statistiche ricercatore

KILSTRUP-NIELSEN, CHARLOTTE

Distribuzione geografica

Continente	#
NA - Nord America	4.310
EU - Europa	3.000
AS - Asia	692
AF - Africa	10
OC - Oceania	6
SA - Sud America	6
Continente sconosciuto - Info sul continente non disponibili	3
Totale	8.027

Salva come PNG Salva come JPEG

Nazione	#
US - Stati Uniti d'America	4.302
IT - Italia	1.609
UA - Ucraina	521
TR - Turchia	228
SE - Svezia	217
DE - Germania	195
CN - Cina	166
VN - Vietnam	164
IE - Irlanda	147
FI - Finlandia	140
SG - Singapore	104
GB - Regno Unito	83
JP - Giappone	23
BE - Belgio	17
FR - Francia	17
NL - Olanda	12
GH - Ghana	10
RU - Federazione Russa	10
AT - Austria	7
CZ - Repubblica Ceca	7
AU - Australia	6
CA - Canada	5
BR - Brasile	3
DK - Danimarca	3
EU - Europa	3
MX - Messico	3
PT - Portogallo	3
CH - Svizzera	2
CL - Cile	2
ES - Italia	2
IN - India	2
RS - Serbia	2
AE - Emirati Arabi Uniti	1
AZ - Azerbaigian	1
BG - Bulgaria	1
BN - Brunei Darussalam	1
GR - Grecia	1
JO - Giordania	1
LI - Liechtenstein	1
LV - Lettonia	1
MT - Malta	1
MY - Malesia	1
NO - Norvegia	1
PE - Perù	1
Totale	8.027

Salva come PNG Salva come JPEG

Città	#
Milan	1.063
Fairfield	473
Chandler	431
Jacksonville	403
Woodbridge	357
Houston	330
Ashburn	259
Ann Arbor	243
Dearborn	233
Seattle	207
Wilmington	188
Cambridge	168
Dublin	147
Princeton	146
Como	130
Izmir	108
Nyköping	105
Singapore	102
Dong Ket	92
Boardman	88
Rome	81
New York	72
Beijing	49
Chicago	46
San Mateo	41
Kocaeli	36
Ogden	30
San Diego	27
Munich	26
Helsinki	21
Brussels	17
Nanjing	16
Tokyo	16
Hefei	15
London	15
Washington	15
Kunming	14
Monza	14
Düsseldorf	13
Santa Clara	12
Los Angeles	11
Guangzhou	10
Jinan	10
Magnago	10
Verona	10
Gallarate	9
Turin	9
Norwalk	8
Ponte Lambro	8
West Jordan	8
Redmond	7
Edinburgh	6
Kilburn	6
Melbourne	6
Osaka	6
Rosdorf	6
Shenyang	6
Vienna	6
Nanchang	5
Amsterdam	4
Angri	4
Auburn Hills	4
Cattolica	4
Frankfurt am Main	4
Naples	4
Peschiera Borromeo	4
Prescot	4
Toronto	4
Bologna	3
Brno	3
Chiswick	3
Dallas	3
Detroit	3
Falls Church	3
Fuzhou	3
Indiana	3
Legnano	3
Mornago	3
Prague	3
Shanghai	3
Wuhan	3
Amstelveen	2
Andria	2
Barcelona	2
Basel	2
Berlin	2
Cagliari	2
Camerino	2
Changsha	2
Chengdu	2
Chongqing	2
Coimbra	2
Hebei	2
Hounslow	2
Köseköy	2
Market Harborough	2
Melegnano	2
Mountain View	2
Nanning	2
Pune	2
Totale	6.109

