Artemia franciscana: studies in vivo and in vitro 67
A novel interaction between MeCP2 and HIPK2: characterization of its role in cell proliferation and apoptosis 67
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 66
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology 66
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 65
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity 64
Xenopus NF-Y pre-sets chromatin to potentiate p300 and acetylation-responsive transcription from the Xenopus hsp70 promoter in vivo. 62
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome. 62
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms 62
Molecular pathologies and functional interactions of the X-linked MECP2 and CDKL5 genes. 62
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome 61
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized 61
Caratterizzazione di nuovi interattori di MeCP2 e loro coinvolgimento nella sindrome di Rett 61
DNA methylation and Rett Syndrome 60
MOLECULAR AND FUNCTIONAL CHARACTERIZATION OF THE NEWLY IDENTIFIED INTERACTION BETWEEN RETT SYNDROME ASSOCIATED FACTOR MECP2 AND THE PRO-APOPTOTIC FACTOR HIPK2 60
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 58
MeCP2 phopshorylation and related kinases in Rett syndrome and early infantile epileptic encephalopathy 58
Struttura della cromatina e controllo dell'espressione genica 57
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome 56
MeCP2 phopshorylation and related kinases in rett syndrome. 54
Characterization of four proteins that, by interacting with MeCP2, could be involved in Rett syndrome 53
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett syndrome 53
Proteomic approaches for the molecula characterization of CDKL5, a novel protein invoved in severe forms of mental retardation associated with infantile spasms. 53
alpha test 2 52
European Working Group on Rett Syndrome 50
Identification and characterization of proteins that, by interacting with MeCp2, could be involved in Rett synrome 50
Molecular mechanisms of gene silencing by DNA methylation 48
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins 47
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome 46
Role of the methyl-binding protein 2, MeCP2, and its target genes in prostate cancer. 46
Chromatin structure modifications induced by the oncogenic protein PML-RAR 45
Cromatina e controllo dell'espressione genica 44
Totale 7.353
Categoria #
all - tutte 18.007
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 18.007


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019632 0 0 0 2 2 1 10 88 14 73 185 257
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
2022/20231.205 111 78 70 127 87 260 10 178 171 43 31 39
2023/2024910 300 272 308 30 0 0 0 0 0 0 0 0
Totale 7.353