statistiche ricercatore

LANDSBERGER, NICOLETTA

Distribuzione geografica

Continente	#
NA - Nord America	4.518
EU - Europa	3.290
AS - Asia	811
Continente sconosciuto - Info sul continente non disponibili	5
OC - Oceania	2
SA - Sud America	2
Totale	8.628

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Nazione	#
US - Stati Uniti d'America	4.506
IT - Italia	1.511
UA - Ucraina	674
TR - Turchia	300
SE - Svezia	284
DE - Germania	248
VN - Vietnam	195
CN - Cina	185
FI - Finlandia	178
IE - Irlanda	163
SG - Singapore	101
GB - Regno Unito	98
RU - Federazione Russa	76
FR - Francia	26
JP - Giappone	21
BE - Belgio	14
CA - Canada	12
EU - Europa	5
CZ - Repubblica Ceca	4
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
HK - Hong Kong	1
IR - Iran	1
LU - Lussemburgo	1
LV - Lettonia	1
MY - Malesia	1
PL - Polonia	1
PT - Portogallo	1
Totale	8.628

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Città	#
Milan	1.133
Jacksonville	513
Fairfield	503
Chandler	465
Woodbridge	347
Ashburn	305
Houston	280
Ann Arbor	244
Wilmington	208
Seattle	198
Dearborn	197
Princeton	172
Dublin	163
Cambridge	157
Nyköping	145
Izmir	137
Singapore	99
Dong Ket	98
Boardman	96
Rome	84
San Mateo	74
Como	53
Beijing	50
New York	41
San Diego	34
Chicago	33
Ogden	26
Washington	21
Kocaeli	20
Hefei	18
Nanjing	16
Verona	16
Kunming	15
Munich	15
Norwalk	15
Brussels	14
Düsseldorf	14
Tokyo	14
Helsinki	13
Santa Clara	13
Dallas	11
Auburn Hills	10
Berlin	10
Los Angeles	10
Frankfurt am Main	8
London	8
Guangzhou	7
Jinan	7
Monza	6
Osaka	6
Ottawa	6
Changsha	5
Ponte Lambro	5
Angri	4
Chengdu	4
Chongqing	4
Naples	4
Pune	4
Siderno	4
Toronto	4
Brno	3
Chiswick	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
San Francisco	2
Shanghai	2
Shenyang	2
Sofia	2
Torre San Patrizio	2
Turin	2
Villa D'alme	2
Wuhan	2
Andria	1
Bandar Seri Begawan	1
Catania	1
Cattolica	1
Central	1
Cincinnati	1
Clifton	1
Dubai	1
Eden Prairie	1
Totale	6.266