Salva come PNG Salva come JPEG

Nome	#
CDKL5 and shootin1 interact and concur in regulating neuronal polarization	198
Cannabidivarin completely rescues cognitive deficits and delays neurological and motor defects in male Mecp2 mutant mice	192
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	172
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex	165
Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization	164
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	157
CDKL5 localizes at the centrosome and midbody and is required for faithful cell division	145
PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain	142
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome	141
CDKL5 influences RNA splicing activity by its association to the nuclear speckle molecular machinery.	141
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?	141
Synaptic synthesis, dephosphorylation and degradation: a novel paradigm for an activity-dependent neuronal control of CDKL5.	139
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH	138
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors	135
CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail	134
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties	133
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy.	131
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms	131
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain.	128
Characterization of CDKL5 transcript isoforms in human and mouse	128
The antidepressant tianeptine reverts synaptic AMPA receptor defects caused by deficiency of CDKL5	127
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	126
CDKL5 ensures excitatory synapse stability by reinforcing NGL1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons	119
Brain phosphorylation of MeCP2 at serene 164 is developmentally regulated and globally alters its chromatin association	117
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation	116
Genetics and mechanisms of disease in Rett Syndrome	113
Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis	113
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis	112
DNA methylation and Rett syndrome	106
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome	106
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation	103
Rescue of prepulse inhibition deficit and brain mitochondrial dysfunction by pharmacological stimulation of the central serotonin receptor 7 in a mouse model of CDKL5 Deficiency Disorder	103
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	100
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.	96
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	95
Identification and Characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	94
Microtubules: A Key to Understand and Correct Neuronal Defects in CDKL5 Deficiency Disorder?	94
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome	93
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms.	93
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS.	93
La cromatina e controllo dell'espressione genica.	92
2nd European Working Group on Rett Syndrome	92
Characterization of a novel MeCP2 interacting protein	90
DNA methylation in the control of gene silencing during development and human disorders (DisChrom)	90
The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo	90
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity	88
Pregnenolone and pregnenolone-methyl-ether rescue neuronal defects caused by dysfunctional CLIP170 in a neuronal model of CDKL5 Deficiency Disorder	88
Molecular characterization of the CDKL5 gene involved in mental retardation and infantile spams	86
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis.	84
Functional Characterization of CDKL5, a novel gene involved in the onset of Rett syndrome	84
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	83
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	82
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome.	81
Functional characterization of CDKL5, a novel gene involved in Rett syndrome and infantile spams associated with mental retardation	81
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	80
Functional characterization of CDKL5, a novel gene involved in Rett Syndrome and infantile spams	79
Functional characterization of CDKL5, a novel gene involved in the onset of Rett Syndrome	77
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology	77
Functional characterizationof CDKL5, a novel gene involved in the onset of Rett Syndrome	76
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	75
Functional characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	75
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders	75
Molecular and functional characterization of CDKL5, a novel X-linked kinase, mainly involved in female mental retardation	74
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	74
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized	74
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	66
European Working Group on Rett Syndrome	64
Loss of CDKL5 Causes Synaptic GABAergic Defects That Can Be Restored with the Neuroactive Steroid Pregnenolone-Methyl-Ether	62
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	60
Identification and characterization of proteins that interacting with MECP2, could be involved in Rett Syndrome	60
Therapeutic potential of pregnenolone and pregnenolone methyl ether on depressive and CDKL5 deficiency disorders: Focus on microtubule targeting	53
Cromatina e controllo dell'espressione genica	51
Pregnenolone-methyl-ether enhances CLIP170 and microtubule functions improving spine maturation and hippocampal deficits related to CDKL5 deficiency	46
Characterization of the molecular mechanism underlying GABAA-receptor defects in CDKL5 deficiency disorder	34
CDKL5 interacts with inhibitory postsynaptic scaffolding proteins and regulates synaptic GABAA receptor levels	34
Novel role of CDKL5 in the inhibitory synapse and a possible therapeutic strategy for CDKL5-related defects	28
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	25
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	22
Rett syndrome: from the involved gene(s) to treatment	10
Totale	8.086

Salva come PNG Salva come JPEG

Categoria	#
all - tutte	30.984
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	30.984

Salva come PNG Salva come JPEG

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	1.033	0	0	0	0	87	206	237	169	98	101	41	94
2020/2021	1.100	24	116	25	99	45	103	57	80	186	95	116	154
2021/2022	669	87	92	50	33	23	21	26	32	36	100	80	89
2022/2023	1.082	107	82	56	114	70	227	9	149	131	38	50	49
2023/2024	1.829	282	261	293	289	322	181	20	47	59	29	12	34
2024/2025	396	7	38	238	36	77	0	0	0	0	0	0	0
Totale													8.086