statistiche ricercatore

KILSTRUP-NIELSEN, CHARLOTTE

Distribuzione geografica

Continente	#
NA - Nord America	4.125
EU - Europa	2.878
AS - Asia	559
AF - Africa	9
SA - Sud America	6
Continente sconosciuto - Info sul continente non disponibili	3
OC - Oceania	2
Totale	7.582

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Nazione	#
US - Stati Uniti d'America	4.118
IT - Italia	1.553
UA - Ucraina	521
TR - Turchia	226
SE - Svezia	217
DE - Germania	167
VN - Vietnam	164
CN - Cina	156
IE - Irlanda	147
FI - Finlandia	123
GB - Regno Unito	80
BE - Belgio	16
FR - Francia	16
GH - Ghana	9
JP - Giappone	9
RU - Federazione Russa	8
AT - Austria	6
CA - Canada	5
CZ - Repubblica Ceca	4
NL - Olanda	4
BR - Brasile	3
DK - Danimarca	3
EU - Europa	3
AU - Australia	2
CH - Svizzera	2
CL - Cile	2
ES - Italia	2
IN - India	2
MX - Messico	2
PT - Portogallo	2
BG - Bulgaria	1
BN - Brunei Darussalam	1
GR - Grecia	1
LI - Liechtenstein	1
LV - Lettonia	1
MT - Malta	1
MY - Malesia	1
NO - Norvegia	1
PE - Perù	1
RS - Serbia	1
Totale	7.582

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Città	#
Milan	1.049
Fairfield	473
Chandler	431
Jacksonville	403
Woodbridge	357
Houston	330
Ashburn	257
Ann Arbor	243
Dearborn	233
Seattle	207
Wilmington	188
Cambridge	168
Dublin	147
Princeton	146
Como	125
Izmir	108
Nyköping	105
Dong Ket	92
Rome	80
New York	72
Beijing	49
San Mateo	41
Kocaeli	36
Ogden	30
San Diego	27
Brussels	16
Hefei	15
Nanjing	15
Washington	15
Kunming	14
Monza	14
Düsseldorf	13
London	13
Guangzhou	10
Jinan	10
Los Angeles	10
Magnago	10
Verona	10
Norwalk	8
Ponte Lambro	8
West Jordan	8
Boardman	7
Redmond	7
Edinburgh	6
Kilburn	6
Osaka	6
Rosdorf	6
Shenyang	6
Helsinki	5
Nanchang	5
Vienna	5
Angri	4
Auburn Hills	4
Cattolica	4
Chicago	4
Naples	4
Peschiera Borromeo	4
Prescot	4
Toronto	4
Turin	4
Bologna	3
Chiswick	3
Detroit	3
Falls Church	3
Fuzhou	3
Indiana	3
Mornago	3
Prague	3
Wuhan	3
Amsterdam	2
Andria	2
Barcelona	2
Basel	2
Berlin	2
Changsha	2
Chongqing	2
Coimbra	2
Frankfurt am Main	2
Hebei	2
Hounslow	2
Market Harborough	2
Melbourne	2
Melegnano	2
Mountain View	2
Nanning	2
Pune	2
Rozzano	2
Secaucus	2
Shanghai	2
São Paulo	2
Tokyo	2
Torre San Patrizio	2
Utrecht	2
Varese	2
Villa D'alme	2
Wandsworth	2
Zhengzhou	2
Acton	1
Aigaleo	1
Andover	1
Totale	5.767

