statistiche ricercatore

LANDSBERGER, NICOLETTA

Distribuzione geografica

Continente	#
NA - Nord America	5.886
EU - Europa	3.563
AS - Asia	2.329
SA - Sud America	239
AF - Africa	38
Continente sconosciuto - Info sul continente non disponibili	5
OC - Oceania	2
Totale	12.062

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Nazione	#
US - Stati Uniti d'America	5.821
IT - Italia	1.520
SG - Singapore	761
UA - Ucraina	677
CN - Cina	509
VN - Vietnam	369
TR - Turchia	312
SE - Svezia	294
DE - Germania	288
HK - Hong Kong	248
FI - Finlandia	213
BR - Brasile	200
IE - Irlanda	164
GB - Regno Unito	128
FR - Francia	106
RU - Federazione Russa	99
IN - India	41
JP - Giappone	35
MX - Messico	34
CA - Canada	26
PL - Polonia	15
BD - Bangladesh	14
BE - Belgio	14
ES - Italia	12
AR - Argentina	9
NG - Nigeria	9
ZA - Sudafrica	9
EC - Ecuador	7
UZ - Uzbekistan	7
CZ - Repubblica Ceca	6
IQ - Iraq	6
KE - Kenya	6
NL - Olanda	6
VE - Venezuela	6
AT - Austria	5
EU - Europa	5
MA - Marocco	5
BG - Bulgaria	4
MY - Malesia	4
SA - Arabia Saudita	4
BO - Bolivia	3
CO - Colombia	3
ID - Indonesia	3
LT - Lituania	3
PY - Paraguay	3
UY - Uruguay	3
AO - Angola	2
AU - Australia	2
CL - Cile	2
DK - Danimarca	2
DZ - Algeria	2
EG - Egitto	2
GY - Guiana	2
HN - Honduras	2
LB - Libano	2
PK - Pakistan	2
PS - Palestinian Territory	2
RS - Serbia	2
AE - Emirati Arabi Uniti	1
AZ - Azerbaigian	1
BH - Bahrain	1
BN - Brunei Darussalam	1
CI - Costa d'Avorio	1
GD - Grenada	1
GR - Grecia	1
IR - Iran	1
JM - Giamaica	1
JO - Giordania	1
KG - Kirghizistan	1
LU - Lussemburgo	1
LV - Lettonia	1
LY - Libia	1
NP - Nepal	1
OM - Oman	1
PA - Panama	1
PH - Filippine	1
PT - Portogallo	1
RO - Romania	1
SR - Suriname	1
TN - Tunisia	1
Totale	12.062

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Città	#
Milan	1.134
Jacksonville	513
Fairfield	503
Chandler	465
Ashburn	458
San Jose	449
Singapore	417
Woodbridge	348
Houston	285
Ann Arbor	244
Hong Kong	240
Wilmington	208
Seattle	200
Dearborn	197
Princeton	172
Dublin	164
Dallas	160
Cambridge	157
Beijing	145
Nyköping	145
Izmir	138
The Dalles	125
Dong Ket	98
Boardman	96
Rome	84
Ho Chi Minh City	77
Chicago	74
Lauterbourg	74
San Mateo	74
New York	70
Como	54
Los Angeles	51
Munich	43
Hanoi	34
Helsinki	34
San Diego	34
Council Bluffs	30
Tokyo	28
Ogden	26
Buffalo	23
London	23
Santa Clara	23
Mexico City	22
Orem	21
Washington	21
Chennai	20
Kocaeli	20
Hefei	19
Guangzhou	18
São Paulo	17
Kunming	16
Nanjing	16
Verona	16
Norwalk	15
Brussels	14
Düsseldorf	14
Turku	14
Warsaw	14
Brooklyn	13
Frankfurt am Main	12
Denver	11
Stockholm	11
Atlanta	10
Auburn Hills	10
Berlin	10
Abuja	9
Haiphong	8
Shanghai	8
Boston	7
Changsha	7
Hangzhou	7
Jinan	7
Nuremberg	7
Charlotte	6
Monza	6
Mumbai	6
Nairobi	6
Osaka	6
Ottawa	6
Pune	6
Rio de Janeiro	6
Salvador	6
Tashkent	6
Tianjin	6
Ankara	5
Da Nang	5
Johannesburg	5
Manchester	5
Nanchang	5
Ponte Lambro	5
Porto Alegre	5
San Francisco	5
Shenzhen	5
Toronto	5
Angri	4
Baghdad	4
Chengdu	4
Chongqing	4
Columbus	4
Detroit	4
Totale	8.471