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Nome	#
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action	189
MeCP2 related studies benefit from the use of CD1 as genetic background	173
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex	165
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms	161
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction	160
DNA methylation directs a time-dependent repression of transcription initiation.	155
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration.	145
Highly repetitive DNA sequence in parthenogenetic Artemia.	143
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome	143
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?	142
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery.	141
Role of chromatin and Xenopus laevis heat shock transcription factor in regulation of transcription from the X. laevis hsp70 promoter in vivo.	140
Molecular mechanisms of gene silencing mediated by DNA methylation	139
A binding protein (p82 protein) recognizes specifically the curved heterochromatic DNA in Artemia franciscana.	136
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy.	136
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties	133
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms	131
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	129
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain.	129
Purification and characterization of a proteolytic active fragment of DNA topoisomerase I from the brine shrimp Artemia franciscana (Crustacea Anostraca)	126
Chromatin and transcriptional activity in early Xenopus development.	121
The heat shock response in Xenopus oocytes, embryos and somatic cells: a regulatory role for chromatin.	120
Incorporation of mouse zona pellucida proteins into the envelope of Xenopus laevis oocytes.	120
The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA	118
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation	118
Phylogenetic study of bisexual Artemia using random amplified polymorphic DNA.	116
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis	115
Nucleotide variation and molecular structure of the heterochromatic repetitive AluI DNA in the brine shrimp Artemia franciscana.	114
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis	114
DNA ricombinante	112
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription.	111
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome	110
Oligomerization of RAR and AML1 transcription factors as a novel mechanism of oncogenic activation	108
The cDNA encoding Xenopus laevis heat-shock factor 1 (XHSF1): nucleotide and deduced amino-acid sequences, and properties of the encoded protein.	104
Biologia molecolare del gene	102
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	101
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	97
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.	97
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS.	95
Biologia molecolare del gene	95
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome	94
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms.	94
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins	94
Heterochromatic bent DNA influences the topology and the compaction of a structural DNA domain	94
In vitro reconstitution of Artemia satellite chromatin	93
2nd European Working Group on Rett Syndrome	93
Caratterizzazione funzionale di CDKL5, un nuovo gene coinvolto nella sindrome di Rett	93
Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte. EMBO J. 16, 4361-4373.	91
Characterization of a novel MeCP2 interacting protein	90
Sequence-directed curvature of repetitive AluI DNA in constitutive heterochromatin of Artemia franciscana.	88
Molecular pathology and functional interactions of the CDKL5 and MECP2 genes: molecular bases and clinical consequences of an altered neurobiological network.	88
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity	88
Regulatory roles for chromatin.	86
A novel interaction between MeCP2 and HIPK2: characterization of its role in cell proliferation and apoptosis	86
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis.	85
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	84
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	84
DNA ricombinante Geni e genomi	83
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome.	82
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	82
Topoisomerase I action on the heterochromatic DNA from the brine shrimp Artemia franciscana: studies in vivo and in vitro	80
Caratterizzazione di nuovi interattori di MeCP2 e loro coinvolgimento nella sindrome di Rett	80
Molecular pathologies and functional interactions of the X-linked MECP2 and CDKL5 genes.	78
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology	78
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	77
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	76
MeCP2 phopshorylation and related kinases in Rett syndrome and early infantile epileptic encephalopathy	76
Xenopus NF-Y pre-sets chromatin to potentiate p300 and acetylation-responsive transcription from the Xenopus hsp70 promoter in vivo.	75
MOLECULAR AND FUNCTIONAL CHARACTERIZATION OF THE NEWLY IDENTIFIED INTERACTION BETWEEN RETT SYNDROME ASSOCIATED FACTOR MECP2 AND THE PRO-APOPTOTIC FACTOR HIPK2	75
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized	74
Proteomic approaches for the molecula characterization of CDKL5, a novel protein invoved in severe forms of mental retardation associated with infantile spasms.	70
Struttura della cromatina e controllo dell'espressione genica	70
MeCP2 phopshorylation and related kinases in rett syndrome.	68
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett syndrome	67
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	66
Identification and characterization of proteins that, by interacting with MeCp2, could be involved in Rett synrome	66
Characterization of four proteins that, by interacting with MeCP2, could be involved in Rett syndrome	66
DNA methylation and Rett Syndrome	65
European Working Group on Rett Syndrome	65
alpha test 2	63
Chromatin structure modifications induced by the oncogenic protein PML-RAR	61
Role of the methyl-binding protein 2, MeCP2, and its target genes in prostate cancer.	61
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins	60
Molecular mechanisms of gene silencing by DNA methylation	53
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	51
Cromatina e controllo dell'espressione genica	51
Totale	8.648

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Categoria	#
all - tutte	31.161
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	31.161

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	1.026	0	0	0	0	0	191	253	195	102	148	20	117
2020/2021	1.119	15	132	16	122	34	126	40	99	200	54	107	174
2021/2022	774	86	85	82	35	33	27	23	37	56	124	76	110
2022/2023	1.180	111	78	70	127	87	260	0	178	168	35	30	36
2023/2024	1.835	297	272	304	353	344	157	11	18	42	7	10	20
2024/2025	395	17	29	217	11	58	63	0	0	0	0	0	0
Totale													8.648