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Nome	#
CDKL5 and shootin1 interact and concur in regulating neuronal polarization	193
Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action	187
Cannabidivarin completely rescues cognitive deficits and delays neurological and motor defects in male Mecp2 mutant mice	185
MeCP2 related studies benefit from the use of CD1 as genetic background	165
MeCP2 affects skeletal muscle growth and morphology through non cell-autonomous mechanisms	158
The neurosteroid pregnenolone reverts microtubule derangement induced by the loss of a functional CDKL5-IQGAP1 complex	158
Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization	157
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction	152
PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain	140
CDKL5 localizes at the centrosome and midbody and is required for faithful cell division	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
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH.	136
MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?	135
Synaptic synthesis, dephosphorylation and degradation: a novel paradigm for an activity-dependent neuronal control of CDKL5.	133
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors	130
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties	129
CDKL5 expression is modulated during neuronal development and its subcellular distribution is tightly regulated by the C-terminal tail	129
Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms	129
Characterization of CDKL5 transcript isoforms in human and mouse	125
What We Know and Would Like to Know about CDKL5 and Its Involvement in Epileptic Encephalopathy.	124
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	123
A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain.	123
The antidepressant tianeptine reverts synaptic AMPA receptor defects caused by deficiency of CDKL5	120
CDKL5 ensures excitatory synapse stability by reinforcing NGL1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons	116
Brain phosphorylation of MeCP2 at serene 164 is developmentally regulated and globally alters its chromatin association	112
Extrasynaptic N-methyl-D-aspartate (NMDA) receptor stimulation induces cytoplasmic translocation of the CDKL5 kinase and its proteasomal degradation	111
Genetics and mechanisms of disease in Rett Syndrome	110
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
DNA methylation and Rett syndrome	101
Characterization of HIPK2 that, by Associating with MeCP2, Might Function as a Modifier Gene in Rett Syndrome	101
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	101
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation	100
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells	98
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
La cromatina e controllo dell'espressione genica.	89
Identification and Characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	88
CHARACTERIZATION OF THE CDKL5 GENE INVOLVED IN MENTAL RETARDATION AND INFANTILE SPASMS.	88
2nd European Working Group on Rett Syndrome	88
Identification and characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome	88
Microtubules: A Key to Understand and Correct Neuronal Defects in CDKL5 Deficiency Disorder?	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
Characterization of a novel MeCP2 interacting protein	84
The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo	84
DNA methylation in the control of gene silencing during development and human disorders (DisChrom)	83
Molecular characterization of the CDKL5 gene involved in mental retardation and infantile spams	83
Functional Characterization of CDKL5, a novel gene involved in the onset of Rett syndrome	82
CDKL5 levels quickly respond to neuronal activity, reinforcing its involvement in synaptic plasticity	82
Pregnenolone and pregnenolone-methyl-ether rescue neuronal defects caused by dysfunctional CLIP170 in a neuronal model of CDKL5 Deficiency Disorder	81
Functional Characterization of CDKL5, an X-Linked Gene Involved in Mental Retardation and Epileptic Crisis.	78
Disruption of the Cellular Regulation of CDKL5 Might be Relevant for Rett Syndrome	78
Functional characterization of CDKL5, a novel gene involved in Rett syndrome and infantile spams associated with mental retardation	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
Molecular characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	76
Functional characterization of CDKL5, a novel gene involved in Rett Syndrome and infantile spams	75
Revealing a novel and unexpected function of MeCP2, possibly involved in RTT pathophysiology	75
Functional characterizationof CDKL5, a novel gene involved in the onset of Rett Syndrome	74
Functional characterization of CDKL5, a novel kinase involved in Rett syndrome and infantile spasms	73
Functional characterization of CDKL5, a novel gene involved in the onset of Rett Syndrome	73
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders	72
Molecular and functional characterization of CDKL5, a novel X-linked kinase, mainly involved in female mental retardation	71
Molecular genetics of Rett syndrome: when epigenetic signals go unrecognized	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
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome	63
European Working Group on Rett Syndrome	60
Identification and characterization of proteins that interacting with MECP2, could be involved in Rett Syndrome	58
Therapeutic potential of pregnenolone and pregnenolone methyl ether on depressive and CDKL5 deficiency disorders: Focus on microtubule targeting	47
Cromatina e controllo dell'espressione genica	46
Loss of CDKL5 Causes Synaptic GABAergic Defects That Can Be Restored with the Neuroactive Steroid Pregnenolone-Methyl-Ether	42
Pregnenolone-methyl-ether enhances CLIP170 and microtubule functions improving spine maturation and hippocampal deficits related to CDKL5 deficiency	37
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	35
Characterization of the molecular mechanism underlying GABAA-receptor defects in CDKL5 deficiency disorder	20
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	20
Novel role of CDKL5 in the inhibitory synapse and a possible therapeutic strategy for CDKL5-related defects	19
The functional role of CDKL5 at the inhibitory synapse and its interaction with the cytoplasmatic collybistin-gephyrin complex	13
CDKL5 interacts with inhibitory postsynaptic scaffolding proteins and regulates synaptic GABAA receptor levels	9
Rett syndrome: from the involved gene(s) to treatment	2
Totale	7.641

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Categoria	#
all - tutte	23.909
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	23.909

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	413	0	0	0	0	0	0	0	0	0	62	149	202
2019/2020	1.441	56	37	65	250	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	1.780	282	261	293	289	322	181	20	47	59	26	0	0
Totale													7.641