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Nome	#
MeCP2 related studies benefit from the use of CD1 as genetic background	235
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction	221
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action	216
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex	211
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome	207
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?	207
DNA methylation directs a time-dependent repression of transcription initiation.	196
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms	196
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration.	190
Highly repetitive DNA sequence in parthenogenetic Artemia.	189
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	187
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery.	187
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain.	184
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy.	184
Molecular mechanisms of gene silencing mediated by DNA methylation	183
A binding protein (p82 protein) recognizes specifically the curved heterochromatic DNA in Artemia franciscana.	183
Role of chromatin and Xenopus laevis heat shock transcription factor in regulation of transcription from the X. laevis hsp70 promoter in vivo.	172
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties	170
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms	168
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis	167
Chromatin and transcriptional activity in early Xenopus development.	165
The heat shock response in Xenopus oocytes, embryos and somatic cells: a regulatory role for chromatin.	162
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis	161
Incorporation of mouse zona pellucida proteins into the envelope of Xenopus laevis oocytes.	160
Purification and characterization of a proteolytic active fragment of DNA topoisomerase I from the brine shrimp Artemia franciscana (Crustacea Anostraca)	157
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome	157
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.	156
Biologia molecolare del gene	153
Biologia molecolare del gene	153
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome	152
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription.	152
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation	152
DNA ricombinante	152
Characterization of a novel MeCP2 interacting protein	150
The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA	150
Nucleotide variation and molecular structure of the heterochromatic repetitive AluI DNA in the brine shrimp Artemia franciscana.	149
Phylogenetic study of bisexual Artemia using random amplified polymorphic DNA.	147
Heterochromatic bent DNA influences the topology and the compaction of a structural DNA domain	141
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity	140
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	139
The cDNA encoding Xenopus laevis heat-shock factor 1 (XHSF1): nucleotide and deduced amino-acid sequences, and properties of the encoded protein.	138
Oligomerization of RAR and AML1 transcription factors as a novel mechanism of oncogenic activation	138
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS.	138
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	137
2nd European Working Group on Rett Syndrome	136
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins	136
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms.	132
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis.	128
Caratterizzazione funzionale di CDKL5, un nuovo gene coinvolto nella sindrome di Rett	128
A novel interaction between MeCP2 and HIPK2: characterization of its role in cell proliferation and apoptosis	127
Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte. EMBO J. 16, 4361-4373.	126
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome.	125
In vitro reconstitution of Artemia satellite chromatin	124
Molecular pathology and functional interactions of the CDKL5 and MECP2 genes: molecular bases and clinical consequences of an altered neurobiological network.	123
Molecular pathologies and functional interactions of the X-linked MECP2 and CDKL5 genes.	122
Topoisomerase I action on the heterochromatic DNA from the brine shrimp Artemia franciscana: studies in vivo and in vitro	121
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	121
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	121
Sequence-directed curvature of repetitive AluI DNA in constitutive heterochromatin of Artemia franciscana.	120
DNA ricombinante Geni e genomi	119
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	119
Regulatory roles for chromatin.	118
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	117
Caratterizzazione di nuovi interattori di MeCP2 e loro coinvolgimento nella sindrome di Rett	117
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	112
European Working Group on Rett Syndrome	112
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology	112
Xenopus NF-Y pre-sets chromatin to potentiate p300 and acetylation-responsive transcription from the Xenopus hsp70 promoter in vivo.	111
MeCP2 phopshorylation and related kinases in Rett syndrome and early infantile epileptic encephalopathy	108
alpha test 2	106
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	104
MOLECULAR AND FUNCTIONAL CHARACTERIZATION OF THE NEWLY IDENTIFIED INTERACTION BETWEEN RETT SYNDROME ASSOCIATED FACTOR MECP2 AND THE PRO-APOPTOTIC FACTOR HIPK2	104
Characterization of four proteins that, by interacting with MeCP2, could be involved in Rett syndrome	104
MeCP2 phopshorylation and related kinases in rett syndrome.	100
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized	96
Proteomic approaches for the molecula characterization of CDKL5, a novel protein invoved in severe forms of mental retardation associated with infantile spasms.	95
Changes in chromatin structure and transcriptional regulation mediated by leukemic oncofusion proteins	94
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett syndrome	93
Cromatina e controllo dell'espressione genica	91
Struttura della cromatina e controllo dell'espressione genica	91
DNA methylation and Rett Syndrome	90
Chromatin structure modifications induced by the oncogenic protein PML-RAR	89
Identification and characterization of proteins that, by interacting with MeCp2, could be involved in Rett synrome	87
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	84
Molecular mechanisms of gene silencing by DNA methylation	84
Role of the methyl-binding protein 2, MeCP2, and its target genes in prostate cancer.	83
Totale	12.082

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Categoria	#
all - tutte	43.558
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	43.558

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	335	0	0	0	0	0	0	0	0	0	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	1.208	17	29	217	11	58	63	34	50	142	117	141	329
2025/2026	2.621	227	190	115	373	263	218	620	162	332	121	0	0
Totale													12.082